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Article |
PR-Set7–dependent lysine methylation ensures genome replication and stability through S phase
Correspondence to Claude Sardet: claude.sardet{at}igmm.cnrs.fr; or Eric Julien: eric.julien{at}igmm.cnrs.fr
PR-Set7/SET8 is a histone H4–lysine 20 methyltransferase required for normal cell proliferation. However, the exact functions of this enzyme remain to be determined. In this study, we show that human PR-Set7 functions during S phase to regulate cellular proliferation. PR-Set7 associates with replication foci and maintains the bulk of H4-K20 mono- and trimethylation. Consistent with a function in chromosome dynamics during S phase, inhibition of PR-Set7 methyltransferase activity by small hairpin RNA causes a replicative stress characterized by alterations in replication fork velocity and origin firing. This stress is accompanied by massive induction of DNA strand breaks followed by a robust DNA damage response. The DNA damage response includes the activation of ataxia telangiectasia mutated and ataxia telangiectasia related kinase–mediated pathways, which, in turn, leads to p53-mediated growth arrest to avoid aberrant chromosome behavior after improper DNA replication. Collectively, these data indicate that PR-Set7–dependent lysine methylation during S phase is an essential posttranslational mechanism that ensures genome replication and stability.
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Introduction |
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PR-Set7 (also known as SET8) is a single polypeptide with an evolutionary conserved SET domain that specifically catalyzes monomethylation of histone H4-K20 (H4-K20me1; Fang et al., 2002; Nishioka et al., 2002; Couture et al., 2005; Xiao et al., 2005), whereas dimethylation (H4-K20me2) and trimethylation (H4-K20me3) of the same lysine are triggered by several other histone methyltransferases, including Suv420h1/2 (Schotta et al., 2004), NSD1 (Rayasam et al., 2003), and Ash1 (Beisel et al., 2002). H4-K20 trimethylation (H4-K20me3) selectively marks constitutive pericentromeric heterochromatin (Schotta et al., 2004) and imprinting control regions (Delaval et al., 2007), whereas mono- and dimethylation are broadly distributed but principally enriched in euchromatin regions (Nishioka et al., 2002; Karachentsev et al., 2005). Although the biological function of H4-K20me remains poorly understood, several studies have suggested that H4-K20me2 is involved in the guidance of DNA repair proteins to DNA strand breaks (Sanders et al., 2004; Botuyan et al., 2006), whereas H4-K20me1 is associated with chromatin condensation processes (Trojer et al., 2007). Furthermore, changes in H4-K20me3 patterns are frequently observed in human cancers (Fraga et al., 2005), suggesting that the epigenetic signal achieved with this methyl residue can affect important chromatin-templated processes with far-reaching consequences for normal and neoplastic development.
As part of the initial characterization of PR-Set7 functions, its levels in HeLa cells were found to be cell cycle regulated with a peak during M phase (Rice et al., 2002). Furthermore, PR-Set7 becomes phosphorylated at the G2/M transition (Georgi et al., 2002) and remains associated with chromosomes during mitosis (Rice et al., 2002). Collectively, these observations suggested that this enzyme might be involved in some aspects of cell division control. Consistent with this hypothesis, inactivation of the Drosophila melanogaster PR-Set7 orthologue causes defective mitotic progression and activation of DNA damage checkpoints in highly dividing cells of larval tissues, including imaginal disc cells and third instar larval neuroblasts (Karachentsev et al., 2005; Sakaguchi and Steward, 2007). Conversely, up-regulation of mammalian PR-Set7 expression upon loss of the transcriptional regulator HCF-1 leads to improper mitotic H4-K20 methylation levels and cytokinesis defects in HeLa cells (Julien and Herr, 2004). However, it remained unclear whether these mitotic defects were the effect of PR-Set7 functions in the mitotic process or whether they were the end point of cellular alterations generated before the onset of mitosis, thereby raising the question of PR-Set7 functions during the different phases of the cell cycle.
In this paper, we study the functions of human PR-Set7. Our results show that PR-Set7 regulates cell cycle progression by playing a key role during S phase. PR-Set7 associates with sites of DNA synthesis and regulates replication-fork progression. Inhibition of its catalytic activity causes improper DNA replication and loss of H4-K20 mono- and trimethylation. These defects are associated with massive induction of DNA breaks that leads to a p53-dependent DNA damage response to avoid entry into mitosis and aberrant chromosome behavior. Collectively, our results establish that PR-Set7–dependent lysine methylation is an essential posttranslational modification that contributes to genome replication and stability through S phase.
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Results |
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35% showing a small, punctated nuclear staining (Fig. 1 A, left).
Importantly, transient transfection of an HA epitope–tagged PR-Set7 in U2OS cells resulted in the same punctated pattern (Fig. S1 B), whereas it was not observed in cells depleted for PR-Set7 by siRNA treatment (not depicted). Because PR-Set7 has been described as a chromatin-associated protein, we checked whether these PR-Set7 foci colocalized with previously described chromatin/DNA foci (Baus et al., 2003; Peters et al., 2003). Strikingly, they did not colocalize with HP1 heterochromatin foci or with 
-H2A.X DNA damage foci after bleomycin treatment (Fig. 1 A, merged panels). In contrast, PR-Set7 foci colocalized with the sites of DNA synthesis detected by a short pulse (10 min) of BrdU incorporation (Fig. 1 B, merged panel). Accordingly, coimmunostaining was also detected with the proliferating nuclear antigen A and the DNA polymerase epsilon, two components of the replication machinery (Fig. 1 C, merged panels). This colocalization was observed at all stages of S phase based on the size and nuclear localization of BrdU-positive replication foci (unpublished data). Collectively, these results suggested that PR-Set7 might be important for DNA replication and S-phase progression.
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Other studies have shown that human PR-Set7 also associates with mitotic chromosomes (Rice et al., 2002), raising the possibility that PR-Set7 also plays a role during M phase of the cell cycle. To determine whether the improper S-phase progression of PR-Set7–depleted cells resulted from S-phase alterations or from alterations that occurred during the previous M phase, we synchronized U2OS and U2OSSR cells at the G1/S border 36 h after shRNA expression. At this time, shPR7 U2OS cells still contained PR-Set7, as shown in Fig. 2 D (top left). 20 h later, once PR-Set7 was efficiently depleted (Fig. 2 D, top right), cells were released and pulse labeled with BrdU for 1 h at the indicated times to follow their progression through S phase. The results are shown in Fig. 2 D (bottom). 4 h after release, BrdU incorporation and DNA content of shLuc U2OS, shPR7 U2OS, and shPR7 U2OSSR indicated that entry into S phase was similar in the three cell populations. However shLuc U2OS and shPR7 U2OSSR cells underwent progression through S phase over an 10-h time period, with 70% of cells emerging in G2/M stage (Fig. 2 D, bottom; left and right), whereas shPR7 U2OS cells failed to complete S phase for the duration of the experiment (Fig. 2 D, bottom; middle). These results indicate that accurate completion of DNA replication is indeed directly dependent on PR-Set7 functions during S phase.
PR-Set7 silencing leads to massive DNA strand breaks during S phase and activation of a DNA damage response
Improper S-phase progression followed by a G2-phase arrest in PR-Set7–depleted cells led us to hypothesize that these cells had activated their DNA damage checkpoint. As shown in Fig. 3 A, alkaline comet assays, which monitor mainly single-strand breaks and alkali labile sites, revealed extensive DNA strand breaks in U20S cells 3 d after shPR7 expression.
Close to 80% of the PR-Set7–depleted U2OS cells displayed comets with a tail moment greater than five (Fig. 3 B), whereas no significant signature of damage was observed in control cells (shLuc-treated U2OS and shPR7 U2OSSR cells). Strikingly, spontaneous DNA strand breakage upon PR-Set7 silencing led to a robust DNA damage response. As shown in Fig. 3 C, the molecular signature of this response was easily detectable by immunoblotting in shPR7 U2OS cellular extracts with the presence of the activated/phosphorylated forms of the DNA damage kinases ataxia telangiectasia related (ATR) and ataxia telangiectasia mutated (ATM) and their phosphorylated targets CHK1 (phosphoserine 345), H2A.X (-H2A.X), and p53 (phosphoserine 15). A p53-dependent response was also activated in these cells, as indicated by the sustained up-regulation of the cyclin-dependent kinase inhibitor p21Waf1 (Fig. 3 C), a transcriptional target of p53 implicated in the maintenance of G2 arrest after DNA damage (Taylor and Stark, 2001). Importantly, this activation of the DNA damage signaling cascade was not detected in cellular extracts prepared from shLuc U2OS cells and shPR7 U2OSSR control cells (Fig. 3 C).
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-BrdU antiserum (to identify cells that had entered S phase) and with an antiserum against the phosphorylated form of histone H2A.X (-H2A.X). The results are shown in Fig. 3 D. As expected, only 3% of shLuc U2OS cells and 7% of shPR7 U2OSSR cells displayed both BrdU and -H2A.X staining during S-phase progression (Fig. 3 D). In contrast, whereas no -H2A.X staining was detected in shPR7 U2OS cells before release from the G1/S block, an intense -H2A.X immunostaining was observed in S phase–progressing cells, with up to 65% of BrdU-positive cells showing -H2A.X staining 5 h after their release (Fig. 3 D, top and bottom). Interestingly, digital sectioning images of asynchronous shPR7 U2OS cells incubated with BrdU for 10 min to detect active replication foci showed that a significant fraction of BrdU-positive foci colocalized with DNA damage foci (Fig. 3 E). A partial colocalization may lie in the fact that the appearance of DNA damage at replication foci rapidly causes the arrest of replication (Sancar et al., 2004), thereby preventing the incorporation of BrdU. Collectively, our results strongly suggest that the absence of PR-Set7 causes DNA breaks at replication sites, thereby leading to a DNA damage response characterized by activation of the ATM and ATR kinase–mediated pathways.
PR-Set7 regulates replication fork activity
The appearance of DNA breaks during S phase of PR-Set7–depleted cells could reflect some defects in replication fork activity. To adress this question, we monitored DNA replication dynamics at the level of individual DNA molecules by DNA combing experiments (Michalet et al., 1997; Pasero et al., 2002). 3 d after shLuc and shPR7 expression, we measured the velocity of replication forks by pulse labeling shRNA-treated cells consecutively with the thymidine analogues iododeoxyuridine (IdU) and chlorodeoxyuridine (CldU). Staining of combed DNA with anti-IdU and -CldU antibodies identified ongoing forks either as a stretch of IdU framed by CldU labeling or IdU label followed by a single CldU label. Representative examples of immunostaining are shown in Fig. S2 A (available at http://www.jcb.org/cgi/content/full/jcb.200706179/DC1). As shown in Fig. 4 A, quantification of the length of IdU/CldU signals indicated that the rates of elongation were dramatically reduced in PR-Set7–depleted cells (mean speed of 578 bp/min) compared with controls (750 bp/min and 892 bp/min in shPR7-treated U2OSSR cells and shLuc-treated U2OS cells, respectively), suggesting that replication fork velocity is impaired in the absence of PR-Set7.
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These results were surprising because a decrease in fork velocity is often compensated by an increase in replication fork density (Anglana et al., 2003). We assumed that this might reflect the inhibition of late replication origins by the ATR and ATM kinase pathways in response to DNA damage (Sancar et al., 2004). To test this hypothesis, replication fork activity (Fig. 4, B–D) and cell cycle progression (Fig. 4 E) were analyzed in shPR7 U2OS cells that were treated for 5 h with 10 mM caffeine (an inhibitor of ATM and ATR kinases). Although the length of replicated tracks remained severely reduced in these caffeine-treated shPR7 U2OS cells (Fig. 4 B, bottom), the density of their active replication forks was largely increased (Fig. 4, C [bar 4] and D), and they were then able to bypass S-phase arrest upon PR-Set7 depletion (Fig. 4 E). Thus, these results support a scenario in which the absence of PR-Set7 at replication foci impairs the progression of the replication machinery, leading to DNA breaks and activation of a DNA damage response that delays S-phase progression by regulating the origin-firing timing.
The p53 response induced by DNA damage in PR-Set7–depleted cells is required to prevent aberrant mitotic chromosome behavior
Inactivation of the Drosophila PR-Set7 orthologue also causes an activation of a DNA damage response in neuroblasts of the third instar larval brains (Sakaguchi and Steward, 2007). However, in contrast to our results, this activation is associated with extensive mitotic defects, including improper mitotic chromosome structure and progression (Karachentsev et al., 2005; Sakaguchi and Steward, 2007). In our case, we did not observe significant alterations of these mitotic events in shPR7 U2OS cells (unpublished data). This might reflect the fact that the Drosophila p53 orthologue does not possess the growth arrest functions like its mammalian counterpart (De Nooij and Hariharan, 1995; Sogame et al., 2003).
To address this point, we investigated whether human p53 was required to prevent the onset of mitosis in PR-Set7–depleted cells that were able to exit S phase with DNA damage. Thus, shRNA-mediated depletion of PR-Set7 was performed in HNFs or in the same cells expressing the human papillomavirus oncoprotein E6 (HNFE6), which targets p53 for degradation (Scheffner et al., 1993). Although E6 has targets other than p53, HNFE6 cells are commonly used as a human cellular model deficient for p53 functions (Baus et al., 2003; Mallette et al., 2007). As shown in Fig. 5 A, cell cycle profile analyses showed that both shPR7 HNF and shPR7 HNFE6 cells gradually accumulated in S phase and then in the G2/M stage 3 d after shRNA expression.
Consistent with our data in U20S cells, none of the shPR7 HNF cells with DNA damage had entered into mitosis, as indicated by the fact that we did not detect fluorescent coimmunostaining of these cells probed with the DNA damage marker -H2A.X and the mitotic marker phosphohistone H3-S10 (unpublished data). In contrast, this costaining was readily observed in 90% of shPR7 HNFE6 mitotic cells, as shown in Fig. 5 B. Strikingly, these cells displayed abnormal mitotic chromosome morphology (Fig. 5 B).
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80%) as shown in Fig. 5 (C, b and c) or condensed chromosomes (20%) but with a significant number of aberrations, including chromosome breaks (Fig. 5 C; d, d-1, d-2, and d-3) and sister chromatid fusion (Fig. 5 C; d and d-4). Conspicuously, such mitotic defects are reminiscent of those observed in Drosophila PR-Set7–depleted neuroblasts (Sakaguchi and Steward, 2007). These data illustrate the importance of the DNA damage–induced p53 response to prevent abnormal chromosome behavior upon PR-Set7 depletion in human cells.
PR-Set7 depletion in U2OS cells is associated with reduced levels of H4-K20 mono- and trimethylation
To gain insights into the mechanisms by which PR-Set7 regulates DNA replication and genome stability, we examined the levels of H4-K20 methylation in PR-Set7–depleted cells displaying improper S-phase progression. 3 d after shRNA expression, total histones of U2OS and U2OSSR cells were acid extracted and subjected to immunoblot analysis with the different antimethylated H4-K20 antibodies. The results are shown in Fig. 6 A.
The levels of the three methyl marks were similar between shLuc U2OS and shPR7 U2OSSR cells (Fig. 6 A). In contrast, the levels of H4-K20me1 as well as of H4-K20me3 were strongly reduced in shPR7 U2OS cells, suggesting that PR-Set7 plays a key role in the maintenance of both H4-K20 mono- and trimethyl marks during S phase. For H4-K20me2, we observed only a slight reduction in shPR7 U2OS cells (Fig. 6 A), suggesting that changes in H4-K20me2 levels are not associated with the DNA replication defects described here. Consistent with the preservation of H4-K20me2 in PR-Set7–depleted U2OS cells, p53-binding protein 1 (53BP1), which associates primarily with H4-K20me2 in response to DNA damage (Botuyan et al., 2006), was still colocalized with spontaneous as well as irradiation-induced DNA damage foci (Fig. S3, available at http://www.jcb.org/cgi/content/full/jcb.200706179/DC1).
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PR-Set7–mediated lysine methylation is essential for S-phase progression and genomic stability
To further demonstrate that loss of the histone methyltransferase activity of PR-Set7 is indeed the key event that causes defective DNA replication and genomic instability during S phase, we examined the ability of shRNA-resistant PR-Set7 (PR-Set7SR) mutants to rescue the PR-Set7 loss of function phenotype. Fig. 6 B shows the structure of the different PR-Set7SR mutants tested. Among them, only PR-Set7SR/
141–322 deleted for the SET domain and PR-Set7SR/R265G, which contains an arginine to glycine substitution at position 265 within the entire SET domain, lack PR-Set7 methyltransferase activity (Nishioka et al., 2002).
The PR-Set7SR mutants were stably expressed in U2OS cells and infected with either shLuc or shPR7 retrovirus. 4 d after shRNA expression, we monitored (1) defective S-phase progression by measuring the levels of BrdU incorporation and DNA content by flow cytometry and (2) DNA damage by immunofluoresence with -H2A.X staining. The results are shown in Fig. 6 (C and D, respectively). Importantly, the different PR-Set7 mutants themselves did not induce defective cell cycle progression and DNA breaks compared with untransfected cells (unpublished data). As expected, PR-Set7 inhibition led to an accumulation of cells in S and G2/M stages associated with DNA breaks (Fig. 6, C and D). Analysis of the different PR-Set7SR mutants reveals that PR-Set7 methyltransferase activity is essential to preserve genome stability and proper DNA replication. Wild-type PR-Set7SR as well as PR-Set7SR/1–30, PR-Set7SR/37–50, and PR-Set7SR/51–140 (Fig. 6 D, bars 2–5) were generally successful in rescuing both normal S-phase progression (Fig. 6 D) and genome stability (Fig. 6 D), whereas PR-Set7SR/141–322 and PR-Set7SR/R265G were not (Fig. 6 D, bars 6 and 7). Collectively, these results indicate that PR-Set7–mediated lysine methylation, likely H4-K20me, is essential for the accurate completion of DNA replication and for preservation of genome integrity through S phase.
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Discussion |
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To characterize the PR-Set7 loss of function phenotype in mammalian cells, we used shRNA viral vectors to silence PR-Set7 expression. The main limitation of this approach is the off-target effects of the shRNA sequences (for review see Cullen, 2006). Therefore, we created shRNA-resistant wild-type PR-Set7 molecules in U2OS cells and sucessfully rescued all aspects of the PR-Set7 loss of function phenotype. Finally, the use of mutant shRNA-resistant PR-Set7 molecules revealed that the PR-Set7 methyltransferase activity was essential for genome replication and stability through S phase.
Regulation of H4-K20 methylation levels by PR-Set7
In mammalian cells, mono- and trimethylation of H4-K20 appear relatively stable during the cell cycle, whereas dimethylation follows a cyclic pattern with maximum levels in S phase, suggesting that H4-K20me1 and H4-K20me3 are regulated differently than the dimethyl mark (Fang et al., 2002; Karachentsev et al., 2007). Accordingly, our results in U2OS cells indicate that PR-Set7 functions during S phase are important for the maintenance of H4-K20me1 and H4-K20me3 but not for H4-K20me2 (Fig. 6). A role for PR-Set7 in the regulation of H4-K20me3 was unexpected because this enzyme is clearly defined as a methyltransferase that specifically monomethylates histone H4-K20 (Couture et al., 2005; Xiao et al., 2005), whereas H4-K20me3 was triggered by the Suv4-20h1 and Suv420h2 enzymes (Schotta et al., 2004). Importantly, the levels of Suv4-20h1 and Suv420h2 are not altered in PR-Set7– depleted cells (unpublished data), indicating that the decrease in H4-K20me3 is likely caused by loss of the monomethyl mark. This interdependence between the lysine mono- and trimethylation state, as suggested here for histone H4-K20, has been previously described for another mark of silent chromatin domains, histone H3-K9me (Peters et al., 2003; Schotta et al., 2004). In this case, the H3-K9 trimethylating enzymes appear to use an H3-K9 monomethyl residue as their in vivo substrate (Peters et al., 2003). Accordingly, knockout of the H3-K9 trimethylating enzymes in mouse embryonic stem cells resulted in a significant decrease in H3-K9me3 and, conversely, an increase in H3-K9me1 (Peters et al., 2003, Schotta et al., 2004). Although the PR-Set7 loss of function phenotype described here provides the first evidence that this scenario might also apply to H4-K20me, it will be important to study the phenotype of the loss of function of Suv4-20h genes to fully address this question, a compound model that is now available (Benetti et al., 2007).
PR-Set7 functions during DNA replication
An important finding of our studies is that PR-Set7–depleted cells can initiate DNA replication, at least during early S phase, but then they fail to proceed properly with the elongation step of DNA replication. How might PR-Set7 ensure proper replication fork progression? In Drosophila, the PR-Set7 orthologue suppresses position effect variegation (Nishioka et al., 2002; Karachentsev et al., 2005), raising the possibility that it functions as a transcriptional repressor. Although we cannot exclude that mammalian PR-Set7 may indirectly promote replication fork progression by regulating gene expression, localization of the enzyme at sites of DNA synthesis (Fig. 1) and our results with synchronized cells (Fig. 2 D) support a model in which PR-Set7 would directly participate in the replication machinery. Intriguingly, our results show that localization of PR-Set7 at replication foci is strongly enhanced upon proteasome inhibition (Fig. 1), suggesting a rapid exchange of the pool of PR-Set7 proteins associated with these foci during S phase. The biological significance of this proteasome-mediated turnover of PR-Set7 is still unclear; however, our current hypothesis is that this might represent a novel and important regulatory step in the control of DNA replication. Among many other possible scenarios, this might be linked with rapid and local changes of chromatin structure that are necessary for the activation and displacement of replication forks along the DNA template (Nishitani et al., 2006; Senga et al., 2006).
Recruitment of a histone methyltransferase to sites of DNA synthesis is not unprecedented, as it has been observed for the histone H3-K9 methyltransferases G9a (Esteve et al., 2006) and SETDB1 (Sarraf and Stancheva, 2004). This is thought to contribute to the restoration of H3-K9 methylation patterns on newly assembled chromatin behind the replication fork. A similar function of PR-Set7 in the maintenance of H4-K20 methylation patterns during S phase would be consistent with our data and would notably explain why PR-Set7 inhibition causes an acute DNA replication stress. Indeed, structural analysis of nucleosomal particles revealed that the position of K20 within the N-terminal tail of histone H4 makes an interparticle contact between the histone H2A-H2B dimer and DNA (Davey et al., 2002), an observation that suggests that methylation of this lysine can directly affect the nucleosome structure. Furthermore, it has been recently shown that binding of the protein L3MBTL1 to nucleosomes is directly regulated by the specific methylation state of H4-K20 (Trojer et al., 2007), which is thought to contribute to chromatin compaction. Therefore, alterations in H4-K20 methylation could result in a rapid regulatory dead end for the packaging of nascent DNA into chromatin, thereby leading to the generation of DNA breaks, as we have observed in PR-Set7–depleted cells.
An alternative but not mutually exclusive possibility is that PR-Set7 may also modify other components of chromatin, including the replication machinery itself, that are essential for proper replication fork progression and stability. For example, the acetyltransferase HBO1, which is required for S-phase initiation and fixing replication origins (Doyon et al., 2006), can acetylate histone H4 as well as replication proteins (Iizuka et al., 2006). Recently, PR-Set7 has been reported to monomethylate the tumor suppressor p53 at lysine 382, which represses p53 transcriptional activation on a subset of target genes (Shi et al., 2007). Importantly, inhibition of p53-K382me without affecting H4-K20me did not cause any growth defects in U2OS cells (Shi et al., 2007), suggesting that abnormal PR-Set7–mediated methylation of p53 is not the prime cause of the replication defects described here. Other nonhistone targets of PR-Set7 have not been identified yet, and further work will be necessary to identify such targets. If they exist, it will be of great interest to determine whether their methylation plays a role in genome replication and stability.
Does PR-Set7 play a role in tumorigenesis?
The S phase of the cell cycle is a period of high vulnerability for the genome. Either intrinsic or external events can lead to the stalling of replication forks, which, if not managed properly, can have devastating consequences for the integrity of the genome. Indeed, there is now clear evidence that DNA damage during S phase can lead to genomic instability, thereby creating clones of cells that proliferate uncontrollably (Bartkova et al., 2005; Gorgoulis et al., 2005). Our findings that PR-Set7 catalytic activity ensures proper DNA replication and stability during S phase suggest that PR-Set7–mediated lysine methylation is a safeguarding posttranslational modification for the genome. This is particularly evident in cells defective for the tumor suppressor p53 and depleted from PR-Set7, in which improper DNA replication and generation of DNA damage lead to aberrant mitotic chromosome behavior (Fig. 5), a hallmark of cancer cells (for review see Duesberg and Li, 2003). Given the importance of deregulated DNA replication in tumorigenesis (Bartkova et al., 2006; Di Micco et al., 2006) and that loss of H4-K20me3 patterns are observed in almost all human cancers (Fraga et al., 2005), it will be interesting to explore whether PR-Set7 is a putative target for cellular transformation and contributes to tumor development.
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Materials and methods |
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shRNA preparation and transfection
A human PR-Set7 shRNA directed against the PR-Set7 mRNA sequence GATGCAACTAGAGAGACA (nucleotides 854–871) was checked against the human genome sequence to ensure that only the PR-Set7 mRNA would be targeted. A firefly luciferase nonspecific control shRNA was used. The shRNA sequences were introduced into the puromycin retroviral vector RNAi Ready pSiren (BD Biosciences) according to the manufacturer's instructions. Cells were infected with the corresponding retroviral particles as described previously (Le Cam et al., 2006) and were selected 24 h later in 10 µg/ml puromycin.
Mutagenesis and generation of PR-Set7SR cell lines
A hygromycin retroviral vector pMSCV was modified to encode the HA epitope tag downstream of the ATG, creating pMSCV-HA vector. The HA epitope tag sequence is followed by an SpeI–BamH1 polylinker. Spe1–BamH1 cDNA fragments encoding the different PR-Set7 truncations were cloned into pMSCV-HA vector. The PR-Set7SR constructs were prepared by introducing five silent mutations into PR-Set7 cDNA as described previously (Julien and Herr, 2003). For stable PR-Set7SR expression, U2OS cells were infected as described previously (Le Cam et al., 2006) and selected with 60 µg/ml hygromycin B.
Flow cytometry
Cells were incubated with 300 µM BrdU (Sigma-Aldrich) for 1 h, fixed with a 70% ethanol solution, and permeabilized with 0.2% Triton X-100 for 10 min. Then, cells were treated with 0.2 N HCl before staining with mouse antibody to BrdU (1:30 diluted in PBS with 0.2% Tween 20 and 1% BSA; Becton Dickinson) for 1 h at room temperature followed by 1-h incubation with an FITC-conjugated antibody (1:300; BD Biosciences). DNA was then counterstained by overnight incubation with 7-amino-actinomycin D (7AAD; 1:50; Sigma-Aldrich) in the presence of RNase. Cell cycle profiles were analyzed by a flow cytometer (FACScan; Becton Dickinson) using CellQuest software (Becton Dickinson).
Western blot analysis
For immunoblot analysis, cells washed with PBS were lysed in laemmli buffer (for histones, acid extraction was performed according to the Abcam protocol). After measuring protein quantity by Bradford, equal amounts of protein were resolved by SDS-PAGE, transferred to a nitrocellulose membrane (Whatman), and probed with one of the following antibodies: mouse antiphospho-ATM-Ser1981 (1:1,000; Cell Signaling Technology), rabbit antiphospho-ATR-Ser428 (1:1,000; Cell Signaling Technology), rabbit antiphospho-Chk1-Ser345 (1:1,000; Cell Signaling Technology), mouse anti-Chk1 (1:1,000; gift from V. Gire), rabbit anti-p21 (1:500; gift from V. Dulik, Institut de Génétique Moléculaire, Montpellier, France), rabbit antiphospho-p53-Ser15 (1:500; gift from V. Gire), mouse anti-p53 (1:1,000; gift from V. Gire), rabbit anti–PR-Set7 (1:1,000; Millipore), mouse anti–β-actin (1:20,000; Sigma-Aldrich), mouse antiphospho-H2A.X-Ser139 (1:1,000; Millipore), rabbit antiphospho-histone H3-Ser10 (1:1,000; Millipore), rabbit anti–H4-K20-1xMe, -2xMe, or -3xMe (1:1,000; Millipore), rabbit anti–histone H4 (1:1,000; Millipore), and mouse anti-HA tag (12CA5; Cold Spring Harbor Laboratory). Membranes were then incubated with the appropriate HRP-conjugated secondary antibodies. The immunoreactive bands were detected by chemiluminescence (Thermo Fisher Scientific).
Immunofluorescence
For immunofluorescence, shRNA-infected cells grown on glass coverslips were fixed in 3% PFA for 15 min, permeabilized with 0.2% Triton X-100 in PBS for 15 min, and blocked for 1 h with 1% BSA (Roche) at room temperature. To visualize PR-Set7, cells on coverslips were pretreated with 15 µM MG132 for 1 h and incubated for 10 min at 4°C with a solution of PBS and 0.5% Triton X-100 before PFA fixation. Incubation with primary antibodies against PR-Set7 (1:600; Millipore), HA tag (12CA5; 1:500), phospho-H2A.X-Ser139 (1:500; Millipore), phosphohistone H3-Ser10 (1:600; Millipore), proliferating cell nuclear antigen (1:500; gift from J. Piette), DNA polymerase 
(1:800; gift from D. Fischer, Institut de Génétique Moléculaire, Montpellier, France), and 53BP1 (1:500; Millipore) was conducted at room temperature for 1 h. After washing, cells were incubated with AlexaFluor568- or 488-conjugated goat anti–mouse or goat anti–rabbit secondary antibodies (Invitrogen) for 1 h. Cells were finally stained with DAPI, and coverslips were mounted using Prolong Antifade (Invitrogen). Samples were examined at room temperature with a microscope (Imager.Z1; Carl Zeiss, Inc.) equipped with a 63x NA 1.4 or 40x NA 1.25 oil immersion objective and an Apotome device (Carl Zeiss, Inc.). Pictures were captured using a camera (CoolSNAP HQ2; Photometrics) interfaced with MetaMorph software 7.1 (MDS Analytical Technologies), and levels were adjusted with Photoshop 7 (Adobe). Digital sectioning images (Apotome) were captured using Axiovision 4.6 software (Carl Zeiss, Inc.).
Chromosome spreading
3 d after shPR7 or shLuc expression, HNFE6 cells were incubated for 30 min with 10 µg/ml colchicine. After washing in PBS, cells were resuspended in a hypotonic solution of 75 µM KCl for 15 min at 37°C. They were then fixed twice with a methanol/acetic acid buffer for 10 min at 4°C and spotted on frozen microscope glass slides. After drying, slides were stained with a solution of PBS and 0.1% Tween 20 containing Hoescht (1:10,000) mounted using Prolong Antifade, and images were captured at room temperature using an Imager.Z1 microscope with a 100x NA 1.4 oil immersion objective (Carl Zeiss, Inc.) equipped with a CoolSNAP HQ2 camera interfaced with MetaMorph software 7.1. Levels were adjusted with Photoshop 7.0.
DNA combing
U2OS cells were pulse labeled for 15 min with 50 µM BrdU and were harvested. For IdU-CldU labeling experiments, cells were successively labeled for 1 h with 25 µM IdU and 200 µM CldU for 1 h. Nuclei (from 2.5 x 104 cells) were embedded in agarose plugs, stained with YOYO-1 (Invitrogen), and resuspended in 50 mM MES, pH 5.6, after digestion of the plugs with agarase (Roche). Then, DNA combing was performed as described previously (Michalet et al., 1997). In brief, combed DNA fibers were denatured for 25 min with 0.2 N NaOH, and BrdU and CldU were detected with a rat anti-BrdU antibody (clone BU-75; Sera Laboratory) and a secondary antibody coupled to AlexaFluor488 (Invitrogen). IdU was detected with a mouse monoclonal anti-IdU antibody (clone B44; Becton Dickinson) and a secondary antibody coupled with AlexaFluor546 (Invitrogen). DNA molecules were counterstained as previously described (Pasero et al., 2002) with an antiguanosine antibody (Argene) and an anti–mouse IgG coupled to AlexaFluor546 (Invitrogen). DNA fibers were examined, and images were captured at room temperature using a microscope (DMRX; Leica) with a 40x NA 1.25 oil immersion objective (Leica) and equipped with a CoolSNAP FX camera interfaced with MetaMorph software 7.1. Levels were adjusted with Photoshop 7.0. Replicated track sizes were measured with MetaMorph using adenovirus DNA molecules as a size standard (one pixel = 680 bp). Fork speed was calculated by dividing track sizes by labeling time, and the nonparametric test of Mann-Whitney was used.
Comet assay
DNA break repair was assayed by alkaline single-cell agarose gel electrophoresis essentially as described previously (Murr et al., 2006). In brief, cells were infected with shRNA luc (control) or shRNA PR-Set7, harvested (105 per pellet) 5 d after infection, mixed with low-gelling temperature agarose (type VII; Sigma-Aldrich), and layered onto agarose-coated glass slides. Slides were maintained in the dark at 4°C to gel and were submerged in lysis buffer (2.5 M NaCl, 0.1 M EDTA, 10 mM Trizma base, 1% Triton X-100, and 10% DMSO) for at least 1.5 h. After washing with Tris buffer, slides were incubated for 1 h in alkaline electrophoresis buffer (300 mM NaOH and 1 mM EDTA, pH 10) or in neutral electrophoresis buffer (300 mM sodium acetate, 100 mM Tris-HCl, and 1% DMSO, pH 8.3). Slides were then subjected to electrophoresis for 40 min at 25 V, air dried, neutralized, and stained with 30 µl ethidium bromide (20 µg/ml–1). Mean comet tail moment was scored for 50 cells/slide by using Comet Imager 1.2.10 software (MetaSystems Inc.).
Online supplemental material
Fig. S1 shows the cell cycle distribution of PR-Set7 in U2OS and normal fibroblasts (A) and in the nuclear localization of HA epitope–tagged PR-Set7 in U2OS cells treated for 1 h with proteasome inhibitor MG132 (B). Fig. S2 shows representative DNA combing pictures in shLuc and shPR7 U2OS cells. Fig. S3 shows 53BP1 localization at spontaneous DNA damage foci in shPR7-depleted U2OS cells and quantification of shPR7 U2OS cells displaying 53BP1 foci after ionizing radiation. Fig. S4 shows the impact of PR-Set7 depletion in proliferation rates and H4-K20me status of HeLa cells. Online supplemental material is available at http://www.jcb.org/cgi/content/full/jcb.200706179/DC1.
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Acknowledgments |
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This work was performed with the institutional support of the Centre National de la Recherche Scientifique and by grants from the Institut National du Cancer and the Association pour la Recherche sur le Cancer to C. Sardet and E. Julien. M. Tardat was supported by a fellowship from the French government.
Submitted: 25 June 2007
Accepted: 27 November 2007
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