FACT Prevents the Accumulation of Free Histones Evicted from Transcribed Chromatin and a Subsequent Cell Cycle Delay in G1

The FACT complex participates in chromatin assembly and disassembly during transcription elongation. The yeast mutants affected in the SPT16 gene, which encodes one of the FACT subunits, alter the expression of G1 cyclins and exhibit defects in the G1/S transition. Here we show that the dysfunction of chromatin reassembly factors, like FACT or Spt6, down-regulates the expression of the gene encoding the cyclin that modulates the G1 length (CLN3) in START by specifically triggering the repression of its promoter. The G1 delay undergone by spt16 mutants is not mediated by the DNA–damage checkpoint, although the mutation of RAD53, which is otherwise involved in histone degradation, enhances the cell-cycle defects of spt16-197. We reveal how FACT dysfunction triggers an accumulation of free histones evicted from transcribed chromatin. This accumulation is enhanced in a rad53 background and leads to a delay in G1. Consistently, we show that the overexpression of histones in wild-type cells down-regulates CLN3 in START and causes a delay in G1. Our work shows that chromatin reassembly factors are essential players in controlling the free histones potentially released from transcribed chromatin and describes a new cell cycle phenomenon that allows cells to respond to excess histones before starting DNA replication.


Introduction
The FACT complex plays an important role by allowing RNA polymerase II (Pol II) to transcribe through chromatin (reviewed by [1,2]), the only factor known to date that is able to stimulate Pol II-dependent transcription elongation through chromatin in a highly purified system [3,4].Yeast FACT is required in vivo to transcribe genes with highly positioned nucleosomes at the 59 end of the transcribed region [5], and several lines of evidence of other organisms also support that FACT plays an important role in transcription elongation in vivo [6][7][8][9][10].In spite of its role in elongation, several in vivo and in vitro approaches indicate an additional role of yFACT in establishing transcription initiation complexes by promoting TBP binding to core promoters in a TFIIA-dependent manner [11,12]).Finally and in addition to its role in transcription, FACT also plays an important function during DNA replication [13][14][15].
In humans, the FACT complex is composed of two proteins, p140 and SSRP1, which are highly homologous to the essential yeast proteins Spt16/Cdc68/Ssf1 (hereafter referred to as Spt16) and Pob3, respectively [16].SPT16 had been previously identified as both a CDC gene [17], and also as a recessive suppressor of the deletion of SWI4, a transcription factor required for the high-level expression of the G1 cyclin genes, CLN1 and CLN2 [18].Besides, Spt16 had also been described as a protein involved in transcription since several spt16 alleles suppress the transcriptional effects of Ty insertions in yeast (Spt-phenotype) [19].
yFACT has been reported to interact physically or genetically with other factors related to histone modifications and chromatin remodeling, like the Paf complex, the ATP-dependent chromatin factor Chd1 and the NuA3 histone acetyltransferase complex [11,[20][21][22].A reciprocal regulation of the FACT function by H2B ubiquitination has also been described [23].In agreement with these findings, yFACT and the HMG-box protein Nhp6 have been shown to form a heterodimer capable of binding nucleosomes [24] and of reorganizing them in vitro [25,26].Both the yFACT subunits are able to bind H3/H4 tetramers and H2A/ H2B dimers, sometimes in a functionally redundant manner [27,28].These interactions are thought to allow FACT to destabilize nucleosomes during transcription [26,29].Some spt16 alleles are synthetically lethal with mutations affecting chromatin assembly [30].Moreover, they lead to the activation of cryptic transcription initiation sites within coding regions, indicating that FACT, together with other factors like Spt6, also plays a role in maintaining the integrity of the chromatin structure during transcription [9,[31][32][33][34].
Several spt16 mutants show defects while progressing through START, the main regulatory event in the G1 phase of the cell cycle [17,35].At a non-permissive temperature, the G1 phenotype of these spt16 mutants has been accounted for by the drastic reduction in the expression of CLN1, CLN2 and CLN3, the genes encoding the three G1 cyclins [35,36].CLN1 and CLN2 are able to self-regulate their expression by a positive feed-back mechanism [37], but the regulation of G1 length requires the activation of the cyclin-dependent kinase Cdc28 (Cdk1) by Cln3 [38][39][40][41].Cln3associated Cdk1 binds SBF (Swi4-Swi6) to the CLN1 and CLN2 promoters where it phosphorylates the negative regulator of START, Whi5 [42].This phosphorylation promotes its release from SBF and leads to the activation of the CLN1 and CLN2 promoters [43,44].SBF-dependent recruitment of FACT plays an important role in this activation, which promotes the G1/S transition [45].Notably, the kinase activity of Cln1,2-Cdk1 triggers the degradation of the cyclin-dependent kinase inhibitor Sic1 which no longer inhibits the S phase-promoting complex Clb5,6-Cdc28 [46,47].
Another key regulatory process during the G1/S transition is the induction of histone genes, which allows the coupling of bulk histone synthesis to ongoing DNA replication.In proliferating cells, the synthesis of the vast majority of histones occurs during the S-phase of the cell cycle.The tight cell cycle regulation of the histone genes results from their transcriptional repression in phases G1 and G2, their transcriptional activation just before the S-phase and the post-transcriptional regulation of their mRNAs.During the S-phase, histone genes can also respond to changes; for instance, the accumulation of histones in response to the genotoxic agents interfering with DNA replication induces their repression (reviewed by [48]).
In recent years, a novel mechanism in budding yeast preventing the accumulation of free histones and which is superimposed upon the regulation of histone gene transcription and mRNA stability has been described [49].This mechanism involves the use of the DNA damage checkpoint protein kinase Rad53 as part of a surveillance process that not only monitors the accumulation of excess histones, but also induces their degradation.This degradation is controlled by phosphorylation and is carried out by the proteosome in an ubiquitylation-mediated manner [50].Excess histones are thought to be generated at the end of the normal S-phase or in response to an abrupt decrease of DNA synthesis following DNA damage.This mechanism is dependent on neither the checkpoint kinases Mec1 and Tel1 nor other DNAdamage checkpoint proteins (reviewed in [51]).
Some aspects of the G1 phenotype of the spt16 mutants remain unknown.It is not clear whether FACT plays a direct role in the regulation of CLN3.Alternatively, the decreased expression of CLN3 might be a physiological response to FACT inactivation.We investigated this question and found that the inactivation of FACT down-regulates the CLN3 promoter in START.This phenomenon coincides with the accumulation of free histones and is enhanced by the mutation of the free histones controller, RAD53.We also found that the forced entry of FACT-deficient cells into the Sphase lowers their viability.Finally, we discovered that the overexpression of histones in the wild-type cells decreases CLN3 transcription in START and leads to a delay in G1.We propose that the accumulation of free histones triggers the down-regulation of CLN3, thereby contributing to control the excess histones before starting DNA replication.We further propose that the main potential source of free histones is transcribed chromatin and that chromatin reassembly factors play an essential protective role in this respect.

FACT inactivation causes a down-regulation of the CLN3 promoter in START
The arrest of yeast cells in G1 after Spt16 inactivation has been suggested to be a possible direct consequence of a very strict requirement of Spt16 for CLN1, CLN2 and CLN3 transcription [35].FACT has been shown to participate directly in the activation of the CLN1 and CLN2 promoters after START [45].In order to explore the effect of FACT inactivation on the previous step, we quantified the mRNA levels of CLN3 in alpha factorsynchronized spt16-197 cells at a non-permissive temperature (see Materials and Methods for the ranges of permissive and nonpermissive temperatures ranges).We treated cells for two hours with the pheromone at 30uC, then for one a further hour at either 30uC or 35uC in the continuous presence of alpha-factor.Next we released the cells from the arrest and analyzed CLN3 mRNA by Northern blotting (Figure 1).In agreement with previously published results based on asynchronous cells [35], the CLN3 mRNA levels in the pheromone-treated spt16-197 cells at 35uC were clearly lower than in the wild-type cells (see time 0 in Figure 1B).When cultures were released from alpha-factor, the wild-type cells progressed into the S-phase at any temperature, whereas spt16-197 cells entered the S-phase only at 30uC, with most spt16-197 cells remaining in G1 at the restrictive temperature (see times 10, 20 and 45 min in Figure 1A).The CLN3 mRNA levels in the spt16-197cells released from alpha-factor at 37uC

Author Summary
Lengthy genomic DNA is packed in a highly organized nucleoprotein structure called chromatin, whose basic subunit is the nucleosome which is formed by DNA wrapped around an octamer of proteins called histones.Nucleosomes need to be disassembled to allow DNA transcription by RNA polymerases.An essential factor for the disassembly/reassembly process during DNA transcription is the FACT complex.We investigated a phenotype of yeast FACT mutants, a delay in a specific step of the cell cycle division process immediately prior to starting DNA replication.The dysfunction caused by the FACT mutation causes a downregulation of a gene, CLN3, which controls the length of that specific step of the cell cycle.FACT dysfunction also increases the level of the free histones released from chromatin during transcription, and the phenotype of the Spt16 mutant is enhanced by a second mutation affecting a protein that regulates DNA repair and excess histone degradation.Moreover, we show that the overexpression of histones causes a cell cycle delay before DNA replication in wild-type cells.Our results point out a so-far unknown connection between chromatin dynamics and the regulation of the cell cycle.remained very low.In contrast, the mRNA levels of ADH1, a constitutive non-cycling gene, were only partially affected by Spt16 inactivation (Figure 1B), which is in agreement with the limited effect of spt16-197 at restrictive temperatures in a broad set of noncyclin genes [35,36].The occupancy of CLN3 and ADH1 by the RNA polymerase II (RNApol II) paralleled their mRNA levels.As Figure 1C depicts, the amount of RNApol II bound to the CLN3 transcribed region at 35uC was significantly lower in spt16-197 (52%) than in the wild type, whereas the variation of RNApol II binding to ADH1 was slighter.
The fact that the CLN3 expression markedly reduced in response to Spt16 inactivation might be due to either a direct effect of FACT dysfunction on CLN3 transcription or a yet unidentified signaling pathway targeting the CLN3 promoter in response to FACT inactivation.In order to distinguish between these possibilities, we first analyzed the response of a reporter fused to the CLN3 promoter upon Spt16 inactivation in alpha-factorsynchronized cells.To construct this fusion, we combined the entire intergenic region between the neighboring CLN3 and CYC3 coding regions and the coding region of E. coli lacZ (Figure 2A).We chose lacZ since we had previously showed that the transcription elongation of this reporter gene is not sensitive to FACT dysfunction [5].As shown in Figure 2B, lacZ mRNA was hardly detectable when the synchronized spt16-197 cells were incubated at the restrictive temperature, indicating that the CLN3pr::lacZ reporter (fusion 1) behaved similarly to the endogenous CLN3 mRNA.In contrast, the mRNA levels of an ADH1pr::lacZ transcriptional fusion did not lower under the same conditions.This result indicates that the promoter region of CLN3 mediates the drop in its mRNA levels after FACT inactivation.
We further constructed additional CLN3pr::lacZ fusions containing different segments of the CLN3-CYC3 intergenic region (Figure 2A).No difference in copy number among the reporter plasmids was detected by quantitative PCR (Figure S1).We measured the lacZ mRNA levels expressed by these fusions in the spt16-197 cells synchronized in START.The expression patterns of the complete CLN3pr::lacZ (fusion 1) and ADH1pr::lacZ were in agreement with the experiments described above (Figure 2C).Fusion 2, which contains the entire intergenic region, except the CLN3 59UTR and the CYC3 termination region (2999, 2339) (Figure 2A), retained sensitivity to Spt16 inactivation as it dropped as the lacZ mRNA levels did after Spt16 inactivation (Figure 2C).A significant influence of mRNA instability in this decrease was ruled out because two completely different mRNAs (lacZ and CLN3) responded similarly to FACT inactivation when they were driven by the same promoter (CLN3pr).In contrast, when lacZ mRNA was driven by the ADH1 promoter, it did not show any significant variation in spt16-197 at the restrictive temperature (Figure 2C).In short, spt16-197 does not influence the expression of CLN3 at a post-initiation level.However, Spt16 may also play a role in transcription initiation by facilitating TBP binding to the core promoters.We constructed CLN3pr::lacZ fusion number 3 (2472, 2389), which contains the minimal core promoter of CLN3 (Figure 2A).In spite of the weak expression of this fusion (five fold lower than fusion number 2 in asynchronous cultures), its mRNA level was not significantly influenced by Spt16 inactivation (Figure 2C).These results, in addition to the absence of FACT binding to the CLN3 promoter during START (David Stillman, personal communication), indicate that the effect of Spt16 inactivation on the expression of CLN3 in START is not due to the specific involvement of FACT in the transcription of this gene in this particular step of the cell cycle.Instead, our results suggest the existence of a control mechanism mediated by the promoter of CLN3 which regulates the G1/S transition in response to FACT dysfunction.Such a mechanism might protect the cell from the deleterious effect of entering the S-phase under these conditions.We tested this hypothesis by forcing the entry of spt16-197 cells into the S-phase.First, we went about this by overexpressing CLN3 with a Tet off ::CLN3 construct (negatively regulated by doxycycline) which suppressed the accumulation of spt16-197 cells in G1 at a restrictive temperature (Figure 3A).We observed a negative effect of the overexpression of CLN3 on the viability of spt16-197 cells at a semi-permissive temperature (Figure 3B).Similar results were obtained in those cells lacking Sic1, the inhibitor of the Cdc28-Clb complexes that negatively regulates entry into the S-phase (Figure 3C and 3D).These data reveal that the forced progression of spt16-197 cells into the S-phase at semi-permissive temperatures is deleterious; therefore, the G1 delay triggered by the inactivation of FACT is cell-protective.

The lethality associated with FACT dysfunction relates to the accumulation of the free histones evicted during transcription
The association between impairment of transcription elongation and genome instability is well established [52][53][54].Since FACT plays a role during elongation, we wondered whether the G1 delay induced by FACT inactivation could be due to the action of the canonical DNA-damage checkpoint.To test this hypothesis, we investigated the possible implication of Rad9, a component of the DNA-damage sensor machinery operating in G1 [55,56].We performed a FACS analysis with strains carrying the spt16-197 and rad9D mutations.The profile of the spt16-197 rad9D double mutant after four hours at a restrictive temperature was almost identical to that of the single spt16-197 mutant (Figure S2A), indicating that the G1 arrest produced by FACT inactivation is proficient in the absence of Rad9.Accordingly, no genetic interaction between spt16-197 and rad9D was detected when we analyzed the thermosensitivity of the double mutant (Figure S2B).We further tested whether spt16-197 exhibited any aggravation of its ts phenotype in the absence of Mec1, the key kinase of the DNAdamage checkpoint pathway [57].As with rad9D, the deletion of MEC1 in spt16-197 did not affect its thermosensitive (ts) phenotype (Figure 4A).
It was intriguing to note that of all the DNA-damage checkpoint genes we tested, only the mutation of RAD53, which encodes another essential protein kinase for the DNA-damage checkpoint [58], led to a clear genetic interaction with spt16-197.Indeed the rad53K227A allele, which abolishes most Rad53 kinase activity, dramatically enhanced the thermosensitive phenotype of spt16- CLN3 expression is down-regulated after Spt16 inactivation.Wild-type (FY120) and spt16-197 (FY348) cells grown asynchronously (AS) were synchronized at START by treatment with alpha-factor for two hours at 30uC (ST), followed by one additional one hour at 30uC or 35uC in the presence of the mating pheromone.Cells were then released from the arrest at time 0 at either 30uC or 35uC by washing out the alpha-factor.Samples were taken at different time points to analyze the DNA content by flow cytometry and the proportion of unbudded cells by microscopy (A), and to quantify the mRNA levels of the indicated genes by Northern blot analysis (B).Transcripts levels were represented as arbitrary units (AU) after normalization with 18S rRNA.The results of a typical experiment and the quantification of three independent experiments are shown.(C) Relative RNApol II binding to the transcribed region of CLN3 and ADH1 in spt16-197.Cells were synchronized with alpha-factor for two hours at 30uC, followed by one additional one hour at 30uC or 35uC in the presence of the mating pheromone.The 8WG16 antibody, recognizing the CTD repeats of Rpb1, was used.doi:10.1371/journal.pgen.1000964.g001with the plasmids bearing lacZ fusion number 1 (CLN3pr::lacZ) or ADH1pr::lacZ, was grown until the mid-log phase (AS), and was then synchronized at START (ST) by alpha-factor treatment for 2h at 30uC, followed by one additional hour of incubation at 30uC or 37uC in the presence of the mating 197.While the growth of the spt16-197 and rad53K227A single mutants was virtually not affected at 32uC, the double spt16-197 rad53K227A mutant was unable to grow at this temperature (Figure 4A).Similar results were obtained with the complete deletion of RAD53 (Figure S3).Unlike what happens following DNA damage, Rad53 was not hyperphosphorylated in the spt16-197 mutant at a restrictive temperature (Figure 4B).Hence we conclude that Rad53 kinase activity is required to alleviate the deleterious effects of the spt16-197 mutation, irrespectively of the role it plays in the DNA damage response.
As we mentioned in the Introduction, Rad53 is involved in the detection and subsequent degradation of excess histones without becoming phosphorylated and independently of its role in the DNA damage checkpoint [49].Since FACT is involved in chromatin transactions during transcription, we hypothesized that the dysfunction of Spt16 might cause an increase in free histones, which would need to be targeted for degradation by Rad53.The mutations lowering the H2A-H2B dosage have been described to enhance the viability of the spt16 mutants [30].Accordingly, we observed how the deletion of HTA2-HTB2, one of the two loci encoding H2A and H2B, partially suppressed the ts phenotype of spt16-197 at restrictive (Figure 4C) and semi-restrictive temperatures (Figure S4A).The hta2Dhtb2D deletion also suppressed the accumulation of spt16-197 cells in G1 at a restrictive temperature (Figure 4D).In contrast, the deletion of the HTA1-HTB1 locus caused no suppression in either the ts phenotype (Figure 4C and Figure S4A) or the G1 delay (Figure 4D).The HTA1-HTB1 locus has been shown to be essential for viability and the hta1Dhtb1D strain we used (FY710) is only alive because of an extrachromosomal copy of HTA2-HTB2 [59].We confirmed the presence of this extra-chromosomal copy of HTA2-HTB2 not only in FY710, but in the isogenic spt16-197 hta1/htb1D double mutant (Figure S4B).The main difference between these two histone loci lies in their regulation.The expression of HTA1-HTB1 is sensitive to the levels of histones, whereas HTA2-HTB2 is not [60].In order to properly compare the effect of the two loci on the ts phenotype of spt16-197, we engineered new strains containing all the viable combinations of the H2A/H2B-encoding loci.We found that the presence of two copies of the HTA2-HTB2 (non responsive to free H2A and H2B) led to a more severe thermosensitivity than the presence of two copies of the HTA1-HTB1 locus (repressible by free histones) (Figure S4A).Moreover the deletion of the regulatory sequence (NEG), which mediates the repression of HTA1-HTB1 in response to histone levels, enhanced the ts phenotype of spt16-197 (Figure S4A).Taken together, these results suggest that the accumulation of free H2A and H2B contributes to the lethality of spt16-197 at high temperatures and that the accumulation of spt16-197 cells in G1 responds to free histones.
In order to confirm this hypothesis, we analyzed the amount of non chromatin-associated histones in spt16-197 in either the absence or presence of Rad53 kinase activity.The huge amount of histones present in the chromatin fraction makes it extremely difficult to quantify reproducibly free histones pools in a direct manner.Instead, we measured the amount of histones associated with soluble histone chaperones, a well-characterized procedure that allows a reproducible measurement of free histones [49,50].
We performed co-immunoprecipitation assays using the H2A-H2B chaperone Nap1 (Figure 5A) and the H3-H4 histone chaperone Asf1 (Figure 5B) fused to the FLAG epitope.The spt16-197 mutation did not produce a significant effect on the levels of Nap1-FLAG and Asf1-FLAG detected in the extracts (Figure S5A and S5B).We quantified the amount of H2A co-immunoprecipitated with Nap1 in exponentially growing cells after switching them to the non-permissive temperature.We saw a clear increase in the accumulation of free H2A in Nap1 in the spt16 and rad53 mutants compared to the wild-type cells, and an even higher level of co-immunoprecipitated H2A in the double mutant (Figure 5A).Next we performed a similar experiment with Asf1-FLAG.Wildtype cells exhibit very little H4 associated with Asf1 under normal growth conditions at 25uC (Figure 5B).We found that, even at this permissive temperature, the spt16-197 mutation increased the amount of histones associated with Asf1 up to levels close to those shown by rad53K227A (Figure 5B).One again, the accumulation of free H4 in the double mutant exceeded the levels of the single mutants (Figure 5B).To test whether this increase of free histones in FACT-deficient cells was taking place in G1, independently of the histone synthesis that takes place during the S-phase, we incubated alpha factor-synchronized spt16-197 cells for two hours at either 25uC or 35uC.As expected, the amount of free histones associated with Asf1 in the spt16-197 mutant increased at the restrictive temperature.We also observed that inhibiting RNApol II transcription with alpha-amanitin prevented this increase (Figure 5C).Northern blot experiments showed no misregulated expression of the histone genes in spt16-197 during START (Figure S5D).Taken together, these results are compatible with a scenario in which Pol II-dependent transcription in the absence of active FACT causes an accumulation of the evicted histones, which become toxic to the cell if not targeted for degradation by Rad53.

Excess histones induce a G1 cell cycle delay
Our results pose an intriguing question about a possible link between the CLN3-dependent G1 delay and the presence of excess histones, both induced by FACT dysfunction.We addressed this question by testing whether the enhancement of the spt16-197 thermosensitivity caused by rad53K227A correlated with the observed delay in G1.As Figure 6A depicts, an asynchronous culture of the double mutant exhibited a stronger and faster accumulation of cells in G1 compared to the single spt16-197 mutant when they were shifted to a restrictive temperature.Moreover, the alpha-factor-synchronized spt16-197 rad53K227A cells also displayed a much slower entry into the S-phase than the single spt16-197 or rad53K227A mutants when the mating pheromone was removed from the medium at a semi-permissive temperature.Even at 25uC, the double mutant displayed a slower exit from G1, although the double mutant exhibited a proportionally stronger defect in the G1-S progression at 32uC, as compared to the single mutants (Figure 6B).
In order to establish a correlation between the excess histones and the CLN3 mRNA levels in START, we measured them under conditions in which the mutant's general transcriptional capacity is not significantly affected, but the level of free histones increases.To pheromone.Cells were then transferred to a fresh medium without alpha-factor (time 0h) to allow cells to progress at 30uC or 37uC.At the indicated times, samples were taken to analyze the transcript levels by Northern blot analysis with the indicated probes.The results of a typical experiment are shown.(C) The spt16-197 (FY348) cells were transformed with the plasmids bearing the three lacZ fusions described in (A) or ADH1pr::lacZ.These transformants were grown until the mid-log phase (AS) and were synchronized with alpha-factor at 30uC (START), followed by an additional hour at 30uC or 37uC in the presence of the mating pheromone, as indicated.The transcript levels were quantified by Northern blot analysis.The results of a typical experiment and the quantification of three independent experiments are shown.The CLN3 levels were normalized to ADH1.AU: arbitrary units.doi:10.1371/journal.pgen.1000964.g002do this, we pre-synchronized the spt16-197 rad53K227A cells with alpha-factor and analyzed the CLN3 mRNA levels one hour after switching them to 32uC in the continued presence of pheromone.
The results show a more marked reduction of CLN3 mRNA after one hour at 32uC in the double spt16-197 rad53K227A mutant than in the single spt16-197 mutant (Figure 6C).Therefore, the absence  If our hypothesis that transcriptionally evicted histones trigger the G1 delay of spt16-197 is true, we should then expect the other mutants affected in chromatin reassembly to also exhibit similar cell cycle defects.In addition to FACT, another important factor that participates in chromatin reassembly during transcription is Spt6 [61].We found that the viability of cells bearing the mutant allele spt6-1004 clearly lowered in the absence of Rad53 kinase activity, but remained unchanged in the absence of Mec1 (Figure 7A).We also found that spt6-1004 cells clearly accumulated in G1 when shifted to a restrictive temperature in both asynchronous and alpha factor-synchronized cells (Figure 7B and  7C).As in the spt16-197 cells, the CLN3 mRNA levels, or the lacZ mRNA levels when driven by the CLN3 promoter, decreased when alpha factor-synchronized spt6-1004 cells were shifted to a restrictive temperature (Figure 7D).
Given these results, we thought it would be interesting to determine whether the overexpression of histones in G1 induces a cell cycle delay in wild-type cells.We found that an additional copy of the HTA1-HTB1 locus produced a very slight delay in cell cycle progression when alpha factor-synchronized cells were released from the pheromone.In contrast, a copy of the same locus lacking the regulatory sequence that mediates its repression in response to histone levels (DNEG) led to a clear accumulation of cells in G1 (asynchronous culture) and a more marked delay in the entry of synchronized cells into the S-phase (Figure 8A).Accordingly, we detected a more significant decrease of the CLN3 mRNAs in START, in those cells bearing the deregulated HTA1-HTB1 copy (DNEG) than in those transformed with the intact allele (Figure 8B).Since all the cells in this experiment were held in START by the presence of the mating pheromone, the drop in CLN3 mRNA could not be an indirect consequence of free histones inhibiting cell cycle progression.We conclude, therefore, that excess histones downregulate CLN3 in the wild-type cells during G1 and subsequently delay their progression through the G1/S transition.

Discussion
The primary objective of our study was to understand the defects in the G1/S progression exhibited by the spt16-197 mutant.The genetic and molecular evidence described in the Results section indicates that the dysfunction of Spt16 downregulates the expression of CLN3 in START by triggering a regulatory mechanism that specifically represses the CLN3 promoter.Our results also reveal that the G1 delay undergone by the spt16 mutant is not mediated by the DNA-damage checkpoint, although the rad53K227A mutation enhances both the thermosensitivity of spt16-197 and its G1 phenotype.This result, in combination with the lack of phosphorylation of Rad53 after Spt16 inactivation, indicates that excess histones are involved in this phenomenon.We confirm that this hypothesis is true by showing that the Spt16 dysfunction produces an accumulation of free histones associated with histone chaperones in G1 (Figure 5C), and that excess histones induce a delay in the otherwise wild-type cells during the G1/S transition concomitantly with CLN3 downregulation.

Chromatin as a potential source of free histones
It is well known that the accumulation of non-nucleosomal histones in the cell is toxic [62] and that this toxicity is normally avoided by regulating the histone gene expression at both the transcriptional and posttranscriptional levels [60].Obviously, these mechanisms are incapable of controlling excess histones when they originate by eviction from chromatin due to a dysfunction in chromatin reassembly during transcription.We demonstrate herein that Spt16 inactivation results in the accumulation of non-chromatin bound histones in G1.The only way for the cell to avoid the toxic effects of these excess histones is to degrade them in a process that is mediated by Rad53 [49].Our results show that the absence of Rad53 kinase activity lowers the viability of the spt16-197 mutant and suggest that one of the roles of the Rad53-dependent histone degradation mechanism is the elimination of those histones evicted by the transcriptional activity that are not reassembled into chromatin.Beyond the S-phase, transcribed chromatin is probably the main source of free histones in yeast cells, presumably due to minor imbalances between histone supply and demand during chromatin reassembly.The general similarities between histone trafficking during all the chromatin transactions suggests that DNA repair or DNA replication might also result in the excess of free histones when chromatin assembly is dysfunctional [63].
Our results suggest that FACT, in addition to avoiding initiation from cryptic promoters [9,31], is a protective factor against the toxic risk represented by evicted histones.A recent publication reports how Spt16 promotes the redeposition of the original H3 and H4 histones evicted by elongating Pol II [34].Our results agree with this conclusion since we have detected a clear accumulation of free H3 and H4 in Spt16-deficient cells.However, we have also noted an increase in the free H2A pool.This result and the genetic interactions between spt16-197 and the H2A-H2B loci also indicate that Spt16 plays a role in preventing the accumulation of evicted H2A and H2B.In fact, a high H2A-H2B/H3-H4 gene ratio impairs the spt16-11 growth, whereas a low H2A-H2B/H3-H4 gene ratio improves it [30], suggesting that the accumulation of free H2A-H2B caused by Spt16 dysfunction may be more relevant for the phenotypes observed.
It has been recently demonstrated that FACT promotes the transition between the canonical nucleosome configuration and a looser, more dynamic structure that involves changes in the interaction of the four core histones with the DNA [26].According to this view, FACT would be essential for the maintenance of this altered configuration during transcription elongation by limiting the amount of the four histones joining the free pools.One prediction of this model is that those histone mutations which destabilize this alternative nucleosomal configuration would promote free histone accumulation.Some H4 mutations affecting H3-H4 tetramer/H2A-H2B dimer interactions show delayed G1/S transition and reduced CLN3 expression levels [64].Accordingly, we detected a negative synthetic interaction between one of these mutations (hhf1-36, bearing the H4-Y72G mutation) and rad53K227A (Figure S6).
The protective role against evicted histones is probably not an exclusive function of FACT, but is also a function of the other factors that cooperate during chromatin reassembly, like Spt6, for which we show some evidence.It is likely that Asf1, Nap1, the Hir FY348, FY710, DMY10, DMY11, and DMY12) were grown in YPD medium at 25uC.10-fold serial dilutions of the indicated strain were plated on YPD plates and incubated for three days at the indicated temperatures.(D) Cells of strains FY120 (WT), FY348 (spt16-197), FY710 (hta1D-htb1D), DMY10 (hta2D-htb2D), DMY11 (spt16-197 hta1D-htb1D), and DMY12 (spt16-197 hta2D-htb2D), exponentially growing in YPD at 25uC, were shifted to 37uC for four hours or kept at 25uC.Samples were taken to analyze the DNA content by flow cytometry.Numbers indicate the proportion of G1 cells.doi:10.1371/journal.pgen.1000964.g004Figure 5. FACT dysfunction causes a transcription-dependent accumulation of free histones.(A) Histone H2A levels associated with chaperone Nap1.The indicated strains carrying Nap1-FLAG were grown exponentially at 25uC and then shifted for two hours to 37uC, prior to harvesting the cells for whole cell extract (WCE) preparation.Co-immunoprecipitation assays were carried out as described in the Materials and Methods.The levels of immunoprecipitated (IPed) Nap1 and co-immunoprecipitated (co-IPed) H2A are indicated.The histogram shows the relative complex or Nsr1 also protect against evicted histones.Asf1 has been seen to act as an intermediary in the parental histone disassembly/reassembly during replication as it associates with the MCM proteins at the replication fork [65].An analogous situation might exist during transcription whereby Asf1 or the HIR complex, both of which have been shown to be capable of chromatin assembly outside the S-phase [66,67], may act as an intermediary in the histone eviction and reassembly process in conjunction with FACT.Nap1 promotes nucleosome assembly by eliminating nonnucleosomal H2A-and H2B-DNA interactions and it prevents aberrant transcription by avoiding excessive H2A-H2B binding to DNA [68].
In this study we also show how the overexpression of H2A-H2B results in G1 delays in the wild-type cells.Similar effects, but to a lesser extent, were obtained by overproducing H3-H4 (data not shown).These results demonstrate that a histone-mediated G1 delay can be obtained in a background with no possible indirect effect mediated by either the role of FACT in the expression of the G1-S regulators, or the function of Rad53 in the control of early replication.

CLN3-dependent G1 delay in response to free histones
Our results show that the G1-delay caused by Spt16 dysfunction correlates with a down-regulation of the transcriptional activity of the CLN3 promoter.Cln3 shortage can only explain a transient G1-delay as cells can enter the S-phase after a prolonged G1 in the absence of Cln3.Therefore it is likely that the permanent G1 arrest shown by spt16-197 cells at high temperatures (over 37uC) is caused by a combination of the CLN3mediated transient delay and additional defects on the expression of other G1/S regulators caused by Spt16 inactivation.For instance, the MluI cell-cycle boxes (MCB)-mediated activation of SWI4 and SWI6 is also negatively affected by FACT dysfunction [18].The CLN1 and CLN2 promoters are two other clear targets of Spt16 inactivation, since FACT binds them during G1 and participates in their activation after START [45].However, the marked reduction in the CLN3 expression following FACT inactivation cannot be caused by a direct involvement of FACT in the transcriptional activity of the CLN3 promoter during G1 because it does not bind this promoter during this phase of the cell cycle (David Stillman, personal communication).We show herein that a CLN3pr::lacZ fusion lacking any sequence in common with CLN3 mRNA is also responsive to the inactivation of Spt16 or Spt6 under conditions in which a constitutively expressed ADH1pr::lacZ is not.Furthermore, rad53K227A enhances the level of CLN3 down-regulation caused by spt16-197.Finally, the overexpression of H2A-H2B in an otherwise wild-type strain decreases the CLN3 expression.Taken together, these results support the existence of a mechanism which down-regulates the CLN3 promoter during G1 in response to the accumulation of free histones caused by either defects in cotranscriptional chromatin reassembly or histone genes deregulation.
CLN3 mediates several regulatory pathways by coupling the cellcycle progression in G1 to physiological conditions, including nitrogen deprivation [69], daughter cell G1-delay [70,71] and changes in glucose levels [72].In the last case, the up-regulation of the CLN3 promoter is due to the binding of the Azf1 transcriptional activator.Another transcription factor shown to regulate the CLN3 promoter is the Mcm1-containing early cellcycle box (ECB) binding complex [73].Homeodomain repressors, Yox1 and Yhp1, restrict the ECB-dependent activation of the CLN3 transcription to the M/G1 phase [74].The deletion of AZF1, YOX1 or YHP1 does not alter the accumulation of cells in G1, as indicated by spt16-197 at the restrictive temperature (data not shown).Moreover, the binding of Mcm1 to the CLN3 promoter, measured by chromatin immunoprecipitation, was not affected by Spt16 inactivation (data not shown).We conclude that the transcriptional regulation of CLN3 in response to the accumulation of free histones is not mediated by any of the known transcription factors operating on the CLN3 promoter.It is even conceivable that the promoter itself acts as a sensor of free histone concentration and is repressed in response to the excess histones.
In mammalian cells, histone overexpression slows down entry into and progression through the S-phase [65].Interestingly, depletion of human Spt16 leads to the repression of the H1, H2A and H2B genes [75], which could be the result of the accumulation of the free histones in human cells after FACT dysfunction.Given the analogy between the G1-S regulators in yeast (Cln3-SBF-Whi5-Rpd3) and mammals (CyclinD1-E2F-Rb-HDAC1) [42,45], the functional link between the accumulation of free histones and the regulation of the G1-S transition may be evolutionarily conserved.

Chromatin repair
The free histones evicted by the transcriptional activity of cells can potentially associate non-specifically with DNA via electrostatic interactions, and may give rise to aberrant chromatin structures which can be considered a form of chromatin damage.As with DNA damage, which enhances the risk of genome instability, excess free histones may have serious implications for the normal progression of DNA replication since the toxicity of free histones is maximal in the S-phase [49].Consistently with this hypothesis, the experimental conditions under which the spt16induced G1 delay is overcome (CLN3 overexpression, SIC1 deletion) involve an overall decrease in cell viability.The G1 delay should allow cells to reduce the free histone levels through the Rad53-mediated histone degradation pathway before entering the S-phase.The persistence of excess histones, as in the spt16-197 rad53K227A double mutant, would lead to severe replication dysfunctions.Accordingly, chromatin repair would be the combination of DNA repair, chromatin reassembly and excess histone degradation.In this sense, it is interesting to note that Rad53, which participates in both the DNA damage checkpoint and the excess histone degradation pathway, may act as a super-integrator accumulation of H2A on Nap1 compared to the wild-type cells (the data have been normalized to the amount of Nap1 actually IPed).The total levels of H2A in WCE are shown to demonstrate that roughly equal amounts of WCE were used for the immunoprecipitation reactions.(B) The histone H4 levels associated with Asf1 in the spt16-197 cells.The indicated strains carrying FLAG-tagged Asf1 were grown in YPD media at 25uC, while the exponentially growing cells were harvested for WCE preparation.The co-immunoprecipitation assays for Asf1-H4 were carried out as indicated in the Materials and Methods.The total histone H4 and the total Asf1-FLAG levels in the WCE are shown to demonstrate that roughly equal amounts of WCE were used for the immunoprecipitation reactions.The histogram displays the relative accumulation of H4 on Asf1 if compared to the wild-type cells (the data have been normalized to the amount of Asf1 actually IPed).(C) The accumulation of the free histones in G1 upon FACT dysfunction is dependent on transcription.The spt16-197 cells (FY348) carrying FLAG-tagged Asf1 were grown in YPD at 25uC, alpha factor-treated for two hours at 25uC, divided into four equal aliquots, and finally incubated with or without alpha-amanitin for two hours at 25uC or 35uC in the continued presence of the pheromone.Following this, cells were harvested and processed as described for (A).The Asf1-FLAG and histone H3 levels in WCE were shown to demonstrate that roughly equal amounts of WCE were used for the immunoprecipitation reactions.doi:10.1371/journal.pgen.1000964.g005

Materials and Methods
For further details, see Text S1.

Yeast strains and general procedures
All the yeast strains used in this study were derived from the S288C genetic background, unless otherwise indicated, and are listed in Table S1.In our background, temperatures over 33uC were restrictive for spt16-197 growth, whereas temperatures below 31uC were permissive.All the experiments including spt16-197 mutants were performed at several temperatures.For each experiment shown in the Results section, we chose the maximal restrictive temperature at which specific reproducible results were obtained.Standard procedures were followed for cell culturing, synchronization at START and flow cytometry [76,77].

Northern blot analyses
The Northern blot analyses were performed as previously described [5].Six micrograms of total RNA prepared from yeast cells underwent electrophoresis on formaldehyde-agarose gels transferred to Hybond-N filters and UV crosslinked prior to hybridization at 65uC in 0.5M sodium phosphate buffer pH7 7% SDS with a [ 32 P]dCTP-labeled DNA probe.Quantification of the mRNA levels was performed in a phosphorimager (FLA-3000, FujiFilm); the data are provided in arbitrary units.All the values were normalized in relation to the amount of 25S rDNA detected by hybridization with a 32 P-oligolabeled 589 bp 25S rRNA internal fragment obtained by PCR and by using the 19-mer oligonucleotides TTGGAGAGGGCAACTTTGG and CAG-GATCGGTCGATTGTGC.For the mRNA histone analysis, the whole coding regions of HTA1 and HHT1 were used as probes.

Chromatin immunoprecipitation
Pol II ChIPs were performed as in [78], using the 8WG16 monoclonal antibody.Amplicons for Q-PCR quantification extended from +110 to +193 for CLN3, and from +6 to +95 for ADH1, in relation to the transcription start sites.

Rad53p phosphorylation assay
Yeast cultures were grown at 25uC to OD = 1.Cultures were kept at 25uC, or shifted at 37uC and incubated for two hours.Protein extracts for the Western blot analyses were prepared from trichloroacetic acid (TCA)-treated yeast cells.Protein extracts were resolved on a 7.7% SDS-PAGE (35:0.2acrylamide/bis-acrylamide).Immunoblots were done with the goat anti-Rad53 polyclonal antibody from Santa Cruz Biotechnology.

Detection of non chromatin-bound ''free'' histones associated with the histone chaperones Nap1 and Asf1
For the determination of histones associated with Nap1 and Asf1 in Figure 5A and 5B, one-liter cultures of the indicated strains carrying Nap1-FLAG [79] or Asf1-FLAG were grown exponentially in YPD media at 25uC.Cells were then harvested as such at a density of 2.5610E7 cells/ml for the Asf1-FLAG experiment shown in Figure 5B.For the Nap1-FLAG experiment shown in Figure 5A, cells were grown at 25uC until they reached a density of 1.5610E7 cells/ml at which point they were switched to the restrictive temperature of 37uC for two hours prior to harvesting the cells at a density of 2.5610E7 cells/ml.Whole cell extracts (WCEs) were prepared as previously described [49], and FLAG-tagged Nap1 (pRS316-Flag-yNap1) or Asf1-FLAG was immunoprecipitated using FLAG M2 agarose (Sigma).The immunoprecipitated material was resolved on precast 4-12% polyacrylamide gradient gels in MES buffer (BioRad), and were processed for Western blotting as previously described [49].FLAG M2 antibodies (Sigma) were used to detect Nap1-FLAG and Asf1-FLAG, while histone H4 and H2B were detected using the previously described polyclonal antibodies [49].Histone H2A was detected using an H2A antibody from Millipore (Cat.# 07-146).
The influence of transcription on free histone accumulation shown in Figure 5C was tested as follows.One liter of overnight culture of the spt16-197 (FY348) cells carrying FLAG-tagged Asf1 was grown in YPD at 25uC.Once the cells had reached a density of 1.5610E7 cells/ml, they were treated with alpha-factor for two hours at 25uC.Cells were treated with additional amounts of alpha-factor, divided into four equal aliquots, and were treated with or without 200mg/ml alpha-amanitin for 2 hours at 25uC or 35uC in the continued presence of alpha-factor.Afterward, cells were harvested and processed as described before, except histone H3, which was detected using a polyclonal antibody directed against the C-terminus of histone H3, as previously described [49].The inhibition of Pol II by alpha-amanitin was controlled by monitoring the mRNA levels of ACT1 in relation to ribosomal RNA levels (that are unaffected at the alpha-amanitin concentration used) using quantitative RT-PCR (Figure S5C).

Supporting Information
Figure S1 Quantification of the relative copy number of the plasmids described in Figure 2. The indicated plasmids were detected by quantitative PCR as described in Text S1.The ratio between the amplicon localized in the Amp gene of the plasmid and another amplicon localized in the chromosomal GAL1 genes is shown.1.0 corresponds to the empty vector.Found at: doi:10.1371/journal.pgen.1000964.s001(0.18 MB PDF) Figure S2 The G1 delay provoked by Spt16 inactivation was not prevented by the deletion of RAD9.(A) Wild-type (MMY20.4),rad9D (MMY20.1),spt16-197 (MMY20.2) and spt16-19 rad9D (MMY20.3)cells growing exponentially in YPD at 30uC were shifted to 37uC for four hours.Cells were then analyzed by flow cytometry.(B) Wild-type and mutant cells exponentially growing in YPD at 30uC were spotted onto YPD plates and incubated at 30uC, 32uC and 33uC, as indicated.Found at: doi:10.1371/journal.pgen.1000964.s002(0.19 MB PDF) unbudded cells was quantified by microscopy.(B) The wild-type (FY120), spt16-197 (FY348), spt16-197 rad53K227A (VO7) and rad53-K227A (V03) cells were synchronized at START by a treatment with alpha-factor for two hours at 25uC, followed by an additional one hour at 25uC or 32uC in the presence of mating pheromone.Cells were then released from the G1-arrest at time 0 at either 25uC or 32uC by washing out the alpha-factor.Samples were taken at the different time points to analyze the DNA content by flow cytometry and to measure the proportion of unbudded cells by microscopy.(C) Those samples from asynchronous cultures and from the time 0 of B were taken to analyze the CLN3 mRNA levels by Northern blot.The results of a significant experiment and the average quantification of three independent experiments are shown.The CLN3 mRNA levels were normalized to ADH1.doi:10.1371/journal.pgen.1000964.g006 Figure S3 rad53D enhances the thermosensitivity of spt16-197 independently of the DNA damage checkpoint.Cells were grown in YPD medium at 25uC.10-fold serial dilutions of the indicated strain were plated on YPD plates (or YPD+0.02%methyl methane sulfonate, MMS) and incubated for three days at the indicated temperatures.The mRNA levels of CLN3 and CLN3pr::lacZ in spt6-1004.The wild-type (FY120) and spt6-1004 (FY2180) cells were transformed with the plasmids bearing the CLN3pr::lacZ fusion number 1 (see Figure 2A) or ADH1pr::lacZ.These transformants were grown until the mid-log phase (AS) and were alpha factor-synchronyzed at 25uC (START), followed by one additional hour at 37uC in the continued presence of pheromone.The RNA samples were taken to analyze the transcript levels.mRNAs were quantified by Northern blot analysis.The results of a typical experiment and the average quantification of three independent experiments are shown.The CLN3 mRNA levels were normalized to ADH1, and the values of each strain at 37uC were represented in relation to 25uC.doi:10.1371/journal.pgen.1000964.g007Found at: doi:10.1371/journal.pgen.1000964.s003(0.17 MB PDF) Figure S4 hta2/htb2D partially suppresses the thermosensitivity of spt16-197.(A) Strains FY120, FY348, FY710, DMY10, DMY11, and DMY12 were transformed with pRS316 (empty vector), pRS316-HTA1-HTB1 or pRS316-HTA1-HTB1DNEG. Transformants were grown in SC-Ura medium at 25uC.10-fold serial dilutions of the indicated strain were plated on SC-Ura plates and incubated for three days at the indicated temperatures.The chromosomal, extrachromosal or plasmidic copies of HTA1-HTB1 and HTA2-HTB2 presented in each transformant are indicated.Red squares indicate the results of those strains containing two copies of H2A/H2B-encoding loci.(B) An extrachromosomal amplification of the HTA2-HTB2 locus was detected by PCR in FY710 (hta1/htb1D) and DMY11 (spt16-197 hta1/htb1D), following the protocol described in (Libuda and Winston, 2006).Found at: doi:10.1371/journal.pgen.1000964.s004(1.22 MB PDF) Figure S5 spt16-197 does not affect the levels of histone chaperones Nap1 and Asf1 or alter histone gene regulation.(A) Nap1 levels were unaffected in spt16-197.Nap1-FLAG was detected in WCEs of 4 independent generated wild type and spt16-197 strains by Western blotting using an anti-FLAG antibody.A non-specific band was used as the loading control.(B) Asf1 levels were unaffected in spt16-197.Asf1-FLAG was detected in WCE by Western blot with an anti-FLAG antibody.H2A was used as the loading control.(C) Alpha-amanitin inhibited RNA pol II transcription in alpha-factor-synchronized spt16-197 cells.The mRNA levels of the constitutively expressed ACT1 gene were measured by quantitative RT-PCR in the FY348 cells grown exponentially at 25uC and synchronized with alpha factor for four hours.The data was normalized to the levels of ribosomal RNA which is not affected by the concentration of alpha-amanitin used.(D) Repression of histones genes in G1 was not abolished by spt16-197.Wild-type (FY120) and spt16-197 (FY348) cells grown asynchronously (AS) were synchronized at START (ST) by treatment with alpha-factor for two hours at 25uC (ST), followed by an additional one hour at 25uC or 35uC in the presence of the mating pheromone.Cells were then released from the arrest at time 0 at either 25uC or 35uC by washing out the alpha-factor.Samples were taken at the indicated time points to analyze mRNA levels by Northern blot.H2A indicate the signal corresponding to HTA1 and HTA2, and H3 indicate the signal of HHT1 and HHT2.Found at: doi:10.1371/journal.pgen.1000964.s005(0.24 MB PDF) Figure S6 hhf1-36 and rad53K227A exhibit a negative synthetic interaction.Strains MSY623, DMY15, MSY781, and DMY16 exponentially grown in YPD at 30uC were spotted onto YPD plates and incubated for three days at 30uC and 37uC, as indicated.Found at: doi:10.1371/journal.pgen.1000964.s006(0.16 MB PDF) Table S1 The yeast strains used in this work.Found at: doi:10.1371/journal.pgen.1000964.s007(0.03 MB DOC) Text S1 Supplementary material and methods and supplementary references.Found at: doi:10.1371/journal.pgen.1000964.s008(0.03 MB DOC)

Figure 1 .
Figure1.CLN3 expression is down-regulated after Spt16 inactivation.Wild-type (FY120) and spt16-197 (FY348) cells grown asynchronously (AS) were synchronized at START by treatment with alpha-factor for two hours at 30uC (ST), followed by one additional one hour at 30uC or 35uC in the presence of the mating pheromone.Cells were then released from the arrest at time 0 at either 30uC or 35uC by washing out the alpha-factor.Samples were taken at different time points to analyze the DNA content by flow cytometry and the proportion of unbudded cells by microscopy (A), and to quantify the mRNA levels of the indicated genes by Northern blot analysis (B).Transcripts levels were represented as arbitrary units (AU) after normalization with 18S rRNA.The results of a typical experiment and the quantification of three independent experiments are shown.(C) Relative RNApol II binding to the transcribed region of CLN3 and ADH1 in spt16-197.Cells were synchronized with alpha-factor for two hours at 30uC, followed by one additional one hour at 30uC or 35uC in the presence of the mating pheromone.The 8WG16 antibody, recognizing the CTD repeats of Rpb1, was used.doi:10.1371/journal.pgen.1000964.g001

Figure 2 .
Figure 2. The CLN3 promoter mediated the down-regulation of its mRNA levels after Spt16 inactivation.(A) Diagram of the plasmidborne lacZ fusions, encoding E. coli ß-galactosidase, that were generated by introducing different fragments of the CLN3 promoter region.Constructions were numbered 1 to 3. The positions of the early cell cycle boxes (ECB) and the TATA box are indicated.An ADH1 promoter-lacZ fusion was used as a constitutively expressed control.(B) The mRNA levels of CLN3pr::lacZ and ADH1pr::lacZ fusion.The spt16-197 (FY348) strain, transformed with the plasmids bearing lacZ fusion number 1 (CLN3pr::lacZ) or ADH1pr::lacZ, was grown until the mid-log phase (AS), and was then synchronized at START (ST) by alpha-factor treatment for 2h at 30uC, followed by one additional hour of incubation at 30uC or 37uC in the presence of the mating

Figure 3 .
Figure3.The forced entry of Spt16-deficient cells into the S-phase lowered their viability.(A) Wild-type (FY120) and spt16-197 (FY348) cells, containing the centromeric pTet off -CLN3-HA plasmid, were grown in a synthetic medium (SC without uracil) at 30uC in the presence (+) or absence (2) of doxycycline (5mg/ml).Exponentially growing cells were then transferred to 37uC for four hours and analyzed by flow cytometry.(B) The wild-type and spt16-197 cells containing the pTet off -CLN3-HA plasmid were grown until the mid-log phase in a synthetic medium (SC-URA) at 30uC in the presence (+) or absence (2) of doxycycline.Then, 10-fold serial dilutions were spotted onto the same media and incubated at the permissive (30uC) or semi-permissive (32uC) temperature.The first spot on the left corresponds to 5 ml of the undiluted culture.Pictures correspond to three days of incubation.No growth was detected on the forth spot of spt16-197 minus doxycycline at 32uC, even after five days of incubation.(C) The wild-type (MMY18.10),sic1D (MMY18.12),spt16-197 (MMY18.11)and spt16-19 sic1D (MMY18.9)cells growing exponentially in YPD at 30uC were shifted to 37uC for four hours.Cells were then analyzed by flow cytometry.(D) The exponentially growing cells from the strains mentioned in (C) were spotted onto YPD plates, as described in (B), and incubated at 30uC and 32uC as indicated.Pictures correspond to three days of incubation.No growth was detected on the fifth spot of the double mutant at 32uC, even after five days of incubation.doi:10.1371/journal.pgen.1000964.g003

Figure 6 .
Figure 6.Excess histones induce a cell cycle delay in G1. (A) The spt16-197 (FY348) and spt16-197 rad53K227A (VO7) cells growing exponentially in YPD at 25uC were shifted to 32uC at the indicated times.DNA content was analyzed by flow cytometry and the proportion of

Figure 7 .
Figure 7. Spt6 dysfunction provokes G1/S defects and lowers cell viability in combination with rad53K227A.(A) Strains FY120, FY2180, VO1, VO3, DMY5, VO4, VO2, DMY6, DMY7, and DMY8 were grown in YPD at 25uC, spotted onto YPD plates and incubated for three days at the indicated temperature.(B) The wild-type (FY120), spt16-197 (FY348), and spt6-1004 (FY2180) cells exponentially growing in YPD at 25uC, were shifted for two hours at the indicated temperatures.Samples were then taken to analyze the DNA content by flow cytometry.(C) The wild-type (FY120) and spt6-1004 (FY2180) cells were synchronized at START by alpha-factor treatment for 2h at 25uC, followed by an additional one hour at 37uC in the presence of the mating pheromone.Cells were then released from the G1-arrest at time 0 at 37uC by washing out the alpha-factor.Samples were taken at the different time points to analyze the DNA content by flow cytometry and to measure the proportion of unbudded cells by microscopy.(D)The mRNA levels of CLN3 and CLN3pr::lacZ in spt6-1004.The wild-type (FY120) and spt6-1004 (FY2180) cells were transformed with the plasmids bearing the CLN3pr::lacZ fusion number 1 (see Figure2A) or ADH1pr::lacZ.These transformants were grown until the mid-log phase (AS) and were alpha factor-synchronyzed at 25uC (START), followed by one additional hour at 37uC in the continued presence of pheromone.The RNA samples were taken to analyze the transcript levels.mRNAs were quantified by Northern blot analysis.The results of a typical experiment and the average quantification of three independent experiments are shown.The CLN3 mRNA levels were normalized to ADH1, and the values of each strain at 37uC were represented in relation to 25uC.doi:10.1371/journal.pgen.1000964.g007

Figure 8 .
Figure 8.The overexpression of histones in the wild-type cells induces G1 delay.(A) Wild-type cells were transformed with pRS316 (empty vector) or with the analogous centromeric plasmids expressing either HTA1-HTB1 or a mutant version of this locus lacking the sequence that mediates its transcriptional repression in response to the free histones (HTA1-HTB1DNEG).The transformants were grown exponentially in a selective medium (AS), synchronized at START by treatment with alpha-factor for two hours (ST) and released from the arrest by washing out the alpha-factor.Samples were then taken at the different time points to analyze the DNA content by flow cytometry and the proportion of unbudded cells by microscopy.(B) Aliquots from the synchronized cells used in (A) were taken to analyze the CLN3 mRNA levels in START by Northern blot.The results of a typical experiment and the average quantification of three independent experiments are shown.The CLN3 mRNA levels have been normalized to ADH1.doi:10.1371/journal.pgen.1000964.g008