PMC:546168 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/546168","sourcedb":"PMC","sourceid":"546168","source_url":"http://www.ncbi.nlm.nih.gov/pmc/546168","text":"Translocation of XRCC1 and DNA ligase IIIα from centrosomes to chromosomes in response to DNA damage in mitotic human cells \n\nAbstract\nDNA single-strand breaks (SSBs) are the most frequent lesions caused by oxidative DNA damage. They disrupt DNA replication, give rise to double-strand breaks and lead to cell death and genomic instability. It has been shown that the XRCC1 protein plays a key role in SSBs repair. We have recently shown in living human cells that XRCC1 accumulates at SSBs in a fully poly(ADP-ribose) (PAR) synthesis-dependent manner and that the accumulation of XRCC1 at SSBs is essential for further repair processes. Here, we show that XRCC1 and its partner protein, DNA ligase IIIα, localize at the centrosomes and their vicinity in metaphase cells and disappear during anaphase. Although the function of these proteins in centrosomes during metaphase is unknown, this centrosomal localization is PAR-dependent, because neither of the proteins is observed in the centrosomes in the presence of PAR polymerase inhibitors. On treatment of metaphase cells with H2O2, XRCC1 and DNA ligase IIIα translocate immediately from the centrosomes to mitotic chromosomes. These results show for the first time that the repair of SSBs is present in the early mitotic chromosomes and that there is a dynamic response of XRCC1 and DNA ligase IIIα to SSBs, in which these proteins are recruited from the centrosomes, where metaphase-dependent activation of PAR polymerase occurs, to mitotic chromosomes, by SSBs-dependent activation of PAR polymerase.\n\nINTRODUCTION\nDNA single-strand breaks (SSBs) are generated directly by the action of DNA-damaging agents, such as ionizing radiation and active oxygen species. In addition, they arise as reaction intermediates during lagging strand DNA synthesis and DNA excision repair. There is compelling evidence that the DNA repair protein XRCC1 plays a critical role in the repair of SSBs [reviewed in (1)]. Notably, XRCC1 mutant cells exhibit an elevated frequency of spontaneous chromosomal aberrations and deletions (2), and inactivation of the mouse Xrcc1 gene by gene targeting results in embryonic lethality (3), suggesting the importance of XRCC1-dependent repair in maintaining genome stability.\nAlthough XRCC1 protein has no known catalytic activity, it does interact with many different protein partners, including OGG1 (4), PARP-1 (5,6,7), PARP-2 (7), DNA polymerase β (8,9), AP endonuclease (10), polynucleotide kinase (11) and DNA ligase IIIα (LIGIIIα) (12,13). These multiple interactions suggest that XRCC1 co-ordinates the repair of SSBs by acting as a scaffolding factor upon which the other SSB repair proteins assemble. The interaction between XRCC1 and LIGIIIα is constitutive and stabilizes LIGIIIα (14). Interestingly, studies, in which the LIGIIIα-interacting BRCT domain of XRCC1 was inactivated, revealed that XRCC1 repair functions are LIGIIIα-dependent in G1 phase cells and non-cycling cells but are LIGIIIα-independent in S phase cells (15). These results suggest that the XRCC1/LIGIIIα complex participates in SSBs repair and the repair of base lesions by the short patch sub-pathway of BER, whereas XRCC1 functions in certain S phase-specific repair events that are not well understood.\nPARP-1 is the first member of a growing family of enzymes that synthesize poly(ADP-ribose) (PAR). PARP-1 is an abundant nuclear protein that binds avidly to DNA strand breaks, in particular DNA SSBs via two tandem arrayed N-terminal zinc fingers. The binding to SSBs activates the polymerase activity of PARP-1, resulting in the poly(ADP-ribosylation) of PARP-1 itself and other proteins. Although the exact role of PARP-1 in DNA repair remains the subject of conflicting reports, the spontaneous genetic instability and hypersensitivity to DNA-damaging agents of parp-1 mutant cells provides compelling evidence that PARP-1 plays an important role in maintaining genomic integrity [reviewed in (16,17)]. Both XRCC1 (5,6,7) and LIGIII (18) preferentially bind to poly(ADP-ribosylated) PARP-1, suggesting that auto-modified PARP-1 molecules in the vicinity of SSBs may serve as the signal for the recruitment of SSBs repair proteins. In support of this idea, it has been shown that local ultraviolet (UV) irradiation of human nucleotide excision repair-deficient XPA cells expressing UV damage endonuclease (UVDE), which generates SSBs at UV-irradiated restricted regions in nucleus (19) or local laser irradiation (20), resulted in massive synthesis of PAR only within the irradiated regions. Moreover, it was shown that the accumulation of XRCC1 at SSBs is dependent upon PAR synthesis (19,20), and accumulation of polymerase β as well as proliferating cellular nuclear antigen (PCNA) at SSBs is dependent on the presence of XRCC1 (20). Thus, the accumulation of XRCC1 at SSBs is essential for both polymerase β-dependent short-patch and PCNA-dependent long-patch repair pathways.\nRecently, it has been shown that several members of the PARP family, PARP-1 (21,22), PARP-3 (23), tankyrase (24) and PAR glycohydrolase (25), which degrades PAR polymers, localize to the centrosome in mitotic cells. This prompted us to examine whether XRCC1 and LIGIIIα exhibit similar behavior. By using immunofluorescence and confocal microscopy, we show that both XRCC1 and LIGIIIα are mainly localized within centrosomes during mitosis and that this sub-nuclear localization is dependent upon PAR synthesis. In response to DNA damage, both XRCC1 and LIGIIIα translocate from the centrosomes region to the chromosomes providing the first evidence for the repair of SSBs in mitotic chromosomes.\n\nMATERIALS AND METHODS\n\nCell lines and culture conditions\nHeLa, XPA-UVDE and XPA-Vector cells (26) were grown in Eagle's minimal essential medium (Nissui) supplemented with 10% fetal bovine serum.\n\nDNA transfection\nDNA constructs were made according to the standard procedures (27). Briefly, the cDNA of full-length human LIGIIIα was amplified by using PCR with 5′ and 3′ primers containing SalI and EcoRV sites, respectively. The amplified DNA fragments were subcloned into the SalI and SmaI sites of pEGFP-C1 (Clontech). A CHPL-GFP plasmid (obtained from Dr Phanglang Chen) contains a CMV promoter and drives the expression of an in-frame N-terminal green fluorescent protein (GFP) protein. The cDNA of full-length LIGIIIβ was subcloned into the NotI site of the modified CHPL-GFP plasmid. The plasmid expressing full-length XRCC1 tagged with GFP is described previously (20). The DNA constructs were verified by sequencing. These plasmids were introduced into cells using Fugene 6 (Roche) according to the manufacture's protocol.\n\nImmunofluorescence microscopy\nFor immunolabeling, asynchronous HeLa cells were grown for 2 days in glass bottom culture dishes. To examine the effect of inhibitors of PARP, the cells were incubated for 1 h in medium supplemented with 3-aminobenzamide (3-AB) (8 mM; Sigma), fixed with methanol:acetone (1:1) for 10 min at −20°C, then dried. In some cases, the cells were fixed by incubation in 4% formaldehyde in phosphate-buffered saline (PBS) for 10 min at RT, then permeabilized in 0.2% Triton X-100 in PBS for 2 min at RT. Local UV-irradiation, in which XPA-UVDE or XPA-Vector cells were irradiated through tiny pores in polycarbonate membrane filter, was performed essentially as described previously (19). XPA-UVDE or XPA-Vector cells were incubated for 1 h in medium supplemented with or without 1,5-dihydroxyisoquinoline (DIQ) (100 μM; Sigma) before irradiation, and washed twice with Hanks' solution (Nissui) with or without DIQ. Then, the cells were irradiated with UV (20 J/m2). After local UV-irradiation, the cells were incubated in medium with or without DIQ at 37°C for 2 min, and then fixed as described above. Fixed cells were rinsed once with TNT buffer (0.1 M Tris–HCl, 0.15 M NaCl, 0.05% Tween 20, pH 7.5) and then incubated in TNB buffer [TNT buffer containing blocking reagent (NEN)] at 30°C for 30 min. After incubation with anti-XRCC1 antibody (ab144, Abcam) at 1:150 dilution in TNB buffer at 30°C for 1 h, the cells were washed three times with TNT buffer prior to incubation with Alexa Fluor 594 goat anti-rabbit immunoglobulin G (IgG) conjugate (Molecular Probes) at 1:400 dilution in TNB buffer for 1 h. The cells were washed with TNT buffer and then incubated with anti-γ-tubulin (1:200 dilution, GTU-88; Sigma), anti-PAR (1:200 dilution; Trevigen) or anti-DNA LIGIII (1:50 dilution; GeneTex 1F3 or 4C11) in TNB buffer for 1 h. After washing with TNT buffer, the cells were incubated with Alexa Fluor 488 goat anti-mouse IgG conjugate (Molecular Probes) at 1:400 dilution in TNB buffer for 1 h. The cells were washed and then incubated with TOPRO-3 (2 μg/ml, Molecular Probes) and RNaseA (100 μg/ml; Sigma) in PBS at 37°C for 15 min. After washing, the cell samples were mounted in drops of PermaFluor (Immunon), and cover-slips were added. Confocal imaging was performed using an Olympus FV-500 confocal laser system connected to an Olympus microscope (IX81) with a 60× oil immersion objective lens (PlanApo).\n\nRESULTS AND DISCUSSION\n\nDNA ligase IIIα is recruited to SSB in response to the synthesis of PAR\nPreviously, using local UV-irradiation of human nucleotide excision repair-deficient XPA cells expressing UVDE, we had shown that PAR synthesis occurred only within the UV-irradiated regions and that the recruitment of XRCC1 to these regions was dependent upon PAR synthesis (19). Since there is evidence that XRCC1 functions independently of LIGIIIα under certain circumstances (15,28), we asked whether LIGIIIα was also recruited to the sites of SSBs induced by the action of UVDE in XPA cells after local UV-irradiation. As shown previously (19), XRCC1 accumulated at the irradiated spots 2 min after irradiation (Figure 1, column b, upper panel). LIGIIIα was also recruited to the same sites of DNA damage (Figure 1, column b, middle and bottom panels). As was observed with XRCC1, the recruitment of LIGIIIα to the DNA damage sites was dependent upon the expression of UVDE (Figure 1, column e) and was prevented by DIQ (100 μM), an inhibitor of PARP (Figure 1 column c). To confirm that the DNA damage-dependent sub-nuclear location of LIGIIIα was not an artifact of the immunocytochemistry, we transiently expressed a GFP-tagged version of LIGIIIα in XPA-UVDE cells. In accord with the results described above, GFP-LIGIIIα was observed in the nucleolus as well as in the nucleoplasm of undamaged cells (Figure 2, column a) and was recruited to the sites of DNA damage induced by irradiation through a membrane filter (Figure 2, column b). Together, these results demonstrate that LIGIIIα, like its protein partner XRCC1, translocates to the sites of SSBs and that this DNA damage-induced sub-nuclear relocation is dependent upon PAR synthesis. This is consistent with our recent results using local laser irradiation (20). To examine whether the recruitment of LIGIIIα to SSBs is dependent upon XRCC1 and not on PARP-1, we transiently expressed a GFP-tagged version of DNA ligase IIIβ (LIGIIIβ), which is normally only expressed in meiotic cells (29). Importantly, LIGIIIβ interacts with poly(ADP-ribosylated) PARP-1 (18) but does not bind to XRCC1. In undamaged cells, LIGIIIβ was present in the nucleolus as well as in the nucleoplasm (Figure 2 column d), but, unlike LIGIIIα, LIGIIIβ was not recruited to the sites of DNA damage (Figure 2, column e). By a more sensitive assay using UVA laser irradiation and GFP-tagged LIGIIIα, we found a weak accumulation of LIGIIIα at SSBs in XRCC1-deficient cells (L. Lan and A. Yasui, unpublished results), which may be explained by direct interaction between PARP-1 and LIGIIIα. Thus, although LIGIIIα binds to poly(ADP-ribosylated) PARP-1 in vitro, the in vivo recruitment of LIGIIIα to SSBs is mainly dependent upon its C-terminal BRCT domain, which is required for the interaction with XRCC1 (29,30).\n\nXRCC1 and LIGIIIα localize to the centrosomes\nWhen exponentially growing HeLa cells were stained with an XRCC1 antibody, a unique staining pattern that appeared to correspond to the centrosomes was observed in both interphase and mitotic cells. To confirm the co-localization of XRCC1 with the centrosomes, we conducted a series of double-staining experiments using antibodies specific for XRCC1 and γ-tubulin, which is a component of pericentriolar matrix of the centrosome (31). As reported previously (19), the majority of XRCC1 in interphase cells is in the nucleoli, but a small fraction co-localized precisely with the two closely spaced dots of γ-tubulin located near the nuclear envelope (Figure 3A), which correspond to the duplicated centrosomes. The co-localization of XRCC1 with unduplicated centrosomes in interphase cells was also observed (data not shown). As described later, the presence of PAR in the centrosomes is crucial for the centrosomal localization of XRCC1. Detection of XRCC1 in the fraction of the centrosomes by antibodies failed, possibly because the amount of PAR polymers present in the centrosomes is limited partially due to the presence of PAR glycohydrolase and, therefore, the amount of XRCC1 molecules is too low to be detected by western blotting analysis. Therefore, to confirm the centrosomal location of XRCC1, we transiently expressed a GFP-tagged XRCC1 in HeLa cells. Indeed, in interphase cells, GFP-tagged XRCC1 was observed in the centrosomes (Figure 3B).\nThe association of a small fraction of XRCC1 with the centrosomes in interphase cells prompted us to examine the behavior of XRCC1 during mitosis. Using TOPRO-3 to stain cellular DNA, we determined the distribution of XRCC1 and γ-tubulin (Figure 4A), XRCC1 and LIGIIIα (Figure 4B), and XRCC1 and PAR (Figure 4C) at different stages of mitosis. As shown in these figures, in metaphase cells the majority of XRCC1 co-localized with γ-tubulin in the centrosomes. XRCC1 was also detected at the periphery of the centrosomes in metaphase. XRCC1 accumulated at mitotic centrosome and its immediate vicinity in the cells from prophase to metaphase (Figures 5 and 4C, upper panels). However, the pericentriolar localization of XRCC1 disappeared during anaphase (Figure 4A). A similar XRCC1 staining pattern was observed by using paraformaldehyde fixation (Figure 4B), and by using an XRCC1 monoclonal antibody (Figure 5) and in several human fibroblast cell lines including ATM-deficient (AT5BI-VA) cells (Figure 5). The staining pattern of LIGIIIα detected with two different monoclonal antibodies was indistinguishable from that of XRCC1 (Figure 4B). Thus, we conclude that XRCC1 and LIGIIIα are integral components of centrosomes, and that, during the early stages of mitosis, they also concentrate around the pericentriolar matrix.\n\nLocalization of XRCC1 and LIGIIIα to the centrosomes is dependent upon PAR synthesis\nTo examine whether poly(ADP-ribosyl)ation is involved in the centrosomal localization of XRCC1, the cells were incubated with antibodies for PAR and XRCC1. PAR is reported to be present in the centrosomes in both interphase and mitosis (22). During mitosis, PAR co-localized with XRCC1 in the centrosomes and their immediate vicinity (Figure 4C). The change in the amount of PAR in the centrosomes and their immediate vicinity was completely correlated with that of XRCC1 (Figure 4C), suggesting the presence of yet unknown DNA damage-independent mechanisms of PARP activation and the recruitment of XRCC1 to the centrosomal region during mitosis. When cells were incubated for 1 h in the presence of 3-AB (8 mM), a potent inhibitor of PARP, neither PAR nor XRCC1 was observed at or near centrosomes in metaphase cells (Figure 4A–C). Similarly, treatment with 3-AB abolished the localization of LIGIIIα to the centrosomes of metaphase cells (Figure 4B). Moreover, in interphase cells, the centrosomal localization of XRCC1 was also prevented by 3-AB (data not shown). Together, these results show that the synthesis of PAR at or near the centrosomes is a prerequisite for the localization of both XRCC1 and LIGIIIα.\n\nXRCC1 and LIGIIIα translocate from centrosomal region to chromosomes after treatment of cells with H2O2\nSince PARP-1 is present in both centrosomes and chromosomes in mitotic cells (21), we examined whether during mitosis PARP is activated by DNA-damaging agents and whether this activation affects the localization of XRCC1 and LIGIIIα. Following treatment of metaphase cells with H2O2, PAR was synthesized on the metaphase chromosomes (Figure 4C). In response to the PAR synthesis, both XRCC1 and LIGIIIα were translocated from the centrosomes to the metaphase chromosomes (Figure 4A–C). Similar results were obtained by treating the cells with 100 μM of DNA alkylating agent, MMS, for 10 min (data not shown). Thus, it appears that, as in interphase cells (19), the synthesis of PAR by PARP-1 at DNA strand breaks signals the recruitment of SSBs repair factors in mitotic cells. This suggests that DNA repair of SSBs occurs in the condensed chromatin of metaphase chromosomes.\n\nCONCLUSION\nAneuploidy is a characteristic feature of cancer cells. The presence of an abnormally high number of centrosomes in human tumor cells including those lacking p53 suggests that dysregulation of centrosomes function may contribute to cancer formation (32,33). Recently, it has been reported that the PARP inhibitor 3-AB frequently causes centrosome hyperamplification (22). Here, we have shown that XRCC1 and LIGIIIα, both of which interact with PARP-1, are present within the centrosomes in various stages of cell cycle. This effect is particularly evident in mitotic cells when the majority of these cellular proteins are localized at or near the centromeres. Thus, it is possible that XRCC1 and LIGIIIα are involved in the regulation of centrosome function. In this regard, it is worth noting that several single nucleotide polymorphisms associated with a variety of cancer types have been identified in the XRCC1 gene [reviewed in (34)]. Alternatively, it is possible that the association of XRCC1 and LIGIIIα with centrosomes in mitotic cells ensures the redistribution of these key DNA repair proteins to the daughter cells. Nonetheless, the DNA damage-dependent translocation of XRCC1 and LIGIIIα from the centrosomes to the metaphase chromosomes provides evidence for DNA repair in the condensed chromatin of mitotic chromosomes. Further analysis of the roles of XRCC1 and LIGIIIα in centrosome function and the repair of mitotic chromosomes will be important for understanding the causes of genomic instability in mitotic cells. 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