HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS		QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

J. Biol. Chem., Vol. 277, Issue 35, 31663-31672, August 30, 2002

This Article Abstract Full Text (PDF) All Versions of this Article: 277/35/31663    most recent M203494200v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Sugiyama, T. Articles by Kowalczykowski, S. C. Search for Related Content PubMed PubMed Citation Articles by Sugiyama, T. Articles by Kowalczykowski, S. C. Social Bookmarking                      What's this?

Rad52 Protein Associates with Replication Protein A (RPA)-Single-stranded DNA to Accelerate Rad51-mediated Displacement of RPA and Presynaptic Complex Formation^*

Tomohiko Sugiyama and Stephen C. Kowalczykowski

From the Sections of Microbiology and of Molecular and Cellular Biology, and Center for Genetics and Development, University of California, Davis, California 95616-8665

Received for publication, April 11, 2002, and in revised form, June 7, 2002

	ABSTRACT

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

The Rad51 nucleoprotein filament mediates DNA strand exchange, a key step of homologous recombination. This activity is stimulated by replication protein A (RPA), but only when RPA is introduced after Rad51 nucleoprotein filament formation. In contrast, RPA inhibits Rad51 nucleoprotein complex formation by prior binding to single-stranded DNA (ssDNA), but Rad52 protein alleviates this inhibition. Here we show that Rad51 filament formation is simultaneous with displacement of RPA from ssDNA. This displacement is initiated by a rate-limiting nucleation of Rad51 protein onto ssDNA complex, followed by rapid elongation of the filament. Rad52 protein accelerates RPA displacement by Rad51 protein. This acceleration probably involves direct interactions with both Rad51 protein and RPA. Detection of a Rad52-RPA-ssDNA co-complex suggests that this co-complex is an intermediate in the displacement process.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

The Rad52 epistasis group of proteins, including Rad51 protein, Rad52 protein, and replication protein A (RPA),¹ are important for both mitotic and meiotic recombination, mating-type switching, and repair of DNA double strand breaks in Saccharomyces cerevisiae. Rad51 protein, which is a homologue of the Escherichia coli RecA protein (1-3), is conserved in a wide variety of eukaryotic organisms from yeast to humans (4). Like RecA protein, Rad51 protein binds single-stranded DNA (ssDNA) to form the functional presynaptic complex, which mediates DNA strand exchange (5). However, unlike RecA protein, Rad51 protein readily binds double-stranded DNA (dsDNA), and the binding to dsDNA strongly inhibits DNA strand exchange (6). Therefore, not unexpectedly, the binding of Rad51 protein to dsDNA present as secondary structure in ssDNA severely limits DNA strand exchange (7). For this reason, Rad51 protein-mediated DNA strand exchange depends strongly on a ssDNA-binding protein to eliminate DNA secondary structure.

RPA, which is a heterotrimeric ssDNA-binding protein (8, 9), greatly stimulates DNA strand exchange by Rad51 protein, provided that RPA is added to a preexisting complex of Rad51 protein and ssDNA (5). However, RPA will inhibit DNA strand exchange when it is allowed to bind ssDNA before Rad51 protein. Previously, we offered an interpretation for this dichotomous role of RPA in Rad51 protein-mediated DNA strand exchange (7). According to this view, RPA aids DNA strand exchange by disrupting DNA secondary structure, which is an impediment to presynaptic complex formation. However, because RPA and Rad51 protein both compete for these same ssDNA binding sites, RPA can also be an impediment to presynaptic complex formation. Nevertheless, when the molecular ratios of Rad51 protein and RPA to ssDNA are appropriate (2-3 nucleotides per Rad51 protein and 10-20 nucleotides per RPA), the steady-state product of this competitive process is a uniform Rad51 protein-ssDNA complex with little DNA secondary structure. Based on this model, after disruption of DNA secondary structure, RPA is expected to be displaced by Rad51 protein. Previously, however, we did not directly demonstrate the release of RPA from ssDNA.

Purified yeast Rad52 protein has DNA binding activity (10), and it also interacts with both Rad51 protein and RPA (1, 11). Recent biochemical studies show that Rad52 protein has at least two activities important to recombination. One activity is the stimulation of Rad51 protein-mediated DNA strand exchange (12-15). Both Rad52 protein-RPA and Rad52 protein-Rad51 protein interactions are necessary for stimulation. This stimulatory function of Rad52 protein, however, is revealed under conditions where RPA inhibits Rad51 protein activity: i.e. when RPA is bound to ssDNA prior to Rad51 protein. Therefore, it was hypothesized that Rad52 protein acts by stimulating the displacement of RPA by Rad51 protein (14). The second activity of Rad52 protein is the annealing of complementary ssDNA (10). This activity is consistent with the importance of this protein in the ssDNA annealing pathway of double strand break repair (16). Yeast Rad52 protein can also anneal ssDNA that is complexed with yeast RPA, due to a specific interaction with RPA (11, 17).

The precise mechanism by which Rad52 protein stimulates DNA strand exchange is not clear. Because Rad52 protein stimulates DNA strand exchange when RPA is prebound to ssDNA, Rad52 might simply displace RPA from the ssDNA, permitting Rad51 protein to bind. In this paper, we examine the fate of RPA during presynaptic complex formation. Our results indicate that Rad52 protein alone cannot displace RPA from ssDNA. Instead, Rad52 protein forms a co-complex with the RPA-ssDNA complex, and it recruits the Rad51 protein onto ssDNA, and then Rad51 protein displaces RPA. Our results also reveal the dynamic nature of the complex protein exchange and assembly process that underlies DNA recombination.

	EXPERIMENTAL PROCEDURES

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

DNA and Proteins-- Poly(dT) was purchased from Amersham Biosciences. The 100-mer synthetic DNA 5'-TGGCCTGCAA CGCGGGCATC CCGATGCCGC CGGAAGCGAG AAGAATCATA ATGGGGAAGG CCACCAGCCT CGCGTCGCGA ACGCCAGCAA GACGTAGCCC was purchased from Operon and purified by electrophoresis using 7.5% polyacrylamide gels containing 7 M urea. The 100-mer was labeled with ³²P at its 5'-end by T4-polynucleotide kinase (New England Biolabs). Bluescript SK dsDNA and ssDNA (Stratagene) were prepared as described (18). The nucleotide concentrations of poly(dT), ssDNA, and dsDNA were measured using extinction coefficients of 7.3 × 10³, 8.1 × 10³, and 6.5 × 10³ M¹ cm¹, respectively. Rad51 and Rad52 proteins (14), RPA (19), and E. coli SSB protein (20, 21) were prepared as described. Rabbit polyclonal antibody against RPA was obtained from W. D. Heyer (University of California, Davis).

ATPase Assay-- ATP hydrolysis by Rad51 protein was analyzed at 37 °C essentially as described (7, 22). For the standard reaction, 10 µM ssDNA, 5 µM Rad51 protein, and 1 µM RPA were added in the indicated order to buffer (final volume of 120 µl) containing 2.5 mM ATP, 10 units/ml pyruvate kinase, 10 units/ml lactate dehydrogenase, 0.3 mM phosphoenolpyruvate, 256 µM NADH, 50 µg/ml bovine serum albumin, 1 mM dithiothreitol, 5 mM magnesium acetate, 50 mM KCl, and 30 mM Tris acetate (pH 7.5). The hydrolysis of ATP is coupled to the oxidation of NADH, which results in a decrease in absorbance at 340 nm. The decrease of absorbance was monitored every 25 s by a Hewlett Packard 8452A diode array spectrophotometer. The instantaneous rate of ATP hydrolysis was calculated from the rate of change in absorbance based on 5 or 6 time points using the following formula: rate of A₃₄₀ decrease (s¹) × 9880 = rate of ATP hydrolysis (µM/min). For Fig. 2, we used 2.4 mM magnesium acetate instead of 5 mM, because the displacement was slower and the result was more apparent under these conditions (data not shown).

DNA Binding by RPA Monitored by Fluorescence Quenching-- RPA has an intrinsic fluorescence that is quenched when it binds to ssDNA (19). On the other hand, Rad51 protein, which has no tryptophan residue, has much lower fluorescence (~50-fold lower per molecule than RPA), and it does not change upon DNA binding (data not shown). Although Rad52 protein has ~40% of the fluorescence of RPA, the fluorescence is unchanged by interaction with either ssDNA, Rad51, or RPA (data not shown). Therefore, the dissociation of RPA from ssDNA in the presence of Rad51 protein can be monitored in real time by monitoring the intrinsic fluorescence quenching of RPA. Reactions were done in a quartz cuvette containing 300 or 400 µl of buffer containing 2.5 mM ATP, 1 mM dithiothreitol, 5 mM magnesium acetate, 50 mM KCl, and 30 mM Tris acetate (pH 7.5) at 37 °C. RPA (1 µM), ssDNA (10 µM), and Rad51 protein (5 µM) were added in the order indicated. Between each addition of protein or DNA, the components were allowed to equilibrate for 1.5-2 min. When indicated, Rad52 protein (1 µM) was added to the reaction mixture ~30 s after the addition of Rad51 protein. Throughout the reaction, the fluorescence of RPA was continuously monitored with an SLM8000 spectrofluorimeter set to excitation and emission wavelengths of 284 and 345 nm, respectively. The bandwidth for excitation and emission was 1 and 4 nm, respectively. The percentage of RPA that was displaced from ssDNA was calculated from the fluorescence value relative to free RPA. The contributions of Rad51 and Rad52 proteins to the fluorescence were subtracted.

Gel Mobility Shift Assay-- Proteins were mixed with 10 µM ³²P-labeled synthetic 100-mer ssDNA in the indicated order and incubated for 15 min at 37 °C in 10 µl of buffer containing 30 mM K-MOPS (pH 7.3), 20 mM NaCl, 3 mM magnesium acetate, 1 mM dithiothreitol, and 2 mM ATP (when indicated). When more than one protein was present, the samples were incubated for 10 min at 37 °C between each addition, and for 15 min after the addition of the last protein. After the reaction, samples were analyzed by one of the following electrophoresis methods. For "conventional" electrophoresis, samples were mixed with 5 or 10 µl of loading buffer A (50% glycerol and 0.1% bromphenol blue in TBE buffer (45 mM Tris borate (pH 8.3) and 1 mM EDTA)) and separated with 6% polyacrylamide gel in TBE buffer. Alternatively, electrophoresis was conducted in the presence of ATP and Mg²⁺; samples were mixed with 10 µl of the loading buffer B (50% glycerol, 20 mM NaCl, 5 mM magnesium acetate, 0.5 mM ATP, 0.1% bromphenol blue, and 45 mM Tris borate (pH 8.3) and separated with 6% polyacrylamide gel in 20 mM KCl, 5 mM magnesium acetate, 0.5 mM ATP, and 45 mM Tris borate (pH 8.3). For both methods, retardation of the labeled ssDNA was detected using an Amersham Biosciences Storm 840 PhosphorImager with Image-QuaNT software.

Quantification of Protein-ssDNA Complexes by SDS-PAGE-- The protein content of complexes detected in the gel mobility shift experiments was analyzed in the following way. Gel pieces containing protein-ssDNA complexes were excised and cut into smaller pieces, and then radioactivity was quantified by Cerenkov counting to measure the amount of ssDNA in each sample. Based on the relative radioactivity, the number of pieces used for SDS-PAGE were adjusted so that all samples had the same radioactivity. That enabled comparison of the amount of protein present, normalized to the ssDNA content. The gel pieces (approximate volumes of 10-50 µl) were then mixed with 50 µl of TE buffer and 20 µl of SDS loading buffer (350 mM Tris-HCl (pH 6.8), 1% SDS, 6% 2-mercaptoethanol, 36% glycerol, and 0.1% bromphenol blue) and incubated for 3 h at room temperature and then 4 min at 100 °C. Samples, including gel pieces and buffer, were analyzed by SDS-PAGE followed by staining with Coomassie Brilliant Blue R-250.

Quantification of RPA Bound to ssDNA Complex by Western Blotting-- Protein-DNA complexes were eluted from excised gel pieces overnight into 0.5 ml of TE buffer containing 0.1% SDS at room temperature. After reducing the volume to ~50-100 µl by vacuum concentration, 2 µl of the eluates were spotted on DEAE paper, and relative amounts of ssDNA were quantified by measuring the radioactivity using an Amersham Biosciences Storm 840 PhosphorImager and Image-QuaNT software. Western blotting analysis, using 12% SDS-PAGE, was performed with anti-RPA rabbit polyclonal antibody. As standards, the indicated amounts of RPA were also loaded on the gel. The amount of protein in each sample was determined from the relative intensity of the protein band to the standards, measured using Image-QuaNT software.

	RESULTS

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Rad51 Protein and RPA Compete in ssDNA Binding-- Previously, we suggested that RPA eliminates DNA secondary structure, which impedes presynaptic complex formation by Rad51 protein (7). Since RPA competes with Rad51 protein for binding to ssDNA, we also proposed that bound RPA must be removed from the ssDNA to permit contiguous presynaptic filament formation. Experimentally, the competitive nature of RPA is most clearly manifest by preforming an RPA-ssDNA complex and then introducing Rad51 protein; in this situation, Rad51 protein must displace the RPA from the ssDNA to form a presynaptic complex, and activation of Rad51 protein function is slow (Fig. 1A, RPA-first process). On the other hand, if Rad51 protein is added to native ssDNA that is free of RPA, it makes a discontinuous presynaptic complex that is interrupted by Rad51 protein-dsDNA regions; the addition of RPA stimulates presynaptic complex formation relatively quickly (Fig. 1A, Rad51-first process). To better understand the nature of presynaptic complex formation in the presence of RPA, we examined the time course of filament formation by each process. The binding of Rad51 protein to ssDNA was measured by monitoring the ATP hydrolysis that accompanies formation of a Rad51 protein-ssDNA complex (Fig. 1B), from which the rate of ATP hydrolysis was calculated (Fig. 1C). When Rad51 protein was added to a preformed RPA-ssDNA complex, ATP hydrolysis did not occur instantly. Rather, the ATP hydrolysis rate increased gradually and reached a steady state (2.6 µM/min) ~30 min after the addition of Rad51 protein (Fig. 1, B and C, RPA-first). Without RPA, the discontinuous Rad51 protein-ssDNA complex showed a slower ATP hydrolysis (1.2 µM/min; Fig. 1B, Rad51-first) before the addition of RPA. When RPA was added to this Rad51 protein-ssDNA complex (Fig. 1, B and C, Rad51-first), the ATP hydrolysis rate increased relatively instantly. In the Rad51-first process, 70% of the increase in ATP hydrolysis rate occurred in less than 2 min, whereas it took ~15 min in the RPA-first process.

View larger version (21K): [in this window] [in a new window]   Fig. 1.   RPA displacement from ssDNA coincides with presynaptic complex formation by Rad51 protein. A, schematic drawing of presynaptic complex formation where either RPA (RPA-first) or Rad51 protein (Rad51-first) is prebound to ssDNA. B, ATP hydrolysis measures presynaptic complex formation. Rad51 protein (5 µM) and RPA (1 µM) were added to pBluescript SK ssDNA (10 µM) as indicated. C and D, comparison of the development of Rad51 protein-dependent ATPase activity (i.e. presynaptic complex formation) with the displacement of RPA from ssDNA. Time courses for the ATP hydrolysis rate (C) were calculated as the first derivative of the data in B. Displacement of RPA from ssDNA (D) was monitored as described under "Experimental Procedures." For both C and D, the reactions were started by adding Rad51 protein to the RPA-ssDNA complex () or by adding RPA to a preformed Rad51 protein-ssDNA complex (). The dashed line in C indicates the ATP hydrolysis rate of the Rad51-first reaction before the addition of RPA. The RPA fluorescence is quenched 41% by binding to ssDNA under these conditions in the absence of Rad51 protein, and this quenched level is defined as 0% RPA released.

In parallel with the ATPase assays that measured the Rad51 protein-ssDNA binding status, we also measured the DNA binding status of RPA by fluorescence spectroscopy. RPA has an intrinsic tryptophan fluorescence that is quenched by binding to ssDNA (19). Therefore, the change in fluorescence reflects a change of the RPA-ssDNA binding status. We performed experiments similar to those in Fig. 1C, except that we monitored the intrinsic fluorescence of RPA (Fig. 1D). As expected, when Rad51 protein was added to an RPA-ssDNA complex, RPA was released from the ssDNA slowly (Fig. 1D, RPA-first) and reached a plateau level ~30 min after the addition of Rad51 protein. On the other hand, when RPA was added to a Rad51 protein-ssDNA complex, almost all of the RPA remained unbound throughout the measurement (Fig. 1D, Rad51-first). For both RPA-first and Rad51-first processes, the time courses for RPA release coincided with the time courses for Rad51 protein-ssDNA complex formation that were measured by monitoring ATP hydrolysis. These results indicate that Rad51 protein displaces RPA from ssDNA upon formation of the presynaptic filament. In addition, the RPA-first process is slower than the Rad51-first process. These characteristics can explain why RPA has opposite effects on Rad51 protein-mediated functions, which depend on the order of protein-ssDNA complex formation. This behavior of RPA is similar to that of E. coli SSB protein with regard to RecA protein function; displacement of SSB protein by RecA protein is faster for the RecA-first than for the SSB-first process (23, 24).

Displacement of RPA from ssDNA Is Limited by Nucleation of a Rad51 Protein-ssDNA Complex-- Formation of the RecA nucleoprotein filament is initiated by a rate-limiting nucleation of the protein-DNA complex, followed by cooperative elongation of the filament (25-29). The different rates of RPA displacement in Rad51-first and RPA-first processes suggest that the rate-limiting step in the RPA-first process for RPA displacement is nucleation of the Rad51-ssDNA complex rather than elongation of the filament. To confirm this possibility, we varied the amount of RPA that was prebound to ssDNA, and then Rad51 protein was added to start the displacement reaction (Fig. 2). In this experiment, we used poly(dT) instead of pBluescript ssDNA to eliminate any complications arising from DNA secondary structure, since Rad51 protein will bind to both the ssDNA and dsDNA regions. Because the Rad51 protein-dsDNA complex shows much less ATPase activity than the Rad51 protein-ssDNA complex (7), the ATP hydrolysis rate with native ssDNA would not be proportional to the amount of Rad51 protein that bound the DNA. In contrast, by using poly(dT), the ATPase activity will be proportional to formation of the Rad51 protein-ssDNA complex.

View larger version (17K): [in this window] [in a new window]   Fig. 2.   Saturation of ssDNA with RPA limits the ability of Rad51 protein to displace RPA. A, ATP hydrolysis was monitored in RPA-first experiments like those in Fig. 1B, using 0, 0.27, 0.53, 0.8, 0.9, 1.2, 1.7, or 2.7 µM of RPA (lines from left to right; 1.7 and 2.7 µM curves are overlaid), which were preincubated with 13.7 µM poly(dT). Rad51 protein (5 µM) was added to start the reactions. B, the ATP hydrolysis rate after 10 min was plotted against the concentration of RPA.

When Rad51 protein was added to various subsaturating RPA-poly(dT) complexes (Fig. 2A, left four curves), the steady-state rate of ATP hydrolysis was rapidly attained; however, when Rad51 protein was added to saturated RPA-ssDNA complexes (Fig. 2A, right four curves), a markedly slower increase in ATP hydrolysis occurred. Under the latter saturating conditions, the rate of ATP hydrolysis even after 60 min of incubation was about 30% of that without RPA and was still increasing slowly. The ATPase activities at 10 min after reaction initiation (Fig. 2B) show that concentrations of RPA greater than 0.9 µM precipitously reduced ATP hydrolysis. This concentration of RPA coincides with the concentration required to saturate the poly(dT) (~20 nucleotides per RPA (7)). A slightly lower concentration (0.8 µM) of RPA showed a rather limited reduction of ATP hydrolysis (less than 40%) compared with that of the saturated RPA-poly(dT) complex, although ~90% of ssDNA would be covered by RPA at this concentration. This suggests that the rate-limiting step for displacement at saturating RPA concentrations is the nucleation of Rad51 protein on the RPA-ssDNA complex. Once nucleation occurs, the kinetic curves show that Rad51 protein quickly displaces RPA from ssDNA, presumably by its cooperative assembly along ssDNA. However, in contrast to RecA protein, the distinction between the nucleation and growth phases for Rad51 protein is smaller.

Rad52 Protein Stimulates Rad51 Protein-mediated Displacement of RPA from ssDNA-- Rad52 protein stimulates DNA strand exchange by Rad51 protein under conditions where RPA is bound to ssDNA before Rad51 protein (11, 12, 14). To examine whether this stimulation is due to an accelerated displacement of RPA, we tested the effect of Rad52 protein on both ATP hydrolysis and the displacement of RPA from ssDNA by Rad51 protein. As expected, in the presence of Rad52 protein, the rate of Rad51 protein-dependent ATP hydrolysis increased faster than in the absence of Rad52 protein (Fig. 3A). Similarly, the displacement of RPA from ssDNA by Rad51 protein was accelerated by Rad52 protein (Fig. 3B). We also examined whether Rad52 protein itself could displace RPA from ssDNA in the absence of Rad51 protein. When Rad52 protein was added to a RPA-ssDNA complex in the absence of Rad51 protein, no RPA displacement was observed (Fig. 3B, +Rad52 (no Rad51)). These results show that Rad52 protein alone does not displace RPA from ssDNA, but rather, it facilitates Rad51 protein to do so.

View larger version (26K): [in this window] [in a new window]   Fig. 3.   Rad52 protein helps Rad51 protein to displace RPA from ssDNA. Time courses of ATPase activity (A) and the release of RPA from ssDNA (B) were monitored using the RPA-ssDNA complex as a starting substrate. The reactions were started by the addition of Rad51 protein (5 µM) to a preformed complex of RPA (1 µM) and pBluescript SK ssDNA (10 µM). Where indicated (+Rad52), Rad52 protein (1 µM) was added 20-30 s after the addition of Rad51 protein. For the +Rad52 (no Rad51) reaction, Rad52 protein was added to preformed RPA-ssDNA complexes in the absence of Rad51 protein. The fluorescence of Rad51 and Rad52 proteins was subtracted in the fluorescence analyses.

We also analyzed the effect of Rad52 protein on RPA displacement at various concentrations of Rad51 protein (Fig. 4). At all concentrations, Rad52 protein stimulated displacement. At the lower concentrations of Rad51 protein (stoichiometric relative to ssDNA concentration or lower; Figs. 3A and 4, A, B, and E-G), the stimulation was clear throughout the reaction period; at the higher concentrations of Rad51 protein, stimulation was more modest (Fig. 4, C, D, and E-G). The final rate of ATP hydrolysis, when the Rad51 protein concentration exceeds that needed to saturate the ssDNA, was approximately the same in the presence and the absence of Rad52 protein, supporting the idea that Rad52 protein does not stimulate the ATPase activity of Rad51 protein beyond that of the fully contiguous Rad51 protein-ssDNA complex. These results indicate that the Rad52 protein-mediated stimulation of Rad51 protein function is caused by an acceleration of the loading of Rad51 protein onto an RPA-ssDNA complex with the concomitant release of RPA from the ssDNA.

View larger version (37K): [in this window] [in a new window]   Fig. 4.   Rad52 protein facilitates both the rate and extent of RPA displacement from ssDNA. A-D, ATP hydrolysis was measured as in Fig. 3A, using 2 µM (A), 3 µM (B), 7 µM (C), and 10 µM (D) Rad51 protein in the presence () or the absence () of Rad52 protein (1 µM). E-G, ATP hydrolysis rate after 2 min (C), 5 min (D), and 40 min (E), in the presence () or absence () of Rad52 protein, plotted against the Rad51 protein concentration.

Rad52 Protein-mediated Stimulation of Presynaptic Filament Formation Is Species-specific-- Rad52 protein-mediated stimulation of DNA strand exchange is species-specific (14). Rad52 protein cannot stimulate the reaction either if RPA is replaced by E. coli SSB protein or if Rad51 protein is replaced by E. coli RecA protein. To test whether this species specificity is caused by the specific acceleration of Rad51 protein-ssDNA complex formation by Rad52 protein, we next examined the effect of Rad52 protein on presynaptic complex formation by E. coli RecA and SSB proteins. When Rad51 protein was added to SSB-ssDNA complexes, the ATP hydrolysis rate increased gradually to a plateau level in 40 min (Fig. 5A, Rad52), showing that SSB protein can be displaced by Rad51 protein from ssDNA. Rad52 protein, however, did not affect the time course of SSB displacement by Rad51 protein, showing that the stimulation by Rad52 protein is species-specific (Fig. 5A, +Rad52). When RecA protein was added to an RPA-ssDNA complex, RecA protein also displaced RPA from ssDNA (Fig. 5B, Rad52). However, Rad52 protein did not stimulate but rather blocked displacement (Fig. 5B, +Rad52). This result is consistent with our previous report, which showed that Rad52 protein inhibits DNA strand exchange by RecA protein and RPA (14). Rad52 protein also slowed SSB displacement by RecA protein (Fig. 5C), suggesting that Rad52 protein inhibits either DNA binding or ATP hydrolysis by RecA protein by an unknown mechanism.

View larger version (25K): [in this window] [in a new window]   Fig. 5.   The RPA displacement function of Rad52 protein is species-specific. Presynaptic complex formation by either Rad51 protein or RecA protein, in the presence of either E. coli or yeast ssDNA-binding protein, was examined by measuring ATP hydrolysis. A-C, the ATP hydrolysis reactions were started by adding Rad51 (5 µM; A) or RecA protein (3.3 µM; B and C) to pBluescript SK ssDNA (10 µM) which was prebound with 1 µM RPA (B) or 1.2 µM SSB protein (A and C). Rad52 protein was added immediately after the reaction start (at ~15 s). For the RecA protein reactions, the reaction conditions were the same as for the Rad51 protein reactions except that KCl was omitted, and 1.5 mM phosphoenolpyruvate, 15 units/ml pyruvate kinase, and 15 units/ml lactate dehydrogenase were added. Open triangles with dashed lines and filled circles with solid lines represent the reactions with and without 1 µM Rad52 protein, respectively.

We also examined the effect of various Rad52 protein concentrations on presynaptic complex formation, using all combinations of homologous and heterologous proteins. Experiments such as those shown in Fig. 5, A-C, were performed, and the relative ATPase activity at 5 min after the addition of Rad51 protein was plotted against the concentration of Rad52 protein (Fig. 6), because both stimulation and inhibition were clear at this early stage of the displacement. Rad52 protein stimulated the ATP hydrolysis activity of Rad51 protein only when RPA was used. The optimum Rad52 protein concentration for the stimulation (~0.5 µM) was similar to the concentration of RPA, which was bound to ssDNA. This suggests that a stoichiometric co-complex of Rad52 protein and RPA on ssDNA is involved in the displacement. The displacement of SSB protein by Rad51 protein was not affected at any concentration of Rad52 protein. RecA-mediated displacement of both RPA and SSB protein was inhibited by Rad52 protein in a concentration-dependent manner. These results confirm the need for cognate, species-specific interactions in the Rad52 protein-mediated stimulation of presynaptic complex formation.

View larger version (26K): [in this window] [in a new window]   Fig. 6.   Rad52 protein facilitates ssDNA binding protein displacement only by the cognate DNA strand exchange protein at all concentrations. Experiments, as in Fig. 5, were performed in the presence of various amounts of Rad52 protein, and the ATP hydrolysis rates at 5 min after the addition of Rad51 protein were plotted against the concentration of Rad52 protein. The ATP hydrolysis rates are shown as relative to the rate obtained without Rad52 protein. The reactions with Rad51 protein and RPA (), Rad51 protein and SSB protein (), RecA protein and RPA (), and RecA protein and SSB () are shown.

Detection of a Rad52 Protein-RPA-ssDNA Co-complex-- In the experiments presented so far, we analyzed both ATP hydrolysis by Rad51 protein to follow its binding to ssDNA and the fluorescence of RPA to follow its binding to DNA. Although each method detects the respective status of which protein was bound to ssDNA, neither provides any information regarding the interaction of Rad52 protein with the RPA-ssDNA complex. Because T4 phage UvsY protein and E. coli RecO protein, which are functional homologues of Rad52 protein, can form a co-complex with the gp32-ssDNA complex and the SSB protein-ssDNA complex, respectively (30, 31), it was of special interest to test whether Rad52 protein could also produce a co-complex with the RPA-ssDNA complex. Therefore, we examined the binding of Rad52 protein to RPA-ssDNA complexes using a gel mobility shift assay.

Incubation of RPA and 100-mer ssDNA produced an RPA-ssDNA complex with a reduced electrophoretic mobility (Fig. 7A); titration with RPA showed that 0.7 µM is sufficient to saturate the 10 µM ssDNA. Similarly, titration of the ssDNA with Rad52 protein also produced Rad52 protein-ssDNA complexes, which either entered the gel or stacked in the wells (Fig. 7B). These results are consistent with previous reports regarding the binding of RPA and Rad52 protein to ssDNA (10, 19). Interestingly, adding an increasing amount of Rad52 protein to the saturated RPA-ssDNA complex changed the mobility of the complex to one that is stacked in the wells (Fig. 7C, indicated as Super-shifted complex). To examine which proteins are components of the supershifted complex, the bands corresponding to the supershifted complex were excised and analyzed by SDS-PAGE. To enable direct comparison of the amounts of the proteins present in each complex, we normalized the amount of protein present to the amount of ssDNA present, which was measured from radioactivity of the ssDNA. Compared with the control RPA-ssDNA complex (Fig. 7D, lane 6), the supershifted complexes (lanes 7-9) contained similar amounts of RPA per ssDNA molecule, despite the presence of increasing amounts of Rad52 protein (Fig. 7, D and E). Importantly, these complexes also contained Rad52 protein, the amount of which depended on the concentration of Rad52 protein added to the RPA-ssDNA complex. These results indicate that Rad52 protein and RPA can form a co-complex that is bound to ssDNA. This complex is not just a mixture of RPA-ssDNA and Rad52-ssDNA complexes, because the amount of RPA in the co-complex remains constant with increasing amounts of Rad52 protein. To exclude the possibility of a DNA-independent aggregation of Rad52 protein or of RPA in the mobility shift experiments, we performed the same experiment as for lane 9 of Fig. 7D but in the absence of ssDNA. The gel piece corresponding to the co-complex contained an undetectable amount of RPA or Rad52 protein in this control (Fig. 7D, lane 10).

View larger version (51K): [in this window] [in a new window]   Fig. 7.   Formation of a RPA and Rad52 protein co-complex bound to ssDNA. A and B, the indicated amounts of RPA (A) and Rad52 protein (B) were incubated with 32P-labeled 100-mer ssDNA (10 µM) under the standard conditions without ATP, and samples were analyzed by "conventional" electrophoresis (see "Experimental Procedures" for details). C, RPA-ssDNA complexes were first formed by incubating ssDNA with 0.7 µM RPA, and then various amounts of Rad52 protein were added to produce ssDNA-RPA-Rad52 protein co-complex. The reaction did not contain ATP, since it had no effect on the co-complex formation (data not shown). Samples were analyzed by "conventional" electrophoresis. D, analysis of the Rad52 protein-RPA-ssDNA co-complex. The gel mobility shift experiments as shown in lane 1 of C (RPA-ssDNA complex, lane 6) and lanes 4, 6, and 7 of C (Super-shifted complex, lanes 7-9), and lane 7 of B (Rad52-ssDNA complex, lane 11) were done in 3-fold larger volume, and the supershifted complexes containing an equivalent amount of ssDNA were analyzed by SDS-PAGE followed by staining with Coomassie Brilliant Blue R-250. Lane 10 is the same as lane 9 except that the gel shift experiment had no ssDNA, and twice the amount of gel piece was loaded on the gel. Lanes 1-5 are standards showing 0.03, 0.1, 0.3, 1, and 3 µg of RPA and Rad52 protein, respectively. Lane M, prestained markers, showing 116, 78.0, 49.3 and 34.7 kDa. E, relative molar amount of RPA and Rad52 protein in RPA-ssDNA complex, Rad52-RPA-ssDNA co-complexes, and Rad52 protein-ssDNA complex were calculated based on D. The amount of RPA in RPA-ssDNA complex was defined as 1.

RPA Is Absent from the Presynaptic Filament-- Our fluorescence experiments indicated only the ssDNA binding status of RPA (Figs. 1D and 3B). We could not distinguish whether RPA was free in solution or whether it remained bound to the Rad51 protein-ssDNA complex via protein-protein interactions after being removed from ssDNA. To address this issue, we asked whether Rad51 protein and RPA could form a complex. Initially, we incubated various amounts of Rad51 protein with the 100-mer ssDNA in the absence of RPA using the standard gel mobility shift protocol. Rad51 protein produced only a faint shift under these conditions (Fig. 8A). However, when ATP, NaCl, and magnesium acetate were added to both the gel and the electrophoresis buffer, the Rad51 protein-ssDNA complex was observed more clearly, as a species that stacked in the sample well (Fig. 8B; see "Experimental Procedures" for details). This finding suggested that the Rad51 protein-ssDNA complex was unstable without those components and that it dissociated during electrophoresis. Therefore, electrophoresis was performed using the latter conditions. When an increasing amount of Rad51 protein was added to a saturated RPA-ssDNA complex, the mobility of the ssDNA changed to that of the Rad51 protein-ssDNA complex (Fig. 8C, lanes 1-6). To examine whether RPA was present within this new complex, we measured the amount of RPA in the complexes (Fig. 8, D and E). Consistent with our RPA displacement interpretation, the new complex contained a lower amount of RPA (one-fifth or less) than the control RPA-ssDNA complex (compare lanes 6 and 7 of D and lanes 5 and 7 of E). This result confirms our conclusion that Rad51 protein displaces RPA from ssDNA and, furthermore, that RPA is not forming a stable interaction with the Rad51 protein-ssDNA presynaptic complex after having been displaced.

View larger version (69K): [in this window] [in a new window]   Fig. 8.   Binding of Rad51 protein to ssDNA and displacement of RPA monitored by gel mobility shift assay. A, the indicated amounts of Rad51 protein were incubated with 32P-labeled 100-mer ssDNA (10 µM) under standard conditions with ATP, and the samples were analyzed by "conventional" electrophoresis. B, the same Rad51 protein titration experiment as A was done except that the samples were analyzed by electrophoresis in the presence of ATP and Mg2+ (see "Experimental Procedures" for details). C, RPA-ssDNA complexes were first formed by incubating ssDNA with 0.7 µM RPA for 10 min in the buffer containing ATP and then with (lanes 7-12) or without (lanes 1-6) 0.7 µM Rad52 protein for 10 min; finally, the indicated amounts of Rad51 protein were added and incubated for 15 min. Samples were analyzed by electrophoresis in the presence of ATP and Mg2+. D, analysis of the Rad51 protein-ssDNA complex after displacement. The same gel mobility shift experiments as shown in B and C were done in a 3-fold larger volume, and the RPA-ssDNA complex, which was recovered from lane 1 of C (lane 6), the Rad51 protein-ssDNA complexes, which were recovered from lanes 6 and 12 of C (lanes 7 and 8) and from lane 7 of B (lane 9), each containing an equivalent amount of ssDNA, were analyzed by SDS-PAGE followed by staining with Coomassie Brilliant Blue R-250. Lanes 10 and 11 are the same as lanes 7 and 8, respectively, except that the gel shift experiments had no DNA and twice the amount of gel pieces were loaded on the gel. Lanes 1-5 are standards showing 0.03, 0.1, 0.3, 1, and 3 µg of RPA, Rad51 protein, and Rad52 protein. Lane M, prestained markers, showing 116, 78.0, 49.3, and 34.7 kDa. E, RPA-ssDNA complex in lane 1 of C (lane 5), RPA-ssDNA complex in lane 7 of C (lane 6), Rad51 protein-ssDNA complex in lane 6 of C (lane 7), and Rad51 protein-ssDNA complex in lane 12 of C (lane 8) were analyzed by Western blotting using anti-RPA. The amount of sample was normalized by DNA content. Lanes 1-4 are standards showing 5, 10, 20, and 50 ng of RPA. Lane M, markers.

Rad52 protein (0.7 µM) did not affect the formation of the new complex (Fig. 8C, lanes 7-12). This was not surprising, because we did not detect Rad52 protein-mediated stimulation of DNA pairing with synthetic oligonucleotides and because RPA-displacement measured by ATPase activity showed that the displacement occurred too quickly on such short ssDNA to permit detectable stimulation by Rad52 protein (data not shown). Nevertheless, the amount of RPA also decreased in the Rad51 protein-ssDNA complex (Fig. 8, D and E, compare lanes 6 and 8), showing that the majority of RPA molecules were released from the presynaptic complex even in the presence of Rad52 protein, which can interact with both Rad51 protein and RPA. Finally, we found Rad51 protein in the gel pieces corresponding to Rad51 protein-ssDNA complex (Fig. 8D, lanes 7-9); however, the majority of this signal is due to DNA-independent aggregation of Rad51 protein under these gel electrophoresis conditions, because negative control experiments without ssDNA also detected a similar amount of Rad51 protein (lanes 10 and 11). Therefore, we could not quantify the amount of Rad51 protein in the complexes formed with ssDNA.

	DISCUSSION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

RPA can greatly stimulate Rad51 protein-mediated DNA strand exchange, provided that RPA is added to a preformed complex of Rad51 protein and native ssDNA. One possible explanation for this stimulation is that RPA forms a co-complex with the Rad51 protein-ssDNA complex that is more active in DNA strand exchange. However, the results in this and in our previous work (7) suggest otherwise; instead, they indicate that RPA and Rad51 protein compete with each other for the same ssDNA binding sites. In this paper, we present direct evidence showing that RPA is released from ssDNA by Rad51 protein and that this release correlates exactly with formation of the Rad51 protein-ssDNA complex. This means that the presynaptic complex, which is assembled in the presence of RPA, is simply a complex of Rad51 protein and ssDNA rather than a co-complex of Rad51-ssDNA-RPA. We also showed that the time course for presynaptic complex formation depends on the order that the proteins are bound to ssDNA. The displacement of RPA by Rad51 protein from a preformed RPA-ssDNA complex takes a relatively long period of time (20-30 min), but RPA acts on Rad51 protein-ssDNA complexes instantly, without the detection of a significant level of RPA-ssDNA complex as an intermediate. In addition, the experiments that vary the occupancy of ssDNA by RPA (Fig. 2) suggest that the rate-limiting step of the displacement reaction is the nucleation of Rad51 protein onto ssDNA. Once nucleation occurs, extensive displacement of RPA occurs by growth of the Rad51 filament along ssDNA. These characteristics are similar to the behavior of E. coli RecA and SSB proteins, whereby SSB protein stimulates RecA presynaptic filament formation by a related mechanism (23, 24). We could not detect interaction of RPA with the filament at this stage, even in the presence of Rad52 protein. Rad52 protein may be interacting with the Rad51 presynaptic complex via a protein-protein interaction, but such a hypothetical complex has no effect on the DNA pairing activity, since Rad52 protein has no stimulatory effect on the preformed Rad51 presynaptic complex (12, 14, 32).

Based on the observations in this paper and others, we conclude that Rad51 protein and RPA compete for binding to ssDNA. Although this competition can have a detrimental effect, when the ssDNA has secondary structure, RPA is needed to melt the DNA secondary structure. In the absence of RPA, Rad51 protein binds the duplex regions and inhibits DNA strand exchange. RPA is needed to prevent this binding, but then Rad51 protein nevertheless displaces RPA from ssDNA. When the ssDNA is fully saturated with RPA, nucleation of Rad51-ssDNA binding is a relatively inefficient process. However, once Rad51 protein nucleates on ssDNA, filament extension along ssDNA creates a contiguous Rad51 filament on the DNA that concomitantly displaces the bound RPA. The function of Rad52 protein, therefore, is to help Rad51 protein displace RPA from ssDNA since Rad52 protein alone cannot displace RPA from ssDNA.

Our results also show that Rad52 protein and RPA form a co-complex on ssDNA. This function of yeast Rad52 protein is similar to that of T4 phage UvsY protein and E. coli RecO (or RecOR) protein (see Ref. 33 for a review). Each of these "recombination mediator" proteins recruits its DNA strand exchange proteins to ssDNA to overcome the inhibitory effect of ssDNA-binding proteins, but none of them can displace ssDNA-binding proteins by themselves. Instead, each mediator protein specifically interacts with its cognate ssDNA-binding protein, an interaction that is a universal property of the DNA strand exchange mediators. Since RPA is a relatively abundant protein in the cell, it is reasonable to expect that ssDNA produced in vivo is first coated with RPA. In fact, cytological observations confirm the temporal order of protein appearance that we have elaborated in vitro (34). These analyses also showed that RPA and Rad52 protein co-localize in subnuclear foci at double strand breaks, as an early step of recombination. This co-localization may involve the co-complex formation of RPA and Rad52 protein on ssDNA, which is produced by processing of the DNA breaks, prior to their displacement by Rad51 protein.

Since Rad52 protein by itself cannot displace RPA from ssDNA, there are several possible mechanisms by which Rad52 protein could facilitate assembly of Rad51 protein on ssDNA. Perhaps the simplest one is that Rad52 protein serves as a nucleus for Rad51 protein filament assembly, via an interaction with the RPA-ssDNA complex. Because the rate-limiting step for RPA displacement is the nucleation step of Rad51 protein filament assembly, facilitation of nucleation accelerates the displacement process. Similar mechanisms were proposed for E. coli RecO protein (31, 35) and for T4 UvsY protein (33, 36). Alternatively, Rad52 protein might increase the elongation phase of Rad51 filament assembly. However, this possibility is less likely, because elongation of Rad51 filament is not strongly inhibited by RPA. Finally, a third possibility relies on protein-protein interactions that exist between Rad52 protein and RPA and between Rad52 and Rad51 protein; in principle, these three proteins could form a transient Rad51-Rad52-RPA-ssDNA nucleoprotein co-complex as an intermediate. In the T4 phage system, a three-protein and DNA co-complex was proposed as an intermediate (30), but recent studies have shown that the gp32-ssDNA interaction is destabilized by interaction with UvsY protein to facilitate loading of UvsX protein onto ssDNA (37). So far, however, we have not detected any destabilization of the RPA-ssDNA complex by Rad52 protein.² In this paper, we detected a Rad52-RPA-ssDNA co-complex in vitro. Since the amount of Rad52 protein that is needed for the displacement of RPA is approximately the same as the amount of RPA that is bound to ssDNA, the active species of the displacement may be a stoichiometric complex of Rad52 protein and RPA on ssDNA (Fig. 9b). In addition, both Rad52 protein and UvsY protein form ring-like structure (heptamer for Rad52 protein and hexamer for UvsY), and this multimerization is required for UvsY function (11, 38, 39). Therefore, for the reasons outlined above, we favor the facilitated nucleation model as depicted in Fig. 9.

View larger version (14K): [in this window] [in a new window]   Fig. 9.   A model for presynaptic complex formation by Rad51 and Rad52 proteins and RPA. Rad52 protein binds to RPA-ssDNA complex (a) to form a Rad52-RPA-ssDNA nucleoprotein co-complex (b). This co-complex facilitates the nucleation of Rad51 protein onto ssDNA. The ring form of Rad52 protein may be involved in this step (c). Nucleation is followed by rapid elongation of the Rad51 filament to form a contiguous Rad51-ssDNA presynaptic complex (d).

	ACKNOWLEDGEMENTS

We thank Dr. Richard Kolodner for the RPA-overproducing strain; Dr. Wolf-D. Heyer for anti-RPA antibody; and Piero Bianco, Mark Dillingham, Naofumi Handa, Cynthia Haseltine, Noriko Kantake, Alex Mazin, Katsumi Morimatsu, Jim New, and Yun Wu for comments on the manuscript.

	FOOTNOTES

^* This work was supported by National Institutes of Health Grants AI-18987 and GM-62653 and Human Frontier Science Program Grant RG63 (to S. C. K.).The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

To whom correspondence should be addressed: Section of Microbiology, Briggs Hall, University of California, Davis, CA 95616-8665. Tel.: 530-752-5938; Fax: 530-752-5939; E-mail: sckowalczykowski@ucdavis.edu.

Published, JBC Papers in Press, June 19, 2002, DOI 10.1074/jbc.M203494200

² Tomohiko Sugiyama and Stephen C. Kowalczykowski, unpublished observations.

	ABBREVIATIONS

The abbreviations used are: RPA, replication protein A; ssDNA, single-stranded DNA; dsDNA, double-stranded DNA; MOPS, 4-morpholinepropanesulfonic acid.

	REFERENCES

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

CiteULike

Complore

Connotea

Del.icio.us

Digg

Reddit

Technorati

This article has been cited by other articles:

				Y. Wu, N. Kantake, T. Sugiyama, and S. C. Kowalczykowski Rad51 Protein Controls Rad52-mediated DNA Annealing J. Biol. Chem., May 23, 2008; 283(21): 14883 - 14892. [Abstract] [Full Text] [PDF]

				G. Octobre, A. Lorenz, J. Loidl, and J. Kohli The Rad52 Homologs Rad22 and Rti1 of Schizosaccharomyces pombe Are Not Essential for Meiotic Interhomolog Recombination, but Are Required for Meiotic Intrachromosomal Recombination and Mating-Type-Related DNA Repair Genetics, April 1, 2008; 178(4): 2399 - 2412. [Abstract] [Full Text] [PDF]