Targeted protein destruction of critical cellular regulators during the G1 phase of the cell cycle is achieved by anaphase-promoting complex/cyclosomeCdh1 (APC/CCdh1), a multisubunit E3 ubiquitin ligase. Cells lacking Cdh1 have been shown to accumulate deoxyribonucleic acid (DNA) damage, suggesting that it may play a previously unrecognized role in maintaining genomic stability. The ubiquitin-specific protease 1 (USP1) is a known critical regulator of DNA repair and genomic stability. In this paper, we report that USP1 was degraded in G1 via APC/CCdh1. USP1 levels were kept low in G1 to provide a permissive condition for inducing proliferating cell nuclear antigen (PCNA) monoubiquitination in response to ultraviolet (UV) damage before DNA replication. Importantly, expression of a USP1 mutant that cannot be degraded via APC/CCdh1 inhibited PCNA monoubiquitination during G1, likely compromising the recruitment of trans-lesion synthesis polymerase to UV repair sites. Thus, we propose a role for APC/CCdh1 in modulating the status of PCNA monoubiquitination and UV DNA repair before S phase entry.
Genotoxic stress, such as exposure to UV light, induces the accumulation of different types of DNA lesions and a wide range of cellular responses (Stokes and Comb, 2008). To maintain cell viability, replication forks that encounter damaged DNA must efficiently bypass these lesions to complete replication of the genome in a timely manner during S phase. DNA synthesis across damaged DNA is achieved by specialized DNA polymerases that incorporate nucleotides opposite to damaged bases in a process known as trans-lesion synthesis (TLS; Lehmann et al., 2007). However, overuse of TLS polymerases can increase mutagenesis because of their highly accommodating active sites and lack of proofreading activity (Waters et al., 2009). The recruitment of TLS polymerases for lesion bypass requires the monoubiquitination of proliferating cell nuclear antigen (PCNA; Kannouche et al., 2004; Watanabe et al., 2004; Bienko et al., 2005; Garg and Burgers, 2005; Plosky et al., 2006). Regulatory factors that control the level of PCNA ubiquitination, such as ubiquitin ligases and proteases, are important to promote an optimal balance between TLS-associated cell survival and TLS-associated mutagenesis (Prives and Gottifredi, 2008). This has been previously described in a series of elegant work that suggest the recruitment of Pol-η (a member of the Y family of TLS polymerases) to UV lesions by the Rad18-dependent monoubiquitination of PCNA (Kannouche et al., 2004; Watanabe et al., 2004). The model predicts that the blockage of replicative polymerases activates PCNA monoubiquitination at replication-stalled sites (Hoege et al., 2002; Friedberg et al., 2005). This event in turn promotes the recruitment of TLS polymerases to bypass the lesion and allow continuation of DNA replication. It has been suggested that the switch back from TLS to normal processive polymerases is regulated by ubiquitin-specific protease 1 (USP1), the deubiquitinating enzyme for PCNA (Huang and D’Andrea, 2006; Huang et al., 2006; Ulrich, 2006).
However, recent studies have shown that PCNA monoubiquitination can occur outside of S phase both in mammalian and yeast systems (Frampton et al., 2006; Soria et al., 2006, 2009; Daigaku et al., 2010; Karras and Jentsch, 2010; Ogi et al., 2010). Moreover, Pol-η and other TLS polymerases can be recruited to sites of UV lesions in quiescent or noncycling cells, which is in line with possible roles in gap-filling of DNA damage tracks left behind the replication forks (Lehmann and Fuchs, 2006; Lopes et al., 2006). As such, the gap-filling pathway is likely not limited to S phase but also occurs in G0, G1, and G2/M phases. PCNA monoubiquitination and TLS polymerase recruitment to UV lesions have also been recently implicated in nucleotide excision repair (NER), a DNA repair process that can take place outside of S phase (Ogi et al., 2010). It is currently unclear whether specific cell cycle phases, such as G1 or S phase, can dictate the mechanism of how the cell responds to UV-mediated DNA damage through the activation of PCNA monoubiquitination and subsequent DNA repair.
The anaphase-promoting complex/cyclosome (APC/C) is a multisubunit ubiquitin ligase that targets many key cell cycle regulators for proteolysis (Qiao et al., 2010). The activation of APC/C is dependent on two WD-40 repeat domain–containing proteins, Cdc20 and Cdh1. Whereas APC/CCdc20 principally regulates mitotic progression, APC/CCdh1 shows a broad spectrum of G1-specific substrates, including proteins that function beyond cell cycle control (Skaar and Pagano, 2008; Qiao et al., 2010). Previous studies have shown that Cdh1 knockout or depletion in mammalian cells can cause genomic instability, but the precise cause of this instability is unclear (Engelbert et al., 2008; García-Higuera et al., 2008). Recently, however, the stability of several proteins involved in the DNA damage checkpoint response and DNA repair, such as Claspin, Rad17, thymidine kinase 1, and the ribonucleotide reductase subunit RRM2, has been shown to be regulated by APC/CCdh1 (Chabes et al., 2003; Ke et al., 2005; Bassermann et al., 2008; Gao et al., 2009; Zhang et al., 2010). Moreover, although APC/CCdh1 is active only at the very end of mitosis and during G1, it is reactivated in G2 in response to DNA damage to target the mitotic kinase Plk1 for proteasomal degradation (Bassermann et al., 2008). It is likely that more Cdh1 substrates will be identified with roles in the DNA damage response (DDR) pathways, further underscoring the relevance and importance of APC/C in maintaining cellular genomic integrity.
In humans, protein deubiquitination is controlled by a family of nearly 100 deubiquitinases (DUBs), but the function of many of these ubiquitin proteases is unknown (Nijman et al., 2005b; Reyes-Turcu et al., 2009). The majority of DUBs are cysteine proteases that cleave ubiquitin from specific mono- and polyubiquitinated substrates or from linear ubiquitin polypeptides. The DUB USP1 is a critical regulator of genomic stability in mammalian cells (Kim et al., 2009). USP1 has been shown to regulate the monoubiquitination levels of three protein substrates involved in DNA repair: FANCD2 and FANCI (the Fanconi anemia [FA] effector proteins involved in DNA cross-link repair) and PCNA (the DNA replication processivity factor whose function is important for the recruitment of specialized TLS polymerases to sites of UV DNA lesions; Nijman et al., 2005a; Huang et al., 2006; Sims et al., 2007; Smogorzewska et al., 2007). However, it is unclear how USP1 negatively regulates the monoubiquitination of substrates involved in two distinct DDR pathways.
In this study, we explore whether the control of USP1 levels during cell cycle progression modulates the cellular response to UV DNA damage. We show that during G1, USP1 is targeted for degradation by APC/CCdh1 to ensure that USP1 levels are kept in check before S phase entry. Low levels of USP1 enable robust UV-induced PCNA monoubiquitination during G1, which is likely to allow the recruitment of TLS polymerases to UV lesions. These findings suggest that APC/CCdh1 plays a direct role in modulating the DNA repair choice in G1 and further solidify the link between cell cycle regulation and DNA repair.
Results and discussion
USP1 levels are low during the G1 phase of the cell cycle
To investigate whether USP1 activity is cell cycle regulated, we examined whether USP1 protein levels fluctuate in cells progressing through the cell cycle. We synchronized both U2OS and HeLa cells in prometaphase and then let them progress from mitosis into the next cell cycle. We found that USP1 levels are low during G1 and high during S phase (Fig. 1, A and B). We also observed low levels of USP1 in serum-starved and G1 T98G cells, similar to other proteins known to be degraded in G0/G1, such as Plk1 and cyclin A (Fig. 1 C). USP1 DUB activity depends on the interaction with its catalytic cofactor WDR48 (also called UAF1; Cohn et al., 2007). In contrast to USP1, WDR48 levels did not change throughout the cell cycle (Fig. 1 B and not depicted).
APC/CCdh1 regulates USP1 levels in G1
The down-regulation of USP1 in the G1 phase of the cell cycle led us to ask whether a ubiquitin ligase may be responsible for the degradation of USP1. As the APC/CCdh1 complex is critical for promoting the degradation of cell cycle regulators in G1, we tested whether this ubiquitin ligase also regulates the G1 levels of USP1. To this end, we silenced Cdh1 expression in both synchronized T98G and synchronized U2OS cells using well-established siRNA oligonucleotides (Bashir et al., 2004). We found that USP1 accumulated in both asynchronous and G1 cells depleted of Cdh1 (Fig. 2, A and B). This accumulation appears to be caused by USP1 stabilization, as shown by measuring USP1 half-life (Fig. 2 C). As expected (APC/CCdh1 is inactive during prometaphase), the accumulation of USP1 after Cdh1 silencing was not as prominent in M phase cells (Fig. 2 B). Similarly, upon Cdh1 silencing, Plk1, a known Cdh1 substrate, was also more accumulated in asynchronous and G1 cells than in M phase synchronized cells (Fig. 2 B).
Next, we determined whether USP1 DUB activity is functional during the G1 phase. To this end, we measured the ability of USP1 to react with a chemically modified ubiquitin suicide substrate probe (ubiquitin vinyl sulfone [UbVS]; Borodovsky et al., 2002). We found that G1-stabilized USP1 was still catalytically active (Fig. 2 D). This suggests that USP1 proteolysis is likely a critical mechanism to inhibit USP1 activity during the G1 phase. Thus, we predict that a stable mutant of USP1 that could not be targeted by APC/CCdh1 during G1 would still interact with WDR48 (which is expressed in G1 as shown in Fig. 1 B) and deconjugate specific monoubiquitinated substrates.
To ensure that the Cdh1 knockdown effect on USP1 stability was direct, we addressed whether Cdh1 could interact with USP1 in vivo. We found that both exogenously and endogenously expressed USP1 can interact with members of the APC/CCdh1 complex (Fig. 2, E–G). In T98G cells that are accumulating in G0/G1 (serum starvation time course), we also show that endogenous USP1 can interact with Cdh1 before its degradation (Fig. 2 G).
Characterization of a USP1 mutant that cannot be degraded via APC/CCdh1
To search for a USP1 mutant that is stable in G1, we attempted to map the degradation motif (degron) in USP1. APC/CCdh1-mediated degradation typically requires the RXXL degron (known as destruction box or D box) in its target proteins (Glotzer et al., 1991). Although human USP1 contains three putative D box motifs and a KEN box (Fig. S1; Pfleger and Kirschner, 2000; Littlepage and Ruderman, 2002; Reis et al., 2006), their mutation, singly or in combination, had no appreciable effect on USP1 stability in G1 (not depicted). Thus, we suspected that USP1 possesses a noncanonical degron, which is similar to those found in Aurora A (Littlepage and Ruderman, 2002), Cdc20 (Reis et al., 2006), or Claspin (Bassermann et al., 2008). To map the USP1 degron, we generated a series of N- and C-terminal deletion mutants (Fig. 3 A) and tested them for their ability to resist degradation in response to Cdh1 overexpression. We found that a region surrounding amino acids 307–330 of human USP1 is required for Cdh1-dependent degradation of USP1 (Fig. 3 B). Accordingly, a near full-length USP1 construct containing an internal deletion of 295–342 amino acids was stable in U2OS cells progressing through G1 (Fig. 3 C), whereas wild-type USP1, a USP1 (C90S) mutant (which is catalytic inactive), or the USP1 (GG670/671AA) diglycine mutant (which is unable to cleave itself) was not (Fig. 3 D). These results show that the catalytic and autocleavage activities of USP1 are not necessary for USP1 to be targeted for degradation by APC/CCdh1 during G1. This strongly suggests that the mechanism for degrading USP1 in G1 is completely different from the UV-initiated autocleavage and degradation of USP1 during S phase, as the proteolysis of USP1 during G1 is independent of its own catalytic activity (Huang et al., 2006).
We also generated a double USP1 mutant that contained both the 295–342 deletion and the GG670/671AA mutation, which was also resistant to proteolysis by APC/CCdh1 during G1 (Fig. 3 E). To further support that USP1 is ubiquitinated via APC/CCdh1, we reconstituted the ubiquitination of USP1 in vitro. USP1 was efficiently ubiquitinated only when Cdh1 was present and a specific E2 combination was used (see Materials and methods section; Figs. 3 F and S2). Under our conditions, it is unclear why UBCH10-UBCH5 (Aristarkhov et al., 1996; King et al., 1996; Yu et al., 1996) works better than the canonical E2 pair UBCH10-UBE2S (Garnett et al., 2009; Williamson et al., 2009; Wu et al., 2010) in promoting USP1 polyubiquitination. Interestingly, both UBCH10 and UBE2S are also degraded in G1 by APC/CCdh1, suggesting that other E2 enzymes may be responsible for ubiquitinating G1 versus M phase substrates of APC/C (Williamson et al., 2009). Importantly, Cdh1-dependent ubiquitination was not observed in the USP1 degron mutant (Fig. 3 G). Unexpectedly, the degron mutant was still capable of binding to Cdh1 in vitro, suggesting that the degron region may be more critical for promoting efficient APC/CCdh1-dependent ubiquitination of USP1 (Fig. S3). We have not ruled out the possibility of multiple Cdh1 binding sites on USP1 that may contribute to its direct association with the APC/CCdh1 complex. Nevertheless, experiments in cell systems and in vitro show that Cdh1 promotes the ubiquitination and subsequent degradation of USP1 in a manner dependent on its degron region.
Degradation of USP1 permits UV-induced monoubiquitination of PCNA during G1
We then investigated the biological significance of USP1 degradation in G1. One possibility is that the repair of UV-induced lesions in G1 requires robust PCNA monoubiquitination. In fact, PCNA monoubiquitination is involved in the recruitment of TLS polymerases to sites of UV damage for repair synthesis (Ogi et al., 2010). To test whether UV-induced DNA damage during G1 induces PCNA monoubiquitination, U2OS cells were synchronized in G1 by releasing them from a prometaphase block. 2 h after release, cells were either left untreated or UV irradiated and followed for up to 10 h. After UV damage, USP1 levels decreased below the G1 levels, whereas in untreated cells, USP1 reaccumulated as they exited G1 and started DNA replication (Fig. 4 A). Accordingly, after UV damage, Cdh1 levels remained elevated, correlating with the loss of USP1 and a delay in S phase entry. Interestingly, robust monoubiquitination of PCNA already occurred by 2 h after UV damage and remained present for up to 10 h (Fig. 4 A). In contrast, detectable PCNA-monoubiquitinated species only started to appear when nonirradiated cells reached S phase. A strong UV-induced PCNA monoubiquitination response was also observed in T98G cells during G1 (Fig. 4 B). Interestingly, the monoubiquitination of FANCD2 and FANCI (FA pathway effector proteins) was not induced by UV damage in G1 (unpublished data). This is likely a result of low levels of UBE2T, the E2 conjugating enzyme for the FA pathway, in G1 that prevent activation of the FA pathway outside of S phase (unpublished data). We also noted that the DDR after UV damage is different in G1 versus S phase. For instance, UV irradiation targets the autocleavage and degradation of USP1 in S phase to promote PCNA monoubiquitination, as previously reported (Fig. 4 B; Huang et al., 2006). However, USP1 levels remain low and unchanged after UV damage in G1 (Fig. 4 B), suggesting that the environment in G1 was already conducive for UV-mediated activation of PCNA monoubiquitination. In addition, Cdh1 is degraded after UV damage in S phase cells (Liu et al., 2008) but not in G1. Also, the checkpoint kinase Chk1 is not activated by phosphorylation after UV damage in G1.
We also found that the mechanism controlling PCNA monoubiquitination in G1 is surprisingly similar to the Rad18-dependent mechanism that governs its activation in S phase (Ogi et al., 2010). The knockdown of Rad18 resulted in the inhibition of UV-induced PCNA monoubiquitination during G1 (Fig. 4 C). The monoubiquitination of PCNA is dependent on lysine 164 (unpublished data). Likewise, expression of stable degron mutants of USP1 also reduced the levels of PCNA monoubiquitination and the recruitment of the TLS polymerase Pol-κ to sites of UV lesions in G1 after UV damage (Fig. 4, D and E). Thus, from our study, we provide a model suggesting that degradation of USP1 by the APC/CCdh1 during G1 is critical for cells to properly recruit TLS polymerases for UV-mediated DNA gap repair (Fig. 4 F).
Proteolytic control of cell cycle regulators by the APC/CCdh1 ubiquitin ligase complex is responsible not only for a stable G1 phase after mitotic exit but also for allowing accurate preparation for DNA replication in the following S phase (Nakayama and Nakayama, 2006). It is known that some of these APC/CCdh1 target proteins are frequently up-regulated in tumor cells, and inactivation of human and mouse Cdh1 interferes with genome integrity (Engelbert et al., 2008; García-Higuera et al., 2008). However, it is still unclear what protein targets of APC/CCdh1 are critical for maintaining genomic stability in human cells. Here, we show that USP1 can be targeted for degradation by the APC/CCdh1 cell cycle regulator. This mainly occurs in the G1 phase before the start of DNA replication. USP1 is an important negative regulator of monoubiquitination for two major DNA repair pathways (FA and TLS) that control genomic stability. Thus, proper dynamic control of USP1 levels throughout the cell cycle and during DNA damage may strongly impact how the cell deals with certain types of DNA lesions. To further validate this point, experimental evidence has suggested that higher than normal levels of USP1 will inhibit the DNA damage–induced monoubiquitination of USP1 targets, such as FANCD2, FANCI, and PCNA (Huang et al., 2006; Oestergaard et al., 2007), whereas the loss of USP1 has been shown to cause chromosomal instability and elevated perinatal lethality in mice (Kim et al., 2009).
Previous works by several groups have hinted at a new role for TLS that is linked to PCNA monoubiquitination outside of S phase. For example, Soria et al. (2009) has suggested that the TLS polymerase Pol-η can be recruited to UV-induced DNA lesions in cells outside S phase, including cells permanently arrested in G1. Work in DT40 cells has shown that PCNA ubiquitination may not be required to maintain normal fork progression on damaged DNA template but is essential for filling postreplicative gaps (Edmunds et al., 2008). More recently, Ogi et al. (2010) has suggested that ubiquitinated PCNA is involved in the recruitment of the TLS polymerase Pol-κ to sites of UV lesions in the G1 phase. The function of ubiquitinated PCNA outside of S phase is tied to a gap-filling role or repair synthesis, which occurs downstream of NER. From our study, we believe that the cell prefers to maintain a low level of USP1 during G0/G1 to establish a permissive environment and allow for robust PCNA monoubiquitination if necessary (Fig. 4 F). Thus, in the absence of its negative regulator, PCNA can be rapidly activated after UV damage to allow repair synthesis to occur downstream of the NER pathway. In contrast, expression of a nondegradable form of USP1 during G1 will lead to less monoubiquitinated PCNA and defective recruitment and repair of UV lesions by the TLS polymerases. The reliance on excision and gap filling–based repair mechanisms becomes more crucial when cells are in quiescence or in the postmitotic phase because of the lack of available sister chromatid for homologous recombination repair (Hoeijmakers, 2001).
Materials and methods
Cell culture and cell cycle synchronization and cell images
T98G, HeLa, and U2OS cells were grown in DME with 10% FBS, 1% penicillin/streptomycin, and 1% glutamine. Cells were synchronized in G0/G1 by serum deprivation (0.05% FBS) for 72 h. After 72 h, cells were split, plated, and refed with normal cell culture media. Cells were synchronized in M phase by incubating cells with 0.1 µg/ml nocodazole for 12–16 h. After 12–16 h, mitotic cells were shaken off, collected, and washed twice with 1× PBS and then plated with fresh media. To verify the cell cycle phase for the cell synchronization experiments, cell samples were stained by propidium iodide (PI) according to the following staining procedure: cell pellets were washed and fixed in 70% ethanol overnight and stained with PI staining buffer (50 µg/ml PI and 10 µg/ml RNase in PBS). Flow cytometry analysis was performed using FACSCaliber and analyzed using CellQuest software (BD) and Modfit LT (V3.1; Verity Software House). Immunocytochemistry was performed according to protocol as previously described (Colnaghi et al., 2011). In brief, for detection of GFP–Pol-κ and Myc-USP1 proteins, U2OS cells were fixed in 100% methanol for 10 min, washed in PBS, blocked in 1% BSA in TBS–Tween 20, and incubated with mouse anti-GFP and rabbit anti-Myc antibodies (Santa Cruz Biotechnology, Inc.). Slides were mounted with Vectashield (Vector Laboratories) with DAPI and analyzed using 60× NA 1.42 objective lenses under oil immersion at 26°C using Alexa Fluor 488 and 546 fluorochromes. Microscope images were captured using a DeltaVision system (Applied Precision) on a base microscope (IX71; Olympus) and a charged-coupled device camera (CoolSnap HQ2; Photometrics). Images were deconvolved, and maximum intensity Quick projections were generated using SoftWorx Suite software (Applied Precision). The images were opened, sized, and placed into figures using ImageJ (National Institutes of Health) or Photoshop (7.0 Professional; Adobe) before transferring to Illustrator (CS3; Adobe).
Transfections, siRNA oligonucleotides, DNA constructs, and antibodies
Transfections with plasmids or siRNA oligonucleotides were performed using Fugene 6 (Roche) or Hiperfect (QIAGEN) reagent. The siRNA oligonucleotide sequences targeting human Cdh1 (5′-AATGAGAAGTCTCCCAGTCAG-3′) and human Rad18 (5′-CCCGAGGTTAATGTAGTTGTT-3′) were used. To generate human Myc-tagged USP1 truncation and deletion mutants, USP1 cDNA was PCR amplified and subcloned into modified pcDNA3 plasmid (Invitrogen) containing the 5′ sequence coding for 2× Myc epitope tag. Point mutations C90S or GG(670/671)AA were made by two-step PCR mutagenesis from the original USP1 template and verified by DNA sequencing as previously described (Huang et al., 2006). Truncation mutants were obtained by PCR amplification using specific 5′ or 3′ USP1 sequences. The internal deletion 295–342 amino acids of USP1 was generated by a site-directed mutagenesis kit (Agilent Technologies) using the primers forward 5′-CCAGTCATTGGAAGAGAAGTCTGCAACTAAGC-3′ and reverse 5′-GCTTAGTTGCAGACTTCTCTTCCAATGACTGG-3′. The following antibodies were used for Western blot analysis and/or immunoprecipitation: WDR48/UAF1 (Evoquest; Invitrogen), USP28 (Bethyl Laboratories, Inc.), Cdh1 (EMD), c-Myc (9E10; Santa Cruz Biotechnology, Inc.), HA (Covance), E2F1 (Bethyl Laboratories, Inc.), Emi1 (Invitrogen), PCNA (PC10; Santa Cruz Biotechnology, Inc.), tubulin (Abcam), Plk1 (Abcam), actin (Abcam), cyclin A (EMD), Rad18 (Abcam), pChk1-317 (Abcam), p21 (Abcam), and USP1, APC1, and Cdc27 (Bethyl Laboratories, Inc.). The GFP–Pol-κ expression construct was a gift from T. Ogi and A. Lehmann (University of Sussex, East Sussex, England, UK). Anti-USP1 and FANCD2 antibodies were a gift from A. D’Andrea (Dana-Farber Cancer Institute, Boston, MA).
In vitro ubiquitination, DUB activity assay, and coimmunoprecipitation
USP1 constructs and Cdh1 were in vitro translated using the TNT T7–coupled wheat germ extract system (Promega) and TNT SP6–coupled reticulolysate system (Promega), respectively, following the manufacturer’s protocol. In vitro translation reactions were stopped using 1 mg/ml cycloheximide. Ubiquitination of in vitro–translated USP1 was performed at 30°C with 50 mM Tris, pH 7.6, 5 mM MgCl2, 2 mM ATP, 2.5 mg/ml ubiquitin, 1 µM ubiquitin aldehyde, 1.5 ng/µl UBE1, 25 ng/µl UBCH10, 5 ng/µl UBCH5 (Boston Biochem), and 10 µM MG132 (EMD) in the presence or absence of in vitro–translated HA-Cdh1. UBCH10 and UBCH5 were chosen as the E2 enzyme pair to use for the in vitro ubiquitination assay after screening several E2 pairs to determine the best E2 combination to use (Fig. S2 A). Cdc6 was used as a positive control for an APC/CCdh1-specific ubiquitination substrate (Fig. S2 B), and methyl ubiquitin was used to confirm chain elongation for the in vitro ubiquitination assay (Fig. S2 C). UbVS DUB activity assay was performed according to Borodovsky et al. (2002) with several modifications. Cells were lysed for 1 h on ice with gentle tapping (250 mM Tris, 150 mM NaCl, 3 mM EDTA, and 0.5% NP-40). Supernatants from cell lysis were collected after a 10-min spin of 14,000 rpm at 4°C. Cell extracts and 50 µM HA-UbVS probe (Boston Biochem) were incubated at 25°C for 1.5 h in DUB buffer (50 mM Tris, 50 mM NaCl, 10% glycerol, and 1 mM EDTA). Reactions were terminated with Laemmli buffer and boiled for Western blot analysis. Coimmunoprecipitation studies were performed overnight at 4°C with the indicated antibodies according to the protocol previously described (Sims et al., 2007). In brief, cell lysis, antibody incubation, and bead washes were performed using low immunoprecipitation buffer (25 mM Tris, pH 7.5, 150 mM NaCl, 2 mM EDTA, and 0.5% NP-40 with protease inhibitor cocktail [Roche]).
Induction of DNA damage and measurement of DNA synthesis
T98G and U2OS cells were treated and harvested between 50 and 80% visible cofluency. 254-nm UV-C irradiation was performed (Stratalinker 2400; Agilent Technologies) in the absence of DME media at 50 J/m2. Recovery after UV damage was in complete medium for the times indicated. Replicating cells were detected using a flow cytometry assay kit (Click-iT EDU; Invitrogen) according to the manufacturer’s instructions. Flow cytometric data were acquired on a flow cytometer (LSR II; BD) using the FACS DiVa (BD) and Modfit LT softwares.
Online supplemental material
Fig. S1 shows the sequence alignment of the USP1 degron region. Fig. S2 shows APC/CCdh1-dependent ubiquitination of USP1 using different E2 pairs and methyl ubiquitin. Fig. S3 shows that the degron mutant can still interact with Cdh1.
We especially would like to thank T. Ogi, A. Lehmann, and A. D’Andrea for valuable tools and reagents for this study and members of the T. Huang, M. Pagano, D. Bar-Sagi, and D. Reinberg laboratories for their reagents, technical assistance, equipment, and helpful discussions. We also thank Peter Lopez at the New York University Flow Cytometry Core Facility for helpful assistance with FACS analysis.
This work was supported by National Institutes of Health grants to T.T. Huang (R01-GM084244) and to M. Pagano (R01-GM057587, R37-CA076584, and R21-CA161108). M. Pagano is an Investigator with the Howard Hughes Medical Institute.