INTRODUCTION

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Replication protein A (RPA) is a highly conserved eukaryotic single-stranded DNA (ssDNA) binding protein that was originally identified as a human factor required for simian virus 40 (SV40) DNA replication in vitro (19, 84, 86). As the eukaryotic equivalent of the Escherichia coli ssDNA binding protein (Ecssb), RPA plays multiple roles in DNA metabolism, including DNA replication, repair, and recombination (85). In addition to participating in both the initiation and elongation of DNA replication, RPA is required for nucleotide excision repair in vitro and physically interacts with XPA, XPG, and XPF (30, 39, 62, 69). RPA is also required for genetic recombination and physically interacts with Rad52 and other factors (1, 22, 47, 75).

RPA is a heterotrimeric complex. In the budding yeast Saccharomyces cerevisiae it is composed of the Rpa1 (69 kDa), Rpa2 (36 kDa), and Rpa3 (13 kDa) subunits, which are encoded by RFA1, RFA2, and RFA3, respectively. Each subunit is essential for viability in yeast, and all three subunits are required for SV40 DNA replication in vitro (12, 18, 25, 31, 32). Rpa1 exhibits strong ssDNA binding activity on its own, and a subcomplex of Rpa2 and Rpa3 binds ssDNA weakly (7, 85). We have shown that yeast Rpa1 consists of four functional domains: an 18-kDa N-terminal domain that lacks ssDNA binding activity (Rpa1N) and three tandem ssDNA binding domains (SBDs; see Fig. 1A) (11, 56). SBD-A and SBD-B are structurally homologous as determined by X-ray crystallographic analysis of human RPA (hRPA), while the C-terminal domain (SBD-C) contains a C4-type zinc-finger motif (6, 8, 11). These three ssDNA binding domains share amino acid sequence similarity with each other and with the central region of Rpa2 (11). All four domains of Rpa1, including Rpa1N, are essential for viability in yeast (11, 56).

The essential function of Rpa1N is unknown but may involve its ability to interact with other proteins. Human Rpa1N has been shown to bind DNA polymerase , p53, T antigen, and VP16 (10, 41). Surprisingly, deletion of this domain in hRPA does not affect its ssDNA binding activity or SV40 DNA replication in vitro (25, 35). In contrast, mutations in yeast Rpa1N result in defects in DNA replication, recombination, and repair, and deletion of more than 10 amino acids from the N terminus is lethal (43, 56, 75). To determine the essential cellular role of Rpa1N, we first isolated the conditional mutation rfa1-Y29H, which maps to this domain. We then performed a synthetic-lethal screen with rfa1-Y29H under permissive conditions to identify mutations that require wild-type Rpa1N function for viability. To confirm that these synthetic-lethal mutations interacted specifically with Rpa1N, we took advantage of a large collection of Rpa1 mutants (75). The results indicate that one of the genes isolated in this screen, RFC4, displays allele-specific interactions with mutations mapping to Rpa1N.

Replication factor C (RFC), the eukaryotic clamp loader, loads the DNA polymerase  processivity factor proliferating cell nuclear antigen (PCNA, or sliding clamp) at primer-template junctions (37, 70, 72, 88). In the presence of RPA, the loading of PCNA by RFC promotes a switch from synthesis by DNA polymerase  to processive synthesis by DNA polymerase  (71, 74, 78, 89). RFC is a heteropentameric complex consisting of one large subunit (Rfc1 [Cdc44]) and four small subunits (Rfc2, -3, -4, and -5), all of which are essential for viability in yeast (15, 40). Mutations in RFC2 and RFC5 cause sensitivity to the DNA synthesis inhibitor hydroxyurea (HU). Consistent with this phenotype and their role in DNA replication, these mutant strains display defects in the DNA replication checkpoint pathway (50, 65, 66). The four small subunits of RFC are also associated with Rad24, one of the major components of the DNA damage checkpoint pathway (26, 27, 60). It has been proposed that the Rad24-Rfc2-5 complex is responsible for loading a PCNA-like complex of Rad17-Mec3-Ddc1 at sites of DNA repair (36, 76). Due to their association with Rad24, the small subunits of RFC might also play a role in DNA damage checkpoints. Indeed, defects in DNA damage checkpoints are exacerbated in an rfc5 rad24 double mutant (48).

In this report we describe the isolation of the rfc4-2 mutation based on its synthetic lethality with a mutation in Rpa1N. We find that the rfc4-2 mutant is sensitive to HU, is lethal in combination with Rpa1N mutations that are themselves HU sensitive, and is partially defective in the replication block checkpoint response and the intra-S DNA damage checkpoint. We also find that RFC4 functions in the RAD24 epistasis group and that RFC4 plays a role in multiple DNA damage checkpoint pathways. Taken together, the results suggest that both DNA replication and DNA checkpoint signaling require a direct physical interaction between Rfc4 and Rpa1N.

	MATERIALS AND METHODS

Top Abstract Introduction Materials and Methods Results Discussion References

Strains, media, and plasmid construction. All yeast strains used in this study are listed in Table 1. Plasmids used in this study are listed in Table 2. Standard genetic techniques and reagents were used in the construction, transformation, and growth of yeast (57). The starting strains for the synthetic-lethal screen, HSY657 and HSY672, were constructed by integrating pHS102, containing the rfa1-Y29H allele, at the TRP1 locus of HSY631 and HSY626, respectively. Following loss of pJM195 (RFA1/URA3/ADE3) by growth on media containing 5-fluoroorotic acid (5-FOA), these strains displayed temperature-sensitive (ts) growth. To reduce the probability of obtaining rfa2 or rfa3 mutations in a synthetic-lethal screen with rfa1-Y29H, second copies of RFA2 and RFA3 were provided by integrating pHS203 at the HIS3 locus of these strains.

Isolation of the rfa1-ts allele. The region of the RFA1 gene encoding the promoter and amino acids 1 to 200 was amplified under mutagenic PCR conditions using plasmid pDS1 (RFA1/LEU2/CEN) as a template (56). This DNA was subjected to 35 cycles of amplification using Taq DNA polymerase and specific primers in the presence of 1 mM MnCl₂. These randomly mutagenized PCR products were combined with an RFA1 plasmid vector lacking the N-terminal coding region of RFA1 (pDS1 digested with NdeI and BamHI) and were cotransformed into strain SBY102 carrying plasmid pJM114 (RFA1/URA3/CEN). The RFA1 gene was repaired by homologous recombination in vivo. Leucine prototrophs were selected and replica plated onto solid media containing 5-FOA at 25°C to shuffle out the wild-type RFA1 plasmid, pJM114. FOA-resistant colonies were replica plated to yeast extract-peptone-dextrose (YPD) plates and incubated at 25 or 37°C for 3 to 4 days. Approximately 20,000 colonies were screened for mutants that failed to grow at 37°C. The plasmids from four ts strains were rescued, and the transformation was repeated. One plasmid that was found to reproducibly confer the ts growth phenotype was sequenced and found to encode a single amino acid change at residue 29 from tyrosine to histidine. An ApaI-SpeI fragment containing the rfa1-Y29H mutation was subcloned into an otherwise wild-type RFA1 gene to confirm that the ts phenotype was due to the Y29H mutation.

Synthetic-lethal screen. A red/white colony-sectoring assay was used to identify mutations that were synthetically lethal with rfa1-Y29H (4). To perform this screen, two rfa1-Y29H strains (HSY657 and HSY672) carrying pJM195 and showing the colony-sectoring phenotype were mutagenized with ethylmethanesulfonate to approximately 30% viability. After 7 days of growth at 25°C, approximately 100,000 colonies were screened for a nonsectoring red colony phenotype. About 200 nonsectoring mutants were obtained and rechecked for the nonsectoring phenotype by streaking on YPD and were checked for lethality on 5-FOA, which selects against uracil⁺ cells (i.e., cells that retain pJM195). The following four experiments were performed on the 20 strains that passed these tests. First, to determine whether these mutants required the wild-type RFA1 gene or the pJM195 plasmid (which also contains the URA3 and ADE3 marker genes), they were transformed with pHS118 (RFA1/LEU2/CEN) or pHS119 (RFA1/LYS2/CEN) and were tested for the sectoring phenotype. Mutants that showed a nonsectoring phenotype were likely due to integration of ADE3 into a chromosome and were excluded by this test. Second, the presence of rfa1-Y29H at the TRP1 locus was confirmed by both PCR and complementation testing. Genomic DNA was prepared and amplified by three sets of oligonucleotides to confirm that the rfa1 mutant gene was present at the TRP1 locus. Mutant strains were also crossed to HSY635 or HSY636. Mutants that had lost rfa1-Y29H produced diploids that required pJM195 and remained sensitive to 5-FOA due to the lack of a chromosomal RFA1 gene. Third, the synthetic-lethal mutations in these strains were shown to be recessive by backcross to HSY657 or HSY672. Lastly, each backcrossed diploid was sporulated and microdissected. The ratio of viable to inviable spores was always near unity, indicating that the synthetic lethality was caused by a single mutation. Three mutants passed these tests and were found to represent three different complementation groups. These groups were named slr51, slr157, and slr44, for synthetically lethal with rpa1.

Cloning of RFC4. To clone the wild-type copy of slr51, the mutant strain was transformed with a yeast genomic plasmid library (LEU2/CEN). The library plasmids that complemented FOA-sensitive growth of slr51 were recovered and sequenced. The overlapping regions of these chromosomal fragments identified the complementing gene as RFC4. Genetic linkage analysis was used to confirm that a mutation in RFC4 caused the synthetic-lethal phenotype with rfa1-Y29H. Strain HSY787, which contains a LEU2 marker integrated adjacent to the RFC4 locus, was crossed to the slr51 strain, and the diploid was sporulated and microdissected. Tetrad analysis revealed that synthetic lethality and leucine auxotrophy always segregated together. This mutant allele was named rfc4-2.

Allele specificity of rfc4-2. To examine allele-specific interactions between RFA1 and RFC4, strain HSY740 (rfc4-2 rfa1 leu2 pJM195) was derived from a cross between HSY737 and HSY635. A series of rfa1 mutant alleles in plasmid pRS415 (LEU2/CEN) were previously isolated by Umezu and colleagues (63, 75). These plasmids were transformed into HSY740 and HSY636 to create 19 rfc4-2 rfa1 double mutants and 19 rfa1 single mutants, each carrying pJM195. Cells were scraped from plates and resuspended at an optical density at 600 nm of 3. Tenfold serial dilutions of cells were then prepared in a microtiter plate, and 5 µl of each dilution was transferred onto YPD plates or synthetic complete media containing 5-FOA to measure synthetic lethality.

UV, MMS, and HU sensitivity. To measure sensitivity to UV light, cells were grown to early log phase. About 500 cells were spread on YPD plates and were irradiated with the indicated levels of UV light using a UV cross-linker (Stratagene). The number of viable cells was determined by counting colonies after 3 days of growth, and the percent viability compared to the unirradiated sample was calculated. To determine methylmethanesulfonate (MMS) sensitivity, cells were grown in liquid YPD and MMS was added to a final concentration of 0.1%. At the indicated times, aliquots were removed and neutralized with an equal volume of 10% sodium thiosulfate. The cells were then washed with water and spread on YPD plates. The number of viable cells was determined by counting colonies after 3 days of growth. To determine HU sensitivity, cells were grown in liquid YPD and HU was added to a final concentration of 200 mM. At the indicated times, aliquots were removed, washed with water, and spread onto YPD plates. Viable cells were determined as described above. HU sensitivity was also tested on solid media by replica plating. HU was added to a final concentration of 100 mM to YPD agar or to the appropriate selective media. Fresh cells were scraped from plates and were resuspended at an optical density at 600 nm of 3. Tenfold serial dilutions of cells were then prepared in a microtiter plate, and 5 µl of each dilution was transferred onto plates with and without HU.

Western blot assay for Rad53 phosphorylation. Yeast cells were grown to early log phase at 30°C. Exponentially growing cells, cells synchronized in G₁ for 2 h with -factor (5 µg/ml), or cells arrested in G₂ for 3 h with nocodazole (20 µg/ml) were released into HU (200 mM)- or MMS (0.1%)-containing media for 1 h. Alternatively, cells were irradiated with 60 J of UV light/m² and then were incubated for 30 min. Cells treated with MMS were neutralized with 10% sodium thiosulfate. To make whole cell extracts, 5 ml of each culture was harvested, washed with water-20% trichloroacetic acid, and then resuspended in 25 µl of 20% trichloroacetic acid. An equal volume of glass beads was added, and cells were lysed by vortexing with glass beads at 4°C. Whole cell extracts were microcentrifuged at 3,000 × g for 15 min at 4°C. Protein precipitates were resuspended in 2× sodium dedocyl sulfate (SDS) loading buffer, heated for 5 min, and then centrifuged at 3,000 × g for 5 min (51). Proteins were separated by SDS-10% polyacrylamide gel electrophoresis (PAGE) and transferred to a nylon membrane. Rad53 proteins were detected with antiserum to Rad53 (90) and horseradish peroxidase-conjugated anti-rabbit secondary antibody and were visualized by a chemiluminescent developer (Amersham).

FACS analysis. Yeast cells were grown to early log phase and were synchronized in G₁ with -factor (5 µg/ml) for 2 h. Cells were washed with water and released into YPD or YPD with 0.038% MMS. Aliquots of cells were removed every 30 min and washed with an equal volume of 10% sodium thiosulfate to neutralize the MMS. Cells were then fixed in 0.5 ml of water and 1.0 ml of 100% ethanol solution by rotating overnight. Fixed cells were washed with 1 ml of 50 mM sodium citrate, were resuspended in 0.5 ml of 50 mM sodium citrate containing 0.1 mg of RNase A/ml, and then were incubated for 2 h at 37°C. This cell suspension was added to 0.5 ml of 50 mM sodium citrate containing 50 µg of propidium iodide/ml and was incubated for at least 1 h at room temperature. DNA content was analyzed on a Coulter-Epics fluorescence-activated cell sorter (FACS) (46).

Rfc4-RPA binding assay. Enzyme-linked immunosorbent assay (ELISA) wells (Immulon) were coated with either 0.5 µg of RPA complex, purified as described previously (13), or bovine serum albumin (BSA) in incubation buffer (20 mM Tris-HCl [pH 7.5], 1 mM EDTA, 2 mM dithiothreitol, 5 mM MgCl₂, 150 mM NaCl, 20% glycerol, 2 mM CaCl₂) for 1 h at 30°C. Wells were washed three times with 1× PBST (29) and then blocked with 5% dried milk in 1× PBST for 10 min at room temperature. ³⁵S-labeled Rfc4 protein was expressed in an in vitro transcription/translation system (Promega) and then was applied to a Superdex 75 column. ³⁵S-Rfc4 protein was eluted in buffer A (25 mM Tris-HCl [pH 7.5], 1 mM EDTA, 0.01% NP-40, 10% glycerol, 0.1 mM phenylmethylsulfonyl fluoride, 1 mM dithiothreitol) containing 0.075 M NaCl and was collected. Purified ³⁵S-labeled Rfc4 was added into wells and incubated for 1 h at 30°C. Unbound Rfc4 protein was removed by washing three times with 1× PBST, and the bound ³⁵S-Rfc4 was measured by scintillation counting.

	RESULTS

Top Abstract Introduction Materials and Methods Results Discussion References

Isolation of the conditionally lethal mutant rfa1-Y29H. As a first step to determine the essential cellular role of the N-terminal domain of Rpa1 (Rpa1N), we isolated a conditional-lethal RFA1 mutation mapping to this domain. A strain lacking RFA1 was constructed and maintained by a copy of RFA1 on a URA3-based plasmid. This strain, SBY102 (rfa1 pJM114/RFA1/URA3/CEN), is unable to grow on media containing 5-FOA since selection against the URA3 plasmid is lethal in this background. Mutagenized RFA1 fragments were introduced into this strain on LEU2-based plasmids and were swapped for the RFA1 plasmid by replica plating on media containing 5-FOA at 25°C. About 20,000 colonies were screened for loss of viability at 37°C, and one recessive rfa1-ts allele was isolated. DNA sequencing of this allele revealed a mutation that changed tyrosine at residue 29 to histidine. Hereafter, we refer to this allele as rfa1-Y29H. As shown in Fig. 1A, rfa1-Y29H and wild-type cells grew well at 25°C while the rfa1-Y29H mutant showed a severe growth defect at 37°C. Additional characterization of the rfa1-Y29H mutation revealed that its function was partially compromised at the permissive temperature because the mutant strain was weakly sensitive to UV or MMS treatment at 25°C relative to the wild type (data not shown).

View larger version (49K): [in this window] [in a new window]   FIG. 1.   Interacting alleles rfa1-Y29H and rfc4-2. (A) A schematic diagram of Rpa1 is shown at the top. To demonstrate the ts growth phenotype caused by rfa1-Y29H, the strains HSY657 (rfa1-Y29H) and HSY679 (RFA1) were streaked onto YPD plates and incubated at 25 or 37°C, as indicated, for 3 days. (B) A schematic diagram of Rfc4 is shown together with the location of the mutation encoded by rfc4-2 and the sequences of the surrounding region obtained from several Rfc4 homologs. To demonstrate the synthetic-lethal phenotype caused by rfa1-Y29H and rfc4-2, the strains HSY657 (rfa1-Y29H) and HSY737 (rfa1-Y29H rfc4-2) were streaked onto YPD or 5-FOA plates, as indicated, and were incubated at 25°C for 3 days. SBD, ssDNA binding domain; Zn, zinc-binding domain; P-loop/DEAE, conserved motifs found in a large family of nucleoside triphosphate-binding domains.

Isolation of rfc4-2 by its synthetic lethality with rfa1-Y29H. To identify mutants that require wild-type Rpa1N for viability, we performed a synthetic-lethal screen with rfa1-Y29H at 25°C. HSY657 and HSY672 are ade2 ade3 strains containing a stably integrated rfa1-Y29H allele and plasmid pJM195 (RFA1/URA3/ADE3/CEN) (Table 1). These strains allow the use of a red/white colony-sectoring assay to measure plasmid stability since the starting strain is red (ade2) and plasmid loss events generate white (ade2 ade3) sectors. About 100,000 ethylmethanesulfonate-mutagenized colonies were screened for strains that require the pJM195 plasmid for viability and produce unsectored red colonies essentially as described previously (4). Three recessive slr (synthetic lethal with rpa1) complementation groups were isolated. Because the slr mutants require the wild-type RFA1 plasmid, pJM195, for viability, they acquire a 5-FOA-sensitive phenotype (Fig. 1B). The mutation in slr51 was identified by transforming the strain with a yeast genomic plasmid library and selecting strains that no longer require pJM195 by growth on 5-FOA. The library plasmids were rescued from the transformants, were sequenced, and were found to contain the RFC4 gene. Linkage analysis confirmed that a mutation in RFC4, hereafter referred to as rfc4-2, caused the synthetic-lethal phenotype with rfa1-Y29H. The rfc4-2 allele was found to have a single nucleotide change from G to A at residue 601, resulting in an amino acid change of aspartate to asparagine at residue 201. This mutation maps to the RFC box VIII/sensor2 motif, one of the conserved motifs found in all RFC subunits (Fig. 1B) (15, 21, 40).

View larger version (20K): [in this window] [in a new window]   FIG. 2.   The rfc4-2 mutant is sensitive to DNA damage. (A) UV sensitivity. Strains HSY636 (RFC4), HSY740 (rfc4-2), and HSY845 (rfa1-t11) were grown to early log phase in liquid culture. A volume containing about 500 cells was spread onto YPD plates and was irradiated with the indicated doses of UV light. The percent viability was determined by counting colonies following 3 days of growth. (B) MMS sensitivity. Cultures of HSY636 (RFC4) and HSY740 (rfc4-2) were grown to early log phase in liquid YPD, and MMS was added to a final concentration of 0.1%. At the indicated times an aliquot of the culture was withdrawn, the MMS was neutralized, and about 300 cells were spread onto YPD plates. The percent viability was determined as described for panel A.

Characterization of the Rfc4-Rpa1 interaction. It has recently been shown that the p140, p40, and p38 subunits of human RFC bind the large subunit of human Rpa1 (89). Since yeast Rfc4 is the homolog of p40, we tested whether there was a physical interaction between Rfc4 and yeast RPA. For this experiment we used an ELISA-type assay in which wild-type or mutant RPA complex or BSA control protein was immobilized on the wells of a microtiter plate. These wells were then incubated with increasing amounts of purified ³⁵S-labeled Rfc4 protein that was synthesized in an in vitro translation reaction. After the wells were washed, the level of bound Rfc4 was determined by scintillation counting. As shown in Fig. 3A, wells coated with wild-type RPA bound increasing amounts of wild-type ³⁵S-Rfc4 compared to the BSA control. This result indicates that the yeast RPA complex directly interacts with yeast Rfc4 protein. When RPA was incubated with mutant ³⁵S-Rfc4-2 protein, much less protein was retained. At maximal input only half as much Rfc4-2 protein bound RPA (Fig. 3A). As described below, we found that rfc4-2 is synthetically lethal with several previously characterized rfa1 alleles. When this assay was performed using RPA containing the rfa1-t11 mutation (RPA-t11), we found that it bound less ³⁵S-Rfc4 than did wild-type RPA. Further, when incubated with mutant ³⁵S-Rfc4-2 protein, the mutant RPA-t11 bound even less Rfc4 protein (Fig. 3A). This combination of mutant proteins revealed an interaction only slightly stronger than that between Rfc4 and the control BSA protein. These results suggest that the synthetic lethality between these mutant alleles is due to a compromised interaction between RPA1 and Rfc4.

View larger version (42K): [in this window] [in a new window]   FIG. 3.   An interaction between Rfc4 and RPA. (A) The physical interaction between Rfc4 and the RPA complex was tested by coating ELISA wells with 0.5 µg of either purified wild-type RPA (squares), mutant RPA-t11 (circles) or BSA (triangles) and treating the wells with increasing amounts of purified 35S-labeled wild-type Rfc4 (closed symbols) or mutant Rfc4-2 (open symbols). The counts per minute (cpm) representing bound 35S-Rfc4 was determined by scintillation counting and is plotted relative to the cpm of input 35S-Rfc4. (B) Allele-specific interaction between RFC4 and RFA1. Strains HSY636 (RFC4 rfa1; left and middle columns) and HSY740 (rfc4-2 rfa1; right column) carrying pJM195 (RFA1/URA3) were transformed with wild-type RFA1 or the indicated rfa1 alleles on a LEU2-based vector. Transformants were streaked onto plates lacking leucine and then were taken from the plates and serially diluted 1:10. Approximately 5 µl of each dilution was transferred to a YPD plate, a YPD plate containing HU, or a plate containing 5-FOA to measure synthetic lethality.

RFC4 is required for the replication block checkpoint response. To determine whether rfc4-2 cells respond appropriately to a DNA replication block, we examined the viability of rfc4-2 mutant cells in the presence of HU. When the assay was carried out in liquid media containing 200 mM HU, rfc4-2 cells showed a mild sensitivity relative to wild-type cells (Fig. 4A). Control cells containing rad53-K227A, a kinase-defective allele of the checkpoint kinase Rad53 (2, 20), were strongly sensitive to HU. Both of these mutants displayed a severe growth defect in the presence of continuous HU exposure, although very tiny rfc4-2 colonies were were able to form on plates containing HU (Fig. 4B).

View larger version (41K): [in this window] [in a new window]   FIG. 4.   The rfc4-2 mutant is defective in the DNA replication block checkpoint response. (A) HU sensitivity of rfc4-2 cells. Strains W303-1a (wild type), HSY1025 (rfc4-2), and Y00684 (rad53-K227A) were grown to early log phase in liquid YPD, and HU was added to a final concentration of 200 mM. At the indicated times an aliquot was removed and a volume containing approximately 300 cells was spread onto a YPD plate. The percent viability was determined by counting colonies after 3 days. (B) Sensitivity of rfc4-2 cells to continuous HU exposure. The three strains used in panel A, along with the rfa1-t69 mutant, were streaked onto YPD plates, with or without 100 mM HU, and were incubated at 30°C for 3 days. (C) Phosphorylation of Rad53 in response to HU treatment. Strains W303-1a (WT), HSY1027 (rfc4), and Y00684 (rad53) were synchronized by treatment with -factor (lanes 1, 2, and 3) and were released into liquid YPD medium containing 200 mM HU for 1 h (lanes 4, 5, and 6). The cells were harvested, and whole cell extracts were prepared. Extracts were resolved by SDS-10% PAGE and were Western blotted using an antiserum against Rad53. Asterisks (*) denote nonspecific bands. Rad53-P denotes phosphorylated forms of Rad53.

RFC4 is required for the intra-S checkpoint. DNA damage by continuous exposure to MMS significantly extends the length of the S phase in wild-type cells (9, 52, 53, 61, 80). This response is distinguished from the replication block pathway in that it requires the function of RAD9 and other genes (53). To determine whether RFC4 is required for the intra-S checkpoint, cells were synchronized in G₁ with -factor and were released into YPD media containing 0.038% MMS, and aliquots of cells were removed every 30 min and treated for microfluorometric analysis. The rate of S-phase progression in wild-type and rfc4-2 mutant cells was then monitored by FACS. In the absence of MMS, wild-type and rfc4-2 mutant cells finished DNA synthesis 60 min after release from the -factor block (Fig. 5A, top two histograms). In the presence of MMS, S-phase length was extended in both wild-type and rfc4-2 cells. However, rfc4-2 cells finished S phase faster than the wild type; rfc4-2 cells completed replication 150 min after -factor release, whereas wild-type cells were still in S phase even at 180 min (Fig. 5A, left).

View larger version (33K): [in this window] [in a new window]   FIG. 5.   The rfc4-2 mutant is defective in the intra-S checkpoint. (A) W303-1a (WT) and HSY1027 (rfc4-2) cells were synchronized in G1 phase with -factor and were released into YPD containing 0.038% MMS. Aliquots were removed every 30 min, and the MMS was neutralized. Cells were then fixed, stained, and analyzed by FACS. As a control, cells of each type were released into YPD in the absence of MMS and were similarly analyzed. The DNA content of untreated control cells 60 min after -factor release is presented in the top histograms as representative of cells having completed S phase. (B) Wild-type and rfc4-2 cells were treated as above, and aliquots were removed every 30 min. To analyze Rad53 phosphorylation, whole cell extracts were prepared, were resolved by SDS-10% PAGE, and were Western blotted using an antiserum against Rad53. The asterisk (*) denotes nonspecific bands. Rad53-P denotes phosphorylated forms of Rad53.

RFC4 is required for the DNA damage checkpoint pathway. As mentioned previously, Rad53 phosphorylation is also required for the activation of the DNA damage checkpoint pathway. To examine whether RFC4 is involved in DNA damage checkpoint control, we analyzed Rad53 phosphorylation in response to MMS and UV irradiation. MMS was added to exponentially growing cells to a final concentration of 0.1%, and the phosphorylation of Rad53 was detected by Western blotting. In wild-type cells, unphosphorylated forms of Rad53 completely disappeared and phosphorylated forms of Rad53 with slower mobility accumulated after MMS treatment (Fig. 6A, lane 4). However, Rad53 phosphorylation was greatly reduced in rfc4-2 mutant cells (Fig. 6A, lane 5). As above, Rad53 disappeared in rad53-K227A cells following MMS treatment (Fig. 6A, lane 6). We conclude that RFC4 is required for the DNA damage checkpoint pathway.

View larger version (39K): [in this window] [in a new window]   FIG. 6.   The rfc4-2 mutant is defective in the DNA damage checkpoint. (A) Exponentially growing cells of the indicated genotype were incubated with or without 0.1% MMS for 1 h. Both MMS-treated (lanes 4, 5, and 6) and -untreated (lanes 1, 2, and 3) cells were analyzed for Rad53 phosphorylation by Western blotting. (B) Exponentially growing wild-type and rfc4-2 cells were treated with or without UV light (60 J/m2), were incubated for 30 min, and then were analyzed for Rad53 phosphorylation by Western blotting (lanes 1 and 2). In addition, wild-type and rfc4-2 cells were synchronized in G1 or G2 with -factor or nocodazole, respectively, and were treated and analyzed as above (lanes 3 to 6). Asterisks (*) denote nonspecific bands. (C) The rfc4-2 mutant was tested for G2/M arrest in response to lesions caused by cdc13. Four cdc13 cdc15 strains, DLY408 (WT), DLY409 (rad9), HSY1202 (rfc4-2), and HSY1204 (rfa1-t11), were synchronized in G1 with -factor at 23°C. Cells were then released from the G1 block, shifted to 36°C, and incubated for 3.5 h. Cells were fixed and stained, and their morphology was analyzed by fluorescence microscopy. The percentage of cells arrested at G2/M (large budded cell with a single nucleus at the neck) or at the cdc15 arrest point (large budded cell with two nuclei) is shown in the table in the lower right panel. Cells with nuclear DNA stretched between the mother and daughter compartments are not represented in the table and account for the percentages summing to less than 100.

Interactions between RFC4, RAD24, and RFA1. DNA damage checkpoints are controlled by the RAD9 and RAD24 epistasis groups (16, 45, 81, 82). To determine whether RFC4 belonged to either or both of these pathways, we constructed the following double mutants and tested their response to MMS treatment: rfc4-2 rad24, rfc4-2 rad9, and rfc4-2 rad53-K227A. The rfc4-2 rad9 strain showed an enhanced sensitivity to MMS whereas the MMS sensitivity of the other two double mutants was no greater than either single mutant (Fig. 7A and data not shown). These results indicate that RFC4 functions as part of the RAD24 epistasis group and not RAD9. This result is consistent with the fact that Rad24 is associated with all four small subunits of the RFC complex (26, 27).

View larger version (52K): [in this window] [in a new window]   FIG. 7.   Genetic interactions between checkpoint genes. (A) RAD24 and RFC4 are epistatic with respect to MMS sensitivity. Strains of the indicated genotype were tested for MMS sensitivity by streaking onto YPD plates with or without 0.012% MMS. (B) Suppression of rfc4-2 HU sensitivity by high-copy-number RAD24 or RAD53. Strain HSY1027 (rfc4-2) was transformed with RAD24 or RAD53 genes on a 2µm plasmid. Cells were serially diluted 1:10, and 5 µl was replica plated to solid media lacking tryptophane. (C) Extragenic suppression of rfc4-2 HU sensitivity by rfa1 mutant alleles. Strain HSY740 (rfc4-2 rfa1) containing plasmid pJM195 (RFA1/URA3/ADE3) was transformed with pHS118 (RFA1), pKU1-t6 (rfa1-t6), and pKU1-t124 (rfa1-t124). Transformants were then streaked onto plates containing 5-FOA to remove pJM195. The resulting strains were serially diluted 1:10, and 5 µl was replica plated onto YPD plates with or without 100 mM HU. The resulting strain genotypes are shown at the right of the figure. Strain HSY636 was used as a wild-type control.

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

A genetic interaction between RFA1 and RFC4. The large subunit of replication protein A (Rpa1) contains three ssDNA binding domains and an amino-terminal domain of approximately 180 amino acids (Rpa1N). Although Rpa1N is dispensable for DNA replication in vitro, it is likely to play an important role in vivo because it is essential for viability in yeast (11, 25, 35, 56, 85). Moreover, the most severe mutations identified in a random mutagenesis to create MMS-sensitive rfa1 alleles map to Rpa1N as opposed to the ssDNA binding domains (75). To investigate the essential function of this domain, we searched for mutations that are lethal in the presence of the rfa1-Y29H mutation. This screen identified an allele of RFC4 (rfc4-2) which encodes a subunit of the eukaryotic sliding clamp loader. Since human Rpa1N is known to bind a number of proteins (10, 41), we considered the possibility of a direct interaction between Rpa1N and Rfc4. The results of binding assays and allele-specific lethality observed in a collection of rfa1 rfc4-2 double mutants are consistent with this notion. The simplest interpretation of these results is that an interaction between Rpa1N and Rfc4 is essential for DNA replication in vivo.

View larger version (27K): [in this window] [in a new window]   FIG. 8.   Role of the Rfc4-Rpa1 interaction in DNA replication and DNA damage checkpoint signaling. (Left) The DNA polymerase switch during lagging-strand synthesis is shown. The model proposes that a direct interaction between Rpa1N, bound to the lagging strand, and Rfc4 is required to target RFC to the primer-template junction. Bound RFC then displaces polymerase , loads the PCNA sliding clamp, and allows processive DNA synthesis by polymerase . This reaction fails in the presence of Rfc4-2 and Rfa1-Y29H, resulting in synthetic lethality. (Right) The DNA damage response at a UV-induced lesion is shown. Again, a direct interaction between Rpa1N, bound at the processed lesion, and Rfc4 is required to target the Rad24-Rfc2-5 complex to the primer-template junction. This complex loads the Rad17-Mec3-Ddc1 sliding clamp and activates the signal transduction pathway. This reaction is compromised in the presence of either Rfc4-2 or Rpa1-Y29H, resulting in partially defective checkpoint signaling.

RFC4 as a sensor in checkpoint control. Examination of the rfc4-2 phenotype revealed a mild sensitivity to HU, consistent with a defect in the DNA replication block checkpoint. The RAD53 protein kinase is an essential transducer in checkpoint pathways and is phosphorylated in response to DNA damage and inhibition of DNA replication (16, 55, 58). G₁-arrested rfc4-2 cells show only partial Rad53 phosphorylation following release into HU; approximately half of the Rad53 remains unphosphorylated. In contrast, when wild-type cells are subjected to this treatment all Rad53 protein is found in the phosphorylated form (Fig. 4). Thus, rfc4-2 cells have a partial defect in the replication block checkpoint response consistent with the mild HU sensitivity of the mutant. A more pronounced defect in Rad53 phosphorylation is observed in response to DNA damage in exponentially growing, G₁- or G₂-arrested rfc4-2 mutant cells. The significant amount of unphosphorylated Rad53 that is detected in UV-irradiated rfc4-2 cells is notable given that the mutant is not strongly sensitive to UV irradiation (Fig. 6B). The reason for this discrepancy is unclear, although the DNA damage response may simply require a lower threshold of Rad53 phosphorylation. We also cannot rule out the possibility of additional pathways for DNA damage signaling. Together, these findings indicate that RFC4 is a common component of the checkpoint response to both unreplicated DNA and DNA damage.

RFC4 and RAD24 checkpoint control. Two epistasis groups have been identified that control DNA damage checkpoints in yeast: the RAD24 group, which includes RAD17, MEC3, and DDC1, and the RAD9 group, which contains no other members (16, 45). RAD24 encodes a 76-kDa protein with limited sequence similarity to the RFC proteins that has been shown to be associated with the four small subunits of RFC (26, 27, 60). Consistent with these findings, our results place RFC4 in the RAD24 epistasis group and extend this group to include genes involved in DNA replication. Rad24 is known to compete with Rfc1 for Rfc2-5, as overexpression of RAD24 exacerbates the growth defect of the rfc1 mutant (44). Surprisingly, we find that RAD24 overexpression partially complements the HU sensitivity of the rfc4-2 mutant, implying that RAD24 plays a role in the replication block checkpoint. Previous studies have not revealed a role for RAD24 in the S/M replication block checkpoint, although there is suggestive evidence for such a role (23). In the present case, increased levels of Rad24/Rfc2-5 mutant complexes may have improved the efficiency of the HU response directly by participating in Rad53 phosphorylation. Alternatively, increased Rad24 protein may have further compromised the Rfc1/Rfc2-5 mutant complex and indirectly improved the HU response by activating an alternate checkpoint pathway. Thus, while the present data suggest that RAD24 functions in the replication block checkpoint, we cannot rule out an indirect mechanism for the suppression of the HU sensitivity of the rfc4-2 mutant.