Open access

Abiotic Stress in Plants

Written By

Yin Gong, Liqun Rao and Diqiu Yu

Submitted: 15 October 2012 Published: 20 February 2013

DOI: 10.5772/55865

From the Edited Volume

Agricultural Chemistry

Edited by Margarita Stoytcheva and Roumen Zlatev

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1. Introduction

Living on the same planet, plants means a lot to us. No matter being taken, as our food or treated with great commercial significance, plants are so indispensable that we have to learn how to protect, make use of, and most important of all, get on well with them. In the first place, what we all understand is: plants are distinguished from us or other animals by being unable to escape from the surrounding circumstances. Thus, when they are confronted with living-threaten pressures, their only choice is to try their best to adjust to them.

The second is "But how?" Plants have developed plenty of physical and biochemical strategies to face up to adverse conditions. Fortunately, thanks to so many excellent researchers' efforts in this field, we have been making so many progresses in identifying and characterizing the mechanisms on how plants perceive outside stress and response to it. Unfortunately, that's far from enough. In this chapter, we will mainly discuss abiotic stress and endeavor to elucidate the mechanism of various reactions plants take at the molecular level.

Before we start our discussion, we probably need to know what abiotic stress is all about. Basically, it includes all the non-living environmental factors that can negatively or even harmfully affect the growth and productivity of plants. Commonly, we choose to put drought, flooding or submergence, salinity, extreme temperatures on our daily researching agenda due to their key roles in producing yield loss of agricultural or industrial crops worldwide. But other kind of abiotic stress is entitled to be paid more attention, such as high light, deficits of inorganic nutrients (nitrogen, phosphorus, potassium et al.), and for sure, they are of definite importance for plants' growth and development. Moreover, one factor we can not set aside is human behavior, which in a large sense put considerable pressure on plants. Residuals of chemicals brought by agricultural practice to improve yield may generate stress, and the inceased modification of the atmosphere by human activities is gaining weight. And what we should really stress on is the compounding damaging effects by multiple stress factors acting simultaneously. Thus for plants exposed in diverse stress conditions, struggling for surviving, they organically adapt a complicated interplay of signaling cascade to percepting stress signal, then amplifying, transmitting, and finally triggering stress responses. Furthermore, there do exist overlap between different kinds of stress responses, which truly explains the cross-tolerance phenomenon, a measure taken by plants facing with combining stresses. Here, we are going to introduce signal transduction mechanisms in plants under stressful circumstances, hoping to give readers a general idea about how plants survive in different stressful situations.


2. Signal transduction

In general, for plant cells, signal transduction starts from the receptor activation, then the generation of second messengers translating the primary external signal to intracellular signals. These intracellular messengers will be further interpreted by their co-workers resulting in the inspiration of downstream pathways. During the whole process, reversible protein phosphorylation frequently happens; this can activate various transcription factors inducing the expression of stress responsive genes. Moreover, other components are also essential for the pathway to process. They have always been mentioned as signaling partners, mainly working in recruiting and assembling signal complexes, targeting signaling molecules, as well as controlling their lifespan.

Simply saying, the signal transduction pathway is a delicate cooperating process conducted by each single participator including receptors/sensors, second messengers, phosphoprotein cascades, transcription factors, and stress-responsive genes. Eventually the precise and optimal response will be triggered to protect plants from damages in a large sense. As far as we know, signal transduction is indispensable for many cellular activities and their coordination, and most of its steps are complicated occurring in a time and space-dependent manner. In the following part, we are going to explore every single step of signal transduction in order to understand how plants cope with various stress in their lifespan.

2.1. Sensors

2.1.1. Complexity in researching on sensors

Sensors act as the molecules pioneering in perceiving stress stimulus and relaying the signal to downstream molecules to initiate the signal transduction pathway. As the first participator in the pathway, they must be of great researching meaning. However, they are also the mainly intricate role for us to recognize.

Firstly, most of the abiotic stress signals themselves are complicated which probably comprise several physical or chemical signals. Taken the cold stress as an example, it can induce both osmotic stress and mechanistic stress. Similarly, drought may be accompanied by osmotic stress, ionic stress, a mechanistic signal, and heat stress in some cases. Based on these facts, it is natural for us to deduce that for plants there probably exists inequality in treating each single stimulus in accordance with the plant status or the stress severity. That is to say, a simple stimulus may diversely deliver complicated information to the plants, that's exactly why it is very likely for plants to have multiple cellular sensors to perceive each stress signal or one attribute of that signal. Secondly, the redundancy of signal perception make it even harder to identify and confirm each sensor relating to each stress stimulus, since knocking out one receptor may not significantly affect stress signaling outputs. Thirdly, even if we find a putative sensor, how to prove our hypothesis could also become a headache. Because different sensors probably vary in molecular identities, signal-perceiving modes, outputs, and also subcellular localizations, no wonder not much is known about plant abiotic stress sensors.

2.1.2. Putative sensors for perceiving stress signal

First of all, how can an external signal turn out to be internal? Where are the receptors/sensors and transporters? These will be the first bunch of questions we are going to ask. Imaging if we are plant cells, what will be the first weapon we use to maintain inner homeostasis when suffering from the outside disturbances? The answer will probably be "plasma membrane". So far, many researchers have demonstrated that the plasma membrane (PM) is responsible for perceiving and transmitting external stress signals, as well as responding to them. For example, when plants are under salinity stress, salt reaches the PM first, which makes the membrane lipids and transport proteins start to regulate permeability of this membrane triggering primary responses (Cooke and Burden, 1991). In many plants, changes in PM lipids, such as sterols and fatty acids, have been observed responding to salt stress and may contribute to the control of membrane fluidity and permeability, as a primary stress-responsive reaction (Elkahoui et al., 2004). Therefore, it is suggested that physical properties of membranes (lipid composition, fatty acid composition) may lead us to find potential sensors perceiving stress signals.

Secondly, let's stress a little bit more on the most common stress signals, cold, drought, and salinity. All of these three stresses have been detected to induce transient Ca2+ influx into the cell cytoplasm (Sanders D et al., 1999; Knight, 2000). Thus we can hypothesis channels responsible for this Ca2+ influx possibly acting as a sensor for these stress signals. Based on what we have discussed above, signaling reception may involve changes in membrane fluidity and cytoskeleton reorganization, which are also confirmed in early cold signaling (Sangwan et al., 2001; Wang and Nick, 2001). Coincidentally, cold-induced Ca2+ influx in plants occurs only after the occurrence of a rapid temperature drop (Plieth et al., 1999). Taken together, physical alterations in cellular structures may activate certain Ca2+ channels under cold stress, which indirectly suggests that Ca2+ channels might be a putative sensor.

Except the ion channel as a whole, other types of functional proteins can hardly be ignored on the list of sensors. So far, studies on plants and other systems have also identified several kinds of sensors. And in order to find sensors effectively in plant abiotic pathways, we need to borrow the experience and results of researches on other species. It is known that for plants, cold, drought, and salt stresses will all induce the accumulation of compatible osmolytes and antioxidants (Hasegawa et al., 2000). In yeast and in animals, mitogen-activated protein kinase (MAPK) pathways are responsible for producing osmolytes and antioxidants, which are activated by receptors/sensors such as protein tyrosine kinases, G-protein coupled receptors, and two-component histidine kinases. For plants, only histidine kinases may have been explored and clarified in a deeper sense compared with others.

Retrospecting the history of histidine kinase, one important discovery is the cyanobacterium histidine kinase Hik33 (Suzuki et al., 2000) and the Bacillus subtilis histidine kinase DesK (Aguilar et al., 2001) being identified as thermosensors. Unfortunately, even if several putative two-component histidine kinases have been found in Arabidopsis thaliana (Urao et al., 2000), none of them can be confirmed as thermosensors. However in yeast, a two-component histidine kinase named SLN1 has been identified as a type of membrane protein sensor for osmotic stress perception (Maeda et al., 1994, 1995). And then later researches found out AtHK1, an Arabidopsis histidine kinase, can complement mutations of SLN1. Therefore AtHK1 may participate in osmotic stress signal transduction in plants (Urao et al., 1999). In conclusion, understanding the function of putative histidine kinases and their relationship with MAPK pathways not only help us dig out more sensors but also, even more important, find out how they work in signal transduction pathways.

Thirdly, in plants, the receptor-like kinases and G-protein are worthy to be mentioned in the searching for stress signal sensors. Why? The stress hormone abscisic acid (ABA) makes us study on them who may contain putative stress sensors. It is well-known that the ABA is of great significance in stress signaling, thus, to understand how ABA is perceived certainly will contribute to revealing the hidden sensing-processes of stress signals. Generally, the researches on ABA perception mechanisms always relate to putative receptor-linked components or those putative receptor molecules regulated by stress or ABA.

Here we are going to mention a different way of osmolyte production that involves the pathways triggering the activation of late embryogenesis-abundant (LEA)-type genes representing damage repair processes (Zhu, 2001; Xiong and Zhu, 2002). And these LEA-like genes under cold, drought, and salt stress are modulated by phosphoinositols who are closely connected with the activity of phospholipase C, which in plants might be regulated by G-proteins. Moreover evidences suggest G-protein coupled receptors may take part in perceiving a secondary signal derived from these stresses (Ullah et al., 2001; Wang et al., 2001), which may brings a hint that G-protein may have a position on primary sensors list.

On the other hand, Arabidopsis heterotrimeric G-proteinαsubunit GPA1 may be a part of ABA response in guard cells but has no relation with ABA-induced stomata closure. Moreover GPA1 interacts with the G-protein couple receptor-like protein GCR1. Researches on gpa1 mutants and gcr1 mutants bring us much more information on finding receptors for ABA. Also some small G proteins are referred to as negative regulator of ABA responses in Arabidopsis, like ROP10. But the really surprising discovery comes into the world in 2009. In that year, two research groups from the USA and Germany reported in Science that they had identified a small protein family binding to ABA interacts with ABA Insensitive 1 and 2 (ABI1 and ABI2), two type 2C protein phosphatases (PP2Cs). And they are negative regulators of ABA signaling (Ma et al. 2009, Park et al. 2009).

With the proceeding of the pathway, we can see that abiotic stresses also give birth to second signaling molecules (discussed below). Therefore, in the next part, we are going to pay attention to the second messengers and their performance in signal transduction pathways.

2.2. Second messengers

Several second messengers are active participators in stress signal transduction. Mainly they are groups of small intracellular signaling molecules or ions, normally locating in the cytoplasm of a cell and responding to a signal received by a cell-surface sensor, which activates various kinases to regulate other enzymes' activities. What we mention frequently as second messengers are reactive oxygen species, lipid phosphates-derived signals, and cyclic nucleotides-related signals. Besides, some plant hormones also work as secondary signal molecules under stress conditions.

2.2.1. Reactive oxygen species (ROS)

ROS are species of oxygen which are in a more reactive state than molecular oxygen, resulting from excitation or incomplete reduction of molecular oxygen. Generally, ROS contains both free radical (O2•−, RO•, HO2•, OH•), and non-radical forms (H2O2, 1O2). For plants, they tend to be a two-edged weapon. On one hand, they are highly reactive and toxic, always taken as unwelcome harmful by-products of normal cellular metabolism, and causes damage to proteins, lipids, carbohydrates, DNA which ultimately results in cell death in plants. On the other hand, it has also been proved that ROS can affect genes' expression and signal transduction pathways, which mean that cells may use it as biological stimuli and signals to activate and regulate various genetic stress-response processes (Foyer and Noctor 2009).

Since it means a lot to plants' life, where and how it can be produced? In photosynthetic tissues, the chloroplast is the prime source of ROS. But for the non-photosynthetic tissues, mitochondria are the leader in production. In chloroplasts, photosystem I and II (PSI and PSII) are the major sites for the production of 1O2 and O2•−. In mitochondria, complex I, ubiquinone and complex III of electron transport chain (ETC) are the major sites for the generation of O2•−. In addition to the mitochondria and NADPH oxidases, additional cellular sources of ROS production include a host of other intracellular enzymes such as xanthine oxidase, cyclo-oxygenases, cytochrome p450 enzymes, and lip-oxygenases for which oxidants act as part of their normal enzymatic function.

Consequently, when plant cells are under stresses, the rate of ROS production usually goes up, inspiring the activities of antioxidants and scavenging enzymes to keep plants live a healthy life. Fortunately, plant cells possess very efficient enzymatic (superoxide dismutase, SOD; catalase, CAT; ascorbate peroxidase, APX; glutathione reductase, GR; monodehydroascorbate reductase, MDHAR; dehydroascorbate reductase, DHAR; glutathione peroxidase, GPX; guaicol peroxidase, GOPX and glutathione-S- transferase, GST) and non-enzymatic (ascorbic acid, ASH; praline; glutathione, GSH; phenolic compounds, alkaloids, non-protein amino acids and a-tocopherols) antioxidant defense systems cooperatively working on controlling the cascades of uncontrolled oxidation and protecting plant cells from oxidative damage by scavenging of ROS. Eventually, the equilibrium has maintained between ROS production and antioxidant defense systems.

However, this balance will always be perturbed by various biotic and abiotic stress factors such as salinity, UV radiation, drought, heavy metals, temperature extremes, nutrient deficiency, air pollution, herbicides and pathogen attacks. Once it has been challenged, various signals pathways start to be proceeded to mediate the disturbances to protect cells from harm brought by extra ROS. For example, when osmotic stress comes, various plant species show an obviously reduced assimilation rate due to stomatal closure (Huchzermeyer and Koyro 2005). This result can be owed to an excessive production of reactive oxygen species (ROS) who are highly destructive to lipids, nucleic acids, and proteins (Kant et al. 2006 ; Türkan and Demiral 2009 ; Geissler et al. 2010).

First and foremost, having been identified as second messengers how does ROS affect stress signal transduction? Several enzymes which are involved in cell signaling mechanisms are also potential targets of ROS. These include guanylyl cyclase (E. Vranova, S. Atichartpongkul, 2002), phospholipase C (C.H. Foyer, G. Noctor, 2003), phospholipase A2 (I.M. Moller, 2001) and phospholipase D (A.G. Rasmusson, K.L. Soole, 2004). Ion channels may be targets as well (G. Noctor, R.D. Paepe, 2006), among which calcium channels was mentioned (D.M. Rhoads, A.L. Umbach, 2006). Since calcium has ubiquitous functions in plant stress signal transduction pathway, we are interested in the relationship between ROS and calcium. Before dive into calcium, let's back to NADPH oxidases that are an important ROS-generating system. RBOHs shorting for respiratory burst oxidase homologs is always an eye-catching topic. Recent evidence points out RBOHs relate to heavy-metal induced accumulation of ROS (Pourrut et al. 2008) and early response to salt stress (Leshem et al. 2007). Subsequently, ROS produced by Rbohs are thought to activate Ca2+ channels leading to further increases in cytosolic Ca2+ (Foreman et al. 2003) and downstream signaling. In general, it has been suggested that ROS took part in the regeneration of Ca2+ signals by activating Ca2+ channels. Then additional signal transduction was triggered through Ca2+-mediated pathways (reviewed in Mori, I.C. and Schroeder, J.I. 2004).

Except the interaction with calcium, another route for ROS to work is that ROS themselves can directly modify signaling molecules through redox regulation. Redox status inside a cell is essential to the correct functioning of many enzymes, which can be used to alter enzyme activity; thus alteration of the redox status could be treated as a signaling mechanism (Gamaley and Klyubin, 1999). One of the most important and well-known redox-sensitive molecules in this respect is glutathione (GSH), which can form the GSH/GSSG couple. The balance between the GSH and GSSG takes the central position to maintain cellular redox state (C.H. Foyer, G. Noctor, 2005). But ROS like H2O2 can affect the process of lowering the cells' GSH content to alter the redox status. Meanwhile, it also has been suggested that enzymes such as ribonucleotide reductase and thioredoxin reductase, as well as transcription factors, might be among the targets for altered redox status. In detail, cysteine residues of molecules may be key active sites as targets for redox regulation. And these molecules can act as potential sensors for ROS (Xiong, L. and Zhu, J.K. 2002).

Secondly, ROS are very likely to play a significant role in the activation of stress-responsive genes, especially those who encode enzymes responsible for antioxidants biosynthesis or enzymes directly detoxify reactive oxidative radicals. For example, H2O2 production is thought to be raised under various abiotic stresses, which can enhance gene expression of active oxygen scavenging (AOS) enzymes. NO, produced under salt stress, could serve as a second messenger for the induction of PM H-ATPase genes' expression, which promote PM H-ATPase activity (Liqun Zhao, Feng Zhang et al., 2004).

Thirdly, we are going to stress a little more on H2O2 and NO. In maize, H2O2 production grows up induced by chilling stress, and exogenously applied H2O2 lifted up chilling tolerance (T.K. Prasad, M.D. Anderson, 1994). Increased H2O2 production has been detected occurring gradually responding to salt stress in rice plants (N.M. Fadzilla, R.P. Finch, 1997). Moreover, H2O2 was also reported to induce small heat shock proteins (HSP26) in tomato and rice (J. Liu, M. Shono, 1999; B.H. Lee, S.H. Won, H.S. Lee, 2000). However, it was recently shown that H2O2 produced by apoplastic polyamine oxidase can influence the salinity stress signaling in tobacco and can play a role in balancing the plant response between stress tolerance and cell death (Moschou et al. 2008). NO has also been suggested to act as a signal molecular mediating responses to biotic and abiotic stresses. Under salt stress, NO could serve as a second messenger for the induction of PM H-ATPase expression, which may account for the enhanced PM H-ATPase activity. Thus, ion homeostasis is reestablished so as to adapt to salt stress (Liqun Zhao, Feng Zhang et al., 2004).

Furthermore, researches on ABA give us much more information on H2O2 and NO in signal transduction. So let's take a look at how they work in ABA signaling and other signal transduction pathways. The process of stomata closure regulated by ABA in a large sense require the generation of H2O2. Moreover, H2O2 production may be a prerequisite for ABA-induced stomatal closure (Zhang, X., Zhang, L. et al. 2001). Experiments have found out mutations in genes encoding catalytic subunits of NADPH oxidase, known as the major source for H2O2 production, will impair ABA-induced ROS production, as well as the activation of guard cell Ca2+ channels and stomata closure (Kwak J.M., Mori, I.C. et al. 2003). In plants, both nitrate reductases and NO synthases (NOS) can contribute to NO generation. Loss-of-function mutations in Arabidopsis NOS, AtNOS1, impair ABA-induced NO production and stomata closure (Guo, F.Q., Okamoto, M. and Crawford, N.M., 2003).

On the other hand, accumulated evidence indicate ROS seem to play a central role in regulating Mitogen-activated protein kinase (MAPK or MPK) cascades (discussed later in detail). However, only the functions of MPK4, MPK3 and MPK6, out of the 20 Arabidopsis MAPKs, have been thoroughly characterized. What really counts is they can all be activated by ROS and abiotic stress. In addition, activities of MPK1 and MPK2 have been shown to be provoked by H2O2 and ABA (Ortiz-Masia et al. 2007). Also MPK7 was found to be activated by H2O2 under specific circumstances (Dόczi et al. 2007). Furthermore, the authors found that H2O2 may probably have a generally stabilizing impact on MAPKKs (MAP kinase kinases). In the future, we still have lots of work to elucidate how ROS regulate MAPK signaling in abiotic stress field.

All in all, even if we are holding a lot of evidence about the functions of ROS in abiotic stress, we still have to face up to those obscure steps relating to different mechanisms, not to mention hundreds of stress responsive genes involved in.

2.2.2. Lipid-derived signal messengers

It is well-known that cellular membranes contains a wide range of different lipids, including sphingo-, neutral-, glyco-, and phospholipids, all with unique biophysical properties. Beyond the structural role, some of them are equipped with direct signal-transducing properties. What we discussed in the sensors part is that membrane lipids can directly response to abiotic stress stimuli by modulating membrane fluidity or its other physiochemical properties, but in this part we will take another angle to demonstrate its significant function in the process of generating intracellular signaling molecules. Moreover lipids and their biogenesis and degradation enzymes play many direct or indirect roles to regulate or affect signaling and stress tolerance. In signal transduction, signaling lipids are distinguished for their low abundance and rapid turnover. They are rapidly formed responding to diverse stimuli through lipid kinases or phospholipases' activation. Thanks to the lipid-binding domains, these lipid signals can activate enzymes or recruit proteins to membranes leading to the activation of downstream signaling pathways resulting in specific cellular events and physiological responses. Studies on them find out, for plants, lipid signaling form a complex regulatory network responding to abiotic stress.

Basically, in eukaryotes, typical signaling lipids includes phosphatidylinositol lipids (polyphosphoinositides; PPIs), certain lyso-phospholipids, diacylglycerol (DAG), and phosphatidic acid (PA) (Munnik and Testerink, 2009; Xue et al.,2009; Munnik and Vermeer, 2010). Among them, PA is of great importance as a lipid second messenger in plants involved in various biotic and abiotic stress conditions. Based on thousands of researches, it is easy to detect almost every environmental cue can trigger a rapid PA response (Testerink and Munnik, 2005; Arisz et al., 2009; Li et al., 2009; Mishkind et al., 2009). How can PA be produced? Two ways in brief. Directly PA is generated through activation of phospholipase D (PLD), and indirectly a phospholipase C/diacylglycerol kinase (PLC/DGK) pathway regulated by two types of PLC enzyme named as the PI-PLCs (phosphoinositide-PLCs) and NPCs (non-specific PLCs). After the rapidly bounce up under stress, PA level will go back to normal when stimuli disappear. (Christa Testerink et al. 2011).

In most of the osmotic stress cases, both PLC/DGK and PLD pathways are activated leading to fast and transient PA accumulation, but exceptions also exist (Zonia and Munnik, 2004; Darwish et al., 2009; Hong et al., 2010). Besides responding to osmotic stress, we also see the PLDα1 enzyme participating in cold, frost, and wound stress signaling (Bargmann et al., 2009; Hong et al., 2010) and probably by promoting responses to ABA, especially in stomata (Mishra et al., 2006). On the other side, PLC/DGK pathways also get activated by salinity (Arisz, 2010). Earlier we knew that AtPLC1, one of the PI-PLCs, was shown to be induced by salinity and drought (Hirayama et al., 1995), which is necessary for ABA-induced inhibition of germination and gene expression (Sanchez and Chua, 2001). Recently, NPC4 (a NPC isoform) was found to modulate responses to ABA and bring enhanced salt and drought tolerance (Peters et al., 2010). In addition, several ABA signaling proteins have been identified as potential PA targets (Mishra et al., 2006), which has further suggested PA could mediate ABA responses. Meanwhile, cooperation between the NADPH oxidase isoforms RbohD, RbohF and PA brings more information for us to understand PA's function in ABA-induced ROS generation and stomatal closure (Zhang et al., 2009). Furthermore, PA also targets other protein kinases like SnRK2 protein kinase (Testerink et al., 2004), MAPK isoform MPK6 (Yu et al., 2010), sphingosine kinase (SPHK) (Liang Guo, XueminWang, 2012) to influence diverse signaling transduction pathways.

Other two important second messenger molecules - inositol phosphates Ins(1,4,5)P3 and DAG (diacylglycerol) are worthy to be mentioned here. Firstly, InsP3 was shown to release Ca2+ from an intracellular store in the early 90s, but recently evidences pops up suggesting that InsP6 was shown to release Ca2+ at a 10-fold lower concentration than InsP3 (Lemtiri-Chlieh et al., 2003; Teun Munnik, 2009), who can be generated by phosphorylating InsP3. By the way data can be found demonstrating that whole-plant IP3 level goes up significantly within 1 min after stimuli occur, and keep the tendency for more than 30 min under stress. Under osmotic stress, in Arabidopsis, phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2) is hydrolyzed to IP3. And IP3 accumulation occurs coincidently in a time frame similar to stress-induced calcium mobilization (Daryll B. DeWald et al., 2001). In conclusion, what we can say is under different stress, to identify the most critical second messenger molecules depends on the research on the network consisting of multiple polyphosphoinositides.

Secondly, diacyglycerol (DAG) is an important class of cellular lipid messengers, but for its function in plants, data is not sufficiently provided. In Arabidopsis thaliana, knocking out NPC4 results in DAG level decrease and compromises plant response to ABA and hyperosmotic stresses. On the other hand, overexpressing NPC4 leads to higher sensitivity to ABA and stronger tolerance to hyperosmotic stress than wild-type. And later experiments indicate that NPC4-produced DAG is converted to PA and NPC4 might be a positive regulator in ABA response and promote plant tolerance to drought and salt stresses (Carlotta Peters et al, 2010). Furthermore, all higher plant genomes sequenced so far lack both InsP3 receptor and the DAG target, PKC (Munnik & Testerink 2009). In conclusion, we have reasons to believe in that PA rather than DAG are more likely to play a central role in stress signaling transduction.

At last, we'd love to say more about other types of phospholipases like secreted phospholipase A2 and patatin-related phospholipase A (pPLA) who were shown to have functions in auxin signal transduction by cooperating with auxin receptors ABP1 or TIR1. (Günther F. E. Scherer et al., 2012 ). And this fact helps us to further confirm the significance of phytohormones in signaling transduction which will be discussed below.

2.2.3. Phytohormones

When it comes to phytohormones, strictly speaking, we can not conclude them as second messengers, but the first and foremost idea needs to be posted here is "The most powerful players in intercellular regulation are plant hormones." (Wolfgang Busch, Philip N. Benfey, 2010). Owing to the broad and diverse functions, many of phytohormones were discovered before the dawn of molecular genetics (Sachs and Thimann, 1967; Thimann and Skoog, 1933). In generation, they are a large bunch of trace amount growth regulators, the best-known group comprises auxin (IAA), cytokinin (CK), gibberellic acid (GA), abscisic acid (ABA), jasmonic acid (JA), ethylene (ET), salicylic acid (SA), but the name list is growing by time. Here we add brassinosteroids (BR), nitric oxide (NO), polyamines, and strigolactone (SL). Indubitably phytohormones have various functions in growth and development. Indeed, they play central roles in nutrient allocation, and source/sink transitions. However based on former description relating to sensors and second messengers, we have to focus on here is that these low-molecular-weight compounds are indispensable for coordinating various signal transduction pathways during responses to various abiotic stresses.

Firstly, they function as systemic signals that can transmit information over large distances. Like ABA, it can be transported and play physiological roles at sites far away from where it is synthesized (Sauter, A. et al., 2001). And different types of cells have their own understanding even for the same hormones signal. And information from diverse hormones always triggers coherent responses of cells. This is signal perception at cellular level. Lucky for us, modern transcriptome profiling technologies have provided a global view of hormones' effects at the molecular level and identified hundreds to thousands of genes, the expression levels of which are modified by individual hormones (Goda et al., 2008). A large number of data have proved that treating plants with exogenous hormones will rapidly and transiently alter genome-wide transcript profiles (Chapman and Estelle 2009).

Secondly, complex networks of gene regulation by phytohormones under abiotic stresses involve various cis- or trans-acting elements. Some of the transcription factors regulated by phytohormones include ARF, AREB/ABF, DREB, MYC/MYB, NAC, WRKY and other key components functioning in signaling pathways of phytohormones under abiotic stresses will be briefly mentioned later. And they often rapidly alter gene expression by inducing or preventing the degradation of transcriptional regulators via the ubiquitin–proteasome system (Santner A, Estelle M, 2010).

Thirdly, the ability of plants to a wide range of environmental stresses is also finely balanced through the interaction of hormonal plant growth regulators and the redox signaling hub. Plant hormones produce reactive oxygen species (ROS) as second messengers in signaling cascades that convey information concerning changes in hormone concentrations and/or sensitivity to mediate a whole range of adaptive responses (Carlos G. Bartoli et al., 2012). For example, Brassinosteroids (BRs) can induce plant tolerance to diverse abiotic stresses by triggering H2O2 generation in cucumber leaves (Cui et al., 2011). In the following part we will simply introduce how phytohormones work in signal transduction, and how they talk with each other when they exchange information.

Let's start from ABA, whose synthesis is one of the fastest responses to abiotic stress for plants. Under water stress, ABA synthesis triggers ABA-inducible gene expression leading to stomatal closure, thereby reducing water loss through transpiration, and consequently, a reduced growth rate (Schroeder, J.I. et al., 2001). ABA also plays a vital role in adapting to cold temperatures. Cold stress induces the synthesis of ABA and the exogenous application of ABA enhances the cold tolerance of plants. A large number of genes associated with ABA biosynthesis and ABA receptors-encoding genes and downstream signal relays have been characterized in Arabidopsis thaliana (reviewed by Cutler SR et al., 2010). ABA activates the expression of many stress-responsive genes independently or synergistically with stresses, which makes it become the most studied stress-responsive hormone.

Other hormones, in particular CK, SA, ET, and JA, also have substantial direct or indirect performances in abiotic stress responses. CK is an antagonist to ABA, and under water shortage situation, CK levels usually decrease. But transgenic tomato rootstocks expressing IPT (isopentenyl transferase, a gene encoding a key step in CK biosynthesis) had improved root CK synthesis shown raised salinity stress tolerance (Ghanem ME et al., 2011). Meanwhile, by checking public microarray expression data for A. Thaliana, numerous genes encoding proteins associated with CK signaling pathways have been found affected by various abiotic stresses (Argueso CT et al., 2009). Although auxins, GAs, and CKs have been implicated primarily in developmental processes in plants, they regulate responses to stress or coordinate growth under stress conditions (Günther F. E. Scherer et al., 2012; F. Eyidogan et al., 2012). Auxins taking part in drought tolerance was postulated by researchers (ZhangS-W et al., 2009). What's more, BR was reported (mainly researches on exogenous application of BR) to induce stress-related genes' expression, which results in the maintenance of photosynthesis activity, the activation of antioxidant enzymes, the accumulation of osmoprotectants, and the induction of other hormone responses (Divi UK et al., 2009). In conclusion, there do exist a complex network for phytohormones to contribute to stress-induced reactions for plants. And due to the overlap between hormone-regulated gene suites in the adaptive responses, we have to discuss cross-talk between the different hormone signaling pathways as a extensive part of that complex network.

Earlier, it was reported that ABA can inhibit the biosynthesis of ethylene and may also potentially reduce the sensitivity of plants to ethylene (Sharp, R.E., 2002). Recently the expression of many other genes associated with auxin synthesis, perception, and action has been shown to be regulated by ethylene (Stepanova AN, Alonso JM, 2009). And it is not surprising that auxin has been found involved in ethylene biosynthesis very early. Meanwhile, CK was shown to be a positive regulator of auxin biosynthesis (Jones B et al., 2010).

Furthermore, GA and BR regulate many common physiological processes like the growth and development in rice seedlings (Wang L et al., 2009). Except BR, GA has another partner - SA. Transgenic A. thaliana plants constitutively overexpressing a GA-responsive gene became more tolerant under abiotic stress and this stronger tolerance was correlated with increased endogenous levels of SA (Alonso-Ramirez A et al., 2009).

Discussed above, ABA can regulate stomatal actions under stress conditions; however, it is not alone in that process. CK, ET, BR, JA, SA, and NO also affect stomatal function (reviewed by Acharya B, Assmann S, 2009). In detail, ABA, BR, SA, JA, and NO induce stomatal closure, CK and IAA promote stomatal opening. And we mentioned before, NO acts as a key intermediate in the ABA-mediated signaling network in stomatal closure. Moreover BR-mediated signaling was regulated by ABA, and in turn, ABA was also shown to inhibit BR-induced responses under abiotic stress (Divi U et al., 2010). And it is not hard to deduce that there are other tricky relationships between different hormone-involved pathways. Cross-talk between the phytohormones results in synergetic or antagonist interactions, which is crucial for plants in abiotic stress responses. To characterize the molecular mechanisms regulating hormone synthesis, signaling, and action means a lot to modificate hormone biosynthetic pathways to develop transgenic crop plants with promoted tolerance to abiotic stress.

2.3. Ca2+ as an intermediate signal molecule

So far, we have already touched some grounds related to Calcium (Ca2+) functioning in signal transduction. Among all ions in eukaryotic organisms, it is likely to be the most versatile one who almost links to all aspects of plant development, not to mention many regulatory processes. The reason why it is so powerful may root in its flexibility in exhibiting different coordination numbers and complex geometries, and this ability makes it easily form complexes with proteins, membranes, and organic acids. However we won't detect high cytosolic or organelle Ca2+ concentrations resulting from the tight management of various Ca2+ pumps and transporters. The reason why the concentration needs to be controlled is that higher Ca2+ concentrations can chelate negatively charged molecules in the cell leading to cytotoxicity. Interestingly, all the secondary signaling molecules we mentioned above may activate transient increases in cytosolic Ca2+, and transient elevations in cytosolic Ca2+ concentration have been documented to have relationship with a multitude of physiological processes linking to abiotic stress responses. So we may wonder concentration control probably will help us tell the story of another famous second messenger--- Ca2+ in signal transduction for plants under abiotic stress.

Earlier in 1982, research on the green algae Chara told us the cytosolic Ca2+ concentration change predicted Ca2+ might work as a second messenger in plants (Williamson and Ashley, 1982). Based on later reports, it has been found various stimuli will spur their own special Ca2+ responses differing in where and how changes happen (Johnson et al., 1995; Tracy et al., 2008), which exactly supports the former concept of Ca2+ signature. For plants, to maintain Ca2+ homeostasis, they need the help from Ca2+ channels, pumps, and exchangers (carriers) to make specific adaptation to every kind of stimulus (Kudla et al., 2010). Later, cellular Ca2+ signals are decoded and transmitted by Ca2+-binding proteins that relay this information into downstream responses. Major Ca2+ signal transduction routes contain Ca2+-regulated kinases mediating phosphorylation events and regulation of gene expression via Ca2+-regulated transcription factors and Ca2+-responsive promoter elements.

Generally speaking, Ca2+ signaling comprises three phases: generation of a Ca2+ signature, sensing the signature and transduction of the signal (Reddy and Reddy, 2004). Having discussed above, we are informed that the concentration change are always triggered by cellular second messengers, such as NAADP, IP3, IP6, Sphingosine-1-Phospate, and cADPR (Allen and Sanders, 1995; Navazio et al., 2000; Lemtiri-Chlieh et al., 2003). Then a specific cellular Ca2+ signature is sensed by Ca2+-binding proteins, the Ca2+ sensors (Dodd et al., 2010; Reddy and Reddy, 2004). The sensors themselves may become active to transduce the signal by themselves, or choose to bind to their interacting proteins and affect their partners’ activity to transduce the signal. In detail, there are three major classes of Ca2+ sensors identified in plants. The first one is calmodulins (CaMs) and calmodulin-related proteins (CMLs). CaMs is a group of small acidic protein, highly conserved in eukaryotes (Snedden and Fromm, 2001), and contains four EF hands (one major Ca2+ binding motif) where bind Ca2+. Moreover this binding action induces a conformational change of CaM, leading to exposure of hydrophobic surfaces and further triggering electrostatic interactions with target proteins - CaM-binding proteins (CBPs) (Hoeflich and Ikura, 2002). CBPs have been found to take part in regulating transcription, metabolism, ion transport, protein folding, cytoskeleton-associated functions, protein phosphorylation and dephosphorylation, as well as phospholipid metabolism (Yang and Poovaiah, 2003; Reddy and Reddy, 2004). Furthermore, different CaM proteins exhibit differential expression and are likely to show differential affinity to Ca2+ and to their target proteins (McCormack et al., 2005; Popescu et al., 2007), which makes CaM be equipped with multiple capabilities in Ca2+ signal transduction. With many similarities to CaMs, CMLs are mostly composed of four EF-hands and lack other known functional domains. Like CaMs, they relay the signal by binding to other proteins resulting in activation or inactivation of interacting proteins. Over 300 proteins that interact with CaMs and CMLs have been identified in plants (Popescu et al., 2007). The second class of Ca2+ sensor is represented by the calcium-dependent protein kinases (CDPKs/CPKs) who are serine/threonine protein kinases contain a catalytic kinase domain and EF-hand motifs (Cheng et al., 2002). The third typical sensor type is the EF-hand-containing Ca2+-modulated protein named SCaBP (SOS3 (Salt-Overly-Sensitive 3)-like Ca2+-biniding proteins)/Calcineurin B-like (CBL) proteins, which is plant-specific (Luan et al., 2002). CBLs interact with a family of protein kinases called CBL-interacting protein kinases (CIPKs) (Luan et al., 2009; Weinl and Kudla, 2009; Batistic et al., 2010). In addition to EF-hand-containing Ca2+ binding proteins, there are other proteins without that motif acting as sensors who also can bind Ca2+, like PLD (introduced in 2.2.2), annexins and C2 domain–containing proteins (Clark and Roux, 1995; Reddy and Reddy, 2004; Laohavisit and Davies, 2011), however their functions in abiotic stress responses haven't been deeply explored, and only some reports suggest PLD and annexin be relevant to stress signal transduction (White et al., 2002; reviewed by Laohavisit and Davies, 2011).

However here we will mainly stress on the EF-hand-containing sensors due to their considerable significance in signal transduction pathways. Based on their functional styles, these sensors are assigned into two camps termed as sensor relays and sensor responders (Kudla et al., 2010). The sensor relays do not have any known enzymatic or other functional domains except the EF hands. They interact with other proteins and regulate their activities, just like CaMs/CMLs, and CBLs (with one exception, CaM7) (McCormack et al., 2005; Luan, 2009; DeFalco et al., 2010). The members of another camp are characterized by an additional a catalytic or functional domain, except EF hands, whose activity is regulated by Ca2+ binding to EF-hand motifs. So definitely CDPKs belong to this camp, and other members are Ca2+-and Ca2+/CaM-dependent protein kinases (CCaMKs), some DNA or lipid binding proteins, and a few enzymes (Day et al., 2002; Yang and Poovaiah, 2003; Harper and Harmon, 2005). Many calcium sensors are coded by multiple genes, and expression of many of these is induced by stresses (DeFalco et al., 2010).

Then, let's take a look at what will be the next move of those Ca2+-activated sensors. Firstly, they can directly bind to cis-elements in the promoters of specific genes and induce or repress their expression. Secondly, they will choose to bind to DNA binding proteins and activate or inactivate them, thereby resulting in activation or repression of gene expression. The third path belongs to the activated Ca2+-regulated protein kinases (CDPK,CaM binding protein kinase (CBK), CIPK and CCaMK) or phosphatases. They phosphorylate/ dephosphorylate a transcription factor (TF), respectively, resulting in activation or repression of transcription, which allow for the perception and transmission of Ca2+ signatures directly into phosphorylation cascades that orchestrate downstream signaling responses (Weinl and Kudla, 2009). The most well-known TFs involved in the phosphorylation include Calmodulin binding transcription activators (CAMTAs; also referred to as signal-responsive proteins or ethylene-induced CaM binding proteins) (Reddy et al., 2000), MYB family (Popescu et al., 2007), the WRKY family (Park et al., 2005; Popescu et al., 2007), basic leucine zipper (bZIP) TFs, like TGA3 (Szymanski et al., 1996) and ABA-responsive TFs ABF1, 2, 3, and 4 (reviewed in Galon et al., 2010), and CBP60s who is a plant-specific CaM binding proteins family (Reddy et al., 1993; Zhang et al., 2010), as well as members of NAC family (Kim et al., 2007; Yoon et al., 2008). However they are TFs binding to Ca2+/CaM under Ca2+ regulation, so we posted here another two TFs who can directly bind Ca2+. One is encoded by Arabidopsis NaCL-INDUCED GENE (NIG) (Kim, J., and Kim, H.Y., 2006), and the other is At-CaM7 (Kushwaha et al., 2008). In sum, Ca2+ and their interacting proteins served as the upstream elements play an important role in regulating of some stress genes expression.

Meanwhile, what performance they will give in each specific abiotic stress condition needs to be simply introduced here. For drought stress, cellular Ca2+ transmits drought signals to regulate the physiological responses induced by drought stress (Dai et al., 2007). It has been found that Ca2+ treatment increased protection against membrane lipid peroxidation and stability of membranes and therefore resulted in the increase of drought resistance of rice seedlings. It is also reported that in wheat Ca2+ may reduce the adverse stress effects by elevating the content of proline and glycine betaine, thus improving the water status and growth of seedlings and minimizing the injury to membranes (Geisler et al., 2000; Munns et al., 2006; Goldgur et al., 2007). Additionally, Ca2+/CaM means a lot to the process of ABA-induced drought signal transferring under PEG stress. And ABA synthesis correlates with cytoplasmic Ca2+ concentrations ([Ca2+]cyt) (Rabbani et al., 2003; Noctor, 2006). We know how important ABA is to the stomatal status, and now more studies have established a close relationship between [Ca2+]cyt oscillation and stomatal status. In addition, in Arabidopisis genome, 9 SOS3 homologs (SCaBP/CBL) and 22 SOS2 homologs (SOS2-like protein kinases -PKS/CBL-interacting protein kinases-CIPK) were identified. By the way, SOS2 is a serine/threonine protein kinase with an SNF1/AMPK–like catalytic domain and a unique regulatory domain (Liu et al., 2000). Individual SCaBP/CBL interacts with PKS/CIPK with different specificities (Gong et al., 2004; Luan et al., 2002). And it is indicatied that the interaction between SCaBP5 and PKS3 may interpret Ca2+ signatures resulting from ABA or drought stress signals. On the other hand, SOS3 interact with and activate the SOS2, whose mutation also confers salt sensitivity. Then the activated SOS2 phosphorylates and regulates ion transporters such as the Na+/H+ antiporter SOS1 controlling long-distance Na+ transport from the root to shoot, which eventually leads to the restoration of ion homeostasis in the cytoplasm under salt stress (Zhu, J.K., 2003).

In light of salt stress, like other stresses, it is perceived at cell membrane and then trigger intracellular-signaling cascade including the generation of secondary messenger molecules like Ca2+ and protons. For instance, it was found that in barley roots, under NaCl stress, Ca2+-CaM system may work in activating tonoplast H+-ATPase and regulating Na+ and K+ uptake with involvement of SOS signal transduction pathway (Brini et al., 2007). In Arabidopsis, experiments to overexpress AtCaMBP25 (a CaM binding protein) who may be a a negative regulator of osmotic stress tolerance find the transgenic Arabidopsis plants show higher sensitivity to osmotic stress, while the antisense plants gain more tolerance under salt stress (Perruc, E. et al., 2004).

Furthermore, when it comes to uncomfortable temperature, is there any position for Ca2+? For sure. The Ca2+ channels have shown their power for the growth of root hairs and the low temperature acclimation of chilling-resistant plants. That's why we find data indicating that the activity and stability of Ca2+-ATPase under 2 °C low temperature are the key factors in the development of cold resistance of winter wheat (Yamaguchi-Shinozaki, 2006). Moreover the studies on Arabidopsis mutants displaying reduced tonoplast Ca2+/H+ antiport (CAX1) activity indicate that CAX1 participates in the development of the cold acclimation response (Lecourieux et al., 2006). On the other field of temperature acclimation, there exists data showing in Arabidopsis, Ca2+/CaM have gotten involved in heat shock response (Zhang et al., 2009). And we also find some researches on overexpression of a CDPK in rice which brings increased tolerance to cold and salt stress (Saijo, Y. et al., 2000).

Taken together, depending on the type of signal or the type of cell, internal and/or external Ca2+ stores could be involved in raising [Ca2+]cyt (Dodd et al., 2010; Kudla et al., 2010). Both types of Ca2+ transporters, namely, Ca2+-ATPases and CAXs involve in plant responses by regulating [Ca2+]cyt. Based on that, regulating cellular and intercellular Ca2+ signaling networks brings improving resistances or tolerances. And seeing from the regulation networks of stress responses to drought, salt and cold stress, we find Ca2+ and its interacting proteins may be the cross-talks among ABA-dependent, MAPK and other stress signaling pathways. Anyway, we can see the core of Ca2+ actions in relaying abiotic stress signaling depends on how to translate Ca2+ signatures to specific protein phosphorylation cascades,which we have mentioned above, so in the following part, we are going to trace the performance of phosphoproteins in signal transduction.

2.4. Role of phosphoproteins in stress signaling

By controlling the phosphorylation status of other proteins, protein kinases and phosphatases play a fundamental role in coordinating the activity of many known signal transduction pathways. For many signal pathways not only in abiotic stress field, protein reversible phosphorylation is the major player in relaying signals. And during this significant process, we highlight the functions of protein kinases and protein phosphatases who are enzymes to catalyze these reversible phosphorylation processes. And they are divided into several categories according to their structure or functional characteristics. And in the following part, we will give a general idea to the readers about their central role in signal transduction in abiotic stress aspect.

2.4.1. MAPK

Obviously, we have seen MAPK many times in formal description in this chapter. Even if it is not found in plants, the mitogen activated protein kinase (MAPK) cascades are known to be involved in plant abiotic stress responses acting as intracellular signal modules that mediate signal transduction from the cell surface to the nucleus. The reason to mention it here is that phosphorylation plays a central role in the progression of the signal through the MAPK cascade. Moreover MAPK cascades, the conserved signaling modules found in all eukaryotes, are fundamental in transducing environmental and developmental cues into intracellular responses bringing changes in cellular organization or gene expression. The simplest constitution of a MAPK cascade contains MAP kinase kinase kinases (MAP3Ks/MAPKKKs/MEKKs), MAP kinase kinases (MAP2Ks/MAPKKs/MEKs/MKKs) and MAP kinases (MAPKs/MPKs) (Mishra NS et al., 2006). And when under stress, stimulated plasma membrane will activate MAP3Ks or MAP kinase kinase kinase kinases (MAP4Ks), who may be the adapters to link upstream signaling steps to the core MAPK cascades (Dan I et al., 2001). Following that, MAP3Ks will phosphorylate two amino acids in the S/T-X3-5-S/T motif of the MAP2K activation loop. Then MAP2Ks phosphorylate MAPKs on threonine and tyrosine residues at a conserved T-X-Y motif at the active site. When signals come to MAPKs, further phosphorylation will tag on a wide range of substrates involving other kinases, cytoskeleton-associated proteins, and/or transcription factors. As for formation and integrity of a specific MAPK cascade, scaffold proteins take control over it (Whitmarsh AJ et al., 1998). And after signaling completed, MKPs (MAPK phosphatases) take the responsibility to shut the pathway down. Generally, the whole cascade is regulated by various mechanisms, including not only transcriptional and translational regulation but through post-transcriptional regulation such as protein-protein interactions (Rodriguez MC et al., 2010).

Thanks to traditional genetic and biochemical methods and lots of excellent research efforts, we can conclude that MAP3K/MAP2K/MAPK signaling modules show overlapping roles in controlling diverse cellular functions by forming complex interconnected networks within cells. These include cell division, development, hormone signaling and synthesis, and response to abiotic stress (high and low temperature, drought and high and low osmolarity, wounding, high salinity, UV radiation, ozone, ROS, heavy metals), as well as biotic stress reactions (Jonak C et al., 2002; Xiong L et al., 2003; Raman, M. et al., 2007; Gohar Taj et al., 2010; Alok Krishna Sinha et al., 2011).

According to the researches on MAPK pathways, we can see that regulated expression of MAPK components shows effects on stress sensitivity. Here are some examples. Expression of an active form of a tobacco MAP3K, NPK1, increases freezing tolerance of transgenic tobacco or maize plants (Kovtun, Y et al., 2000; Shou, H et al., 2004). Meanwhile, MAP2K1 shows transcriptional induction under salt stress, drought and cold, as well as activated by wounding and drought stress. And MAP2K1 can phosphorylate MAPK4. An unsurprised fact is that MAPK4 and MAPK6 are found to be activated by cold, salt and drought (Ichimura K et al., 2000). Indeed, a MAPK module composed of MAP3K1-MAP2K1/MAP2K2-MAPK4/MAPK6 has been confirmed in cold and salt stress by yeast two hybrid analyses and yeast complementation (Teige M et al., 2004). So we can say different MAPKs are activated at different times after the onset of stress and the activities of these MAPKs are activated within different time periods. By the way, during osmolarity signaling MAPKs module seems to be widely involved (reviewed by Gohar Taj et al., 2010).

Due to the interlink between osmotic stress and oxidative stress, we are informed of the relationship between ROS, hormone signaling and MAPKs. ROS like H2O2 is closely associated to MAPKs' activities. In Arabidopsis, H2O2 activates AtMPK6 and the related AtMPK3 via the MAP3K ANP1(Desikan R et al., 1999), and AtMPK6 are involved in cold stress as we knew before. Additionally, in tobacco, under H2O2 and ozone treatment, the ortholog of AtMPK, SIPK1 will be activated as well (Samuel MA et al., 2000). These findings imply that multiple MAPK modules mediate oxidative stress responses and that MAPK cascades are not only induced by ROS but may also regulate ROS levels. Meanwhile, activating SIPK1 (salicylic acid-induced protein kinase), who is an NO-activated protein kinase in tobacco, can not process without SA, which brings a suggestion for the existence of cross-talk between ROS, hormone signaling and MAPKs. Here is some other evidence coming from studies on stomatal movement (Eckardt NA., 2009). In guard cells of Vicia faba, MAP2K is believed to regulate stomatal movement through mediating H2O2 generation induced by ABA (Song XG et al., 2008). Later, in guard cells studies, MAPK9 and MAPK12 have been proved to serve as positive regulators acting downstream of reactive oxygen species and calcium signaling in ABA signaling. In 2.2.4, we talk about ABA- and Ca2+-induced stomatal closure, so we can't help wonder is there any link between MAPK and ABA- and Ca2+-induced pathways? Yes, it has been found that ABA and Ca2+ signals cannot activate anion channels in mpk9/12 mutants, thus indicating that these two MAPKs act between the ABA and Ca2+ signals and the anion channels. (Jammes F et al., 2009).

Even if the role of MAPK in ABA signaling has not yet been directly confirmed, the attempts to clarify the relationship between hormone and MAPKs never stop. Not just for ABA, the role of MAPK signaling cascades in auxin signaling and ethylene biosynthesis has been documented in numerous studies (Dai Y et al., 2006; Xu J et al., 2008). Eventually, the genes in hormone biosynthesis (ethylene) and responses (auxin) are altered, it is of great significance to distinguish the direct targets of MAPK cascade from those that are regulated by altered hormonal and oxidative stress responses. On the other hand, recently in heavy metal stress studies, we find data supporting that MAPK3 and MAPK6 are activated responding to cadmium through ROS accumulation produced by oxidative stress in Arabidopsis (Liu XM et al., 2010), which further demonstrate the close relevance between ROS and MAPKs.

Meanwhile, by searching for the linkage between MAPKs and its various substrates involving other kinases and transcription factors, we gain much more information about MAPK cascades. Over-expression of MAP2K2 affects genes for several transcription factors (such as RAV1, STZ, ZAT10, ERF6, WRKY, and CBF2), disease resistance proteins, cell wall related proteins, enzymes involved in some secondary metabolisms and an 1-aminocyclopropane-1-carboxylic acid synthase (ACS). In the case of ACS, the rate-limiting enzyme of ethylene biosynthesis, the phosphorylation by MAPKs and by CDPKs affects protein stability and turnover, which again shows us the complicated cross-talk network (Bernhard Wurzinger et al., 2011). So it is a big challenge to identifying the targets of MAPK cascades, but the researches on other protein kinases leave us useful clue to find the answer.

2.4.2. Other protein kinases

Whether at the transcript level or activity level, protein kinases are induced by a variety of abiotic stress, which indicates their powerful participation in signaling process. Moreover no matter suppressing or overexpressing these kinases, there both exists data showing that in transgenic plants, stress responses has changed. So far, we know several protein kinases involved in stress tolerance are stimulated by ABA, such as most of SNF1-related kinases (SnRKs) like SnRK2, SnRK3 (CIPK), CDPK and MAPK families. But others like Glycogen synthase kinase 3 (GSK3) ( Jonak and Hirt, 2002; Koh et al., 2007), S6 kinase (S6K) (Mahfouz et al., 2006), SERK (Marcelo O. Santos et al., 2009) also attract a lot of attention.

Now let's start from SnRKs. The SnRK2 family members are plant-specific kinases relating to abiotic stresses responses and abscisic acid (ABA)-dependent plant development. They have been classed into three groups; members of group 1 are not activated by ABA, and group 2 also will not be activated or weekly activated, while group 3 is strongly activated by ABA. In Arabidopsis the SnRK2 subfamily consists of 10 members. Except SnRK2.9, all SnRK2s are activated by osmotic and salt stress (Boudsocq, M. et al., 2004). Take SnRK2.6 (OST1) as an example. SnRK2.6 functions in the ABA signaling pathway upstream ABA-induced ROS production. It is related to the ABA-activated protein kinase AAPK in Vicia faba and also associates with SNF1 protein kinase. NADPH oxidases function in ABA signal transduction, also targeted by the SnRK2.6 kinase (Nakashima et al., 2010). Generally speaking, regulating the response to ABA through SnRK2s pathways is to directly phosphorylate various downstream targets such as ion channels (SLAC1, KAT1) and ABFs and other specific TFs required for expression of stress-responsive genes (Anna Kulik et al., 2011). By the way, the SnRK2 subfamily is conserved in land plants. No wonder their role in ABA signaling and osmotic stress responses have also been found in pea, barley, rice and zea mays (Shen, Q. et al., 2001; Kobayashi et al., 2004; Huai, J. et al., 2008). As for SnRK3 (CIPK), we compact it here that CIPK1/3/8/14/15/20/23/24 take part in ABA signaling. CIPKs play a main role in plant ion homeostasis and abiotic stress tolerance by regulating H+, Na+, Ca2+ and NO3- transporters and K+ channels and interacting with TFs (Kudla, J. et al., 2010). Moreover, the CDPKs that are involved in ABA signaling are CPK3/4/6/11/32. CPK4 and CPK11 are closely related genes and both phosphorylate the transcription factors ABF1 and ABF4. Based on a majority of evidence, it can be concluded that CDPKs target core ABA signaling components (Geiger, et al., 2010). A role for MAPKs in ABA signaling has been shown above, but posted here again (MPK1/2/3/6/9/12). Taken together, none of these protein kinase families function specifically in ABA signaling, which still need us to stress on functional redundancy and complicated cross-talk network in the future research.

As follows, we take a brief look at other kinases. CDKs (Cyclin dependent protein kinases) are a large family of serine/threonine protein kinases and mainly function in ensuring that cells progress in order over the different cell division stages. But their roles in abiotic stress responses turn out to be more eye-catching, which can be reflected in heat, cold, drought and salt stimuli researches (reviewed by Georgios Kitsios, 2011). Other findings like Somatic Embryogenesis Receptor Kinase (SERK) relating to somatic embryogenesis and apomixis (Marcelo O. Santos et al., 2009), AtNEK6, a member of the NIMA (never in mitosis A)-related kinases (NEKs) (Lee SJ et al., 2010), bring us a large amount of information to explore the functional importance of various kinases in abiotic stress.

2.4.3. Protein phosphatases

During phosphorylation process, the job for protein phosphatases is to remove the phosphate added by protein kinases. Based on their substrate specificity, protein phosphatases can be classified, at least three families, as PPP family and PPM family composed by serine/threonine phosphatases, PTP family comprising tyrosine phosphatases, and dual specificity phosphatases (dsPTPs/dsPPase). As the largest group of phosphatases in plants, serine/threonine phosphatases can be further divided into PP1, PP2A, PP2B, and PP2C. For stress signal transduction, involvement of PP2C, PP2A, PTP, dsPPase have been reported in ABA or stress signal transduction, but the best-known example is the PP2C. On the other hand, many experiments have found that the relationship between MAPKs and phosphatases both exists in animals and plants. It has been shown that tyrosine-specific phosphorylation is associated with plant MAPKs, which again demonstrate the essential position phosphatases take in signaling pathways.

For the biggest branch of protein phosphatases in plants, in Arabidopsis alone, 76 PP2C genes have been identified early (Kerk et al. 2002). Further researches say ABA and other abiotic stress stimuli can induce A-type PP2C expression. Furthermore the A-type PP2C phosphatases, ABI1, ABI2, HAB1 (P2CHA) and PP2CA (AHG3) have been proved to directly interact with PYR/RCAR ABA receptors, however they always act as negative regulators at different layers of ABA signaling. (Merlot et al., 2001; Umezawa et al., 2009; Nishimura et al., 2010).

Working on other phosphatases like PP1, we find data in Vicia faba studies supporting its involvement in stomatal opening during the response to blue light (Takemiya et al. 2006). As to PP2A, five genes encoding its catalytic subunit has been identified in rice, and three of them show expression alteration under abiotic stress (Yu et al. 2003, 2005). And the activity of PP2B needs the help from calcium (Luan 2003). Some others like DSP4, a dual-specificity phosphatase, has been demonstrated to bind starch and interact with AKIN11, a SNF 1-related kinase in Arabidopsis (Fordham-Skelton et al. 2002; Kerk et al. 2006). Anyway we do need more facts to clarify the function network between phosphatases and other signals like hormone, ion channels, kinases actions.

Finally, we can see that the biggest challenge for abiotic stress signal research is to elaborate the network of kinases and phosphatases, and their relationship with a wide range of substrates, as well as understand the phosphorylation states and how phosphorylation-dependent activity culminates in the process of coping with a particular environmental stress.

2.5. The role of TFs and genes in certain abiotic stress situations

By the end of signaling, the biggest assignment is to temporally and spatially regulate stress-induced genes expression, and it is almost done at transcriptional level(Rushton and Somssich 1998). Obviously the most contributing workers are transcription factors (TFs) who modulate genes expression by binding to specific DNA sequences in the promoters of target genes (Chaves and Oliveira 2004). Thanks to coordination between TFs and genes, new transcripts are synthesized and stress adaptations have been realized within just a few hours. Consequently, that is why TFs are such a group of powerful targets being so popular in genetic engineering field aiming at improving stress resistance in crop plants. But, who are they? While, most of them belong to several big families, naming AP2/ERF (ethylene responsive element binding factor), Zn finger, basic leucine zipper (bZIP), basic helix-loop-helix (bHLH), WRKY, MYB, and NAC. Indeed we frequently mentioned them in formal description. So let's start to wander in their complicated regulatory network designed for the also complex stress situations.

2.5.1. Drought

Based on recent data, the rate of land area experiencing drought is uprising and probably goes up to 30% by the end of this century (Yi et al. 2010). And that is a big threaten for plants lives, for drought is very likely to give rise to arrest of photosynthesis, disturbance of metabolism and finally plant death (Jaleel et al. 2008). But plants will react efficiently. With a few second of water loss, phosphorylation status of a protein will be triggered and later when the suffering time reached hours or days long, gene expression and plant morphology occur (Verslues and Bray, 2006). By researching on Arabidopsis plants under water-deficit stress, more than 800 induced genes have been identified (Bray, 2004), who play key roles in signal transduction, transcriptional regulation, cellular metabolism and transport, as well as cellular structures protection. Meanwhile, when water deficit comes two major transcriptional regulatory pathways of gene expression show up. One group is TFs called dehydration response element binding protein (DREB) coming from AP2/ERF family and another is NAC, AREB/ABF, WRKY and MYB group. The former work in the ABA-independent pathway, latter known to be as the most responsive to ABA signaling under drought.

The DREB proteins contain an ERF/AP2 DNA-binding domain that is quite conserved. The TFs containing it are widely found in many plants, including Arabidopsis (Okamuro et al. 1997 ), tomato (Zhou et al. 1997 ), tobacco (Ohme-Takagi and Shinshi 1995 ), rice (Weigel 1995 ) and maize (Moose and Sisco 1996 ). And a conserved Ser/Thr-rich region next to ERF/AP2 domain is considered to be responsible for DREB proteins phosphorylation (Liu et al., 1998). Latter, Agarwal et al. found high sequence similarity exists in different DREB proteins by amino acid alignment analysis (Agarwal et al., 2006).

Generally, The DREB TFs could be divided into DREB1 and DREB2, and they participate in signal transduction pathways under low temperature and dehydration respectively. They belong to plants-distinctive ERF family. ERF proteins share a conserved domain binding to the C-repeat CRT/dehydration responsive element (DRE) motif engaged in the expression of cold and dehydration responsive genes (Agarwal et al., 2006). The expression of DREB2A and its homolog DREB2B are induced by dehydration and high salt stress (Liu et al., 1998; Nakashima et al., 2000 ). Furthermore, the expression of DREB genes is induced by abiotic stresses at different time periods (Liu et al. 1998; Dubouzet et al. 2003). But for the character of tissue-specific expression, the data is still in short.

For the ABA-dependent gene induction under water-deficit condition, we want to stress on another group of TFs. Firsly, MYB, MYC, homeodomain TFs and a family of transcriptional repressors (Cys2/His2-type zinc-finger proteins) are involved in the ABA response to water deficit. The promoter region of Responsive to Dehydration 22 (RD22), who is induced by ABA, contains MYC and MYB cis-element recognition sites. And MYC and MYB TFs only accumulate after an increase of ABA concentration, and Over-expressing these TFs lead to promoted ABA sensitivity and drought tolerance (Abe et al. 2003). Also other data indicate that two R2R3-MYB TFs (AtMYB60 and AtMYB61) are directly involved in stomatal dynamics in Arabidopsis regulated by light conditions, ABA and water stress (Liang et al. 2005). Very recently, in Arabidopsis, it has been strongly suggested that WRKY TFs possibly act downstream of at least two ABA receptors, the cytoplasmic PYR⁄PYL⁄RCAR protein phosphatase 2C-ABA complex and the chloroplast envelope–located ABAR–ABA complex. And the promoter-binding experiments show that the target genes for WRKY TFs involved in ABA signalling include ABF2/4, ABI4/5, MYB2, DREB1a/2a, RAB18, RD29A and COR47. Other findings in a large sense prove us ome WRKY TFs are positive regulators of ABA-mediated stomatal closure being relevant with drought responses (reviewed by Deena L. Rushton et al., 2011). On the other hand, it has been realized earlier that the ABA response element (ABRE) is bound by basic Leucine Zipper Domain (bZIP-type) TFs, and three Arabidopsis bZIP TFs (AREB1/ABF2, AREB2/ABF4, and ABF3) are activated through phosphorylation reacting to water deficit and ABA treatment. Other NAC domain proteins ANAC019, ANAC055, and ANAC072 are also induced by the same treatment. And in guard cells, it has been shown that the strong induction of Stress Responsive–NAC1 (SNAC1) gene expression by drought also affect stomatal closure (Hu et al. 2006).

2.5.2. Flooding stress

Flooding and submergence are two stresses lead to anoxic conditions in the root system. Under this stress condition, both anoxia and hypoxia are defined by O2 shortage. But diverse plants have their own way to adjust to it. Some lowland rice cultivars, such as FR13A, can survive submergence by suppressing shoot elongation. At the molecular level, Submergence-1 (Sub1), which is derived from FR13A, is a major quantitative trait locus contributing to great submergence tolerance (Xu et al. 2006). And three sequentially arrayed genes (designated Sub1A, Sub1B, and Sub1C) has been identified. Sub1A has been proved to encode an ERF domain–containing TF associated with the induction of low oxygen escape syndrome (LOES) (Bailey-Serres and Voesenek, 2008 ).

In plants, different cell types exhibit a conserved response to low oxygen levels at the molecular level (Mustroph et al. 2010). This response includes the induction of genes after 30 min under hypoxia, whose expression is maintained for several hours (Klok et al. 2002; van Dongen et al. 2009). The increased transcript levels of these genes are further accompanied by active combination between mRNAs and polysomes reflecting promoted translation process (Branco-Price et al. 2008). Unfortunately, in plants the mechanism by which oxygen is perceived has not been clarified. But researches on hypoxia-responsive TFs can help us a lot to investigate the regulation of the hypoxic response. Usually these TFs are detected in families like MYB, NACs [Arabidopsis Transcription Activation Factor (ATAF) and Cup-shaped Cotyledons (CUC)], Plant Homeodomain (PHD) and ERF families (Hoeren et al. 1998; Christianson et al. 2009; Licausi et al. 2010b). And on the other hand, Microarray data in Arabidopsis and rice research find us several transcription factors whose expression increases induced by oxygen deprivation, such as heat shock factors, MADS-box proteins, and WRKY factors (Lasanthi-Kudahettige et al., 2007). Recently Licausi et al. (2010a) have identified TFs that are differentially expressed under hypoxic conditions. The results indicate members of the AP2 ⁄ ERF-type family are the most common upregulated TFs, followed by Zinc-finger and basic helix-loop-helix (bHLH-type) TFs. TFs belonging to the bHLH family also appear in the downregulated part, together with members from the bZIP and MYB families.

On the other hand, by silico experiments and trans-activation assays it has been confirmed that five hypoxia-induced TFs (At4g29190; LBD41, At3g02550; HRE1, At1g72360; At1g69570; At5g66980) from different TF families [Zinc Finger, Ligand Binding Domain (LBD)/Lateral Organ Boundary Domain, ERF, DNA binding with one finger (DOF), ARF] respectively showed the ability to regulate the expression of hypoxia responsive genes (Licausi et al. 2010b). Other evidence relating to TFs and adaptive response to low oxygen will refer to redox-sensitive TFs. ZAT12, a putative zinc finger-containing TF, is identified as an important link in the oxidative stress response signalling network in Arabidopsis (Rizhsky et al. 2004), for its transcript levels were remarkably mounted up in response to hypoxia and anoxia in several independent analyses (Branco-Price et al. 2005).

2.5.3. Salinity

Plants growing in high salt concentrations, as we know, will suffer from osmotic stress and take actions like closing stomata and reducing cell expansion in young leaves and root tips. Subsequently, accumulation of ions, especially sodium (Na+), in the photosynthetic tissues, will hit photosynthetic components such as enzymes, chlorophylls, and carotenoids (Davenport et al. 2005), followed by secondary stresses (oxidative stress and nutritional disorders) (Hasegawa et al. 2000; Chinnusamy et al. 2006).

One of the main strategies taken to improve plant salt tolerance is to re-establish ion homeostasis by counteracting the osmotic component of the stress to avoid toxic concentrations within the cytoplasm (Munns and Tester 2008). Recently, in Arabidopsis it has been confirmed that the effective establishing and maintaining ion homeostasis is mediated mainly by a Salt Overly Sensitive (SOS) signal pathway, which we refer to in Ca2+ part. Recently, SOS4 and SOS5 have also been characterized (Mahajan et al. 2008). Similar to SOS1, Arginine Vasopressin1 (AVP1) and A. thaliana Na+/H+ exchanger1 (AtNHX1) genes contribute to ion homeostasis also (Gaxiola et al. 2001; Zhang et al. 2001). Besides these genes, overexpression of genes encoding LEA proteins, such as the barley HVA1 (Xu et al. 1996) and wheat dehydrin-5 (DHN-5) (Brini et al. 2007), is confirmed to be able to enhance plant salt tolerance. And regulating Lea gene expression is mediated by both ABA dependent and independent signalling pathways, both of which use Ca2+ signaling to induce Lea gene expression during salinity.

Meanwhile, what do TFs do in salt stress signaling? Based on researches on Cor/Lea salinity stress responsive genes, whose expression is mediated Ca2+and ABA in salt stress signaling, it has been indicated that various upstream TFs will activate DRE/CRT, ABREs, MYC recognition sequence (MYCRS) and MYB recognition sequence (MYBRS) cis-elements. Also, with or without the involvement of ABA makes them differs from each other. On one hand, ABRE and MYB/MYC element-controlled gene expression is ABA-dependent, which activates bZIP TFs called AREB binding to ABRE element to induce the stress responsive gene (RD29A). However, even if ABA makes these TFs function in their own regulating ways, it has been shown that ABA-dependent and -independent TFs may also cross talk to each other in a synergistic way to amplify the response and improve stress tolerance (reviewed by Dortje Golldack et al., 2011).

2.5.4. Extremes of temperature

Signals of extreme temperature, from freezing to scorching, is perceived by membrane and transduced by different transduction components results in transcription of several genes. Cold stress directly inhibit metabolic reactions and indirectly produce harm through cold-induced osmotic prevents the expression of full genetic potential of plants owing to its direct inhibition of metabolic reactions and, indirectly, through cold-induced osmotic, oxidative and other stresses such as water uptake barriers caused by chilling and cellular dehydration induced by freeze. Cold stress, based on temperature range, are defined as chilling (<20°C) and/or freezing (<0°C) temperatures, both of which hurt plants in different ways. The former leads to slow biochemical reactions related to enzymes and membrane transport activities, while the latter forming ice crystal can cause membrane system disruption (Chinnusamy et al. 2007).

Numerous TFs in cold stress circumstances have been identified in Arabidopsis, homologs of which have been reported in other plants also. Significant progress has been made in the past decade in elucidating the transcriptional networks regulating cold acclimation. Firstly, AP2/ERF family TFs, CBFs play essential role in controlling genes in phosphoinositide metabolism, osmolyte biosynthesis, ROS detoxification, hormone metabolism and signalling (Lee et al. 2005). They can bind to cis-elements in the promoters of COR genes to activate gene expression. Earlier it was proved that DREB1A/CBF3, DREB1B/CBF1 and DREB1C/CBF2 genes, lying tandemly in the Arabidopsis genome, are induced by cold but not by dehydration or high salinity (Shinwari et al. 1998). CBF genes showed high expression under low temperature treatment and the transcript was detectable after 30 min exposed to 4 °C and reached maximum expression at 1 h (Medina et al. 1999). However this time-linking phenomenon differs from various plants. In rice, detecting OsDREB1A and OsDREB1B transcript might need to wait 40 min after cold exposure. By the way, CBF pathway might also have a crucial role in constitutive freezing tolerance (Hannah et al. 2006).

Moreover for many studies, emphasize has been laid on the ICE-CBF-COR transcriptional cascade. In Arabidopsis, ICE1 (Inducer of CBF Expression1), a MYC-type bHLH TF, can bind to MYC recognition elements in the CBF3 promoter affecting its expression during cold acclimation (Chinnusamy et al. 2003). Besides being the inducer of CBFs transcription, ICE1 is also a transcriptional inducer of ZAT12, NAC072 and HOS9 in Arabidopsis (Benedict et al. 2006). Furthermore, by studying on ice1 mutation under cold stress, the genes in calcium signaling, lipid signaling or encoding receptor-like protein kinases are found to be affected (Lee et al., 2005). In conclusion, there do exists network between these components in cold signaling. Constitutive expressed ICE1 is actived through sumoylation and phosphorylation induced by cold stress, which then induce the transcription of CBFs and reprime MYB15. For CBFs expression, CBF2 acts as a negative regulator of CBF1 and CBF3 expression. Meanwhile, the expression of CBFs is negatively regulated by upstream TF MYB15 and ZAT12(Chinnusamy et al. 2007).


3. Conclusion

Thanks to so much efforts made by researchers in various fields, we have a pretty clear idea about how to develop our researching methods in abiotic stress field. That is exactly what we should concentrate on in the future. For plants’ reactions to different kinds of stress, we must make more efforts in taking measures in focusing on systematic studies which so far can be taken as the best way to figure out what plants will do under certain circumstances.

As we all know, it is of incredibly great importance to understand more about abiotic stress which impacts a lot on plants, which will not only change our understanding of current environment we live, but also bring a plenty of benefits for improving human beings living standards. That is why at this part we hope we can get everyone’s attention to how to explore plants kingdom and develop researches in a systematic way.


  1. 1. CookeD. TMunkongeF. MBurdenR. SJamesC. SFluidity and lipid composition of oat and rye shoot plasma membrane: effect of sterol perturbation by xenobiotics.Biochim Biophys Acta, 1991156 EOF62 EOF
  2. 2. ElkahouiSSmaouiAZarroukMGhrirRLimamFSalt-induced lipid changes in Catharanthus roseus cultured cell suspensions.Phytochemistry20041911 EOF7 EOF
  3. 3. BewellM. AMaathuisF. JAllenG. JSandersDCalcium-induced calcium release mediated by a voltage-activated cation channel in vacuolar vesicles from red beetFEBS letters199941 EOF44 EOF
  4. 4. KnightB. WOmurtagASirovichLThe approach of a neuron population firing rate to a new equilibrium: An Exact Theoretical Result.Neural Computation20001045 EOF55 EOF
  5. 5. SangwanVFouldsISinghJDhindsaR. SCold-activation of Brassica napus BN11 EOF12 EOFpromoter is mediated by structural changes in membranes and cytoskeleton, and requires Ca2+ influx.The Plant Journal, 2001
  6. 6. WangQ. YNickPCold acclimation can induce microtubular cold stability in a manner distinct from abscisic acidPlant Cell Physiology, 2001999 EOF1005 EOF
  7. 7. PliethCTemperature sensing by plants: calcium-permeable channels as primary sensors-A Model.The Journal of Membrane Biology1999121 EOF7 EOF
  8. 8. HasegawaP. MBressanR. AZhuJ-KBohnertH. JPlant cellular and molecular responses to high salinityAnnual Review of Plant Physiology and Plant Molecular Biology2000463 EOF500 EOF
  9. 9. SuzukiILosD. AKanesakiYMikamiKMurataNThe pathway for perception and transduction of low-temperature signals in Synechocystis.The EMBO Journal20001327 EOF34 EOF
  10. 10. AguilarP. SHernandez-arriagaA. MMolecular basis of thermosensing: a two-component signal transduction thermometer in Bacillus subtilis.The EMBO Journal20011681 EOF91 EOF
  11. 11. UraoTYamaguchi-shinozakiKShinozakiKTwo-component systems in plant signal transduction. Trends in Plant Science, 2000
  12. 12. MaedaTWurgler-murphyS. MSaitoHA two-component system that regulates an osmosensing MAP kinase cascade in yeast.Nature1994242 EOF5 EOF
  13. 13. UraoTYakubovBSatohRYamaguchi-shinozakiKA transmembrane hybrid-type histidine kinase in Arabidopsis functions as an osmosensor.The Plant Cell19991743 EOF54 EOF
  14. 14. ZhuJ-KPlant salt tolerance. Trends in Plant Science, 2001
  15. 15. XiongLZhuJ-KMolecular and genetic aspects of plant responses to osmotic stressPlant, Cell & EnvironmentCell & Environment, 2002131 EOF139 EOF
  16. 16. UllahHChenJ-GYoungJ. CImK-HModulation of cell proliferation by heterotrimeric G protein in Arabidopsis.Science, 20012066 EOF9 EOF
  17. 17. WangX-QUllahHJonesA. MAssmannS. MG protein regulation of ion channels and abscisic acid signaling in Arabidopsis guard cells.Science, 20012070 EOF2 EOF
  18. 18. MaYSzostkiewiczIKorteARegulators of 2Cphosphatase activity function as abscisic acid sensors.Science, 2009
  19. 19. ParkS-YFungPNishimuraNAbscisic acid inhibits type 2C protein phosphatases via the PYR/PYL family of START proteins.Science, 20091068 EOF71 EOF
  20. 20. FoyerC. Hand NoctorGAscorbate and glutathione: the heart of the redox hub. Plant Physiology, 2011
  21. 21. HuchzermeyerBKoyroH. WSalt and drought stress effects on photosynthesis. Handbook of Photosynthesis (2nd edition)., 2005
  22. 22. KantSKantPRavehEBarakSEvidence that differential gene expression between the halophyte, Thellungiella halophila, and Arabidopsis thaliana is responsible for higher levels of the compatible osmolyte proline and tight control of Na+ uptake in T. Halophila. PlantCell & Environment, 20061220 EOF1234 EOF
  23. 23. TürkanIDemiralTRecent developments in understanding salinity toleranceEnvironmental and Experimental Botany2 EOF9 EOF2009
  24. 24. GeisslerBTungekarRSatchell KJF. Identification of a conserved membrane localization domain within numerous large bacterial protein toxinsProc Natl Acad Sci U S A., 2010
  25. 25. VranovaEAtichartpongkulSComprehensive analysis of gene expression in Nicotiana tabacum leaves acclimated to oxidative stress.Proc Natl Acad Sci U S A., 2002
  26. 26. FoyerC. HNoctorGRedox sensing and signalling associated with reactive oxygen in chloroplasts, peroxisomes and mitochondriaPhysiologia Plantarum2003355 EOF364 EOF
  27. 27. MollerI. MPlant mitochondria and oxidative stress: electron transport, NADPH turnover, and metabolism of reactive oxygen speciesAnnual Review of Plant Physiology and Plant Molecular Biology2001561 EOF591 EOF
  28. 28. RasmussonA. GSooleK. LElthonT. EAlternative NAD (P) H dehydrogenases of plant mitochondria. Annual Review of Plant Biology, 2004
  29. 29. NoctorGMetabolic signalling in defence and stress: the central roles of soluble redox couplesPlantCell & Environment, 2006409 EOF425 EOF
  30. 30. RhoadsD. MUmbachA. LSubbaiahC. CSiedowJ. NMitochondrial reactive oxygen species. Contribution to oxidative stress and interorganellar signalingPlant Physiology, 2006
  31. 31. PourrutBPerchetGSilvestreJCecchiMGuiresseMPinelliEPotential role of NADPH-oxidase in early steps of lead-induced oxidative burst in Vicia faba rootsJournal of Plant Physiology2008571 EOF579 EOF
  32. 32. LeshemYSeriLLevineAInduction of phosphatidylinositol 3kinase-mediated endocytosis by salt stress leads to intracellular production of reactive oxygen species and salt toleranceThe Plant Journal2007
  33. 33. ForemanJDemidchikVBothwellJ. HMylonaPReactive oxygen species produced by NADPH oxidase regulate plant cell growth.Nature2003442 EOF6 EOF
  34. 34. MoriI. CSchroederJ. IReactive Oxygen Species Activation of Plant Ca2+ Channels. A Signaling Mechanism in Polar Growth, Hormone Transduction, Stress Signaling, and Hypothetically Mechanotransduction.Plant Physiology, 2004
  35. 35. GamaleyI. AKlyubinI. VRoles of reactive oxygen species: signaling and regulation of cellular functions.International Review of Cytology1999203 EOF55 EOF
  36. 36. FoyerC. HNoctorGRedox homeostasis and antioxidant signaling: a metabolic interface between stress perception and physiological responsesThe Plant Cell, 2005
  37. 37. ZhaoLZhangFGuoJYangYLiBZhangLNitric oxide functions as a signal in salt resistance in the calluses from two ecotypes of reed.Plant Physiology2004849 EOF57 EOF
  38. 38. PrasadT. KAndersonM. DMartinB. AEvidence for chilling-induced oxidative stress in maize seedlings and a regulatory role for hydrogen peroxide.The Plant Cell, 1994
  39. 39. FadzillaN. MFinchR. PBurdonR. HSalinity, oxidative stress and antioxidant responses in shoot cultures of riceJournal of Experimental Botany1997325 EOF332 EOF
  40. 40. LuiJShonoMCharacterization of mitochondria-located small heat shock protein from tomato (Lycopersicon esculentum)Plant Cell Physiology, 19991297 EOF1304 EOF
  41. 41. LeeB. HWonS. HLeeH. SMiyaoMChungW. IKimI. JExpression of the chloroplast-localized small heat shock protein by oxidative stress in riceGene2000283 EOF290 EOF
  42. 42. MoschouP. NPaschalidisK. ADelisI. DSpermidine exodus and oxidation in the apoplast induced by abiotic stress is responsible for H2O2 signatures that direct tolerance responses in tobacco. The Plant Cell20081708 EOF1724 EOF
  43. 43. ZhangXZhangLDongFGaoJGalbraithD. WHydrogen peroxide is involved in abscisic acid-induced stomatal closure in Vicia faba.Plant Physiology20011438 EOF48 EOF
  44. 44. KwakJ. MMoriI. CPeiZ. MLeonhardtNTorresM. ANADPH oxidase AtrbohD and AtrbohF genes function in ROS-dependent ABA signaling in ArabidopsisThe EMBO Journal20032623 EOF2633 EOF
  45. 45. GuoF. QOkamotoMCrawfordN. MIdentification of a plant nitric oxide synthase gene involved in hormonal signaling.Science, 2003100 EOF3 EOF
  46. 46. Ortiz-masiaDPerez-amadorM. ACarbonellJDiverse stress signals activate the C1 subgroup MAP kinases of ArabidopsisFEBS letters20071834 EOF1840 EOF
  47. 47. DócziRBraderGPettkó-szandtnerAThe Arabidopsis mitogen-activated protein kinase kinase MKK3 is upstream of group C mitogen-activated protein kinases and participates in pathogen signaling.The Plant Cell20073266 EOF79 EOF
  48. 48. MunnikTTesterinkCPlant phospholipid signaling: “in a nutshell”.Journal of Lipid Research2009
  49. 49. XueH. WChenXMeiYFunction and regulation of phospholipid signalling in plantsBiochemical Journal, 2009
  50. 50. MunnikTVermeer JEM. Osmotic stress-induced phosphoinositide and inositol phosphate signalling in plants.2010Cell & Environment, 2010655 EOF69 EOF
  51. 51. TesterinkCMunnikTPhosphatidic acid: a multifunctional stress signaling lipid in plants.Trends in Plant Science, 2005
  52. 52. AriszS. ATesterinkCMunnikTPlant PA signaling via diacylglycerol kinase.Biochimica et Biophysica ActaBBA)- Molecular and Cell Biology of Lipids, 2009869 EOF75 EOF
  53. 53. LiMHongYWangXPhospholipaseDand phosphatidic acid-mediated signaling in plants. Biochimica et Biophysica ActaBBA)- Molecular and Cell Biology of Lipids, 2009927 EOF35 EOF
  54. 54. MishkindMVermeer JEM, Darwish E. Heat stress activates phospholipase D and triggers PIP2 accumulation at the plasma membrane and nucleus.The Plant Journal200910 EOF21 EOF
  55. 55. TesterinkCMunnikTMolecular, cellular, and physiological responses to phosphatidic acid formation in plants.Journal of Experimental Botany20112349 EOF61 EOF
  56. 56. ZoniaLMunnikTOsmotically induced cell swelling versus cell shrinking elicits specific changes in phospholipid signals in tobacco pollen tubes.Plant Physiology2004813 EOF23 EOF
  57. 57. DarwishETesterinkCKhalilMPhospholipid signaling responses in salt-stressed rice leavesPlant Cell Physiology, 2009986 EOF997 EOF
  58. 58. HongYZhangWWangXPhospholipaseDand phosphatidic acid signalling in plant response to drought and salinity. Plant, Cell & EnvironmentCell & Environment, 2010627 EOF635 EOF
  59. 59. Bargmann BORLaxalt AM, Riet B. Multiple PLDs required for high salinity and water deficit tolerance in plantsPlant Cell Physiology, 2009
  60. 60. MishraGZhangWDengFZhaoJA bifurcating pathway directs abscisic acid effects on stomatal closure and opening in Arabidopsis.Science, 2006264 EOF6 EOF
  61. 61. AriszSMunnikTDiacylglycerol kinase. Lipid Signaling in Plants, 2010
  62. 62. HirayamaTOhtoCMizoguchiTA gene encoding a phosphatidylinositol-specific phospholipase C is induced by dehydration and salt stress in Arabidopsis thaliana.Proc Natl Acad Sci U S A., 19953903 EOF7 EOF
  63. 63. SanchezJ. PChuaN. HArabidopsis PLC1 is required for secondary responses to abscisic acid signalsThe Plant Cell, 2001
  64. 64. PopescuS. CPopescuG. VBachanSZhangZSeayMGersteinMSnyderMDinesh-kumarS. PDifferential binding of calmodulin-related proteins to their targets revealed through high-density Arabidopsis protein microarrays.Proc Natl Acad Sci U S A., 20074730 EOF5 EOF
  65. 65. PetersCLiMNarasimhanRRothMNonspecific phospholipase C NPC4 promotes responses to abscisic acid and tolerance to hyperosmotic stress in ArabidopsisThe Plant Cell20102642 EOF2659 EOF
  66. 66. TesterinkCDekkerH. LLimZ. YJohnsM. KIsolation and identification of phosphatidic acid targets from plantsThe Plant Journal2004527 EOF536 EOF
  67. 67. YuLNieJCaoCJinYYanMWangFLiuJPhosphatidic acid mediates salt stress response by regulation of MPK6 in Arabidopsis thaliana.New Phytologist, 2010762 EOF73 EOF
  68. 68. GuoLWangXCrosstalk between Phospholipase D and Sphingosine Kinase in Plant Stress Signaling.Frontiers in plant science201251 EOF
  69. 69. Lemtiri-chliehFMacRobbie EAC. Inositol hexakisphosphate mobilizes an endomembrane store of calcium in guard cellsProc Natl Acad Sci U S A., 2003
  70. 70. DewaldD. BTorabinejadJJonesC. ARapid accumulation of phosphatidylinositol 4, 5-bisphosphate and inositol 145trisphosphate correlates with calcium mobilization in salt-stressed Arabidopsis.Plant Physiology, 2001
  71. 71. PetersCLiMNarasimhanRRothMNonspecific phospholipase C NPC4 promotes responses to abscisic acid and tolerance to hyperosmotic stress in ArabidopsisThe Plant Cell20102642 EOF2659 EOF
  72. 72. Scherer GFELabusch C, Effendi Y. Frontiers: Phospholipases and the Network of Auxin Signal Transduction with ABP1 and TIR1 as Two Receptors: A Comprehensive and Provocative Model.Frontiers in Plant Physiology, 201256 EOF
  73. 73. BuschWBenfeyP. NInformation processing without brains-the power of intercellular regulators in plants.Development20101215 EOF1226 EOF
  74. 74. SachsTThimannK. VThe role of auxins and cytokinins in the release of buds from dominanceAmerican Journal of Botany1967136 EOF
  75. 75. ThimannK. VSkoogFStudies on the growth hormone of plants: III. The inhibiting action of the growth substance on bud developmentProc Natl Acad Sci U S A., 1933
  76. 76. SauterADaviesW. JHartungWThe long‐distance abscisic acid signal in the droughted plant: the fate of the hormone on its way from root to shoot. Journal of Experimental Botany, 2001
  77. 77. GodaHSasakiEAkiyamaKThe AtGenExpress hormone and chemical treatment data set: experimental design, data evaluation, model data analysis and data access. The Plant Journal2008526 EOF542 EOF
  78. 78. ChapmanE. JEstelleMMechanism of auxin-regulated gene expression in plants.Annual Review of Genetics2009265 EOF85 EOF
  79. 79. SantnerAEstelleMThe ubiquitin‐proteasome system regulates plant hormone signaling. The Plant Journal, 2010
  80. 80. Bartoli CG, CasalonguéCA, Simontacchi M. Interactions between hormone and redox signalling pathways in the control of growth and cross tolerance to stress. Environmental and Experimental Botany, 2012, 52(3): 139-47.
  81. 81. CuiJZhouYDingJ. GRole of nitric oxide in hydrogen peroxide‐dependent induction of abiotic stress tolerance by brassinosteroids in cucumber. Plant, Cell & Environment, 2011
  82. 82. SchroederJ. IKwakJ. MAllenG. JGuard cell abscisic acid signalling and engineering drought hardiness in plants.Nature2001327 EOF30 EOF
  83. 83. CutlerS. RRodriguezP. LFinkelsteinR. RAbscisic acid: emergence of a core signaling network. Annual Review of Plant Biology, 2010
  84. 84. GhanemM. EHichriISmigockiA. CAlbaceteARoot-targeted biotechnology to mediate hormonal signalling and improve crop stress tolerancePlant Cell Reports2011807 EOF823 EOF
  85. 85. ArguesoC. TFerreirF. JEnvironmental perception avenues: the interaction of cytokinin and environmental response pathways.PlantCell & Environment, 20091147 EOF60 EOF
  86. 86. EyidoganFOzM. TYucelMOktemH. ASignal Transduction of Phytohormones Under Abiotic Stresses. Phytohormonesand Abiotic Stress Tolerance in Plants, 2012
  87. 87. ZhangS. WLiC. HCaoJZhangY. CZhangS. QAltered architecture and enhanced drought tolerance in rice via the down-regulation of indole-3acetic acid by TLD1/OsGH3.13 activationPlant Physiology, 2009
  88. 88. DiviU. KKrishnaPBrassinosteroid: a biotechnological target for enhancing crop yield and stress tolerance.New Biotechnology2009131 EOF6 EOF
  89. 89. SharpR. EInteraction with ethylene: changing views on the role of abscisic acid in root and shoot growth responses to water stressPlantcell & environment, 2002211 EOF222 EOF
  90. 90. StepanovaA. NAlonsoJ. MEthylene signaling and response: where different regulatory modules meet.Current Opinion in Plant Biology2009548 EOF55 EOF
  91. 91. JonesBGunnerasS. APeterssonS. VCytokinin regulation of auxin synthesis in Arabidopsis involves a homeostatic feedback loop regulated via auxin and cytokinin signal transduction.The Plant Cell, 2010
  92. 92. WangLWangZXuYJooS. HKimS. KOsGSR1 is involved in crosstalk between gibberellins and brassinosteroids in riceThe Plant Journal2009498 EOF510 EOF
  93. 93. Alonso-ramirezARodriguezDReyesDEvidence for a role of gibberellins in salicylic acid-modulated early plant responses to abiotic stress in Arabidopsis seedsPlant Physiology20091335 EOF1344 EOF
  94. 94. AcharyaB. RAssmannS. MHormone interactions in stomatal functionPlant Molecular Biology2009451 EOF462 EOF
  95. 95. DiviU. KRahmanTKrishnaPBrassinosteroid-mediated stress tolerance in Arabidopsis shows interactions with abscisic acid, ethylene and salicylic acid pathwaysBMC plant biology, 2010
  96. 96. WilliamsonR. EAshleyC. CFree Ca2++ and cytoplasmic streaming in the alga CharaNature1982647 EOF50 EOF
  97. 97. JohnsonC. HKnightM. RKondoTMasson. P Circadian oscillations of cytosolic and chloroplastic free calcium in plants. Science, 1995
  98. 98. TracyF. EGillihamMDoddA. NNaCl-induced changes in cytosolic free Ca2+ in Arabidopsis thaliana are heterogeneous and modified by external ionic composition.PlantCell & Environment, 20081063 EOF73 EOF
  99. 99. KudlaJBatisticOHashimotoKCalcium signals: the lead currency of plant information processingThe Plant Cell, 2010
  100. 100. VinogradovaM. VReddyV. SReddy ASN. Crystal structure of kinesin regulated by Ca2+-calmodulin. The Journal of Biological Chemistry, 2004
  101. 101. AllenG. JSandersDCalcineurin, a type 2B protein phosphatase, modulates the Ca2+-permeable slow vacuolar ion channel of stomatal guard cells.The Plant Cell, 1995
  102. 102. DoddA. NKudlaJSandersDThe language of calcium signaling. Annual Review of Plant Biology, 2010
  103. 103. SneddenW. AFrommHCalmodulin as a versatile calcium signal transducer in plants. New Phytologist200135 EOF66 EOF
  104. 104. HoeflichK. PIkuraMCalmodulin in action: diversity in target recognition and activation mechanisms. Cell2002739 EOF742 EOF
  105. 105. YangTPoovaiahB. WCalcium/calmodulin-mediated signal network in plantsTrends in Plant Science2003505 EOF512 EOF
  106. 106. McCormack E, Tsai YC, Braam J. Handling calcium signaling: Arabidopsis CaMs and CMLs. Trends in Plant Scienc, 2005, 10(8):383-9.
  107. 107. PopescuS. CPopescuG. VBachanSZhangZSeayMGersteinMSnyderMDinesh-kumarS. PDifferential binding of calmodulin-related proteins to their targets revealed through high-density Arabidopsis protein microarrays.Proc Natl Acad Sci U S A., 20074730 EOF5 EOF
  108. 108. ChengS. HWillmannM. RChenH. CSheenJCalcium signalingthrough protein kinases. The Arabidopsis calcium-dependent protein kinase gene family. Plant Physiology, 2002
  109. 109. LuanSKudlaJRodriguez-concepcionMYalovskySGruissemWCalmodulins and calcineurin B-like proteins: calcium sensors for specific signal response coupling in plants.Plant Cell, 2002Suppl:S389400
  110. 110. LuanSLanWChul Lee S. Potassium nutrition, sodium toxicity, and calcium signaling: connections through the CBL-CIPK network.Current Opinion in Plant Biology2009339 EOF46 EOF
  111. 111. WeinlSKudlaJThe CBL-CIPK Ca2+-decoding signaling network: function and perspectives. New Phytology, 2009
  112. 112. BatisticOWaadtRSteinhorstLHeldKKudlaJCBL-mediated targeting of CIPKs facilitates the decoding of calcium signals emanating from distinct cellular stores.Plant Journal, 2010211 EOF22 EOF
  113. 113. ClarkG. BRouxS. JAnnexins of plant cells.Plant Physiology, 1995
  114. 114. LaohavisitADaviesJ. MAnnexins. New Phytology, 2011
  115. 115. WhiteP. JBowenH. CDemidchikVNicholsCDaviesJ. MGenes for calcium-permeable channels in the plasma membrane of plant root cellsBiochim Biophys Acta, 2002299 EOF309 EOF
  116. 116. McCormack E, Tsai YC, Braam J. Handling calcium signaling: Arabidopsis CaMs and CMLs. Trends in Plant Scienc, 2005, 10(8):383-9.
  117. 117. DefalcoT. AChiassonDMunroKKaiserB. NSneddenW. ACharacterization of GmCaMK1, a member of a soybean calmodulin-binding receptor-like kinase familyFEBS letters20104717 EOF4724 EOF
  118. 118. DayI. SReddyV. SAliG. SReddy ASN. Analysis of EF-hand-containing proteins in Arabidopsis.Genome Biology2002research0056.10056
  119. 119. HarperJ. FHarmonAPlants, symbiosis and parasites: a calcium signalling connection.Nat Rev Mol Cell Biol., 2005555 EOF66 EOF
  120. 120. ReddyA. SReddyV. SGolovkinMA calmodulin binding protein from Arabidopsis is induced by ethylene and contains a DNA-binding motifBiochem Biophys Res Commun., 2000762 EOF769 EOF
  121. 121. ParkC. YLeeJ. HYooJ. HMoonB. CChoiM. SKangY. HLeeS. MKimH. SKangK. YChungW. SLimC. OChoM. JWRKY group IId transcription factors interact with calmodulinFEBS letters20051545 EOF1550 EOF
  122. 122. SzymanskiD. BLiaoBZielinskiR. ECalmodulin isoforms differentially enhance the binding of cauliflower nuclear proteins and recombinant TGA3 to a region derived from the Arabidopsis Cam-3 promoterPlant Cell, 19961069 EOF
  123. 123. GalonYFinklerAFrommHCalcium-regulated transcription in plants.Molecular Plant2010653 EOF69 EOF
  124. 124. B. WPoovaiahASN Reddy. Calcium and signal transduction in plants.Critical Reviews in Plant Sciences1993185 EOF211 EOF
  125. 125. ZhangYXuSDingPWangDChengY. THeJGaoMXuFLiYZhuZLiXZhangYControl of salicylic acid synthesis and systemic acquired resistance by two members of a plant-specific family of transcription factorsProc Natl Acad Sci USA., 201018220 EOF18225 EOF
  126. 126. KimS. GKimS. YParkC. MA membrane-associated NAC transcription factor regulates salt-responsive flowering via FLOWERING LOCUS T in ArabidopsisPlanta2007647 EOF654 EOF
  127. 127. YoonH. KKimS. GKimS. YParkC. MRegulation of leaf senescence by NTL9mediated osmotic stress signaling in ArabidopsisMolecules and Cells2008
  128. 128. KimY. SKimS. GParkJ. EParkH. YLimM. HChuaN. HParkC. MA membrane-bound NAC transcription factor regulates cell division in Arabidopsis.The Plant Cell20063132 EOF44 EOF
  129. 129. KushwahaRSinghAChattopadhyaySCalmodulin7 plays an important role as transcriptional regulator in Arabidopsis seedling developmentThe Plant Cell20081747 EOF1759 EOF
  130. 130. DaiXXuYMaQXuWWangTXueYChongKOverexpression of an R1R2R3 MYB gene, OsMYB3R-2, increases tolerance to freezing, drought, and salt stress in transgenic Arabidopsis. Plant Physiology, 2007
  131. 131. GeislerMAxelsenK. BHarperJ. FPalmgrenM. GMolecular aspects of higher plant P-type Ca2+-ATPases. Biochim Biophys Acta, 2000
  132. 132. MunnsRJamesR. ALäuchliAApproaches to increasing the salt tolerance of wheat and other cerealsJournal of Experimental Botany20061025 EOF1043 EOF
  133. 133. GoldgurYRomSGhirlandoRShkolnikDShadrinNKonradZBar-zviDDesiccation and zinc binding induce transition of tomato abscisic acid stress ripening 1, a water stress- and salt stress-regulated plant-specific protein, from unfolded to folded state. PlantPhysiology, 2007
  134. 134. RabbaniM. AMaruyamaKAbeHKhanM. AKatsuraKItoYYoshiwaraKSekiMShinozakiKYamaguchi-shinozakiKMonitoring expression profiles of rice genes under cold, drought, and high-salinity stresses and abscisic acid application using cDNA microarray and RNA gel-blot analyses. Plant Physiology, 2003
  135. 135. LiuJIshitaniMHalfterUKimC. SZhuJ. KThe Arabidopsis thaliana SOS2 gene encodes a protein kinase that is required for salt toleranceProc Natl Acad Sci USA., 2000
  136. 136. GongDGuoYSchumakerK. SZhuJ. KThe SOS3 family of calcium sensors and SOS2 family of protein kinases in Arabidopsis.Plant Physiology2004919 EOF26 EOF
  137. 137. ZhuJ. KRegulation of ion homeostasis under salt stressCurrent Opinion in Plant Biology2003441 EOF445 EOF
  138. 138. BriniFHaninMMezghaniIBerkowitzG. AMasmoudiKOverexpression of wheat Na+/H+ antiporter TNHX1 and H+-pyrophosphatase TVP1 improve salt- and drought-stress tolerance in Arabidopsis thaliana plants. Journal of Experimental Botany, 2007
  139. 139. PerrucECharpenteauMRamirezB. CJauneauAGalaudJ. PRanjevaRRantyBA novel calmodulin-binding protein functions as a negative regulator of osmotic stress tolerance in Arabidopsis thaliana seedlingsPlant Journal, 2004410 EOF420 EOF
  140. 140. Yamaguchi-shinozakiKShinozakiKTranscriptional regulatory networks in cellular responses and tolerance to dehydration and cold stresses.Annual Review of Plant Biology2006781 EOF803 EOF
  141. 141. Lecourieux D, Ranjeva R, Pugin A. Calcium in plant defence-signalling pathways. New Phytologist, 2006, 171(2):249 EOF269 EOF -69.
  142. 142. SaijoYHataSKyozukaJShimamotoKIzuiKOver-expression of a single Ca2+-dependent protein kinase confers both cold and salt/drought tolerance on rice plants. Plant Journal, 2000
  143. 143. MishraN. STutejaRTutejaNSignaling through MAP kinase networks in plantsArch Biochem Biophys., 200655 EOF68 EOF
  144. 144. DanIWatanabeN. MKusumiAThe Ste20 group kinases as regulators of MAP kinase cascadesTrends Cell Biol., 2001220 EOF230 EOF
  145. 145. WhitmarshA. JCavanaghJTournierCYasudaJDavisR. JA mammalian scaffold complex that selectively mediates MAP kinase activation.Science, 19981671 EOF4 EOF
  146. 146. RodriguezM. CPetersenMMundyJMitogen-activated protein kinase signaling in plants.Annual Review of Plant Biology2010621 EOF49 EOF
  147. 147. JonakCOkrészLBögreLHirtHComplexity, cross talk and integration of plant MAP kinase signallingCurrent Opinion in Plant Biology2002415 EOF424 EOF
  148. 148. XiongLYangYDisease resistance and abiotic stress tolerance in rice are inversely modulated by an abscisic acid-inducible mitogen-activated protein kinase.Plant Cell, 2003745 EOF59 EOF
  149. 149. RamanMChenWCobbM. HDifferential regulation and properties of MAPKs.Oncogene20073100 EOF12 EOF
  150. 150. TajGAgarwalPGrantMKumarAMAPK machinery in plants: recognition and response to different stresses through multiple signal transduction pathwaysPlant Signal Behav., 2010
  151. 151. SinhaA. KJaggiMRaghuramBTutejaNMitogen-activated protein kinase signaling in plants under abiotic stressPlant Signal Behav., 2011196 EOF203 EOF
  152. 152. KovtunYChiuW. LTenaGSheenJFunctional analysis of oxidative stress-activated mitogen-activated protein kinase cascade in plants.Proc Natl Acad Sci USA., 20002940 EOF5 EOF
  153. 153. ShouHBordalloPWangKExpression of the Nicotiana protein kinase (NPK1) enhanced drought tolerance in transgenic maizeJ Exp Bot., 20041013 EOF1019 EOF
  154. 154. IchimuraKMizoguchiTYoshidaRYuasaTShinozakiKVarious abiotic stresses rapidly activate Arabidopsis MAP kinases ATMPK4 and ATMPK6.Plant Journal, 2000655 EOF65 EOF
  155. 155. TeigeMScheiklEEulgemTDócziRIchimuraKShinozakiKDanglJ. LHirtHThe MKK2 pathway mediates cold and salt stress signaling in ArabidopsisMolecular Cell2004141 EOF152 EOF
  156. 156. DesikanRClarkeAAtherfoldPHancockJ. TNeillS. JHarpin induces mitogen-activated protein kinase activity during defence responses in Arabidopsis thaliana suspension cultures.Planta199997 EOF103 EOF
  157. 157. SamuelM. AMilesG. PEllisB. EOzone treatment rapidly activates MAP kinase signalling in plants.Plant Journal, 2000367 EOF76 EOF
  158. 158. EckardtN. ANegative regulation of stress-activated MAPK signaling in Arabidopsis.Plant Cell, 20092545 EOF
  159. 159. X. GSongX. PSheL. YGuoZ. NMengA. XHuangMAPK Kinase and CDP Kinase Modulate Hydrogen Peroxide Levels during dark-induced Stomatal Closure in Guard Cells of Vicia faba. Botanical Studies, 2008
  160. 160. JammesFSongCShinDMunemasaSTakedaKGuDChoDLeeSGiordoRSritubtimSLeonhardtNEllisB. EMurataYKwakJ. MMAP kinases MPK9 and MPK12 are preferentially expressed in guard cells and positively regulate ROS-mediated ABA signalingProc Natl Acad Sci USA., 200920520 EOF20525 EOF
  161. 161. DaiYWangHLiBHuangJLiuXZhouYMouZLiJIncreased expression of MAP KINASE KINASE7 causes deficiency in polar auxin transport and leads to plant architectural abnormality in Arabidopsis.Plant Cell, 2006308 EOF20 EOF
  162. 162. XuJLiYWangYLiuHLeiLYangHLiuGRenDActivation of MAPK kinase 9 induces ethylene and camalexin biosynthesis and enhances sensitivity to salt stress in ArabidopsisJ Biol Chem., 200826996 EOF27006 EOF
  163. 163. LiuX. MKimK. EKimK. CNguyenX. CHanH. JJungM. SKimH. SKimS. HParkH. CYunD. JChungW. SCadmium activates Arabidopsis MPK3 and MPK6 via accumulation of reactive oxygen speciesPhytochemistry2010614 EOF618 EOF
  164. 164. WurzingerBMairAPfisterBTeigeMCross-talk of calcium-dependent protein kinase and MAP kinase signalingPlant Signal Behav., 2011
  165. 165. JonakCHirtHGlycogen synthase kinase 3/SHAGGY-like kinases in plants: an emerging family with novel functionsTrends Plant Sci., 2002457 EOF461 EOF
  166. 166. KohS. HKimYKimH. YHwangSLeeC. HKimS. HInhibition of glycogen synthase kinase-3 suppresses the onset of symptoms and disease progression of G93A-SOD1 mouse model of ALSExp Neurol., 2007336 EOF346 EOF
  167. 167. MahfouzM. MKimSDelauneyA. JVermaD. PArabidopsis TARGET OF RAPAMYCIN interacts with RAPTOR, which regulates the activity of S6 kinase in response to osmotic stress signalsPlant Cell, 2006
  168. 168. SantosM. OAragaoF. JRole of SERK genes in plant environmental responsePlant Signal Behav., 2009
  169. 169. BoudsocqMBarbier-brygooHLauriereCIdentification of nine sucrose nonfermenting 1related protein kinases 2 activated by hyperosmotic and saline stresses in Arabidopsis thaliana.J Biol Chem., 2004
  170. 170. UmezawaTNakashimaKMiyakawaTKuromoriTTanokuraMShinozakiKYamaguchi-shinozakiKMolecular basis of the core regulatory network in ABA responses: sensing, signaling and transportPlant Cell Physiology, 2010
  171. 171. Kulik A, Wawer I, Krzywińska E, Bucholc M, Dobrowolska G. SnRK2 protein kinases--key regulators of plant response to abiotic stresses. OMICS., 2011, 15(12):859-72.
  172. 172. ShenQGomez-cadenasAZhangPWalker-simmonsM. KSheenJHoT. HDissection of abscisic acid signal transduction pathways in barley aleurone layersPlant Mol Biology, 2001437 EOF448 EOF
  173. 173. KobayashiYMurataMMinamiHYamamotoSKagayaYHoboTYamamotoAHattoriTAbscisic acid-activated SnRK2 protein kinases function in the gene-regulation pathway of ABA signal transduction by phosphorylating ABA response element-binding factorsPlant Journal, 2005939 EOF949 EOF
  174. 174. HuaiJWangMHeJZhengJDongZLvHZhaoJWangGCloning and characterization of the SnRK2 gene family from Zea maysPlant Cell Reports20081861 EOF1868 EOF
  175. 175. KudlaJBatisticOHashimotoKCalcium signals: the lead currency of plant information processingThe Plant Cell, 2010
  176. 176. GeigerDScherzerSMummPMartenIAchePMatschiSLieseAWellmannCAl-rasheidK. AGrillERomeisTHedrichRGuard cell anion channel SLAC1 is regulated by CDPK protein kinases with distinct Ca2+ affinitiesProc Natl Acad Sci USA., 2010
  177. 177. LeeS. JChoD. IKangJ. YKimM. DKimS. YAtNEK6 interacts with ARIA and is involved in ABA response during seed germination.Molecules and Cells2010559 EOF66 EOF
  178. 178. KerkDBulgrienJSmithD. WBarsamBVeretnikSGribskovMThe complement of protein phosphatase catalytic subunits encoded in the genome of Arabidopsis.Plant Physiology2002908 EOF25 EOF
  179. 179. MerlotSGostiFGuerrierDVavasseurAGiraudatJThe ABI1 and ABI2 protein phosphatases 2C act in a negative feedback regulatory loop of the abscisic acid signalling pathway.The Plant Journal, 2001295 EOF303 EOF
  180. 180. UmezawaTSugiyamaNMizoguchiMHayashiSMyougaFYamaguchi-shinozakiKIshihamaYHirayamaTShinozakiKType 2C protein phosphatases directly regulate abscisic acid-activated protein kinases in ArabidopsisProc Natl Acad Sci USA., 200917588 EOF17593 EOF
  181. 181. HubbardK. ENishimuraNHitomiKGetzoffE. DSchroederJ. IEarly abscisic acid signal transduction mechanisms: newly discovered components and newly emerging questionsGenes & Development, 2010
  182. 182. TakemiyaAKinoshitaTAsanumaMShimazakiKProtein phosphatase 1 positively regulates stomatal opening in response to blue light in Vicia fabaProc Natl Acad Sci USA., 2006
  183. 183. YuR. MZhouYXuZ. FChyeM. LKongR. YTwo genes encoding protein phosphatase 2A catalytic subunits are differentially expressed in rice.Plant Molecular Biology2003295 EOF311 EOF
  184. 184. YuR. MWongM. MJackR. WKongR. YStructure, evolution and expression of a second subfamily of protein phosphatase 2A catalytic subunit genes in the rice plant (Oryza sativa L.)Planta2005757 EOF768 EOF
  185. 185. LuanSProtein phosphatases in plants. Annual Review of Plant Biology, 2003
  186. 186. Fordham-skeltonA. PChilleyPLumbrerasVReignouxSFentonT. RDahmC. CPagesMGatehouseJ. AA novel higher plant protein tyrosine phosphatase interacts with SNF1related protein kinases via a KIS (kinase interaction sequence) domainThe Plant Journal2002
  187. 187. KerkDConleyT. RRodriguezF. ATranH. TNimickMMuenchD. GMoorheadG. BA chloroplast-localized dual-specificity protein phosphatase in Arabidopsis contains a phylogenetically dispersed and ancient carbohydrate-binding domain, which binds the polysaccharide starchThe Plant Journal2006400 EOF413 EOF
  188. 188. RushtonP. JSomssichI. ETranscriptional control of plant genes responsive to pathogensCurrent Opinion in Plant Biology1998311 EOF315 EOF
  189. 189. ChavesM. MOliveiraM. MMechanisms underlying plant resilience to water deficits: prospects for water-saving agricultureJournal of Experimental Botany20042365 EOF2384 EOF
  190. 190. YiNKimY. SJeongM. HOhS. JJeongJ. SParkS. HJungHChoiY. DKimJ. KFunctional analysis of six drought-inducible promoters in transgenic rice plants throughout all stages of plant growth.Planta2010743 EOF54 EOF
  191. 191. JaleelC. AGopiRSankarBGomathinayagamMPanneerselvamRDifferential responses in water use efficiency in two varieties of Catharanthus roseus under drought stressComptes Rendus Biologies200842 EOF47 EOF
  192. 192. VersluesP. EBrayE. ARole of abscisic acid (ABA) and Arabidopsis thaliana ABA-insensitive loci in low water potential-induced ABA and proline accumulationJournal of Experimental Botany2006201 EOF212 EOF
  193. 193. BrayE. AGenes commonly regulated by water-deficit stress in Arabidopsis thalianaJournal of Experimental Botany20042331 EOF2341 EOF
  194. 194. OkamuroJ. KCasterBVillarroelRVan MontaguMJofukuK. DTheA. Pdomain of APETALA2 defines a large new family of DNA binding proteins in Arabidopsis. Proc Natl Acad Sci USA., 1997
  195. 195. ZhouJTangXMartinG. BThe Pto kinase conferring resistance to tomato bacterial speck disease interacts with proteins that bind a cis-element of pathogenesis-related genes.EMBO Journal, 19973207 EOF18 EOF
  196. 196. Ohme-takagiMShinshiHEthylene-inducible DNA binding proteins that interact with an ethylene-responsive element. The Plant Cell, 1995
  197. 197. WeigelDThe APETALA2 domain is related to a novel type of DNA binding domain. The Plant Cell, 1995
  198. 198. MooseS. PSiscoP. HGlossy15, an APETALA2like gene from maize that regulates leaf epidermal cell identity. Genes & Development, 1996
  199. 199. LiuQKasugaMSakumaYAbeHMiuraSYamaguchi-shinozakiKShinozakiKTwo transcription factors, DREB1 and DREB2, with an EREBP/AP2 DNA binding domain separate two cellular signal transduction pathways in drought- and low-temperature-responsive gene expression, respectively, in Arabidopsis. The Plant Cell, 1998
  200. 200. AgarwalP. KAgarwalPReddyM. KSoporyS. KRole of DREB transcription factors in abiotic and biotic stress tolerance in plants. Plant Cell Reports, 2006
  201. 201. DubouzetJ. GSakumaYItoYKasugaMDubouzetE. GMiuraSSekiMShinozakiKYamaguchi-shinozakiKOsDREB genes in rice, Oryza sativa L., encode transcription activators that function in drought-, high-salt- and cold-responsive gene expression. The Plant Journal, 2003
  202. 202. AbeHUraoTItoTSekiMShinozakiKYamaguchi-shinozakiKArabidopsis AtMYC2 (bHLH) and AtMYB2 (MYB) function as transcriptional activators in abscisic acid signaling. The Plant Cell, 2003
  203. 203. LiangY. KDubosCDoddI. CHolroydG. HHetheringtonA. MCampbellM. MAtMYB61, an R2R3MYB transcription factor controlling stomatal aperture in Arabidopsis thaliana. Current Biology, 2005
  204. 204. RushtonD. LTripathiPRabaraR. CLinJRinglerPBokenA. KLangumT. JSmidtLBoomsmaD. DEmmeN. JChenXFinerJ. JShenQ. JRushtonP. JWRKY transcription factors: key components in abscisic acid signalling. Plant Biotechnology Journal, 2012
  205. 205. HuHDaiMYaoJXiaoBLiXZhangQXiongLOverexpressing a NAM, ATAF, and CUC (NAC) transcription factor enhances drought resistance and salt tolerance in rice. Proc Natl Acad Sci USA., 2006
  206. 206. XuKXuXFukaoTCanlasPMaghirang-rodriguezRHeuerSIsmailA. MBailey-serresJRonaldP. CMackillD. JSub1A is an ethylene-response-factor-like gene that confers submergence tolerance to rice. Nature, 2006
  207. 207. Bailey-serresJVoesenekL. AFlooding stress: acclimations and genetic diversity. Annual Review of Plant Biology, 2008
  208. 208. MustrophALeeS. COosumiTZanettiM. EYangHMaKYaghoubi-masihiAFukaoTBailey-serresJCross-kingdom comparison of transcriptomic adjustments to low-oxygen stress highlights conserved and plant-specific responses. Plant Physiology, 2010
  209. 209. KlokE. JWilsonI. WWilsonDChapmanS. CEwingR. MSomervilleS. CPeacockW. JDolferusRDennisE. SExpression profile analysis of the low-oxygen response in Arabidopsis root cultures. The Plant Cell, 2002
  210. 210. Van DongenJ. TFrohlichARamírez-aguilarS. JSchauerNFernieA. RErbanAKopkaJClarkJLangerAGeigenbergerPTranscript and metabolite profiling of the adaptive response to mild decreases in oxygen concentration in the roots of arabidopsis plants. Annals of Botany, 2009
  211. 211. Branco-priceCKaiserK. AJangC. JLariveC. KBailey-serresJSelective mRNA translation coordinates energetic and metabolic adjustments to cellular oxygen deprivation and reoxygenation in Arabidopsis thaliana. The Plant Journal, 2008
  212. 212. HoerenF. UDolferusRWuYPeacockW. JDennisE. SEvidence for a role for AtMYB2 in the induction of the Arabidopsis alcohol dehydrogenase gene (ADH1) by low oxygen. Genetics, 1998
  213. 213. ChristiansonJ. AWilsonI. WLlewellynD. JDennisE. SThe low-oxygen-induced NAC domain transcription factor ANAC102 affects viability of Arabidopsis seeds following low-oxygen treatment. Plant Physiology, 2009
  214. 214. LicausiFVan DongenJ. TGiuntoliBNoviGSantanielloAGeigenbergerPPerataPHRE1 and HRE2, two hypoxia-inducible ethylene response factors, affect anaerobic responses in Arabidopsis thaliana. The Plant Journal, 2010
  215. 215. Lasanthi-kudahettigeRMagneschiLLoretiEGonzaliSLicausiFNoviGBerettaOVitulliFAlpiAPerataPTranscript profiling of the anoxic rice coleoptile. Plant Physiology, 2007
  216. 216. RizhskyLLiangHShumanJShulaevVDavletovaSMittlerRWhen defense pathways collide. The response of Arabidopsis to a combination of drought and heat stress. Plant Physiology, 2004
  217. 217. Branco-priceCKawaguchiRFerreiraR. BBailey-serresJGenome-wide analysis of transcript abundance and translation in Arabidopsis seedlings subjected to oxygen deprivation. Annals of Botany, 2005
  218. 218. DavenportRJamesR. AZakrisson-ploganderATesterMMunnsRControl of sodium transport in durum wheat. Plant Physiology, 2005
  219. 219. HasegawaP. MBressanR. AZhuJ. KBohnertH. JPlant cellular and molecular responses to high salinity. Annu Rev Plant Physiol Plant Mol Biol., 2000
  220. 220. ChinnusamyVZhuJ. KSunkarRGene regulation during cold stress acclimation in plants. Methods in Molecular Biology, 2010
  221. 221. MunnsRTesterMMechanisms of salinity tolerance. Annual Review of Plant Biology, 2008
  222. 222. MahajanSPandeyG. KTutejaNCalcium- and salt-stress signaling in plants: shedding light on SOS pathway. Arch Biochem Biophys., 2008
  223. 223. GaxiolaR. ALiJUndurragaSDangL. MAllenG. JAlperS. LFinkG. RDrought- and salt-tolerant plants result from overexpression of the AVP1 H+-pump. Proc Natl Acad Sci USA., 2001
  224. 224. ZhangH. XBlumwaldETransgenic salt-tolerant tomato plants accumulate salt in foliage but not in fruit. Nature Biotechnology, 2001
  225. 225. XuDDuanXWangBHongBHoTWuRExpression of a Late Embryogenesis Abundant Protein Gene, HVA1, from Barley Confers Tolerance to Water Deficit and Salt Stress in Transgenic Rice. Plant Physiology, 1996
  226. 226. BriniFHaninMLumbrerasVAmaraIKhoudiHHassairiAPagesMMasmoudiKOverexpression of wheat dehydrin DHN-5 enhances tolerance to salt and osmotic stress in Arabidopsis thaliana. Plant Cell Reports, 2007
  227. 227. GolldackDLükingIYangOPlant tolerance to drought and salinity: stress regulating transcription factors and their functional significance in the cellular transcriptional network. Plant Cell Reports, 2011
  228. 228. ChinnusamyVZhuJZhuJ. KCold stress regulation of gene expression in plants. Trends Plant Sci., 2007
  229. 229. LeeB. HHendersonD. AZhuJ. KThe Arabidopsis cold-responsive transcriptome and its regulation by ICE1. The Plant Cell, 2005
  230. 230. ShinwariZ. KNakashimaKMiuraSKasugaMSekiMYamaguchi-shinozakiKShinozakiKAn Arabidopsis gene family encoding DRE/CRT binding proteins involved in low-temperature-responsive gene expression. Biochem Biophys Res Commun., 1998
  231. 231. MedinaJBarguesMTerolJPérez-alonsoMSalinasJThe Arabidopsis CBF gene family is composed of three genes encoding AP2 domain-containing proteins whose expression Is regulated by low temperature but not by abscisic acid or dehydration. Plant Physiology, 1999
  232. 232. HannahM. AWieseDFreundSFiehnOHeyerA. GHinchaD. KNatural genetic variation of freezing tolerance in Arabidopsis. Plant Physiology, 2006
  233. 233. ChinnusamyVOhtaMKanrarSLeeB. HHongXAgarwalMZhuJ. KICE1: a regulator of cold-induced transcriptome and freezing tolerance in Arabidopsis. Genes & Development, 2003
  234. 234. BenedictCGeislerMTryggJHunerNHurryVConsensus by democracy. Using meta-analyses of microarray and genomic data to model the cold acclimation signaling pathway in Arabidopsis. Plant Physiology, 2006

Written By

Yin Gong, Liqun Rao and Diqiu Yu

Submitted: 15 October 2012 Published: 20 February 2013