Transcriptome Analysis in Chickpea (Cicer arietinum L.): Applications in Study of Gene Expression, Non-Coding RNA Prediction, and Molecular Marker Development

Extensive analyses of transcriptome have been carried out in chickpea, which is the third most important legume valued as a source of dietary protein and micronutrients. Over the last two decades, several laboratories have used a wide range of techniques encompassing expressed sequence tag (EST) analysis, serial analysis of gene expression (SAGE), microarray and next-generation sequencing (NGS) technologies for analysing the chickpea transcriptomes. However, chickpea transcriptome analysis witnessed significant progress with the advent of the NGS platforms. Gene expression analyses using NGS platforms were carried out in the vegetative and reproductive tissues such as shoot, root, mature leaf, flower bud, young pod, seed and nodule by various groups which resulted in identification of several tissue-specific transcripts. Some laboratories have utilized transcriptomics to explore the response of chickpea to abiotic and biotic stresses such as drought, salinity, heat, cold, Fusarium oxysporum and Ascochyta rabiei differentially expressed genes and also established crosstalk between biotic and abiotic stress responses. Transcriptome analysis has been utilized extensively to identify non-coding RNAs such as miRNAs and long intergenic non-coding (LINC) RNAs. Transcriptome analysis has facilitated the development of molecular markers such as simple sequence repeats (SSRs), single-nucleotide polymorphisms (SNPs) and potential intron polymorphisms (PIPs) that are being used to expedite the chickpea breeding programmes. The available chickpea transcriptomes will continue to serve as the foundation for devising strategies for chickpea improvement.


Introduction
Chickpea (Cicer arietinum L.) is a diploid (2n = 16), self-pollinated plant which is grown in the cool season and has a genome size of 738 Mb [1].It is the third most produced pulse crop in the world (13.73 million tons) after beans (26.52 million tons) and green pea (17.43 million tons) (FAOSTAT 2014).It is considered to be an ideal crop for the semiarid and arid regions as it exhibits an extensive tap root system.Chickpea seeds are an excellent source of nutrition as they contain ≈40% carbohydrates, ≈6% oil and 20-30% protein and good source of minerals and trace elements such as calcium, magnesium, phosphorus, iron and zinc [2].Moreover, chickpea contributes to improvement of soil fertility since it has the capability to establish symbiotic association with Mesorhizobium ciceri that helps in fixing atmospheric nitrogen to the reduced nitrogen (NH 3 ).Chickpea, through symbiotic nitrogen fixation (SNF), can fulfil up to 80% of its nitrogen requirement [3].All these qualities make chickpea an economically important crop as it is an affordable source that can fulfil the dietary protein requirement of the masses.

Challenges in chickpea production
The world average of chickpea productivity is 982.1 kg/ha (FAOSTAT 2014); however, a simulated study showed that potential productivity of chickpea in rain-fed situations ranged from 1390 to 4590 kg/ha [4].There is a huge yield gap of 408-3608 kg/ha.A number of biotic and abiotic factors affect chickpea plant growth and, therefore, are responsible for poor productivity.
Chickpea is mostly raised on conserved soil moisture under rain-fed conditions [5].Therefore, drought stress generally affects the crop at terminal stage [6] and leads to productivity loss of up to 50% [7].Drought reduces overall biomass, reproductive growth and seed yield and increases flower abortion, pod abscission and number of empty pods [8].Soil salinity affects productivity by delaying the flowering leading to decrease in reproductive success of chickpea [9].Since chickpea is a cool season crop, high temperatures adversely affect the development of the plant [10].Chander [11] reported a decline in yield of chickpea by about 301 kg/ha per 1°C increase in mean seasonal temperature in India [12,13].Biotic factors also adversely affect the yield of chickpea crop.Fusarium wilt, caused by Fusarium oxysporum f.sp.ciceri; Ascochyta blight, caused by Ascochyta rabiei and Botrytis grey mould, caused by Botrytis cinerea mainly affect the leaves of chickpea, whereas Pythium ultimum causes root and seed rot and is common in the areas where the chickpea growing season is cool and humid [14,15].A number of other fungi, such as Alternaria sp., Ascochyta pisi, Uromyces sp., Botrytis sp., Phytophthora medicaginis and so on, cause considerable damage to chickpea crops.Pod borer (Helicoverpa armigera Hubner) is the major pest affecting chickpea worldwide [15][16][17].Therefore, improvement in yield, nutritional quality and stress tolerance are the major targets of chickpea research and breeding programmes which may be facilitated by detailed understanding of biological processes occurring in tissue-specific and developmental pathways.Moreover, responses to various stresses at molecular level also need to be elucidated in detail.
Applications of RNA-Seq and Omics Strategies -From Microorganisms to Human Health

Legume genomics
With the advent of next-generation sequencing technologies, there has been a rapid increase in the efficiency of DNA and RNA sequencing and decrease in the cost involved.Leguminosae is a very important family known due to the economic and nutritional value of its members [18].The recent years have witnessed a spurt in the number of studies utilizing genomic approaches to understand the biology of several agronomic traits in legumes.
Next-generation sequencing (NGS)-based plant genomics has also assisted in understanding of genetic variation within and between species mostly through identification of single-nucleotide polymorphisms (SNPs).In chickpea, a number of studies have been performed to identify SNPs and utilized for various applications such as construction of linkage maps, synteny analysis, anchoring of whole genome sequencing and quantitative trait loci (QTL) analysis [44][45][46][47][48][49].A CicArVarDB has also been developed which includes SNP and InDel variations in chickpea [50].

Transcriptome
A cell undergoing a functional or developmental process has a specific set of genes undergoing transcription at a particular time and is collectively called the 'transcriptome'.Thus, a transcriptome represents up to an extant physical, biochemical and developmental status of a cell.A transcriptome represents a pool of protein coding as well as nonprotein-coding RNAs; moreover, there may be the presence of variants of genes originating from alternative splicing and RNA editing, making the transcriptome more complex than a genome.Study of transcriptome may reveal information regarding spatial and temporal expression patterns of genes, and therefore it is possible to generate global expression profiles of genes representing developmental stages of an organism [34].However, with the advent of NGS and the simultaneous development of in silico analytical tools, global genome and transcriptome analysis has become a standard practice for deriving information to relate genotype to phenotype.However, it is not possible to sequence the transcripts to the full length due to technological limitations.Transcriptome analysis is based on the principle that the depth of coverage of a sequence is proportional to the level of expression of the corresponding gene.Therefore, by mapping and counting the sequenced reads onto the given transcript, expression can be measured, thereby translating sequence information to some biologically significant information.A host of NGS technologies such as sequencing by synthesis (Illumina Inc., USA), SOLiD (ThermoFisher Scientific) and pyrosequencing (454 biosciences/Roche) has provided unprecedented opportunities for high-throughput functional genomic research [51][52][53].Moreover, a number of technologies for transcriptome sequencing are emerging such as The Ion Torrent (ThermoFisher Scientific), single-molecule real time (SMRT) (Pacific Biosciences, USA) and Nanopore (Oxford Nanopore Technologies, UK).

Using transcriptome analysis for studying biological processes in chickpea
Extensive transcriptome analysis has been carried out in chickpea in order to gain insights into the numerous biological processes.Techniques, such as EST sequencing, SAGE and most importantly the NGS, have been used to analyse the transcriptomes of root, shoot, flower, seed and nodule tissues in order to understand the tissue-specific development and function.Several were reported and used to develop the 'Chickpea Root Expressed Sequence Tag Database' [54].
A major advancement in transcriptome analysis for understanding developmental and biological processes occurred with the advent of the NGS platform.Several large-scale NGS-based transcriptome analyses were carried out in chickpea [34][35][36].In one of the first NGS-based  [34].These sequence reads generated by the Roche/454 platform were merged with the Illumina reads from the previous study, and a hybrid assembly was generated [34], which resulted in 34,760 tentative consensus (TC) transcripts.Of these, 1851 transcripts were annotated as transcription factors belonging to 84 families.This analysis also led to the identification of 1132, 695, 513, 408 and 126 TCs specifically expressed in flower bud, young pod, shoot, root and mature leaf, respectively.The complete data were integrated leading to the development of the 'Chickpea Transcriptome Data Base' (CTDB) which provides a searchable interface to the chickpea transcriptome data [34].Further, transcriptome analysis of the wild progenitor of chickpea, i.e.Cicer reticulatum PI489777, was also performed by Jhanwar et al. [37].Moreover, transcriptomes of the kabuli, desi and wild chickpeas were compared [55] and used to create an improved version of the Chickpea Transcriptome Data Base V2.0 [56].
Flower development is an important and specialized process that takes place in angiosperms.
Hence, in order to gain insights into the molecular mechanisms responsible for flower development in chickpea, transcriptome analysis was carried out using the Illumina sequencing platform [38].Transcriptome sequencing of eight successive developing stages of flower (flower buds at sizes 4, 6, 8 and 8-10 mm and flowers with closed petals, partially opened petals, opened and faded petals and senescing petals) along with young leaf, germinating seedling and shoot apical meristem was carried out.Differential expression analysis revealed 1572 genes to be differentially expressed in at least one stage of flower development.A number of 1118 genes (908 upregulated and 201 downregulated) and 966 genes (857 upregulated and 109 downregulated) were found to be differentially regulated in flower bud and flower developmental stages, respectively [38].The majority of the differentially expressed genes were found to be involved in various flower developmental pathways such as floral organ identity; development of corolla, androecium and gynoecium and gametophyte development.Moreover, genes related to cell wall development and transport were also found to be differentially expressed.In addition, 111 TF genes were found differentially expressed in floral bud and flower.
Chickpea is most valued for its seeds since they serve as a source of protein, especially for vegetarian population.Therefore, a thorough understanding of the transcriptional flux during seed development is important in order to get insights into the biological processes that define the seed.Towards this, an NGS-based deep transcriptome analysis of chickpea seed at four developmental stages, i.e. 10 days after anthesis (DAA), 20 DAA, 30 DAA and 40 DAA, was carried out [39].The transcriptome was sequenced using the 454 pyrosequencing on the GS-FLX Titanium platform followed by its assembly into 51,099 transcripts.A gene ontology enrichment of seed-specific genes revealed genes related to reproductive structure development, fruit development and embryonic and post-embryonic development to be highly represented.Many metabolic pathways such as proteolysis, lipid metabolic process, regulation of RNA metabolic process, regulation of transcription, terpenoid metabolic process and gibberellin metabolic processes were also found to be significantly represented [39].In another study, sequencing of ESTs from the chickpea embryo resulted in identification of 1480 unigenes expressed during embryo development [57].The analysis also identified 12 genes encoding for F-box proteins, of which 2 F-box genes (CarFbox_PP2 and CarF-box_LysM) were predicted to be involved in seed development [57].
Another important distinctive feature of chickpea is its ability to form symbiotic relationship with M. ciceri which results in the formation of specialized structures called root nodules.
These are formed by the host plant and protect the oxygen-sensitive, bacterial nitrogen fixing machinery.It is a complex phenomenon and a detailed understanding of the molecular pathways governing that the process of nodule development and nitrogen fixation would certainly help plant scientists in developing sustainable farming strategies for chickpea.Towards this, a DeepSuperSAGE-based transcriptome analysis led to the identification of 71 genes being differentially expressed in root nodules [58].Further, in order to understand the root nodulation in greater depth, a deep transcriptome analysis of the chickpea root nodule at different developing stages was carried out using the 454 pyrosequencing [40].Sequencing of transcriptomes of uninfected root and three developing stages of nodules followed by reference-based assembly resulted in 83,405 transcripts.Of these 3760 were found to be differentially expressed in at least one of the stages of nodule when compared to uninfected root.Also, 1606 transcripts were identified as transcription factors, of which 171 TFs were found to be differentially expressed during nodulation.

Using transcriptome analysis for study of stress response in chickpea
Transcriptome analysis has been utilized exclusively to study different abiotic and biotic stress responses in chickpea.Drought and salinity are the major factors that limit the growth and productivity of the plants.Terminal drought is thought to be a major constraint affecting productivity of chickpea as it can lower the yield of chickpea by about 50% [59].Cold stress also affects susceptible chickpea mainly at the reproductive stage where it leads to pollen sterility and flower abortion [60].Thus, it is important to study the response of chickpea under these stress conditions in order to devise strategies for development of stress-tolerant chickpea.Earlier studies based on EST sequencing, SAGE and microarray provided preliminary evidence for drought responses of chickpea at transcriptome level [61][62][63][64][65][66].An EST sequencing-based study of drought and salinity stress in chickpea resulted in generation of 20,162 ESTs, of which 105 were found to have differential expression during one of the stresses [65].In another comparison between ESTs generated from chickpea, ICC 4958 (drought tolerant) and ICC 1882 (drought resistant) varieties resulted in identification of 5494 drought-responsive ESTs [61].A microarray-based transcriptome analysis of root and leaf of chickpea under drought stress resulted in identification of 4815 differentially expressed genes.
Approximately 2623 and 3969 genes were found to be differentially expressed, whereas 88 and 52 genes were found to be specifically expressed during drought stress in root and leaf tissues, respectively [66].Another microarray analysis in chickpea revealed 109, 210 and 386 Applications of RNA-Seq and Omics Strategies -From Microorganisms to Human Health genes to be differentially expressed in drought, cold and high-salinity stresses, respectively [62].A SuperSAGE-based transcriptome analysis of chickpea drought stressed and control tissues gave rise to 17,493 unique transcripts (UniTags) of which 7532 were differentially expressed in drought stress [63].Another SuperSAGE followed by 454 sequencing of root nodule transcriptome of salt-tolerant variety INRAT-93 identified 363 and 106 genes to be upregulated and downregulated, respectively, in root and nodule tissues [64].
The more global view of stress response in chickpea was provided by the study of Garg et al. [41] in which the transcriptome of chickpea root and shoot under desiccation, salinity and cold stress was analysed.The Illumina sequencing-based transcriptome and comparison revealed 11,640 transcripts to be differentially expressed during at least one of the stresses.Seven hundred forty-five transcription factors (TFs) were also found to be differentially regulated in at least one stress condition.Moreover 3536 unannotated genes from the chickpea transcriptome were also identified [41].A more detailed transcriptome analysis of drought-tolerant (ICC 4958), drought-sensitive (ICC 1882), salinity-tolerant (JG 62) and salinity-sensitive (ICCV2) chickpea varieties resulted in identification of 18,462 transcripts representing 13,964 unique loci in at least one sample/stress condition.The study also revealed 4954 and 5545 genes exclusively regulated in drought-tolerant and salinitytolerant varieties.A number of 775 TFs encoding genes belonging to 80 families were also found differentially regulated in stress conditions.Members of the bHLH, WRKY, NAC, AP2-EREBP and MYB were found among the top differentially expressed TFs in stress condition [42].In order to understand the effect of cold stress, AFLP-based transcript profiling (cDNA-AFLP) approach was used [67], which showed that in cold-tolerant chickpea, 102 transcript-derived fragments (TDFs) were differentially expressed during cold stress.Moreover, transcriptome analysis of cold-tolerant chickpea ICC 16349 using cDNA differential display (DDRT-PCR) resulted in identification of 127 ESTs as differentially expressed in anthers during cold stress conditions.
Ascochyta blight caused by A. rabiei and Fusarium wilt caused by F. oxysporum are major fungal diseases of chickpea.In order to understand the response of chickpea to A. rabiei, an EST library sequencing of blight-resistant chickpea variety ICC 3996 infected with A. rabiei was performed by Coram and Pang [68].The study reported 516 genes of which 4% were related to defense and found to encode for lignin and phytoalexin biosynthesis enzymes, pathogenesisrelated proteins, signalling proteins and putative-defensive proteins [68].For further identification of resistance-related genes, transcriptome analysis of four genotypes, C. arietinum ICC 3996, C. arietinum Lasseter, C. arietinum FLIP94-508C and Cicer echinospermum ILWC245, was performed using 756 featured microarrays.The study revealed 97 genes to be differentially expressed upon infection with A. rabiei.A comparison between resistant and susceptible varieties identified many genes such as pathogenesis-related proteins, SNAKIN2 antimicrobial peptide, proline-rich protein, disease resistance response protein DRRG49-C, environmental stress-inducible protein, leucine-zipper protein, polymorphic antigen membrane protein and Ca-binding protein, which might be responsible for imparting resistance to the tolerant varieties [69].On the other hand, in order to identify genes involved in wilt resistance in chickpea, EST sequencing followed by microarray analysis of chickpea wilt susceptible genotype (JG-62) and resistant genotype (WR-315) was performed after infecting them with F. oxysporum ciceri.The analysis resulted in identification of 257 differentially expressed genes associated with the early signalling pathway [70].In order to understand the differential response of susceptible and tolerant/resistant chickpea varieties to F. oxysporum, transcriptomes of wilt susceptible (JG62) and wilt-tolerant/wilt-resistant (ICCV2, K850 and WR315) chickpea varieties were analysed using the Illumina platform.Comparison among the transcriptomes led to identification of 303 polymorphic SSRs, 14,462 SNPs and 1864 insertions/deletions (InDels).
Moreover, a large number of SNPs and/or InDels were found to be present in defence-related genes [43].
In order to identify common genes between biotic and abiotic responses in chickpea, Mantri et al. [71] performed microarray analysis of chickpea ICC 3996 under three abiotic stresses (drought, cold and high salinity) and biotic stress (infection with A. rabiei).This analysis revealed 46, 54, 266 and 51 genes to be differentially regulated in drought, cold, high salinity and A. rabiei stresses, respectively.A. rabiei stress response was found to be more similar to that of high-salinity stress [71].

Transcriptome analysis for non-coding RNA studies in chickpea
Non-coding RNAs usually act as regulatory elements that have a decisive role in fine regulation of gene activity.Non-coding transcripts comprise of small and long non-coding RNAs.Small non-coding RNAs regulate diverse developmental processes by controlling gene expression at transcriptional and post-transcriptional level [72,73].MicroRNAs (miRNAs) constitute the major class of small non-coding RNAs and are 20-24 nucleotides long key regulatory elements.They are highly conserved and play an important part in various developmental processes in plants such as leaf development, flowering, formation and maintenance of the shoot, floral and axillary meristems, establishment of organ polarity, root nodule symbiosis, vegetative to reproductive phase transition and response to biotic and abiotic stresses [73][74][75][76][77].In chickpea, small RNA libraries were sequenced from normal tissues and those under different stress conditions [78][79][80].Small RNA sequence data were filtered and processed for miRNA prediction using miRDeep pipeline resulting in identification of distinct conserved miRNAs from shoot (302, including Cat-miR156b-5p, Cat-miR156j.1,Cat-miR159.1, Cat-miR169b-5p), root (280, including Cat-miR156c.1,Cat-miR169n, Cat-miR171k-3p), mature leaf (248, including Cat-miR156k, Cat-miR172d.2,Cat-NovmiR319b, Cat-miR167a, Cat-miR167d.2),stem (268, including Cat-miR172c-3p, Cat-miR159.3,Cat-NovmiR319d, Cat-miR171k-3p), flower bud (247, Cat-miR319g.2,Cat-miR167c.2,Cat-miR167d.1,Cat-miR171b-3p.2),flower (293, Cat-miR159.4,Cat-miR159e, Cat-miR171m) and young pod (274, Cat-miR172d.1,Cat-NovmiR159a, Cat-miR167-5p).By ab initio prediction, a total of 109, 76, 123, 100, 106, 98 and 120 novel candidate miRNAs were identified from the above tissues, respectively.Overall 618 miRNAs were identified from all the tissues with the maximum being 373 miRNAs from the shoot and minimum 303 from flower buds.Of the 618 miRNAs predicted, 158 were present in all the tissues, and 29% of the miRNAs were found to be tissue specific.Of the 618 miRNAs, 421 were clustered to 73 miRNA families, and 197 could not find similarity to any miRNA family and were termed putative novel.Chickpea miRNAs targeted a wide range of transcripts involved Applications of RNA-Seq and Omics Strategies -From Microorganisms to Human Health in diverse cellular processes including protein turnover and modification, metabolism, transcriptional regulation and signal transduction [78].A similar kind of study performed in leaf and flower tissue resulted in the prediction of 96 highly conserved miRNAs belonging to 38 miRNA families and 20 novel miRNAs belonging to 17 miRNA families in chickpea [80].In addition to identification of miRNA from different tissues, studies were also conducted for characterization of miRNA in response to different biotic and abiotic stresses.In one such kind of study, three libraries were sequenced for small RNA identification [79].Libraries were constructed from fungal-infected (F.oxysporum f.sp.ciceris), salt-treated and untreated seedlings of chickpea and were sequenced using the Illumina GAIIx platform.The analysis identified 122 conserved miRNAs belonging to 25 different families along with 59 novel miRNAs.
miR156, miR396 and miR319 were upregulated in response to salt stress.miR156 and miR396 expression was found to be 1.5 times upregulated in both wilt and salt stresses, indicating a common mechanism implied by chickpea involving these miRNAs to cope up with both the stresses.miR530 was found to be significantly upregulated during wilt stress and may be involved in defence to fungal infection.Three legume-specific miRNAs, miR2111, miR2118 and miR5213, were also indicated to play a critical role in defence to pathogen attack.Targets of miR2111 include F-box protein and TIR (Toll/Interleukin-1 Receptor) domain-containing NBS-LRR disease-resistance proteins, and miR2118 and miR5213 also target the same class of R genes.Interestingly, miR2118 is upregulated following wilt infection and downregulated following salt stress [79].
Long intergenic non-coding (linc) RNAs belong to a class of non-coding transcripts which have a length of at least 200bp lacking coding potential and are transcribed from intergenic region of protein coding genes [81,82].Linc RNAs control gene regulation at transcriptional and post-transcriptional level by mechanisms including chromatin modification, promoter binding complex attachment and shielding mRNA degradation by acting as sponge against miRNA [83][84][85].RNA-seq data from 11 different tissues of chickpea were used for mining linc-RNA [86].RNA-seq data were processed using TopHat2 and Cufflinks program using chickpea genome as the reference.From 32,984 transcripts obtained, 5782 putative intergenic transcripts were extracted out and subjected to the optimized pipeline for identification of linc-RNA.After removing potential coding transcripts and transcripts having similarity to protein domains, finally a total of 2248 transcripts were retained as putative chickpea linc-RNAs.About 79%, i.e. 1790 linc-RNAs, could be assigned a putative function.Through expression profiling it was evident that a large number of linc-RNAs have tissue-specific expression in distinct tissues.Along with this several linc-RNAs were found to be targets of miRNAs and were involved in various developmental and reproductive processes [86].

Expanding transcriptome data to aid development of molecular markers
A DNA-based molecular marker is a DNA sequence with an identifiable location on the genome that can be transmitted from one generation to the next following the standard laws of inheritance [87].Recent years have witnessed an immense interest in generation and utilization of molecular markers, as they provide the essential tools for a variety of genomic applications such as QTL mapping, map-based cloning, marker-assisted breeding, association mapping and genetic diversity assessment.These approaches can be applied to understand the genomic architecture of the crop and can expand the efficiency of breeding programmes, thereby aiding to expedite agricultural research.The advent of NGS has enabled the exploration of thousands of markers across entire genomes and transcriptomes.Although transcriptomics has been majorly used for gene expression analysis, it has also been utilized to identify molecular markers such as SSRs and SNPs especially in the genic regions.Such gene-based markers located in coding regions of the genes greatly enhance the opportunity of precise mapping of genes linked to important traits.[92].However, currently transcriptomic resources can be easily generated by high-throughput NGS technologies and utilized to identify molecular markers very rapidly and cost-effectively.Hiremath et al. [36] utilizing the Roche platform generated about 3000 gene-based markers from a large subset of transcripts derived from different chickpea tissues.Currently, SNPs are the markers of choice and are preferred over the SSRs and other markers because of their genome-wide presence and amenability to high-throughput genotyping.Theoretically, SNP calling may be defined as the process of identifying a single-nucleotide variation from an accession read that differs from the existing reference genome or a de novo assembly at similar nucleotide position.Read assembly files generated by mapping programs such as BWA, Bowtie and SOAP are used to perform SNP calling.Bioinformatics tools such as HaploSNPer [93], SAMtools [94,95], POLYBAYES [96], SNVer [97] and SOAPsnp [98] have been designed to detect the variations in the NGS data.Comparison of transcriptome datasets from contrasting genotypes could help derive SNPs.To date, several studies have been carried out using NGS technology-based transcriptome sequencing to generate large sets of molecular markers in various crop species including chickpea.For instance, a report by Garg et al. [35] facilitated identification of 4816 SSRs from the de novo assembly of the chickpea transcriptome.
In another study, sequencing the transcriptome of C. reticulatum (PI489777), the wild relative of chickpea, by GS-FLX 454 technology, generated a total of 4072 SSRs and 36,446 SNPs.
Likewise, Agarwal et al. (2012) sequenced the transcriptome of ICCV2 and identified 5409 SSRs.Amongst these, 130 and 493 SSRs were found to be polymorphic after comparing with the transcriptome of desi and wild chickpea.In addition to the SSRs, a total of 1986 and 37,954 SNPs were also identified between the desi, kabuli and wild genotypes.Similarly, in another study, 51,632 genic SNPs were identified by 454 transcriptome sequencing of C. arietinum and C. reticulatum genotypes [99].In a recent study, Srivastava et al. [100] identified 11,621 differentially expressed genes in root vs shoot tissues using RNA sequencing of a wild perennial Cicer microphyllum and integrated above transcriptome profiling with high-resolution QTL mapping in order to identify drought-responsive root-specific genes.The transcriptomic resources, therefore, clearly have remarkable potential to expedite the development of large numbers of molecular markers which can be used in genomic-assisted breeding for developing improved varieties of chickpea.

Future perspectives
The last few years have witnessed legume genomics attaining new heights as genomes, and transcriptomes of many model legumes (M.truncatula, L. japonicus) and crop legumes (G.max, C. cajan, P. vulgaris, Arachis hypogaea, Vignas, etc.) were sequenced.Transcriptomes of both types of cultivated chickpea (desi and kabuli) and its wild progenitor (C.reticulatum) have also been sequenced.Several studies have been carried out to analyse the transcriptome of chickpea which have led to genome-wide determination of transcript levels in various tissues and developmental pathways as well as during biotic and abiotic stresses.This comprehensive analysis of the chickpea transcriptome has advanced the understanding of the molecular mechanisms underlying several critical biological pathways in chickpea.Moreover, analyses of the non-coding RNAs have revealed potential regulators of important pathways affecting the overall development and stress tolerance in chickpea.Further, transcriptome analysis has also facilitated the development of large sets of genic molecular markers such as SSRs and SNPs that will serve as excellent tools for advancing the chickpea breeding programmes.Overall, the transcriptome sequencing of chickpea has not only provided a deep insight into the gene space and quantitation of gene expression but also an opportunity to isolate genes of interest and functional markers for use in chickpea improvement.
groups undertook EST sequencing, and till date (March 2017) 53,333 chickpea ESTs are reported in the NCBI database.In another earlier study of the root transcriptome, an EST library was constructed by subtractive suppressive hybridization (SSH) of two related chickpea varieties, ICC 4958 and Annigeri, as they show different root traits.Sequences of more than 2800 ESTs

. Methods for transcriptome analysis
Applications of RNA-Seq and Omics Strategies -From Microorganisms to Human Health studies, the Illumina sequencing of transcriptome of chickpea genotype ICC 4958 root and shoot followed by de novo assembly resulted in generation of 53,409 transcripts.Of these 34,676 transcripts were annotated, and 6577 transcripts were identified as transcription factors (TFs) belonging to 57 families.Another study by Garg et al. reported the Roche/454-based transcriptomes of 'shoot', 'root', 'mature leaf', 'flower bud' and 'young pod' of chickpea geno- Transcriptome Analysis in Chickpea (Cicer arietinum L.): Applications in Study of Gene... http://dx.doi.org/10.5772/intechopen.69884 Transcriptome Analysis in Chickpea (Cicer arietinum L.): Applications in Study of Gene... http://dx.doi.org/10.5772/intechopen.69884 [90]scriptome sequencing offers another advantagefor those crops in which a reference genome is not available.To identify SSRs from transcriptome data, several bioinformatics tools have been developed such as MISA (MIcroSAtellite identification tool) (pgrc.ipk-gatersleben.de/misa/),RISA(RapidIdentification of SSRs and Analysis of primers) (http://sol.kribb.re.kr/RISA/) and RepeatAnalyzer[88].In chickpea, initially a large number of molecular markers were derived from ESTs.Buhariwalla et al.[89]reported 106 EST-based markers developed from an EST library of root tissue from chickpea.In another study by Choudhary et al.[90], 2131 ESTs were utilized for development of 246 EST-SSR markers.Apart from SSRs, several types of markers such as ESTPs, PIPs and EST-SNPs were developed in chickpea using transcriptome data.For instance, Choudhary et al.