Each time a cell divides it must duplicate its DNA content and segregate it equally between two daughter cells. Once a cell has decided to replicate its DNA, hundreds of different proteins must carefully interact with each other in a very orchestrated process. Defects in any of these steps can lead to cell death and genetic instability and have been shown to be present in many human diseases including cancer . Each step of DNA replication must take place in a correct spatial and temporal window, so cells have evolved complex regulatory networks allowing an efficient regulation of this process. One important feature of eukaryotic cells is that DNA is strongly associated with histones, basic proteins that wrap DNA around octameric structures called nucleosomes. The association of DNA and nucleosomes is commonly known as chromatin.
Nucleosomes are, among others, one of the principal differences between eukaryotic and prokaryotic DNA. Unlike bacteria, eukaryotic cells are not able to live without DNA packed into chromatin . Replication involves dramatic changes in the whole chromatin landscape, since nucleosomes must be removed transiently from the front of the replication machinery and repositioned after it. Nucleosome disassembly and assembly involves the action of chromatin remodeling factors, proteins able to destabilize interactions between histones and DNA allowing the interaction of other complexes with DNA. Restoration of chromatin after the replication bubble is a very important step because nucleosomes are not repetitive units of information and contain a specific epigenetic signature or code . In order to ensure enough histones for the nascent DNA, cells must increase the pool of free histones. In human cells, each passage through S-phase requires the synthesis and assembly of almost 30 million nucleosomes that are synthesized mainly during S-phase and are rapidly packaged to DNA. Histone production is very tightly coupled to DNA synthesis and is rapidly shut off when replication finishes or is halted by treatment with mutagenic agents. Histone regulation is very important and accumulation of free histones in the cell has been shown to be highly deleterious for the cell and lead to chromosome loss .
Chromatin is a structural barrier for replication but can also play an important role in the regulation of some of the steps within. In this chapter, we will focus on how the chromatin landscape influences DNA replication and show that histones and DNA must adapt to each other in order to ensure a correct genomic duplication. We will describe the influence that chromatin plays at the different stages of DNA replication and then jump to the accurate control that cells exert on histone levels during the cell cycle. We will finally show different situations that uncouple DNA replication from histone deposition and synthesis, and discuss if chromatin state can influence the decision of cells to replicate their DNA or not.
2. Replication from a chromatin point of view
2.1. Chromatin influences early steps of replication
The initiation of DNA replication in any organism requires a series of proteins able to recruit and ultimately load two hexameric DNA helicases. These proteins are able to unwind DNA, a process required to start replication. In eukaryotic cells the pre-initiation complex is formed by two MCM2-7 rings that are loaded in an inactive form next to the Origin Recognition Complex (ORC). The MCM helicase must be activated by the sequential action of Dbf4 Dependent Kinase (DDK) and Cyclin Dependent Kinase (CDK), and the addition of other accessory proteins. In mammalian cells, 30,000 to 50,000 origins are sequentially activated each time a cell divides .
The nature of the sequence and the structure of replication origins is still a matter of debate, and most higher eukaryotes lack a specific consensus sequence for ORC binding. Origins of DNA Replication Initiation (ORIs) are normally regions of DNA sequence rich in AT that contain a nucleosome-free region (NFR)   and it has been suggested that the chromatin environment is important for the establishment of the ORC complex  . In
As ilustrated in figure 1, methylation of histone H4 has also been shown to be important for ORC recruitment and artificial tethering of the methyltransferase SET8 to a random locus promotes ORC1 binding . Once ORC is bound to DNA, proteins CDC6 and CDT1 help to load the two MCM2-7 helicases to DNA . Loading could also be influenced by the acetylation of histone H4, since CDT1 is able to recruit the histone acetyltransferase HBO1 to the ORC and enhances the recruitment of MCM2-7 to the origin [12, 13] . Nevertheless, some ORC and MCM subunits are acetylated by Hbo1 in yeast and could therefore be the real targets of this enzyme . Although all origins that are selected are able to load the pre-initiation complex, only one out of every ten will fire. Regulation of firing depends on the activation of the MCM helicases by sequential phosphorylation of some of its subunits by DDK and CDK kinases, that allow the recruitment of CDC45 and the GINS complex . Once these proteins are loaded, the rest of the replication machinery is recruited and replication starts.
Two interesting observations have lead to the hypothesis that chromosome architecture can also be important for origin usage. One of them is that origins seem to be organized into clusters of 5 to 10 origins that fire simultaneously . Cohesins are enriched next to origins and depletion of the RAD21 cohesin subunit greatly reduces the number of active origins. This ring-like complex is able to wrap two chromatin fibers and creates a chromatin loop. It has been suggested that this spatial organization of chromatin could define replication domains that are activated synchronously [16, 17]. In agreement with this hypothesis, analysis of the oriGNA13 replication origin of hamster cells shows that active origins localize close to the base of chromatin loops . The second feature that directly relates chromatin structure and replication is that genome replication does not take place in a single and continuous way. Domains containing several megabases of contiguous DNA are replicated earlier than others  and this replication timing is somehow correlated with acetylation levels of histone H4 at the K16 residue .
Chromatin influences the recruitment and the activity of different elements of the replication machinery. Once this machinery has been set up and is fully active, fork progression must now cope with the fact that approximately every 192 bp there is a nucleosome that must be displaced from DNA in order to continue with replication.
2.2. Nucleosome reorganization around the replication fork
Replication fork progression involves many proteins that interact closely with DNA. Electron micrography of replicating SV40 mini-chromosomes has shown that 300bp ahead of the replication fork, DNA remains
Nucleosome disassembly and reassembly are processes quite well described for transcription. The efficiency of these processes is largely dependent on chromatin-remodeling complexes, proteins able to interact with and change the stability of chromatin, allowing the transcription machinery to interact with DNA. There are many different chromatin-remodeling complexes and all of them are possible candidates for nucleosome eviction during replication. The fact that chromatin disassembly and assembly occur in such a small spatial window makes it very difficult to distinguish between the complexes required for one or the other process. There are two major complexes that could be involved in H2A/H2B displacement during replication: FACT and NAP1, and another two for H3/H4: Asf1 and CAF1.
The FACT complex is composed of two main subunits, SPT16 and SSRP1 (Pob3 in
To date, it is not known if H2A/H2B dimers removed during replication are recycled. On the contrary, it is well established that the original H3/H4 tetramer present in front of the replication fork machinery is restored after the replication fork in a random semi-conservative process . The fact that the H3/H4 tetramer is recycled suggests that a histone chaperone must disassemble this tetramer in front of the replication machinery and reassemble it after. One good candidate for this process is Asf1. This protein along with Chromatin Assembly Factor 1 (CAF1) plays a key role in deposition of new H3/H4 following passage of the replication fork. Asf1 binds PCNA and replication factor C , and can also bind the MCM helicase complex through histones H3 and H4. Upon a replication fork progression block, Asf1 can be found associated with post-translationally modified H3/H4 histones, which most likely belong to the parental chromatin .
Deposition of histone octamers occurs as soon as DNA is long enough to wrap around a nucleosome . Since one H3/H4 tetramer is recycled after DNA replication, one new H3/H4 tetramer must be deposited on the other strand. The mechanism of reposition of the original H3/H4 tetramer remains unclear but probably involves Asf1 (see previous paragraph). Incorporation of the new H3/H4 tetramer on the other hand is more defined and involves the action of CAF1 and Asf1. CAF1 is recruited to both leading and lagging strands by the proliferating cell nuclear antigen PCNA. Depletion of CAF1 produces a clear decrease in the assembly of new chromatin during replication , activates the DNA Damage Checkpoint (DDR), and stalls replication forks , suggesting that efficient chromatin repositioning after replication is important for replication fork progression. Asf1 plays a role in this process as a histone pool protein that delivers H3/H4 dimers to CAF1. After the H3/H4 tetramer is assembled, H2A/H2B becomes incorporated into chromatin in a process that probably involves FACT or NAP1. Finally, H1 protein is incorporated to allow further compacting of chromatin. Incorporation of H1 is probably mediated by the NASP protein and is required for efficient S-phase progression .
One interesting feature recently described is that the chromatin landscape influences the length of the Okazaki fragments synthesized at the lagging strand during DNA replication . Due to the 5´to 3´ polarity of DNA polymerase, synthesis of DNA in the lagging strand is discontinuous and generates short fragments of DNA named Okazaki fragments. These fragments must then join to form a unique DNA strand in a process known as maturation. Okazaki fragment maturation requires the sequential action of the flap endonuclease 1 (FEN1) and DNA ligase I. This group has demonstrated that the ligation junctions of Okazaki fragments are preferentially located in the nucleosome midpoint. The length of Okazaki fragments depends on the chromatin behind the replication fork and mutations that impair chromatin repositioning increase the average size of Okazaki fragments. According to their model, Pol runs into the nucleosome assembled into the previous Okazaki fragment and this triggers termination, flap processing and ligation.
2.3. Chromatin maturation and centromere formation
After nucleosome incorporation to DNA, two major processes must take place: chromatin maturation and centromere formation. Histones start to acquire certain modifications in their tails as soon as they are repositioned to DNA. Nascent chromatin is highly acetylated and must be deacetylated and methylated to reach a more compact state. Deacetylation normally takes place by the histone deacetylases HDAC1-3 and DNA methylation by the DNA methyltransferase 1 (DNMT1). In addition to chromatin compacting, there are also some specific post-transcriptional modifications that must be acquired to establish a specific epigenetic code that is transmitted to daughter cells. Maintaining this “epigenetic memory” of daughter cells is important and has implications during cell differentiation (23). Restoration of all these marks does not take place exclusively in replication and can also take place during mitosis or even in daughter cells [38, 39]. Replication of the chromatin near the centromere is also vital to ensure an efficient segregation during mitosis. This heterochromatin presents a specific variant of histone H3 named CENP-A, which is essential for the efficient binding of the kinetochore during mitosis. The kinetochore is a huge structure that attaches to centromeric DNA and mediates the interaction of chromosomes with the mitotic spindle and their movement to the spindle poles during mitosis . Accurate segregation of chromosomes relies on the correct formation of the spindle apparatus.
CENP-A (also known as CENH3) is an essential protein that replaces histone H3 at centromeric DNA. This protein is highly divergent among different species but is functionally well conserved since the homologue protein of
3. From gene to protein, histones are highly regulated
It is clear that there is a strong interdependency between DNA replication and chromatin reorganization. Nucleosomes are more than structural bricks for DNA, and require the modification of specific residues or the substitution of certain histone variants for others to maintain a correct epigenetic state. Once cells have decided to replicate their DNA, an increase in the abundance of histone proteins is required to pack the new genome that is about to be generated. Histone genes are among the most highly cell-cycle-regulated genes  because cells need to ensure a high demand of histones during replication, but must make sure that these levels are quickly down-regulated when replication slows down or is blocked, to avoid the deleterious effects of free histones on cell survival.
Canonical histone proteins can be regulated at transcriptional, post-transcriptional, translational and post-translational levels. The importance of each pathway on histone metabolism largely depends on the organism. In
3.1. Histones are regulated from the beginning: transcriptional regulation
Histone transcription is tightly regulated during the cell cycle. In some organisms like
In metazoans, entry into S-phase increases the expression of replication-dependent histone genes three to five-fold . Histone genes are clustered and each cluster normally contains at least one copy of the five canonical histones. Although transcription of all histones is carefully coordinated, no obvious common sequence element has been found at their promoters. Nevertheless, common elements can be found for some particular histone variants, like the Octamer-binding Transcription Factor (OTF1) for H2B promoters  or the Coding Region Activating Sequences (CRAS) in H2A, H3 and H4 genes . Activation of histone gene transcription requires the Nuclear Protein Ataxia-Telangiectasia (NPAT), which is essential for S-phase progression . This protein normally locates next to the
Transcriptional regulation of histones in
It has been recently shown that the HIR complex is conserved through evolution [70, 71] . In humans, this complex is formed by three proteins: HIRA, Ubinuclein1 and Cabin1. The role described for HIRA in humans has been mostly associated with chromatin assembly of the transcriptional histone variant H3.3 in cooperation with ASF1 . Nevertheless, several studies suggest that this complex could also play an important role in metazoan histone regulation. Ectopic over-expression of HIRA is able to repress histone gene transcription and block S-phase progression in human cells. This protein localizes to histone gene clusters in an immunofluorescence essay . Cyclin E-CDK2 and cyclin A-CDK2 can phosphorylate HIRA, and this phosphorylation is inhibited by cyclin inhibitor p21, which has been shown to be important for repression of histone synthesis upon replication stress  . HIRA could therefore be acting as a repressor of histone gene expression outside of S-phase regulated through phosphorylation by the cyclin E-CDK2. In this model, phosphorylation by the cyclin E-CDK2 could switch histone expression by activating NPAT and inactivating HIRA.
3.2. Once they are transcribed: post-transcriptional and translational regulation
Mammalian histone mRNAs lack introns and do not have a poly(A) tail as do most mRNAs. Instead, they contain a special 3´UTR sequence that forms a stem-loop structure . Histone clusters localize to specific Cajal Bodies that are enriched in factors required for expression (NPAT) and maturation (U7 snRNA) of histone mRNA named
SLBP is the only known cell cycle regulated protein of all the histone processing machinery. This protein starts accumulating during late G1 and is degraded at the end of S-phase by the phosphorylation of two threonine residues that target it for degradation . There are three major roles for SLBP on histone regulation: 1. Allow an efficient cleavage during mRNA maturation 2. Facilitate circularization of histone mRNAs, required for their efficient translation by polyribosomes [79, 80] and 3. Increase histone mRNA stability preventing degradation of histone mRNAs by the 3´hExo . Nevertheless, histone mRNA are still degraded when SLBP is artificially present at constitutive levels at the end of S-phase  or when DNA replication is inhibited , indicating that although this protein has a major contribution to histone mRNA stability, it is not able to prevent degradation itself.
Canonical histone mRNAs in lower eukaryotes and plants are polyadenylated. The fact that these transcripts lack any known specific structure at their 3´end and have a short half-life has lead to the conclusion that regulation in these organisms mostly takes place at a transcriptional level. Nevertheless, there is quite a lot of recent evidence that strongly suggests the importance of the post-transcriptional regulation of histone mRNAs in
3.3. Last frontier of histone regulation: controling protein levels
In addition to the tight regulation of histone mRNA levels, a mechanism able to control histone protein levels was described some years ago . To date, this pathway has only been described in the yeast
4. Histones: Enough to pack but not too much
Histone levels are regulated as soon as transcription of its mRNA starts. On top of the normal cell cycle regulation, additional mechanisms are able to block histone production when replication slows down or is completely blocked. Eukaryotic cells are unable to live without histones  and inhibition of histone deposition behind the replication fork blocks DNA synthesis and activates the DNA Damage Response (DDR) . Eukaryotes seem to have evolved to a situation in which histones must not be free in the cell and DNA must not be free of histones. In this last part of the chapter, we will focus on how cells cope with situations that break this bidirectional relationship.
4.1. Harmful effects of free histones
Histones are basic proteins that can bind-specifically to negatively charged molecules. Reconstitution experiments show that a slight excess of histones over DNA is sufficient to promote chromatin aggregation, probably due to the neutralization of negative charged DNA. In yeast, high levels of histones increase chromosome loss and enhance DNA damage sensitivity [57, 89]. Defects in histone degradation during replication stress or DNA damage severely decreases cell viability . Free histones show electrostatic interactions with some cellular macromolecules carrying the opposite charge such as RNA molecules. Additionally, an excess of free histones can saturate and inhibit the activity of some histone modifying enzymes, and change the expression pattern of almost 240 genes . Two different studies in the yeasts
4.2. The DNA Damage Response (DDR): Coupling DNA and histone synthesis
DDR is probably one of the most well characterized checkpoints in the cell and is normally activated whenever a cell senses DNA damage. Activation leads to the sequential action of a cascade of kinases that block or delay cell cycle progression to allow the cell to correct the damage. If damage cannot be repaired, human cells enter the apoptosis program and die . Proper functioning of this pathway is essential for genome integrity and mutations in most of the branches of this path are linked to cancer and other diseases. DDR is able to block cells at G1, S and G2/M . In human cells, two kinases ATM and ATR (Tel1 and Mec1 respectively in
In human cells, activation of histone gene transcription requires NPAT phosphorylation by the cyclin E-CDK2 complex at the beginning of S-Phase. Activation of NPAT is essential for S-phase progression and histone expression. Repression of histone synthesis upon DNA damage requires the activation of ATM, which leads to the sequential activation of p53 and then p21. p21 is able to block the activity of the cyclin E-CDK2 complex. Inhibition of this complex leads to a progressive dephosphorylation of NPAT, which no longer localizes to histone clusters to activate transcription . One interesting hypothesis that remains to be tested is if this cascade could also lead to histone repression by a change in the activity or location of HIRA, the human homologue of the HIR complex, at histone promoters (see previous paragraph about transcriptional regulation of histones). DNA damage also promotes post-transcriptional degradation of histone mRNAs. Treatment of cells with hydroxyurea (HU) increases oligouridylation of histone mRNAs in a process that depends on Upf1. Upf1 binds SLBP and helps to recruit a 3’ Terminal Uridylyl Transferase (TUT-ase) required for oligourydilation. These 3′ oligo(U) tails are recognized by the Lsm1–7 complex that triggers mRNA degradation through the exosome and Xrn1 . How Upf1 is recruited to histone mRNAs upon DNA damage remains unknown.
Regulation of histone levels upon DNA damage in
Asf1 is able to form a very stable complex with Rad53. Upon activation of the DNA damage response, Mec1 phosphorylates Rad53 and this phosphorylation dissociates the stable Asf1-Rad53 complex. This mechanism has been linked to a possible connection between checkpoint activation and DNA repair since Asf1 plays a role in chromatin remodeling during DNA repair . Rad53 can also be found in a hypophosphorylated form in normal conditions during G1, G2 and M, stages at which histone transcription is repressed. This phosphorylation seems to depend on Cdc28, the yeast functional homologue of human CDK1 and CDK2. Asf1 is able to co-immunoprecipitate with all the subunits of the HIR complex. This complex has been related to replication-independent nucleosome assembly and
4.3. Generation of free histones in the cell
How can free histones be generated during a normal cell cycle? Taking into account the tight regulation of histone levels, such situations may seem unlikely. There are two scenarios in which it is possible to think that histone supply and DNA replication can be unbalanced during a normal cell cycle. In the first one, this situation could arise from differences between the rate of DNA synthesis and histone supply during replication. Early S-phase cells use more replication forks than late S-phase cells [101, 102] and lesions in DNA or replication stress also affect the speed of the replication fork [103-106]. The second scenario in which a cell can encounter free histones would take place during the G2 stage of the cell cycle. Given the importance of a balanced ratio between histone H3 and CENPA in chromosome segregation, once cells have finished replication, all free histones that are not positioned should be quickly degraded. It is possible to think that an imbalance between these two types of histones could sometimes take place in actively replicating cells and opens a simple explanation to why most cancer cells have a high incidence rate of chromosome loss .
4.4. Transcription as a source of free histones
Transcription of a chromatin template also requires nucleosomes to be disassembled and reassembled after the passage of RNA polymerase II (RNA Pol II). Outside of the S-phase, transcribed chromatin is probably the major potential source of free histones. These free histones could arise due to minor imbalances between histone supply and demand during chromatin reassembly. One very well described essential factor involved in RNA pol II transcription is the FACT complex [108, 109]. This complex is able to stimulate RNA Pol II-dependent transcription elongation through chromatin
4.5. Can the state of chromatin influence the decision of cells to initiate DNA replication?
Histones are able to affect DNA replication right from the beginning; the state of the chromatin influences the timing and organization of origin firing. Replication fork progression also depends on the correct histone deposition behind the replication machinery, since defects in CAF1 lead to checkpoint activation and block cells in S-phase. The state of chromatin is able therefore to influence DNA replication. Work done in our lab, suggests that chromatin state might also influence the decision of cells to enter or not replication during the G1/S transition in the
The commitment to a new round of cell division takes place towards the end of the G1 phase of the cell cycle in a process called START in yeast, and Restriction Point in mammals . In yeast, this is the main regulatory event of the G1 phase of the cell cycle and involves an extensive transcriptional program driven by transcription factors SBF (Swi4-Swi6) and MBF (Mbp1-Swi6) [121, 122]. MBF and SBF activation depends on the cyclin/cyclin-dependent-kinase (CDK) complex Cln3-Cdc28. This complex phosphorylates Whi5, the negative regulator of START, thus promoting its release from SBF (Swi4-Swi6). Activation of MBF-dependent transcription by Cln3-Cdc28 acts through a mechanism independent of Whi5, involving the phosphorylation of Mbp1 . Activation of these two complexes results in the accumulation of G1 (Cln1 and Cln2) and the early S-phase cyclins (Clb5 and Clb6), which promote in last term S-phase entry . The kinase activity of Cln1,2-Cdc28 triggers the degradation of cyclin-dependent kinase inhibitor Sic1 which no longer inhibits the S phase-promoting complex Clb5,6-Cdc28 [125, 126].
FACT plays a role in maintaining the integrity of the chromatin structure during transcription [127-129] but has also been related to a G1/S cell cycle defect in yeast in a genetic screen to identify
In eukaryotes and also some archaebacteria, DNA forms a nucleoprotein complex called chromatin, which allows extensive compaction of genomic DNA in the limited space of the nucleus. This traditional view of chromatin as simple building-bricks has substantially changed since the nucleosome hypothesis was proposed [133, 134]. Cells have evolved a unique and complex machinery to cope with the fact that most of the processes involving DNA are going to need to interact with and probably modify chromatin first. Chromatin acts as a new step of regulation and carries an epigenetic specific code that in some cases can be as important for the cell as the one contained on DNA. In addition, cells must also carefully balance the levels of histones during chromatin formation to avoid the generation of free histones, in order to prevent their deleterious effects.
We thank Akash Gunjan´s and Vincent Geli´s labs for our fruitful collaboration. We would also like to thank people in the lab for such a wonderful work environment and to all those people who are always there to make things easier. The Spanish Ministry of Education and Science (grant BFU2007-67575-C03-02/BMC), the Andalusian Government (grant P07-CVI02623) and the European Union (FEDER) have supported this work. D.M. was covered by a F.P.I. fellowship from the Regional Andalusian Government, and M. M-H. and L.D-R., by fellowships from the Spanish Ministry of Education and Science.
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