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Molecular and Cellular Biology, May 2006, p. 3527-3540, Vol. 26, No. 9
0270-7306/06/$08.00+0     doi:10.1128/MCB.26.9.3527-3540.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Rad18 Regulates DNA Polymerase and Is Required for Recovery from S-Phase Checkpoint-Mediated Arrest

Xiaohui Bi,^1, Laura R. Barkley,^1, Damien M. Slater,¹ Satoshi Tateishi,² Masaru Yamaizumi,² Haruo Ohmori,³ and Cyrus Vaziri^1*

Department of Genetics and Genomics, Boston University School of Medicine, 80 E. Concord St., Boston, Massachusetts 02118,¹ Institute of Molecular Embryology and Genetics, Kumamoto University, Honjo 2-2-1, Kumamoto 860-0811, Japan,² Institute for Virus Research, Kyoto University, 53 Shogoin-Kawaracho, Sakyo-ku, Kyoto 606-8507, Japan³

Received 15 November 2005/ Returned for modification 21 December 2005/ Accepted 14 February 2006

	ABSTRACT

Top Abstract Introduction Materials and Methods Results Discussion References

 
We have investigated mechanisms that recruit the translesion synthesis (TLS) DNA polymerase Pol to stalled replication forks. The DNA polymerase processivity factor PCNA is monoubiquitinated and interacts with Pol in cells treated with the bulky adduct-forming genotoxin benzo[a]pyrene dihydrodiol epoxide (BPDE). A monoubiquitination-defective mutant form of PCNA fails to interact with Pol. Small interfering RNA-mediated downregulation of the E3 ligase Rad18 inhibits BPDE-induced PCNA ubiquitination and association between PCNA and Pol. Conversely, overexpressed Rad18 induces PCNA ubiquitination and association between PCNA and Pol in a DNA damage-independent manner. Therefore, association of Pol with PCNA is regulated by Rad18-mediated PCNA ubiquitination. Cells from Rad18^–/– transgenic mice show defective recovery from BPDE-induced S-phase checkpoints. In Rad18^–/– cells, BPDE induces elevated and persistent activation of checkpoint kinases, indicating persistently stalled forks due to defective TLS. Rad18-deficient cells show reduced viability after BPDE challenge compared with wild-type cells (but survival after hydroxyurea or ionizing radiation treatment is unaffected by Rad18 deficiency). Inhibition of RPA/ATR/Chk1-mediated S-phase checkpoint signaling partially inhibited BPDE-induced PCNA ubiquitination and prevented interactions between PCNA and Pol. Taken together, our results indicate that ATR/Chk1 signaling is required for Rad18-mediated PCNA monoubiquitination. Recruitment of Pol to ubiquitinated PCNA enables lesion bypass and eliminates stalled forks, thereby attenuating the S-phase checkpoint.

	INTRODUCTION

Top Abstract Introduction Materials and Methods Results Discussion References

 
Polycyclic aromatic hydrocarbons (PAHs) are abundant and ubiquitous environmental pollutants with well-documented mutagenic and carcinogenic properties (4). The biological effects of the PAH benzo[a]pyrene (B[a]P) have been studied extensively in vivo and in vitro. B[a]P and many related PAHs are subject to intracellular cytochrome P450-mediated metabolism (11). Cytochrome P450-dependent oxidation of B[a]P generates the reactive species and ultimate carcinogen B[a]P dihydrodiol epoxide (BPDE). BPDE can react covalently with exocyclic deoxyguanosine (majority, 90%) and deoxyadenosine (minority, 10%) residues in genomic DNA to generate bulky adducts (18). The DNA adducts resulting from covalently bound BPDE are believed to account for the mutagenic and carcinogenic properties of B[a]P (19). Potentially, error-prone repair or replication of BPDE-adducted DNA can result in mutations. Propagation of cells containing BPDE-induced mutations in oncogenes or tumor suppressor genes can contribute to multistep carcinogenesis.

Because of the potential threat to genomic stability posed by DNA adducts (as well as other forms of DNA damage), cells have evolved elaborate mechanisms to detect and repair damaged DNA. Cell cycle checkpoints are signal transduction pathways that respond to damaged DNA by inhibiting cell cycle progression (45). The cell cycle delays elicited by checkpoint signaling enable integration of cell cycle progression with DNA repair. Consequently, checkpoints are important for preserving the integrity of the genome. Cells can acquire DNA damage throughout the cell cycle. Therefore, DNA damage-inducible checkpoint mechanisms exist that arrest cells in G₁, S, and G₂/M phases. Individuals with congenital defects in checkpoint genes (such as ATM, ATR, p53, and CHEK2) are prone to cancer, highlighting the importance of checkpoint signaling pathways as important tumor-suppressive mechanisms.

Cell cycle responses to DNA damage acquired during S phase are highly conserved in eukaryotes. During a normal S phase, DNA synthesis initiates at multiple loci (termed origins of replication) that are activated (a process known as firing) in a temporally ordered manner (17). When ongoing replication forks encounter DNA lesions, a signal is generated that prevents initiation of DNA synthesis from unfired origins. The inhibition of DNA synthesis due to delayed firing of late origins is termed the S-phase checkpoint (or the intra-S-phase checkpoint).

Bulky adducts such as those induced by BPDE and UV elicit an S-phase checkpoint pathway involving the proximal checkpoint components ATR (an ATM/RAD3-related protein kinase) and the heterotrimeric Rad9-Rad1-Hus1 (9-1-1) complex (20, 21, 44). ATR and 9-1-1 are recruited separately to damaged DNA (47, 48). Activation of ATR involves its recruitment to RPA-coated single-stranded DNA (ssDNA), which is generated by the uncoupling of replicative helicases from fork progression, via the ATR-interacting protein ATRIP (also termed Rad26) (47, 48). After recruitment to damaged DNA, the concerted actions of ATR and 9-1-1 activate the checkpoint kinase Chk1, which mediates the inhibition of late-firing origins in response to DNA damage. The mechanism by which Chk1 inhibits DNA synthesis at late origins might involve degradation of the Cdc25A protein phosphatase (38) and inhibition of the Dbf4-Cdc7 protein kinase complex (14, 15) which is required for initiation of DNA replication at individual origins throughout S phase. ATM, Nbs1, and Chk2 are dispensable for the BPDE-induced checkpoint pathway (44) and probably also for the UV-induced checkpoint. In addition to inhibiting initiation of late origins, S-phase checkpoint signaling is important for stabilizing stalled replication forks via an unknown mechanism(s) (16, 31, 40).

Replicative DNA polymerases are generally unable to carry out accurate or efficient DNA synthesis when they encounter bulky adducts or other lesions. However, specialized DNA polymerases can be used to replicate past lesions in a process termed translesion synthesis (TLS). Replicative bypass of DNA lesions is an inherently error-prone process due to the low fidelity of TLS polymerases. Thus, error-prone TLS is considered to be one of the causes of mutagenesis and carcinogenesis due to DNA lesions.

TLS DNA polymerases in mammalian cells include Pol, Pol, Pol, Rev1 (the Y family polymerases), and Pol (a B family polymerase comprising the catalytic Rev3 subunit and the noncatalytic Rev7 protein). Pol was the first mammalian TLS polymerase identified (25, 32). Pol is encoded by the XPV gene, which is defective in xeroderma pigmentosum variant patients. The role of mammalian Pol (and that of its Saccharomyces cerevisiae homologue encoded by the Rad30 gene) in TLS has been studied extensively. Pol is unique among eukaryotic DNA polymerases in its ability to replicate templates containing cis-syn thymine-thymine dimers (the species generated by UV radiation).

Studies in vitro with yeast indicate that Pol promotes error-free DNA translesion synthesis in a manner which is stimulated by PCNA and regulated by the Rad6/Rad18 epitasis pathway (22, 39). Rad6 is an E2 ubiquitin (Ub)-conjugating enzyme (also termed UBC2) that forms a tight complex with the RING-containing E3 ligase Rad18. The Rad18-Rad6 complex binds ssDNA and has ssDNA-stimulated ATPase activity (2). Recent reports have demonstrated that in yeast and mammalian cells Rad18 is important for monoubiquitination of PCNA in response to DNA damage (22, 28, 39, 43). Moreover, Pol interacts preferentially with monoubiquitinated PCNA. It has also been shown that Rad18 and Pol interact via their C-terminal motifs and that this interaction is important for guiding Pol to PCNA (43). Therefore, according to current models, Rad18/Rad6-mediated monoubiquitination of PCNA constitutes a molecular switch that recruits Pol to stalled replication forks (41).

In contrast to Pol, which bypasses BPDE-adducted templates very poorly, Pol is able to bypass benzo[a]pyrene-adducted guanine, efficiently inserting the correct C opposite the bulky lesion (36). Pol-deficient mutant mouse embryonic stem (ES) cells are highly sensitive to B[a]P-induced mutagenesis and genotoxicity (35), further suggesting a role for Pol in cellular responses to B[a]P-adducted DNA. BPDE, as well as hydroxyurea (HU) and UV irradiation, can elicit recruitment of Pol to nuclear foci (5, 6, 34), possibly suggesting a general role for Pol in responses to genotoxins and replication stress.

Recently we showed that Pol is specifically recruited to PCNA-containing foci in response to BPDE treatment concomitant with activation of the S-phase checkpoint (6). Furthermore, we showed that, in contrast to wild-type (WT) cells, Pol^–/– mouse embryo fibroblasts (MEFs) arrested irreversibly in S phase after BPDE treatment. In BPDE-treated, Pol-deficient cells, failure to recover from the S-phase checkpoint was associated with persistent activation of ATM, Chk1, and Chk2 kinases, and phosphorylation of the double-strand breakage (DSB) marker H2AX. Taken together, those results suggested that Pol-mediated replicative bypass of BPDE adducts contributes to attenuation of DNA damage signaling and recovery from the S-phase checkpoint.

The specific mechanisms that recruit Pol to the replication machinery in mammalian cells have not been identified. Because of the important role of Pol in the BPDE-induced S-phase checkpoint, we have investigated the mechanisms that recruit Pol to stalled replication forks and promote TLS. Experiments presented here demonstrate an important role for Rad18 in regulating PCNA monoubiquitination, Pol recruitment, and S-phase checkpoint recovery. Importantly, we show that PCNA ubiquitination and associations between PCNA and Pol are regulated by checkpoint signaling.

	MATERIALS AND METHODS

Top Abstract Introduction Materials and Methods Results Discussion References

 
Adenovirus construction and infection. Adenovirus construction and infections were performed as described previously (20). cDNAs encoding hemagglutinin (HA)-Rad18 and HA-PCNA WT and PCNA K164A were subcloned into pAC-CMV to generate pAC-HA-Rad18 and pAC-PCNA WT and pAC-PCNA K164A, respectively. The resulting shuttle vectors were cotransfected into 293T cells with the pJM17 plasmid to generate recombinant adenovirus as described previously. AdGFP-Pol, AdYFP-Pol, and AdChk1KR were described previously (6). H1299 cells were routinely infected with 5 x 10⁹ PFU/ml adenovirus. As controls for adenoviral infection, cells received AdCon (empty adenovirus vector) or AdGFP.

Cell culture. Human lung carcinoma H1299 cells, Rad18^+/+ and Rad18^–/– MEFs, and TERT-immortalized xeroderma pigmentosum variant (XPV) CRL1162 fibroblasts were cultured in Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum, streptomycin sulfate (100 µg/ml), and penicillin (100 U/ml).

ET163 cells from ataxia-telangiectasia patients and a matched cell line designated YZ5, which is complemented with the ATM cDNA (46), were cultured in Dulbecco modified Eagle medium supplemented with 15% fetal bovine serum, streptomycin sulfate (100 µg/ml), and penicillin (100 U/ml).

Genotoxin treatments. BPDE (National Cancer Institute carcinogen repository) was dissolved in anhydrous dimethyl sulfoxide and added directly to the growth medium as a 1,000x stock to give a final concentration of 100 or 600 nM. For HU treatment, HU was dissolved in water and added directly to the growth medium as a 1,000x stock to give a final concentration of 1 µM. For UVC treatment, the growth medium was removed from the cells and replaced with phosphate-buffered saline (PBS). The plates were transferred to a UV cross-linker (Stratagene) and then irradiated. The UVC dose delivered to the cells was confirmed with a UV radiometer (UVP, Inc.). The cells were then refed with complete growth medium and returned to the incubator. For ionizing radiation (IR) treatment, cells were placed in PBS, irradiated with a cesium source, refed with complete growth medium, and then returned to the incubator. In some experiments, cells were incubated in medium containing 5 mM caffeine (Sigma) or 150 nM UCN-01 for 1 h before genotoxin treatment.

RNA interference (RNAi). Cells were plated into six-well culture dishes. At 24 h later, when cells were 50% confluent, the cultures were placed in P_i-free medium (2 ml per well). For each transfection, 6.25 µl of 20 µM stocks of Cy3 (control) small interfering RNA (siRNA), siRPA, or siRAD18 or 10 µl of siATR (Dharmacon smart pool) was diluted into 0.25 ml of Opti-MEM. After 5 min, the siRNA-Opti-MEM solution was mixed with 0.25 ml of Opti-MEM containing 5 µl of Lipofectamine 2000. Twenty minutes later, the resulting mixture was added to culture medium. After incubation overnight, the transfection medium was removed and replaced with standard culture medium. All tubes, tips, and solutions used for RNAi experiments were certified RNase free.

Clonogenic survival assays. Cells were grown to 80% confluence, treated with genotoxins (as described above), and then split into replicate 10-cm plates at a density of 1,000 cells/plate. Cultures were given fresh medium every 3 days. After 1 week, colonies on the plates were fixed in methanol, stained with Giemsa, and counted.

Analysis of PCNA ubiquitination with epitope-tagged Ub. H1299 cells were plated into 10-cm culture dishes. When at 50% confluence, cells were infected with AdCon or AdRad18 for 24 h. Cells were then transfected with a hexahistidine- and Myc-tagged form of Ub (designated H₆M-Ub). Eight micrograms of H₆M-Ub was diluted into 1.5 ml of Opti-MEM. After 5 min, the DNA-Opti-MEM solution was mixed with 1.5 ml of Opti-MEM containing 20 µl of Lipofectamine 2000. Twenty minutes later, the resulting mixture was added to 12 ml of culture medium. After incubation for 6 h, the transfection medium was removed and replaced with standard culture medium. At 24 h after transfection, cells were treated with 600 nM BPDE for 4 h prior to harvest. Cells were washed twice with PBS and then separated into soluble and insoluble fractions with cytoskeleton (CSK) buffer (23). The insoluble fraction was treated with 1,000 U/ml DNase (Roche 10776 785 001) for 30 min at room temperature and then clarified by centrifugation at 10,000 x g for 5 min. The supernatants (containing solubilized chromatin) were normalized for protein content. H₆M-Ub-conjugated proteins were purified by overnight incubation at 4°C with 25 µl of cobalt affinity resin (TALON Clontech 8901-2). The TALON resin was recovered by centrifugation and washed three times with CSK buffer and once with CSK buffer containing 50 mM imidazole. The washed TALON beads were resuspended in an equal volume of 2x Laemmli buffer, boiled for 5 min, and resolved by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). Twenty percent of each input fraction was also analyzed by SDS-PAGE. After transfer to nitrocellulose, immunoblotting was performed with mouse monoclonal anti-PCNA (sc-56; Santa Cruz Biotechnology).

DNA synthesis assays. Cells were plated in 12-well culture dishes and grown to 60% confluence. Genotoxin treatments were performed as described above. To measure DNA synthesis at different time points after genotoxin treatment, replicate wells were given [³H]thymidine (1 µCi/ml; Perkin-Elmer Life Sciences) for 30 min. At the end of the labeling period, the [³H]thymidine-containing medium was aspirated and the monolayers were fixed by addition of 5% trichloroacetic acid. The fixed cells were washed three times with 5% trichloroacetic acid to remove unincorporated [³H]thymidine. The trichloroacetic acid-fixed cells were solubilized in 0.3 N NaOH. A 300-µl aliquot of the NaOH-solubilized material was transferred to a scintillation vial and neutralized by addition of 100 µl of glacial acetic acid. After addition of 5 ml of Ecoscint scintillation fluid, incorporated [³H]thymidine was measured by scintillation counting.

For assays of DNA synthesis in transfected cells, 10-cm plates of Rad18^–/– MEFs at 60 to 80% confluence were placed in 5 ml of Opti-MEM. In a separate tube, 30 µg of plasmid DNA and 50 µl of Lipofectamine 2000 were added to1.5 ml of Opti-MEM and mixed. The resulting mixture was incubated for 25 min at room temperature prior to addition to the cells. After 10 h, transfected cells were transferred to standard culture medium containing 10% FBS. Twelve hours later, the cells were split into 12-well culture dishes for DNA synthesis assays.

Fluorescence microscopy. Cells were plated in four-well chamber slides, grown to 30% confluence, and then infected with various adenovirus vectors. Twenty hours after infection, cells were treated with genotoxins for various times. In some experiments, yellow fluorescent protein (YFP)-Pol and HA-Pol were expressed by transient transfection of plasmid DNA. H1299 cells were seeded into six-well plates and cotransfected the following day with 2 µg each of plasmids pcDNA3-Flag-HA-Pol and pAC.CMV-YFP-Pol (6) by using Lipofectamine 2000 (Invitrogen). Twenty-four hours after transfection, the cells were trypsinized, replated onto glass slides (Colorfrost Plus; Fisher), and grown for an additional 24 h. Cells were then treated with 600 nM BPDE for 6 h, solubilized with cold CSK buffer, and fixed with 1% paraformaldehyde.

To visualize green fluorescent protein (GFP)-Pol or YFP-Pol fluorescence, the cells were fixed with 4% paraformaldehyde for 10 min, washed with PBS, 4',6'-diamidino-2-phenylindole (DAPI) stained, and then mounted with Vectashield solution (Vector Laboratories). To visualize cellular proteins with antibodies, paraformaldehyde-fixed cells were permeabilized with 0.2% Triton X-100 for 5 min. After the slides were washed with PBS, cells were incubated overnight at 4°C with polyclonal HA antibody (Santa Cruz) diluted 1:100 in 1% bovine serum albumin (BSA)-PBS-Triton X-100 (PBST). The slides were washed three times with 1% BSA-PBST and then incubated for 1 h with Cy3-conjugated donkey anti-mouse antibodies (Jackson ImmunoResearch) diluted 1:300 in 1% BSA-PBST. After being washed (three times with 1% BSA-PBST, 30 min per wash), the slides were DAPI stained and mounted with Vectashield solution (Vector Laboratories).

Slides were imaged and analyzed with a DeltaVision image restoration microscopy system (dv1301421; Applied Precision). In some experiments, cell populations were scored for constitutive and genotoxin-induced foci with a Nikon Eclipse E800 fluorescent microscope. In these studies, 500 cells were counted for each experimental condition.

Immunoblotting. Total cell lysates were prepared in lysis buffer containing 50 mM HEPES (pH 7.4), 0.1% Triton X-100, 150 mM NaCl, 1 mM EDTA, 50 mM NaF, 80 mM ß-glycerophosphate, and 1x protease inhibitor mixture (Roche Applied Science). In some experiments, whole nuclei were prepared with CSK buffer as described previously (6). Total cell extracts or nuclear protein samples were separated by SDS-PAGE, transferred to nitrocellulose, and analyzed by immunoblotting with the following antibodies: rabbit anti-Chk1 (FL-476; Santa Cruz Biotechnology), rabbit anti-Chk2 (H-300; Santa Cruz Biotechnology), mouse monoclonal anti-PCNA (catalog no. sc-56; Santa Cruz Biotechnology), rabbit anti-phospho-Chk1 Ser-345 (catalog number 2341; Cell Signaling), rabbit anti-phospho-Chk2 Thr-68 (catalog number 2661; Cell Signaling), polyclonal HA tag antibody (ab9110; abcam Inc.), and polyclonal PCNA antibody (FL-261, catalog no. sc-7907; Santa Cruz Biotechnology).

Coimmunoprecipitation (co-IP) of PCNA and TLS DNA polymerases. H1299 cells were plated in 10-cm culture dishes and infected with adenovirus as described above. Genotoxin treatments were performed at 70% confluence. To isolate chromatin fractions for IP, cells were rinsed twice with PBS and then extracted with 5 ml of CSK buffer for 10 to 15 min. The CSK-extracted cells were rinsed once with PBS and then fixed with 1% formaldehyde in PBS (4.5 ml) for 10 min. Then, 0.5 ml of a 1 M glycine solution in PBS was added for 5 min to quench the cross-linking reaction. The cross-linked nuclei were rinsed with PBS and then lysed in 500 µl of IP lysis buffer (freshly supplemented with protease and phosphatase inhibitors). Lysates were scraped from the plates and transferred into 1.5-ml Microfuge tubes. Samples were sonicated for two 8-s pulses at 30% of the maximum output. Pulses were separated by a 10-s interval on ice to prevent excessive heating. The sonicated samples were clarified by centrifugation at 10,000 x g for 5 min. Supernatants were removed and normalized for protein concentration (approximately 600 µg of protein in 1 ml was used for each IP). PCNA was immunoprecipitated overnight at 4°C with 5 µl of monoclonal PCNA antibody (Santa Cruz). A 25-µl volume of protein A/G beads was added to each sample for 4 h. The beads were recovered by brief centrifugation and washed three times with 1 ml of IP lysis buffer (15 min per wash). The washed immune complexes were boiled in protein loading buffer for 25 min to reverse the cross-links prior to separation by SDS-PAGE.

In some experiments, cells were transfected with siRNA duplexes prior to analysis of PCNA-TLS polymerase associations. For these experiments, cultures were grown to 70 to 80% confluence and then transferred into 5 ml of P_i-free medium. For siRNA transfections, 30 µl of Cy3 control siRNA, siRPA, or siRAD18 stocks (all at 20 µM) or 50 µl of siATR stock solution (Dharmacon smart pool) was added to 1.25 ml of Opti-MEM. After 5 min, this was mixed with 1.25 ml of Opti-MEM containing 30 µl of Lipofectamine 2000. Following a 25-min incubation at room temperature, the transfection mixture was added to the cells. After 24 h, when the cultures were fully confluent, the cells were split 1:2 into fresh 10-cm plates. These were infected with adenovirus vectors (AdGFP-Pol, AdChk1) for 24 h prior to genotoxin treatment. IPs were performed as described above.

Co-IP of Rad18 and TLS polymerases. H1299 cells growing in 10-cm plates were infected at 40 to 50% confluence with the various combinations of adenovirus for 36 h. Infected cells were treated with 600 nM BPDE for 6 h prior to harvest. Isolation of chromatin fractions for IP was performed essentially as described by Watanabe et al. (43). In brief, cells were washed twice with PBS and cross-linked with 9 ml of 1% formaldehyde for 10 min at room temperature. One milliliter of 1 M glycine was then added for 5 min at room temperature to quench the cross-linking reaction. Cells were washed twice in PBS and then fractionated into soluble and insoluble fractions with CSK buffer. The insoluble fraction was sonicated three times for 10 s at 30% of the maximum output and then clarified by centrifugation at 10,000 x g for 5 min. The supernatant (containing solubilized chromatin) and the soluble fraction from the initial cell lysis were normalized for protein content. GFP-Pol and YFP-Pol were immunoprecipitated overnight at 4°C with 3 µl (6 µg) of GFP antibody (Molecular Probes A11122) and 25 µl of protein G beads (Amersham Biosciences 17-0618-01). Immune complexes were washed three times with CSK buffer.

Protein G beads were resuspended in an equal volume of 2x Laemmli buffer, boiled for 5 min, and resolved by SDS-PAGE. Twenty percent of each input fraction was also analyzed by SDS-PAGE. After transfer to nitrocellulose, immunoblotting was performed with GFP antibody (Molecular Probes A11122) at 2 µg/ml and HA-antibody (Santa Cruz sc-805) at 0.2 µg/ml.

Reproducibility. All data shown are representative of experiments that were repeated at least three times with similar results on each separate occasion.

	RESULTS

Top Abstract Introduction Materials and Methods Results Discussion References

 
PCNA is monoubiquitinated in response to BPDE. We previously showed that ectopically expressed GFP-Pol redistributes and colocalizes with replication forks in BPDE-treated cells (6). The Lehman and Yamaizumi laboratories reported that PCNA undergoes monoubiquitination and recruits the TLS enzyme Pol to stalled forks in genotoxin-treated cells (28, 43). In contrast to Pol, mechanisms of Pol regulation are not well understood. Therefore, we asked if similar PCNA-dependent mechanisms recruit Pol and Pol to stalled replication forks.

First, we determined whether BPDE treatment induced PCNA monoubiquitination concomitant with the S-phase checkpoint. H1299 cells were chosen for these experiments. We and others have studied DNA replication extensively in this cell line (6, 20, 42). Importantly, we have demonstrated that the BPDE-induced S-phase checkpoint is intact and that GFP-Pol is recruited to sites of ongoing DNA replication in H1299 cells. H1299 cells were treated with 100 or 600 nM BPDE. At different times after BPDE treatment, nuclear fractions were prepared from BPDE-treated cells and assayed for monoubiquitinated PCNA, which is detected as a distinct band of 40 kDa, in contrast to unmodified PCNA, which is 32 kDa on immunoblots.

The inhibition of DNA synthesis induced by 100 nM BPDE results mainly from inhibition of initiation of replication unfired origins (12, 29). In a previous report, we have shown that 100 nM BPDE elicits a transient inhibition of DNA synthesis that is maximal 1 to 3 h after BPDE treatment (20). As shown in Fig. 1A, 100 nM BPDE induced a modest (1.6-fold) increase in the levels of an anti-PCNA immunoreactive band of 40 kDa, which corresponds to the correct size for monoubiquitinated PCNA. The amount of putative monoubiquitinated PCNA declined to basal levels by 3 to 5 h after BPDE treatment, concomitant with recovery from the S-phase checkpoint. Therefore, the kinetics of PCNA modification induced by 100 nM BPDE were similar to the kinetics of inhibition of DNA synthesis. In contrast to the transient inhibition of DNA synthesis elicited by 100 nM BPDE, 600 nM BPDE results in a persistent inhibition of DNA synthesis due to inhibition of both initiation and elongation steps of DNA synthesis (12, 29). Inhibition of elongation represents a physical stalling of replication forks and is not a regulated checkpoint response. PCNA was also posttranslationally modified in a manner consistent with its monoubiquitination in cells treated with 600 nM BPDE, concomitant with inhibition of elongation. However, both the duration and the levels of PCNA modification were increased in cells treated with the higher dose of BPDE (Fig. 1A, bottom).

View larger version (38K): [in this window] [in a new window]   FIG. 1. PCNA is monoubiquitinated after BPDE treatment. (A) Exponentially growing H1299 cells were treated with 100 nM (top) or 600 nM (bottom) BPDE. At different time points after BPDE treatment, nuclear fractions were prepared. After normalizing for protein content, nuclear samples were separated by SDS-PAGE, transferred to nitrocellulose, and analyzed by immunoblotting with anti-PCNA antibodies. (B) H1299 cells were infected with AdCon or AdRad18 for 24 h. The resulting cultures were transfected with H6M-Ub for 24 h and treated with BPDE (or left untreated). After 4 h, chromatin fractions from the cells were analyzed directly for PCNA levels. Alternatively, H6M-Ub-conjugated proteins were purified with cobalt-agarose resin prior to immunoblot analysis with anti-PCNA.

We expressed a hexahistidine- and Myc-tagged form of Ub (designated H₆M-Ub) in AdCon (empty adenovirus vector)- or AdRad18 (encoding Rad18, a PCNA E3 ligase)-infected H1299 cells by transient transfection. The resulting H₆M-Ub-expressing cells were given BPDE or left untreated as controls. H₆M-Ub-containing proteins were purified from chromatin fractions with metal affinity resin as described in Materials and Methods. The resulting H₆M-Ub-conjugated proteins were resolved by SDS-PAGE and probed with an anti-PCNA antibody. As shown in Fig. 1B, both BPDE and Rad18 induced a 45-kDa PCNA species that was enriched by metal affinity purification. Forty-five kilodaltons corresponds to the expected molecular mass of H₆M-Ub-tagged and monoubiquitinated PCNA. This result demonstrates that PCNA is ubiquitinated in response to BPDE treatment and Rad18 overexpression.

Taken together, these results show that PCNA is ubiquitinated concomitant with the BPDE-induced inhibition of DNA synthesis caused by BPDE doses that inhibit late origin firing (100 nM BPDE) or concentrations that elicit blocks in elongation (600 nM BPDE). The temporal pattern of BPDE-induced PCNA ubiquitination shown here correlates well with the pattern of GFP-Pol focus formation that we described in a previous study (6). These data are consistent with a putative role for PCNA ubiquitination in Pol regulation.

GFP-Pol associates with PCNA in BPDE-treated cells. Our previous study demonstrated colocalization of GFP-Pol with replication forks (as identified by bromodeoxyuridine-labeled regions) in BPDE-treated cells (6). To test specifically if Pol colocalizes with PCNA, we treated GFP-Pol-expressing H1299 cells with BPDE, fixed the resulting cells, and probed them with anti-PCNA antibodies. We detected bound anti-PCNA antisera with Cy3-coupled secondary antibodies. Patterns of PCNA and GFP fluorescence were visualized by deconvolution microscopy. A representative nucleus showing the distribution of BPDE-induced GFP-Pol foci (green) and PCNA (red) staining is shown in Fig. 2A. As shown in Fig. 2A, there was extensive (although not complete) overlap between GFP and PCNA fluorescence, indicating colocalization of Pol and PCNA.

View larger version (39K): [in this window] [in a new window]   FIG. 2. PCNA associates with GFP-Pol in BPDE-treated cells. (A) H1299 cells growing in chamber slides were infected with AdGFP-Pol for 24 h. The resulting cultures were treated with BPDE, and 6 h later cells were fixed with formaldehyde. The resulting slides were probed with anti-PCNA. Bound PCNA antibody was detected with Cy3-coupled secondary antisera. PCNA and GFP-Pol fluorescence were visualized by DeltaVision deconvolution microscopy. DeltaVision 3D object-builder software was used to generate a three-dimensional model of the two-dimensional polygons in each z section of a representative quadrant within the nucleus. The schematic depicts the degree to which green (GFP-Pol) and red (PCNA) signals colocalize in three dimensions. (B) H1299 cells expressing GFP-Pol (left side) or YFP-Pol (right side) were treated with 600 nM BPDE. After 6 h, chromatin fractions from the cells were analyzed directly from Pol or Pol levels (upper blots). Alternatively, chromatin fractions were immunoprecipitated with anti-PCNA antibodies and the resulting immunoprecipitates were analyzed for PCNA and associated GFP-Pol or YFP-Pol with anti-GFP antibodies. IB, immunoblotting.

As shown in Fig. 2B, BPDE treatment had no effect on the levels of GFP-Pol, YFP-Pol, or PCNA in chromatin extracts. However, as expected, PCNA ubiquitination was induced by BPDE. Anti-PCNA immunoprecipitates from the chromatin fractions were resolved by SDS-PAGE and then immunoblotted with anti-GFP (to detect coimmunoprecipitated YFP-Pol and GFP-Pol) or anti-PCNA (to confirm IP of PCNA).

As shown in Fig. 2B, the amount of GFP-Pol that coimmunoprecipitated with PCNA was increased approximately sixfold by BPDE treatment. Interestingly, although YFP-Pol and GFP-Pol were expressed at similar levels, there was a relatively high basal level of association between Pol and PCNA (the association between Pol and PCNA was also increased by BPDE treatment). In our previous study, we noted that YFP-Pol, but not GFP-Pol, forms large numbers of foci in H1299 cells in the absence of genotoxin treatment (6). Therefore, Pol shows a DNA damage-induced association with PCNA concomitant with its redistribution to nuclear foci. In contrast, Pol is associated with PCNA and subnuclear foci in H1299 cells that do not receive genotoxin. In these experiments, we noticed that overexpression of YFP-Pol (but not of GFP-Pol) resulted in increased monoubiquitination of PCNA, even in the absence of DNA damage (Fig. 2B, PCNA immunoblot, right side). YFP-Pol-induced PCNA ubiquitination likely accounts for the high basal association of PCNA with YFP-Pol in H1299 cells.

Previously it was shown that Pol is required for genotoxin-induced association of Pol with nuclear foci (27). To test if Pol is similarly required to recruit Pol to PCNA, XPV cells (which lack functional Pol) were infected with adenovirus encoding GFP-Pol. The resulting cells were treated with 600 nM BPDE for 4 h (or left untreated) and then lysed to prepare chromatin extracts. The resulting chromatin extracts were analyzed directly for PCNA and Pol expression by immunoblotting or solubilized and immunoprecipitated with PCNA antibodies prior to blotting with PCNA or GFP antibodies.

As shown in Fig. 3A, BPDE treatment had no effect on the levels of chromatin-associated GFP-Pol in XPV cells. We consistently observed an increase in levels of chromatin-bound PCNA in XPV cells after BPDE treatment. Nevertheless, as expected, BPDE induced PCNA ubiquitination in XPV cells. Moreover, as also shown in Fig. 3A, BPDE induced association of GFP-Pol with PCNA, similar to results of experiments with Pol-expressing H1299 cells (Fig. 2). Therefore, Pol recruitment to PCNA is BPDE inducible in the absence of Pol.

View larger version (29K): [in this window] [in a new window]   FIG. 3. Pol is not required for BPDE-induced association of Pol with PCNA. (A) CRL1162-TERT XPV cells were infected with 2 x 1010 PFU/ml of AdGFP-Pol. At 48 h after infection, cells were given 600 nM BPDE or left untreated as controls. After 4 h, chromatin fractions were prepared and analyzed directly for Pol and PCNA levels (top). Alternatively, chromatin fractions were immunoprecipitated with anti-PCNA antibody. The resulting immunoprecipitates were resolved by SDS-PAGE, transferred to nitrocellulose, and probed with anti-GFP or anti-PCNA antibodies (bottom). (B) H1299 cells were cotransfected with expression plasmids for YFP-Pol and HA-Pol. At 48 h after transfection, cells were treated with 600 nM BPDE for 6 h. Cells were washed with CSK buffer to remove soluble proteins. The resulting nuclei were fixed in formaldehyde and immunostained with anti-HA antibody. Slides were visualized by DeltaVision deconvolution microscopy. IB, immunoblotting.

As shown in Fig. 3B, and consistent with our previous report (6), YFP-Pol formed nuclear foci in the absence of BPDE. However, there was an increase in the number of YFP-Pol foci in each cell after BPDE treatment. In contrast, HA-Pol foci were observed only after BPDE treatment (Fig. 3B). We observed remarkably little colocalization of HA-Pol and YFP-Pol foci in BPDE-treated cells. These data are consistent with the results of Fig. 3A, which demonstrate that Pol is not required for BPDE-induced recruitment of Pol to replication forks.

Since the experiments whose results are shown in Fig. 1 demonstrated BPDE-induced PCNA ubiquitination and BPDE-induced association between PCNA and GFP-Pol, we asked if this association required PCNA ubiquitination. We generated adenovirus vectors that express HA-tagged WT PCNA and HA-tagged PCNA K164A encoding a ubiquitination-resistant mutant form of PCNA. To verify that the K164A mutant was not ubiquitinated, we expressed HA-PCNA-WT and HA-PCNA-K164A in H1299 cells by adenoviral infection. The resulting cultures were treated with 600 nM BPDE or coinfected with AdRad18. Chromatin extracts were prepared, resolved by SDS-PAGE, transferred to nitrocellulose, and then probed with HA antibodies. As expected, HA-PCNA-WT but not HA-PCNA-K164A underwent a monoubiquitination-induced mobility shift in response to BPDE treatment or Rad18 overexpression (Fig. 4A).

View larger version (38K): [in this window] [in a new window]   FIG. 4. DNA damage-induced association between GFP-Pol and PCNA requires Rad18-dependent PCNA monoubiquitination. (A) H1299 cells were infected with AdHA-PCNA-WT or AdHA-PCNA-K164A individually or in combination with AdHA-Rad18. At 48 h postinfection, some cultures were treated with 600 nM BPDE. Cells were harvested 6 h after BPDE treatment. Chromatin fractions were collected and analyzed for expression of HA-tagged PCNA. (B) H1299 cells were coinfected with AdGFP-Pol and AdHA-PCNA-WT or AdHA-PCNA-K164A. Twenty-four hours after infection, cells were given 600 nM BPDE (BP) or 10 J/m2 of UVC (UV) or left untreated as controls. At 6 h after genotoxin treatment, chromatin fractions were prepared and immunoprecipitated with anti-HA antibody. The resulting immunoprecipitates were resolved by SDS-PAGE, transferred to nitrocellulose, and probed with anti-GFP (top) or anti-PCNA (bottom) antibodies. (C) H1299 cells were infected with AdHA-Rad18 for 24 h. The HA-Rad18-expressing cells were transfected with siRNA oligonucleotides against Rad18 (siRad18) or with control (Cy3) oligonucleotides. The resulting cells were lysed 24 h later. Cell extracts were resolved by SDS-PAGE, transferred to nitrocellulose, and analyzed by blotting with anti-HA antibodies. NS indicates a protein present in H1299 cell lysates that reacts nonspecifically with polyclonal anti-HA antisera and serves as a loading control. (D) H1299 cells were transfected with siRNA oligonucleotides against Rad18 (siRad18) or control siRNA oligonucleotides (Cy3) or infected with AdHA-Rad18. Twenty-four hours later, cells were given 600 nM BPDE for 6 h or left untreated as controls. Chromatin extracts from the cells were immunoprecipitated with anti-PCNA antisera. Immunoprecipitates were analyzed by Western blotting with antibodies against PCNA or GFP. IB, immunoblotting.

Rad18 status influences association between PCNA and Pol. The results shown in Fig. 1 to 3 suggested a role for PCNA monoubiquitination in Pol regulation. Studies with yeast and mammalian cells have shown that PCNA monoubiquitination in response to genotoxins requires the E3 ligase Rad18 (22, 28, 39, 43). Therefore, we used siRNA strategies to test the role of Rad18 in BPDE-induced PCNA ubiquitination and Pol regulation.

We tested the effectiveness of Rad18 siRNA on levels of ectopically expressed HA-tagged Rad18 protein. H1299 cells were infected with Ad-HARad18 adenovirus. The resulting cultures were transfected with siRNA against Rad18 or control Cy3 RNA oligonucleotides. Protein extracts from these cultures were separated by SDS-PAGE, blotted to nitrocellulose, and then probed with anti-HA antibodies. As shown in Fig. 4C, HA-Rad18 was readily detected in extracts from cells transfected with control RNA oligonucleotides. However, expression of HA-Rad18 was ablated by >90% in Rad18 siRNA-transfected cells. Therefore, our Rad18 siRNA oligonucleotides were effective for silencing Rad18 expression.

We tested the effects of Rad18 siRNA on BPDE-induced monoubiquitination of PCNA and PCNA-Pol interactions. H1299 cells were infected with AdGFP-Pol and then transfected with control or Rad18 siRNA oligonucleotides. The resulting cells were treated with BPDE or left untreated as controls. After lysis, chromatin extracts from the cells were immunoprecipitated with anti-PCNA antibodies and analyzed for PCNA modification and coimmunoprecipitated GFP-Pol.

As shown in Fig. 4D, BPDE induced PCNA monoubiquitination and association between PCNA and GFP-Pol in Cy3-transfected (control) cells. However, both the BPDE-induced increase in monoubiquitinated PCNA and PCNA-bound GFP-Pol were ablated in Rad18 siRNA-transfected cells. These data suggest that Rad18 is required for BPDE-induced associations between Pol and PCNA.

We also determined the effect of Rad18 overexpression on PCNA ubiquitination and PCNA-Pol interactions. Adenovirus vectors were used to express GFP-Pol individually or in combination with HA-tagged Rad18. Rad18-overexpressing cells had very high basal levels of monoubiquitinated PCNA, equivalent to levels of monoubiquitination induced by BPDE under our standard experimental conditions (Fig. 4D). The high basal levels of PCNA ubiquitination in AdRad18-infected cells were further increased after BPDE treatment. Interestingly, in HA-Rad18-expressing cells there was also a high-level association between PCNA and GFP-Pol. Therefore, overexpressed Rad18 induces PCNA ubiquitination and associations between PCNA and GFP-Pol in the absence of DNA damage. These results demonstrate an important role for Rad18 in Pol regulation.

Interactions between Rad18 and Pol. Recently, Watanabe et al. showed that Rad18 directly interacts with Pol and that the interaction is required for Pol to form nuclear foci after DNA damage (43). We performed reciprocal co-IP experiments to investigate if similar associations exist between Rad18 and Pol. As a positive control for these experiments, we measured association between Rad18 and Pol. Chromatin fractions from cells expressing HA-Rad18 and YFP-Pol or GFP-Pol were fixed and sheared by sonication as described by Watanabe et al. (43). Solubilized chromatin fractions were immunoprecipitated with anti-GFP antisera, and the resulting immune complexes were analyzed for associated HA-Rad18 by SDS-PAGE and Western blotting.

As expected, Rad18 was present in anti-GFP immunoprecipitates from YFP-Pol-expressing cells (Fig. 5A, lower right part). Interestingly, anti-GFP immunoprecipitates from GFP-Pol- and YFP-Pol-expressing cells contained similar amounts of Rad18, indicating that the two polymerases associated with Rad18 to similar extents. It should be noted, however, that only a small fraction of the cellular HA-Rad18 associated with Pol and Pol in these experiments. Moreover, the association between Pol (or Pol) and Rad18 was only evident in immunoprecipitated chromatin fractions derived from formaldehyde-fixed nuclei. Even when we massively overexpressed GFP-Pol or YFP-Pol and HA-Rad18, we were unable to detect association between soluble pools of polymerase and Rad18 or associations between unfixed chromatin-bound proteins (L.R.B. and C.V., data not shown). Therefore, it is likely that the associations between TLS polymerases and Rad18 that we detected in our chromatin IP assays are indirect and perhaps mediated by PCNA and/or DNA. Alternatively, putative direct associations that exist between Pol or Pol and Rad18 might be weak, transient, and dynamic or poorly preserved in vitro under the experimental conditions used in this study.

View larger version (29K): [in this window] [in a new window]   FIG. 5. Association between Rad18 and Pol. (A) H1299 cells were infected with AdGFP-Pol or AdYFP-Pol individually or in combination with AdHA-Rad18. After 24 h, some cultures were treated with BPDE. Chromatin fractions from the resulting cells were solubilized. Aliquots of total chromatin fractions were analyzed directly for expression of HA-Rad18, GFP-Pol, and YFP-Pol by SDS-PAGE and immunoblotting (input). The remainder of each chromatin fraction was immunoprecipitated with anti-GFP antibodies. The anti-GFP immune complexes were resolved by SDS-PAGE and probed with anti-GFP (to verify IP of GFP and YFP TLS polymerase fusion proteins) or with anti-HA (to test for associated Rad18). (B) H1299 cells were infected with AdGFP-Pol individually or in combination with AdHA-Rad18. At 24 h later, some cultures were given 600 nM BPDE for 6 h. The distribution of GFP-Pol in the resulting cells was determined by deconvolution microscopy. (C) H1299 cells were infected with Ad GFP-Pol and AdHA-Rad18. After 24 h, some cultures received 600 nM BPDE for 6 h. The resulting cells were fixed and stained with anti-HA antibodies as described in Materials and Methods.

Rad18 deficiency perturbs recovery from BPDE-induced S-phase checkpoint. The experiments described above suggested an important role for Rad18 in PCNA modification and Pol recruitment after BPDE treatment. Previously, we reported that Pol deficiency results in defective recovery from the BPDE-induced S-phase checkpoint. Since Rad18 is important for Pol regulation, we expected that Rad18^–/– and Pol^–/– cells would have similar checkpoint recovery defects. To test this prediction, Rad18^–/– and WT MEFs (derived from Rad18 knockout mice and WT animals, respectively) were analyzed for S-phase checkpoint responses to BPDE. Exponentially growing cultures of Rad18^+/+ and Rad18^–/– cells were treated with 100 nM BPDE. Then, at different time points after BPDE treatment, we determined rates of DNA synthesis by using [³H]thymidine incorporation assays.

As shown in Fig. 6A, 2 h after BPDE treatment, DNA synthesis was reduced by 40% in Rad18^+/+ cells. However, 4 h post-BPDE treatment, rates of DNA synthesis recovered to control levels. In Rad18^–/– cells, BPDE inhibited DNA synthesis with kinetics similar to those of WT MEFs, but DNA synthesis failed to recover to control levels within the time frame of this experiment. These data suggest a requirement for Rad18 in recovery from the BPDE-induced S-phase checkpoint. We performed similar experiments to determine the role of Rad18 in recovery from the UV-induced checkpoint. As shown in Fig. 6B, recovery from UV-induced S-phase arrest was also defective in Rad18^–/– cells.

View larger version (24K): [in this window] [in a new window]   FIG. 6. S-phase checkpoint recovery defects in Rad18–/– MEFs. Exponentially growing cultures of Rad18+/+ or Rad18–/– cells were treated with 100 nM BPDE (A), 10 J/m2 UVC (B), 5 Gy of IR (C), or 2 mM HU (D). At different times after genotoxin treatments, rates of DNA synthesis of the resulting cultures were determined by [3H]thymidine incorporation assays. In the experiment shown in panel E, Rad18–/– MEFs were transiently transfected with cytomegalovirus (CMV)-GFP or CMV-HA-Rad18 plasmids. Transfection efficiency was >90% as determined by green fluorescence of transfected cells. Twenty-four hours after transfection, some cells were lysed and analyzed for Rad18 expression by immunoblotting with anti-HA antibodies (left side). Other cultures were treated with 100 nM BPDE. Then, at different times after BPDE treatment, rates of DNA synthesis were determined by [3H]thymidine incorporation assays.

It was formally possible that defects other than Rad18 deletion resulted in the checkpoint recovery defects we observed in Rad18-null MEFs. To address this possibility, we performed transient-expression experiments to reconstitute Rad18 in Rad18^–/– MEFs. As shown in Fig. 6E, ectopic expression of HA-Rad18 corrected the defective checkpoint recovery of Rad18^–/– cells. Taken together, our data show that Rad18 is required for recovery from the BPDE-induced S-phase checkpoint.

Checkpoint signaling in Rad18^–/– cells. S-phase checkpoint signaling is thought to result when replicative enzymes encounter DNA lesions, thereby uncoupling the activities of replicative helicases from fork progression (9). Our results suggested that replication forks in Rad18-null cells fail to carry out TLS of BPDE-adducted DNA and remain stalled. Therefore, we predicted that checkpoint signaling would be elevated in Rad18^–/– cells relative to WT cells (which accumulate fewer blocked replication forks). To test this prediction, we treated cultures of Rad18^+/+ or Rad18^–/– cells with 100 nM BPDE. At different time points after BPDE treatment, the cells were lysed and the resulting protein extracts were analyzed for activation of checkpoint kinases. Chk1 is activated by replication blocks, and we previously showed that Chk1 mediates BPDE-induced S-phase arrest (20). We determined the activation status of Chk1 by using phosphospecific antisera against serine 345. As shown in Fig. 7A, 100 nM BPDE elicited more persistent and higher levels of Chk1 phosphorylation in Rad18-deficient cells compared with WT cells. This result is consistent with the presence of persistent stalled forks resulting from BPDE treatment in a Rad18-null background.

View larger version (50K): [in this window] [in a new window]   FIG. 7. Checkpoint signaling in Rad18–/– MEFs. Rad18+/+ or Rad18–/– MEFs were treated with 100 nM BPDE (A and B) or 10 J/m2 UV (C). At different times after genotoxin treatment, cells were lysed and the resulting protein extracts were analyzed for activation of checkpoint kinases with phosphospecific antibodies against Chk1 (A and B) or Chk2 (C). NS indicates nonspecific bands recognized by the antibodies that served as loading controls.

We showed previously that Pol is important for cell survival after BPDE treatment (6). It was of interest to determine if Rad18 was similarly required for cell viability after acquisition of BPDE-induced DNA damage. Exponentially growing cultures of WT and Rad18^–/– cells were given BPDE or other genotoxins for the purpose of comparison. After 24 h, control and genotoxin-treated cultures were trypsinized and replated at a density of 100 cells/10-cm dish. One week later, viable colonies were visualized by Giemsa staining and enumerated. As shown in the bar chart in Fig. 8, 40% of the Rad18^+/+ cultures survived treatment with 100 nM BPDE. However, Rad18^–/– cells only showed <20% viability after treatment with 100 nM BPDE. Rad18^–/– cells also showed increased sensitivity to UV compared with WT MEFs (Fig. 8). However, Rad18 status did not significantly affect the viability of HU- or IR-treated cultures (Fig. 8). Therefore, Rad18 is important for survival after acquisition of bulky fork-blocking DNA adducts resulting from BPDE or UV but is not required for viability after IR-induced DSBs or HU-induced replication cessation.

View larger version (18K): [in this window] [in a new window]   FIG. 8. Clonogenic survival of Rad18+/+ and Rad18–/– cells after genotoxin treatment. Exponentially growing cultures of Rad18+/+ or Rad18–/– MEFs were treated with BPDE (BP; 100 nM or 600 nM), HU (2 mM for 1 h or 2 h), IR (4 Gy or 8 Gy), or UVC (10 J/m2 or 20 J/m2). Twenty-four hours after treatment, cells were trypsinized and counted and then replated at a density of 1,000 cells/10-cm plate. The resulting plates were returned to the incubator and given fresh growth medium every 3 days. After 7 days, cells were fixed and stained with Giemsa. Giemsa-stained colonies containing >50 cells were scored.

Role of checkpoint signaling in PCNA ubiquitination and Pol recruitment.

We previously showed that the ATM/ATR inhibitor caffeine caused a decrease in the number of Pol nuclear foci induced by BPDE treatment (6). In unpublished experiments, we also found that the Chk1 inhibitor UCN-01 decreased the number of GFP-Pol foci induced by BPDE. Those studies further suggested a role for the ATR/Chk1 pathway in PCNA modification and Pol regulation. A potential complication of studies with caffeine and UCN-01 is that these inhibitors are not entirely specific and might perturb Pol regulation in an ATR- or Chk1-independent manner. Therefore, we used siRNA and dominant-negative strategies to provide a more specific test of the role of ATR/Chk1 signaling in Pol regulation.

To determine the role of ATR in Pol regulation, we performed siRNA experiments to ablate ATR expression. The ssDNA-binding protein RPA is important for activating ATR at stalled replication forks. Therefore, we performed complementary experiments with siRNA against the RPA p34 subunit to test the role of RPA in PCNA modification and Pol regulation. GFP-Pol-expressing H1299 cells were transfected with siRNA oligonucleotides against ATR or RPA or with Cy3 control RNAi duplexes. At 48 h after transfection, we prepared cell extracts and performed immunoblotting with RPA p34 and ATR antisera (Fig. 9A). These analyses verified that ATR and RPA levels were effectively ablated under our experimental conditions.

View larger version (38K): [in this window] [in a new window]   FIG. 9. Roles of RPA, ATR, and Chk1 in BPDE-induced PCNA ubiquitination and Pol recruitment. (A) H1299 cells were transfected with siRNA oligonucleotide duplexes against ATR and RPA or with control Cy3 RNA oligonucleotides. Some cultures were infected with AdChk1KR or AdCon. The resulting cells were analyzed for ATR, RPA, or Chk1 expression with appropriate antibodies. (B) H1299 cells expressing GFP-Pol were transfected with siRNA oligonucleotides against ATR, RPA, and Rad18 or with Cy3 (control) oligonucleotides. Alternatively, some cultures were infected with AdChk1KR. The resulting cultures were given 600 nM BPDE, and 6 h later the cells were lysed. Nuclear fractions were immunoprecipitated with anti-PCNA, and the resulting immune complexes were resolved by SDS-PAGE and immunoblotted (IB) with anti-PCNA or anti-GFP antibodies. (C) ET163 and YZ5 cells were treated with 600 nM BPDE or left untreated as controls. After 4 h, soluble and chromatin fractions were prepared and analyzed directly for PCNA (chromatin fraction) and Thr68-phosphorylated Chk2 (soluble fraction) levels.

Since Chk1 is an important effector of ATR and 9-1-1 in the S-phase checkpoint, we asked if Chk1 was involved in Pol regulation. We previously generated a kinase-inactive dominant-negative mutant form of Chk1 that we expressed with an adenovirus vector. We and others have shown that this reagent can be used to inhibit S and G₂ checkpoints mediated by Chk1 signaling (20, 21). Therefore, we tested the effect of dominant-negative Chk1 on the BPDE-induced association between PCNA and Pol. As shown in Fig. 9B, expression of dominant-negative Chk1 reduced the levels of monoubiquitinated PCNA and the amount of PCNA-associated Pol in BPDE-treated cells by 50% relative to those in control cultures. Therefore, Chk1 signaling contributes to PCNA modification and Pol regulation.

A recent publication by Jazayeri et al. demonstrated that ATR activation by DSBs is regulated by ATM in a cell cycle-dependent manner (24). Therefore, it was of interest to determine if ATM is required for BPDE-induced (and ATR/Chk1-dependent) PCNA ubiquitination. To test the role of ATM in BPDE-induced PCNA ubiquitination, we compared the effect of BPDE treatment on PCNA ubiquitination in ET163 fibroblasts from AT patients and in matched cells designated YZ5 that express reconstituted ATM (46). As shown in Fig. 9C, BPDE-induced PCNA ubiquitination was evident in both ET163 and YZ5 cells and therefore is ATM independent. As expected, DNA damage-induced Chk2 phosphorylation (which is known to be largely ATM dependent) was only observed in YZ5 cells. Taken together, these data suggest that efficient PCNA ubiquitination requires ATR and Chk1, but not the ATM pathway.

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

 
Our previous work demonstrated an important role for Pol in recovery from the BPDE-induced S-phase checkpoint (6). Those studies suggested that Pol is recruited to replication forks stalled by BPDE-adducted DNA and that subsequent Pol-mediated lesion bypass allows attenuation of the S-phase checkpoint. Here we have investigated the mechanism(s) that recruits Pol to stalled replication forks. We show that PCNA is ubiquitinated in a Rad18-dependent manner after acquisition of DNA damage and that Pol associates specifically with monoubiquitinated PCNA. Further, consistent with a role for Rad18-mediated PCNA monoubiquitination in Pol regulation, Rad18^–/– and Pol^–/– cells have similar defects in recovery from the BPDE-mediated S-phase checkpoint.

Although we have shown that Pol forms a complex with monoubiquitinated PCNA, we have not demonstrated that this interaction is direct. Therefore, it is possible that the interaction of Pol with monoubiquitinated PCNA is mediated by another TLS polymerase and/or other factors. For example, Pol and Pol interact directly and Pol is required for genotoxin-induced redistribution of Pol to replication foci (27). In contrast to Pol, we have shown that the recruitment of Pol to ubiquitinated PCNA does not require Pol. Our finding that the association of Pol with PCNA is Pol independent is consistent with previous reports that XPV cells do not show increased sensitivity to BPDE (8, 13) or defects in recovery from the BPDE-induced S-phase checkpoint (6).

Although Pol is not required for BPDE-induced association of Pol with monoubiquitinated PCNA, it is possible that an alternative TLS polymerase helps recruit Pol to the replication fork. However, a recent study showed that Y family polymerases, including Pol, contain novel Ub-binding motifs (7), and it is also likely that Pol and monoubiquitinated PCNA interact directly.

Okada et al. previously found additive effects of Rad18 and Pol deletion in chicken DT40 cells (37), arguing against a dependence of Pol on Rad18 gene function in this experimental system. This contrasts with our finding that Pol is regulated in a Rad18-dependent manner in mammalian cells. It is possible that Pol is regulated via Rad18-independent mechanisms in avian cells. Alternatively, the Rad18 independence of Pol regulation may be an idiosyncrasy of DT40 cells. Recombination activity is very high in DT40, as indicated by the very high efficiency of gene targeting in these cells. It is possible that DNA damage tolerance in DT40 depends more heavily on a DNA recombination pathway than on TLS compared with other systems. Another possibility is that the Rad18 mutant described by Okada and colleagues is not a complete genetic null. Regardless of the reason for the Rad18 independence of Pol regulation in DT40 cells, our data demonstrate a role for Rad18 in Pol regulation in mammalian cell lines. As discussed above, the recent finding that Pol contains a Ub-binding motif (7) provides a plausible molecular basis for direct recruitment of Pol to ubiquitinated PCNA and supports a role for Rad18 in Pol regulation.

Interestingly, our data indicate that ATR/Chk1-mediated S-phase checkpoint signaling may contribute to PCNA ubiquitination and Pol recruitment in response to DNA damage. Taken together, our results suggest the model in Fig. 10, whereby replication blocks initiate ATR/Chk1 signaling. Chk1 activity inhibits late origin firing and stabilizes stalled replication forks. Potentially, stabilization of a stalled fork could facilitate PCNA ubiquitination and recruitment of TLS polymerases indirectly. Alternatively, Chk1 signaling could directly stimulate PCNA ubiquitination, perhaps via Rad18 activation. Subsequently, Pol-mediated lesion bypass recovers the stalled replication fork, thereby attenuating checkpoint signaling and enabling resumption of DNA synthesis. In the absence of lesion bypass, stalled forks collapse to generate DSBs that elicit ATM/Chk2 signaling. A model in which ATR/Chk1 signaling is a prerequisite for TLS is not necessarily implied since overexpression of Rad18 can elicit DNA damage-independent PCNA ubiquitination. Therefore, checkpoint signaling is likely to modulate TLS but is probably not an absolute requirement for PCNA ubiquitination and Pol recruitment.

View larger version (18K): [in this window] [in a new window]   FIG. 10. Hypothetical model describing the roles of Rad18 and Pol in the BPDE-induced S-phase checkpoint. Replication forks stalled by BPDE-adducted DNA activate the ATR/Chk1 pathway. ATR/Chk1 signaling inhibits firing of late origins and also stabilizes stalled replication forks. Stabilization of a stalled fork could facilitate PCNA ubiquitination and recruitment of TLS polymerases indirectly. Alternatively, Chk1 signaling could stimulate PCNA ubiquitination directly, perhaps via Rad18 activation. Pol is recruited to monoubiquitinated PCNA at the stalled fork. Pol-mediated lesion bypass enables recovery of the stalled replication fork, and checkpoint signaling is attenuated. In the absence of Rad18/Pol, stalle