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J. Biol. Chem., Vol. 275, Issue 21, 15895-15904, May 26, 2000

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Functional Interactions among Yeast Rad51 Recombinase, Rad52 Mediator, and Replication Protein A in DNA Strand Exchange^*

BinWei Song and Patrick Sung

From the Department of Molecular Medicine/Institute of Biotechnology, University of Texas Health Science Center, San Antonio, Texas 78245-3207

Received for publication, December 21, 1999, and in revised form, March 7, 2000

	ABSTRACT

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Rad51-catalyzed DNA strand exchange is greatly enhanced by the single-stranded (ss) DNA binding factor RPA if the latter is introduced after Rad51 has already nucleated onto the initiating ssDNA substrate. Paradoxically, co-addition of RPA with Rad51 to the ssDNA to mimic the in vivo situation diminishes the level of strand exchange, revealing competition between RPA and Rad51 for binding sites on ssDNA. Rad52 promotes strand exchange but only when there is a need for Rad51 to compete with RPA for loading onto ssDNA. Rad52 is multimeric, binds ssDNA, and targets Rad51 to ssDNA. Maximal restoration of pairing and strand exchange requires amounts of Rad52 substoichiometric to Rad51 and involves a stable, equimolar complex between Rad51 and Rad52. The Rad51-Rad52 complex efficiently utilizes a ssDNA template saturated with RPA for homologous pairing but does not appear to be more active than Rad51 when an RPA-free ssDNA template is used. Rad52 does not substitute for RPA in the pairing and strand exchange reaction nor does it lower the dependence of the reaction on Rad51 or RPA.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

In eukaryotic organisms, genetic recombination is mediated by genes of the RAD52 epistasis group. These genes were first identified in Saccharomyces cerevisiae and consist of RAD50, RAD51, RAD52, RAD54, RAD55, RAD57, RAD59, RDH54/TID1, MRE11, and XRS2. Mutations in these genes very often result in severe meiotic phenotypes including an arrest in meiotic prophase, low sporulation efficiency, and spore inviability, which arise because of a requirement for the recombination machinery in ensuring the proper disjunction of chromosomal homologs in meiosis I. The RAD52 group genes also mediate the repair of DNA strand breaks by homologous recombination (reviewed in Ref. 1).

The RAD51 gene product is structurally related to RecA (2-4), which plays a central role in recombination processes in Escherichia coli. Studies on RecA, its bacteriophage T4 counterpart UvsX, and eukaryotic Rad51 have indicated that they mediate the homologous DNA pairing and strand exchange reaction that forms heteroduplex DNA during recombination. In the earliest phase of this reaction, referred to as presynapsis, Rad51 polymerizes on ssDNA¹ to form a right-handed nucleoprotein filament that has a highly regular pitch (~95 Å) and in which the DNA is held in a highly extended conformation (axial rise of ~5.4 Å per base or base pair) (5, 6). The formation of heteroduplex DNA with the incoming duplex DNA partner occurs within the confines of this nucleoprotein filament (6). The assembly of this presynaptic Rad51-ssDNA nucleoprotein filament requires ATP binding but not its hydrolysis (7) and is stimulated by the heterotrimeric ssDNA binding factor RPA, which functions to remove secondary structure in the ssDNA (8, 9). Human RAD51 also cooperates with human RPA to yield heteroduplex DNA (10, 11).

Maximal level of strand exchange is obtained when RPA is introduced after Rad51 has already nucleated onto the ssDNA substrate. Paradoxically, a pronounced suppression of the reaction is seen if RPA is added together with or before Rad51 protein to the ssDNA (12-15). Rad52 (12, 13, 15) and the heterodimer of the Rad55 and Rad57 proteins (14) have been found to promote heteroduplex formation when there is a need for Rad51 to compete with RPA for binding sites on the ssDNA. These ancillary protein factors, or mediators (15, 16), are functionally equivalent to the E. coli RecO-RecR complex (17) and T4 UvsY protein (18-21), which allow their cognate recombinases RecA and UvsX to gain access to ssDNA already coated with the ssDNA binding factor. However, the manner in which Rad52 and the Rad55-Rad57 heterodimer overcome the competition by RPA is not known at the present time. Here we describe biochemical studies that enable us to begin understanding the biochemical properties and the mediator function of Rad52 in greater detail.

	MATERIALS AND METHODS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Purification of Recombination Proteins

Rad52-- E. coli strain M15(pREP4) harboring the plasmid expressing His₆-tagged Rad52 under the control of the T5 promoter (gift from Rodney Rothstein) (22) was used. Extract was made from 15 g of cell paste (from 8 liters of culture) in 120 ml of cell breakage buffer (50 mM Tris-HCl, pH 7.5, 10% sucrose, 150 mM KCl, 3 mM EDTA, 1 mM 2-mercaptoethanol) in the presence of protease inhibitors using a French press (23). The lysate was clarified by centrifugation (100,000 × g, 90 min), and the supernatant (fraction I, 120 ml) was applied onto a column of SP-Sepharose (2.5 × 6.1 cm; 30 ml total) equilibrated in buffer K (20 mM KH₂PO₄, pH 7.4, 0.5 mM EDTA, 1 mM DTT) containing 150 mM KCl. The column was developed with a 300-ml gradient of 150-650 mM KCl in buffer K. Rad52 elutes from SP-Sepharose at 360 mM KCl, the pool of which (fraction II, 30 ml) was diluted with 2 volumes of K buffer and applied to a Q-Sepharose column (1.5 × 5.5 cm; 8 ml total), which was developed with a 100-ml gradient of 120-450 mM KCl in K buffer, collecting 2-ml fractions. The pool of Rad52 (fraction III; 10 ml), eluting from Q-Sepharose at about 300 mM KCl, was mixed with 1 ml of nickel-NTA-agarose (Qiagen) for 2 h at 4 °C. The nickel matrix was poured into a glass column (1 cm diameter) and washed with 10 volumes each of 10, 20, and 30 mM imidazole in buffer K containing 500 mM KCl. Rad52 was eluted with 4 ml of 200 mM imidazole in buffer K containing 500 mM KCl and then concentrated to 1 ml using a Centricon microconcentrator (Amicon). The concentrated nickel pool (fraction IV) was subject to sizing in a column of Sepharose 6B (1.6 × 40 cm; 80 ml matrix) in buffer K containing 150 mM KCl. The Rad52 pool (fraction V, 8 ml) was loaded directly onto a Mono S column (HR5/5), which was developed with a 30-ml gradient of 150-500 mM KCl in buffer K. Fractions containing the peak of Rad52 protein, eluting at 350 mM KCl, were pooled (fraction VI; 4 ml) and concentrated to 5 mg/ml and stored in small portions at 70 °C. The concentration of Rad52 protein was measured by densitometric comparison of multiple loadings of Rad52 protein against known amounts of bovine serum albumin and ovalbumin in a Coomassie Blue R-stained polyacrylamide gel.

Rad51 Protein-- Rad51 was purified to near-homogeneity from yeast strain LP2749-9B harboring the plasmid pR51.3 (2 µm, PGK-RAD51), using a combination of ammonium sulfate precipitation and chromatographic fractionation steps in columns of Q-Sepharose, hydroxyapatite, Bio-Rex 70, and Mono Q (7). Rad51 was stored in K buffer containing 350 mM KCl. The concentration of Rad51 protein was measured using molar extinction coefficient of 1.29 × 10⁴ M¹ cm¹ at 280 nm (33).

RPA-- RPA was purified from a yeast strain genetically tailored to co-overexpress the three subunits of RPA (a gift from Richard Kolodner). Extract was prepared and then subjected to fractionation in columns of Affi-Gel Blue, ssDNA cellulose, hydroxyapatite, and Mono Q as described (14). The RPA purified this way was nearly homogeneous and was stored in K buffer containing 200 mM KCl. The concentration of RPA was measured by densitometric comparison of multiple loadings of RPA against known amounts of bovine serum albumin and ovalbumin in a Coomassie Blue R-stained polyacrylamide gel.

Rad51-Rad52 Complex-- Purified Rad51 (3 mg) and Rad52 (3.25 mg) were incubated in 5 ml of buffer K with 300 mM KCl for 12 h on ice and then mixed with 1 ml of nickel-NTA-agarose to immobilize the Rad51-Rad52 complex, which was eluted from the nickel matrix with 3 ml of 200 mM imidazole in buffer K containing 300 mM KCl. The eluate was concentrated to 0.3 ml in a Centricon-30 microconcentrator, diluted to 3 ml with buffer K containing 300 KCl, and reconcentrated to 0.3 ml. This filter-dialysis step was repeated in the same concentrator, and the final concentrate, containing Rad51-Rad52 complex at 150 µM, was stored in small portions at 70 °C.

Nucleic Acids

X174 viral (+) strand was purchased from New England Biolabs, and the replicative form (about 90% supercoiled form and 10% nicked circular form) was from Life Technologies, Inc. The 83-mer oligonucleotides used in the strand exchange experiments were as follows: Oligo 1 with 16% GC content, 5'-AAA TGA ACA TAA AGT AAA TAA GTA TAA GGA TAA TAC AAA ATA AGT AAA TGA ATA AAC ATA GAA AAT AAA GTA AAG GAT ATA AA; Oligo 2, the exact complement of Oligo 1, was labeled at the 5' end with [-³²P]ATP by T4 polynucleotide kinase, and then annealed to Oligo 1. The resulting duplex was purified from 10% polyacrylamide gels by overnight diffusion at 4 °C into TAE buffer (40 mM Tris-HCl, pH 7.4, 20 mM NaOAC, 0.5 mM EDTA).

Sizing by Gel Filtration

A Sepharose 6B column (1 × 45 cm; 35 ml total) was used to monitor the migration of Rad51, Rad52, and the Rad51-Rad52 complex in the experiment described in Fig. 2A. Rad51 protein (11.6 µM in panels I, III, and IV) and Rad52 protein (11.6 µM in panels II and III and 2.3 µM in panel IV) were incubated in 100 µl of column buffer (buffer K containing 150 mM KCl and 1 mM DTT) on ice for 1 h, diluted with 400 µl of column buffer, and then filtered through the sizing column at 0.2 ml/min, collecting 0.5-ml fractions. The indicated column fractions were subject to immunoblot analyses to determine their content of the Rad51 and Rad52 proteins. For calibration of the column, thyroglobulin (669 kDa), catalase (232 kDa), and blue dextran (>2,000 kDa) were used, and their elution positions are marked on the chromatogram in Fig. 2A.

Binding to Nickel-Agarose

In Fig. 2B, Rad51 and Rad52 proteins were incubated at various molar ratios (0.5 µM Rad51 and 2 µM Rad52 or 1:4; 1.5 µM Rad51 and 1.25 µM Rad52 or 1.2:1; 3 µM Rad51 and 1 µM Rad52 or 3:1; or 2 µM Rad51 alone) in 1 ml of K buffer containing 300 mM KCl and 0.01% Nonidet P-40 at 4 °C for 1 h. In Fig. 2C, reaction mixtures containing 1.5 µM Rad51 or a combination of 1.5 µM Rad51 and 1.5 µM Rad52 were incubated in the same buffer with or without 2.5 mM ATP and 3 mM MgCl₂ for 1 h. All the mixtures were gently mixed with 200 µl of nickel-NTA-agarose beads at 4 °C for 3 h. The beads were washed with 2 ml of 20 mM imidazole in the same buffer with or without ATP/MgCl₂ before eluting the bound proteins with 400 µl of 3% SDS by boiling for 1 min.

DNA Binding

DNA Mobility Shift-- The substrates used were X174 viral (+) strand and the replicative form linearized with PstI. In Fig. 3, A-C, the reactions contained both ssDNA (30 µM nucleotides) and dsDNA (20 µM nucleotides) with the indicated amounts of Rad51 protein, Rad52 protein, or Rad51-Rad52 complex in 10 µl of reaction buffer (35 mM K-MOPS, pH 7.2, 1 mM DTT, and 100 µg/ml BSA, with or without 2.5 mM ATP and 3 mM MgCl₂, as indicated). The reaction mixtures were incubated at 25 °C for 10 min, mixed with 2 µl of loading buffer (0.1% Orange G in 30 mM Tris-HCl, pH 7.5, containing 50% glycerol), and then subjected to electrophoresis in 0.9% agarose gels at 100 mA in TAE buffer at 25 °C until the dye front had migrated 4 cm. The gels were stained with ethidium bromide to reveal the DNA species.

Binding to ssDNA Cellulose-- In Fig. 3D, Rad51 (0.45 µM), Rad52 (0.45 µM), or a mixture of these two proteins in 150 µl of buffer T (20 mM Tris-HCl, pH 7.5, 10% glycerol, 0.5 mM EDTA, 1 mM DTT, and 0.01% Nonidet P-40) containing 150 mM KCl and 100 µg/ml BSA was incubated on ice for 45 min and then mixed with 15 µl of ssDNA cellulose beads (1 µg of denatured calf thymus DNA/µl beads; purchased from United States Biochemical Corp.) for 45 min at 25 °C. The beads were collected by a 5-s centrifugation in a microcentrifuge, washed with 150 µl of buffer T containing 300 mM KCl, and treated with 35 µl of 3% SDS at 37 °C for 15 min to elute bound proteins. Equivalent amounts of the input material, the supernatant that contained unbound proteins, the KCl wash, and SDS eluate were subject to immunoblotting to examine the Rad51 and Rad52 contents.

ATPase Assay

Rad51 protein (10 µM) with or without Rad52 protein (4 µM) was incubated with or without X ssDNA (30 µM nucleotides) and 1 mM [-³²P]ATP using the buffer conditions employed in the strand exchange assay. At the indicated times, 1-µl aliquots were removed and directly spotted on a polyethyleneimine-cellulose sheet, which was developed in 0.75 M potassium phosphate. The polyethyleneimine-cellulose sheets were analyzed in the PhosphorImager.

Homologous Pairing and Strand Exchange

X DNA-based System-- The indicated amounts of Rad51 protein in 1 µl of storage buffer were incubated with ssDNA (30 µM) added in 1 µl of TE buffer (10 mM Tris-HCl, pH 7.5, 0.2 mM EDTA) in 10 µl of buffer R (35 mM K-MOPS, pH 7.2, 1 mM DTT) containing 50 mM KCl, 2.5 mM ATP, and 3 mM MgCl₂ for 5 min at 37 °C. After the addition of the indicated amounts of RPA in 0.5 µl of storage buffer, reaction mixtures were incubated at 37 °C for another 5 min before the incorporation of dsDNA (30 µM) in 1 µl of TE and 1 µl of 50 mM spermidine hydrochloride. The reaction mixtures were incubated at 37 °C and stopped by the addition of an equal volume of 1% SDS containing 1 mg/ml proteinase K. Deproteinization of the reaction mixtures was carried out at 37 °C for 20 min. After the addition of 0.2 volume of gel loading buffer, samples were run in 0.9% agarose gels in TAE buffer, stained with ethidium bromide for 60 min, and then destained for at least 4 h in a large volume of H₂O. Images were recorded in a NucleoTech Gel documentation system and analyzed with the software provided. In the time course experiments, the reaction mixtures were scaled up accordingly, and 6-µl portions of the mixtures were withdrawn for analysis at each time point.

Co-addition of Components-- Reaction mixtures (12.5 µl final volume) containing the indicated amounts of Rad51, Rad52, and RPA were incubated on ice for 45 min, followed by the addition of X ssDNA. The reaction mixtures were then incubated at 37 °C for 10 min, followed by the incorporation of the linear dsDNA and spermidine, as described in the standard reaction above.

Oligonucleotide-based System-- In Fig. 6A, 1.0 µM Rad51 or Rad51-Rad52 complex was incubated with Oligo 2 (3 µM) in 10.5 µl of buffer R containing 20 mM KCl, 2.5 mM ATP, and 3 mM MgCl₂ at 37 °C for 5 min, followed by the addition of 1 µl of 50 mM spermidine and the homologous duplex (6 µM) consisting of unlabeled Oligo 1 and ³²P-labeled Oligo 2 in 1 µl. At the indicated times, 4 µl of the reaction mixture was deproteinized and resolved in a 10% polyacrylamide gel in TAE buffer, which was dried onto a sheet of DEAE paper, and the DNA species was quantified in a PhosphorImager. In the experiment in Fig. 7, A and B, unlabeled Oligo 2 (3 µM) was incubated with Rad51 or Rad51-Rad52 complex in 10 µl of buffer R at 37 °C for 5 min before an increasing concentration of RPA (0.07, 0.14, 0.28, and 0.56 µM) was added in 0.5 µl. After a further 5 min, 1 µl of 50 mM spermidine hydrochloride and the homologous ³²P-labeled duplex in 1 µl were incorporated to complete the reactions (12.5 µl final volume). Alternatively, Oligo 2 was co-incubated in 10.5 µl of buffer R with RPA and Rad51 or Rad51-Rad52 complex for 5 min or preincubated with RPA for 5 min before Rad51 or Rad51-Rad52 complex was added and then followed by an additional 5 min of incubation. Subsequent to the addition of labeled duplex DNA and spermidine, all the reaction mixtures (12.5 µl final volume) were incubated at 37 °C for 15 min before being deproteinized and analyzed in 10% polyacrylamide gels in TAE buffer. The gels were dried and the DNA species quantified in the PhosphorImager.

Rescue of Strand Exchange with Non-homologous Duplex

All the reaction mixtures in the experiment in Fig. 5 had a final volume of 37.5 µl. In the experiments in panels I and II of Fig. 5A, Rad51 protein (10 µM in panel I and 20 µM in panel II) was preincubated with X ssDNA (30 µM nucleotides) and then with RPA (1.5 µM) as in the standard reaction. Following the preincubations, 1 µl of either TE or TE containing BsaI-linearized pBluescript DNA (75 µM nucleotides) was added to the reaction mixtures, which were incubated at 37 °C for another 2 min, before the X duplex (30 µM nucleotides) and spermidine were incorporated to complete the reaction. In the experiment in panel III of Fig. 5A, Rad51 (10 µM) and Rad52 proteins (2.5 µM) were preincubated with X ssDNA (30 µM nucleotides) and then with RPA (1.5 µM). Following these preincubations, 1 µl of either TE or TE containing linear pBluescript duplex DNA (75 µM nucleotides) was added to the reaction mixtures, which were incubated at 37 °C for 2 additional min before X duplex DNA (30 µM nucleotides) and spermidine were incorporated to complete the reaction. A 6-µl portion of the reaction mixtures was withdrawn at the indicated times and processed for gel electrophoresis.

Self-aggregation Assay

Self-aggregation reaction (25 µl final volume) was carried out by following the order of addition of reaction components and using the buffer described for the standard strand exchange reaction. After the addition of dsDNA, reaction samples were incubated at 37 °C for 2 min and immediately spun at 12,000 × g for 2 min at 25 °C. After centrifugation, 20 µl of the supernatant was mixed with 20 µl of 1% SDS, and 35 µl of 0.5% SDS was added to the pellet fraction to dissolve the precipitated protein-DNA complex. The supernatant and pellet fractions, 8 µl each, were analyzed for their protein contents by SDS-PAGE and Coomassie Blue staining. To examine the DNA contents, a 10-µl portion of the supernatant and pellet fractions was treated with 0.5 mg/ml proteinase K at 37 °C for 20 min and then subjected to agarose gel electrophoresis as described for the strand exchange experiments. Rad51, RPA, and DNA (ss and ds) were omitted from some of the experiments (Fig. 6, C and D), as indicated, and Oligo 2 replaced the X ssDNA in Fig. 6E.

	RESULTS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Effects of RPA and Rad52 on Rad51-mediated Strand Exchange-- We examined the level of strand exchange reaction products (Fig. 1A) by fixing the amount of Rad51 (10 µM), and we varied the concentration of RPA (0.4-2.8 µM), added either with Rad51 (Fig. 1B, panel I) or after Rad51 has already nucleated onto the ssDNA (Fig. 1B, panel II), as in the standard reaction. At levels of RPA of 2 µM and above, pronounced inhibition of the reaction was observed with the co-addition of components (Fig. 1, B and C). However, at amounts of RPA lower than 2 µM, the extent of suppression of reaction products was much less severe (Fig. 1, B and C). It seems likely that at lower concentrations of RPA, enough Rad51 can still nucleate onto the ssDNA to prime the assembly of the presynaptic nucleoprotein filament.

View larger version (27K): [in this window] [in a new window]   Fig. 1.   Effect of order of addition of Rad51 and RPA on the efficiency of homologous DNA pairing and strand exchange. A, schematic of the homologous DNA pairing and strand exchange reaction. Pairing between the input X viral (+) strand and linear duplex yields a joint molecule, which is processed by strand exchange to produce the final products, nicked circular duplex and displaced ssDNA. B, increasing amounts of RPA (0, 0.4, 0.8, 1.2, 1.6, 2, 2.4, and 2.8 µM in lanes 2-9, respectively) was added together with Rad51 protein to the ssDNA (I) or to preformed Rad51-ssDNA nucleoprotein filament (II). After the incorporation of linear duplex DNA, reaction mixtures were incubated for 40 min before being deproteinized and analyzed by agarose gel electrophoresis to examine the level of pairing and strand exchange products. The concentrations of the other reactants were as follows: Rad51, 10 µM; ssDNA, 30 µM nucleotides; dsDNA, 30 µM nucleotides. jm, joint molecules; nc, nicked circular duplex; ds, input linear duplex; ss, viral (+) strand and displaced linear (+) strand. C, graphical representation of the results shown in B. , level of products obtained in the reaction wherein Rad51 and RPA were added to ssDNA at the same time, as shown in panel I of B; , level of products obtained in the standard reaction as shown in panel II of B. D, strand exchange reactions in which Rad51 (10 µM) and RPA (2 µM) were added together to the ssDNA (30 µM) either without () or with () Rad52 protein (1.2 µM). The results from a standard reaction in which the ssDNA was preincubated with Rad51 are also plotted () for reference. The concentration of dsDNA was 30 µM nucleotides in all the incubations.

We have previously described expression of Rad52 in yeast and its purification to near-homogeneity (15). Since much larger amounts of functionally active and nearly homogeneous Rad52 can be obtained by expression in E. coli (12, 13, 22), we have since used the E. coli system for purifying Rad52 (22). As indicated from recent work (12, 13, 15) and reiterated here (Fig. 1D), the addition of Rad52 at an amount substoichiometric (1.2 µM) to that of Rad51 (10 µM) restored strand exchange to a level comparable to what was obtained in the standard reaction (Fig. 1D). Rad52 by itself, with or without RPA, is devoid of homologous DNA pairing activity (12, 13, 15).

Rad52 Is Multimeric and Forms a Stable, Stoichiometric Complex with Rad51-- As shown in Fig. 2A, panel I, Rad51 (43 kDa) eluted from a Sepharose 6B column with an average V_e/V_t (elution volume/total column volume) of ~0.7, which is slightly before the elution position of catalase (232 kDa), suggesting a multimeric structure under the conditions used. Rad52 (56 kDa) eluted from Sepharose 6B with an average V_e/V_t of ~0.6, slightly before the elution volume of thyroglobulin (669 kDa), indicating that Rad52 also exists as a multimeric structure (Fig. 2A, panel II); the same results were obtained with Rad52 purified from yeast cells (data not shown).

View larger version (40K): [in this window] [in a new window]   Fig. 2.   A stable, stoichiometric complex of Rad51 and Rad52. A, complex formation revealed by sizing. Rad51 protein (I) and Rad52 protein (II) were filtered through a column of Sepharose 6B. In the experiment in panel III, equimolar amounts of Rad51 and Rad52 proteins were mixed, incubated on ice for 1 h, and then filtered, and in panel IV, a mixture of Rad52 and 5 molar excess of Rad51 was incubated on ice for 1 h and then filtered. Identification of the protein peaks was done by immunoblotting of the column fractions. To calibrate the sizing column, a mixture of thyroglobulin (TG; 669 kDa) and catalase (CAT; 232 kDa) was filtered. The column void was determined by filtering dextran blue (DB; >2,000 kDa). I, the input material. B, complex formation revealed by binding to nickel-agarose. Rad51 alone, Rad51 with 4 molar excess of Rad52 (1:4), 1.2 molar excess of Rad51 with Rad52 (1.2:1), and 3 molar excess of Rad51 with Rad52 (3:1) were incubated with nickel-NTA-agarose, and bound proteins were eluted with SDS. The input materials (I) and the SDS eluates (E) were run in a 10% denaturing polyacrylamide gel followed by staining with Coomassie Blue. C, ATP has no measurable effect on complex formation. Rad51 alone, or a mixture of Rad51 and Rad52 at equimolar ratio, was mixed with nickel-agarose in buffer that contained ATP and magnesium or with the ATP and magnesium omitted, and the bound proteins were analyzed as described in B.

When mixed with an equimolar amount of Rad52, the majority of Rad51 (>85%) emerged from the sizing column at a much earlier position (average V_e/V_t of ~0.55) than free Rad51 (V_e/V_t of ~0.7). Consistent with the formation of a stable complex of Rad51 and Rad52, the Rad52 peak was also shifted slightly (Fig. 2A, panel III). When the amount of Rad52 was lowered to one-fifth of the previous level, the portion of the Rad51 shifted to the earlier elution position dropped accordingly to about 20% of the total (see Fig. 2A, panel IV). Similarly, when Rad52 was fixed at the previous level but with the amount of Rad51 being increased five times, the portion of Rad51 found in association with Rad52 was once again about 20% of the total (data not shown). Thus, Rad51 and Rad52 form a stable complex consisting of approximately equimolar amounts of the two proteins. Judging from the elution position of the Rad51-Rad52 complex, it appears that the complex contains multiple molecules of the two proteins.

Complex formation between Rad51 and Rad52 was also examined by mixing different molar amounts of the two proteins and then immobilizing the complex on nickel-NTA-agarose through the histidine tag on Rad52. The results shown in Fig. 2B are again consistent with an approximately equimolar complex between Rad51 and Rad52. The addition of ATP and magnesium did not alter the amount or the stoichiometry of Rad51-Rad52 complex formed, assessed both by immobilizing the complex via the histidine tag on Rad52 (Fig. 2C) or by sizing in Sepharose 6B (data not shown).

Rad52 Targets Rad51 to ssDNA-- The same molar concentrations of Rad51, Rad52, and Rad51-Rad52 complex were incubated with a mixture of ssDNA and dsDNA in the presence of ATP and magnesium, and nucleoprotein complexes were separated from free DNA in an agarose gel and visualized by staining with ethidium bromide. Fig. 3A shows that both Rad52 and the Rad51-Rad52 complex bound specifically to the ssDNA. The experiment presented in Fig. 3A was done in the presence of ATP and magnesium, but we have detected no difference in terms of the amount of ssDNA shifted or the binding specificity of the Rad51-Rad52 complex when ATP was omitted from the reaction mixture (Fig. 3B). No significant shifting of either the ss or ds form of DNA was observed with the concentrations of Rad51 used (Fig. 3A). Much higher concentrations of Rad51 are needed to see ATP-dependent binding to the ssDNA and dsDNA (Fig. 3C).

View larger version (33K): [in this window] [in a new window]   Fig. 3.   Rad52 targets Rad51 to ssDNA. A, DNA mobility shift experiments that used a mixture of ssDNA (30 µM nucleotides) and dsDNA (20 µM nucleotides) and increasing concentrations of Rad51, Rad52, and pre-assembled Rad51-Rad52 complex (0.05 µM in lanes 2, 6, and 10; 0.1 µM in lanes 3, 7, and 11; 0.2 µM in lanes 4, 8, and 12; 0.3 µM in lanes 5, 9, and 13) in reaction buffer that contained ATP and magnesium. B, Rad51-Rad52 complex (0.2 µM in lanes 2, 6, and 10; 0.3 µM in lanes 3, 7, and 11; 0.4 µM in lanes 4, 8, and 12; 0.5 µM in lanes 5, 9, and 13) was incubated with ssDNA (30 µM nucleotides) and dsDNA (20 µM nucleotides) in buffers that contained ATP and magnesium (lanes 2-5), with magnesium only (lanes 6-9), or with both ATP and magnesium omitted (lanes 10-13), as indicated. C, DNA mobility shift experiments that used a mixture of ssDNA (30 µM nucleotides) and dsDNA (20 µM nucleotides) and an increasing concentration of Rad51 (2 µM in lanes 2, 6, and 10; 4 µM in lanes 3, 7, and 11; 6 µM in lanes 4, 8, and 12; 8 µM in lanes 5, 9, and 13), done in buffers that contained ATP and magnesium (lanes 2-5), with magnesium only (lanes 6-9), or with both ATP and magnesium omitted (lanes 10-13), as indicated. D, binding of Rad51 protein to ssDNA cellulose via complex formation with Rad52. Rad51, Rad52, and the Rad51-Rad52 complex (0.45 µM each) were mixed with ssDNA cellulose, which was washed with 300 mM KCl, and then treated with 3% SDS to elute bound proteins. The content of Rad51 and Rad52 in the various fractions was determined by immunoblot analysis. I, input material; S, supernatant after mixing with ssDNA cellulose; W, the KCl wash; E, SDS eluate.

In the DNA mobility shift experiments (Fig. 3, A and B), we could not ascertain that Rad51 was present in the nucleoprotein complex. To demonstrate directly that Rad51 is being targeted to ssDNA by Rad52, we co-incubated Rad51 and Rad52 with ssDNA cellulose and then analyzed the bound proteins by immunoblot analyses after their elution from the matrix by SDS treatment. Under the same conditions, Rad51 alone did not bind to ssDNA cellulose, but Rad52 alone did (Fig. 3D). Importantly, very similar amounts of Rad51 and Rad52 proteins were found in the ssDNA cellulose eluates, indicating that Rad51 bound along with Rad52 to the ssDNA on the matrix. In these experiments, ATP and magnesium were added to all the buffers used. However, the same results were obtained when either ATP or magnesium was omitted from the buffers (data not shown). Taken together, the results suggest that Rad51 is being targeted to ssDNA via complex formation with Rad52.

Excessive Rad52 Inhibits DNA Strand Exchange-- Interestingly, quantities of Rad52 in excess of what was required to give maximal restoration of strand exchange in fact resulted in pronounced inhibition of the reaction. Specifically, at 3 µM Rad52, the level of reaction products was reduced more than 10-fold compared with the maximally restored level (Fig. 4, A and B). This inhibitory effect of Rad52 was also seen in experiments wherein RPA was incorporated after a preincubation of Rad51 and Rad52 with the ssDNA template (data not shown).

View larger version (13K): [in this window] [in a new window]   Fig. 4.   Opposite effects of Rad52 on DNA strand exchange. A, strand exchange reactions in which Rad51 (10 µM), RPA (2 µM), and increasing concentrations of Rad52 protein (0, 0.25, 0.5, 1, 1.5, 2, 2.5, and 3 µM in lanes 2-9, respectively) were preincubated on ice 45 min and added together to the ssDNA (30 µM nucleotides). After the incorporation of the dsDNA (30 µM nucleotides), the reaction mixtures were incubated for 60 min. The 60-min time point of a standard strand exchange reaction is also shown (lane 10; Std). jm, joint molecules; nc, nicked circular duplex; ds, input linear duplex; ss, viral (+) strand and displaced linear (+) strand. B, the results in A are plotted. C, Rad51 protein (10 µM) without () or with 4 µM Rad52 protein () were assayed for ATPase activity in the presence of ssDNA (30 µM nucleotides). ATP hydrolysis by Rad51 without () or with 4 µM Rad52 protein () was also examined in the absence of ssDNA.

We considered the possibility that the suppression of strand exchange by excessive Rad52 might have been due to an exclusion of Rad51 from the ssDNA substrate. Since Rad52 by itself has no ATPase activity and the ssDNA-dependent ATPase activity of Rad51 provides a reliable means for estimating the level of Rad51-ssDNA nucleoprotein filament (8), we measured the Rad51-mediated ssDNA-dependent ATP hydrolysis in the presence of increasing amounts of Rad52 protein; the results of this experiment are shown in Fig. 4C. We found that an amount of Rad52 (4 µM) that would result in almost complete inhibition of pairing and strand exchange did not cause any noticeable inhibition of the Rad51 ATPase activity, strongly suggesting that Rad51 can still gain access to the ssDNA even when Rad52 is present in excess. Consistent with this deduction, we have found that a preassembled Rad51-Rad52 complex shows the same level of ssDNA-dependent ATPase activity as free Rad51 (data not shown).

Rad51 above the level of three nucleotides per protein monomer inhibits strand exchange by binding the duplex molecule (6), and this inhibition is effectively reversed by the addition of the unrelated pBluescript dsDNA to the reaction (Fig. 5, panel II in A and B). Since Rad52 also binds dsDNA, albeit with a much lower affinity than binding to ssDNA (Ref. 24, Fig. 3A), we thought it was possible that the inhibition of strand exchange by excessive Rad52 might have been due to coating of the dsDNA by Rad52. However, the addition of a relatively large amount of pBluescript dsDNA to reaction mixtures containing an inhibitory level of Rad52 did not restore strand exchange (Fig. 5, panel III in A and B; data not shown). We also considered the possibility that an excess of Rad52 may bind to and sequester RPA from the ssDNA, as an interaction between Rad52 and RPA has been described (24, 25). However, increasing the RPA concentration to exceed that of Rad52 was also completely ineffective in restoring strand exchange, regardless of whether the excess of RPA was added with Rad51 and Rad52 to the ssDNA or after a preincubation of Rad51 and Rad52 with the ssDNA (data not shown).

View larger version (30K): [in this window] [in a new window]   Fig. 5.   Inhibition by excessive Rad52 cannot be overcome by heterologous dsDNA. A, panel I, time course of strand exchange reactions in which Rad51 (10 µM) was preincubated with ssDNA (30 µM) and then with RPA (1.5 µM) before the homologous dsDNA (30 µM nucleotides) was added. In lanes 6-9, 2 min prior to the incorporation of the homologous dsDNA, pBluescript dsDNA (75 µM nucleotides) was added to the reaction mixture. Panel II, strand exchange reactions were set up exactly as described in panel I, except that the concentration of Rad51 protein was increased to 20 µM. Panel III, strand exchange reactions were set up as described in panel I, except that 2.5 µM Rad52 was added with Rad51 to the ssDNA. jm, joint molecules; nc, nicked circular duplex; ds, input linear duplex; ss, viral (+) strand and displaced linear (+) strand; pBS, pBluescript linear dsDNA. B, the results in panels I-III in A are plotted in panels I-III, respectively. , reactions without pBluescript DNA; , reactions with pBluescript DNA.

Inhibition by Rad52 Is Likely Due to Intramolecular Aggregation-- One possible explanation for the inhibition seen (Figs. 4A and 5A) was that Rad51-Rad52 complex was inactive in DNA strand exchange and that an excess of it could impair the functionality of the nucleoprotein filament. If this was the cause of inhibition seen with the X substrates, then the complex of Rad51-Rad52 should be inactive in the strand exchange system that employs oligonucleotide-based substrates. To test directly this idea, we assembled and purified the Rad51-Rad52 complex (see "Experimental Procedures") and then compared its ability to promote strand exchange between oligonucleotide-based substrates to that of Rad51. Surprisingly, the Rad51-Rad52 complex was just as active as free Rad51 in promoting strand exchange between the oligonucleotide-based substrates, regardless of whether relatively low concentrations of reactants (3 µM ssDNA, 6 µM dsDNA, 1 µM Rad51 or Rad51-Rad52 complex, as shown in Fig. 6A) or 10 times higher concentrations of reactants were used (data not shown). These results indicate that there is no functional deficit in the Rad51-Rad52 complex compared with free Rad51 in strand exchange activity.

View larger version (29K): [in this window] [in a new window]   Fig. 6.   Rad52 inhibits X DNA-based strand exchange via intramolecular aggregation. A, Rad51-Rad52 complex is active in strand exchange using oligonucleotide substrates. Rad51 or Rad51-Rad52 complex, 1 µM each, was incubated with the oligonucleotide substrates for the indicated times. Strand exchange between the unlabeled oligonucleotide (3 µM nucleotides) and the 32P-labeled homologous duplex (6 µM nucleotides) yields a radiolabeled oligonucleotide (displaced ss), which was resolved from the duplex by electrophoresis in a polyacrylamide gel and visualized by autoradiography of the dried gel in I. The gel was also subject to phosphorimage analysis to yield data points for the graph in II. Symbols used in panel II: , reaction with Rad51; , reaction with Rad51-Rad52 complex. B, aggregation of X ssDNA, Rad51, and Rad52. Strand exchange reactions with final volumes of 25 µl containing ssDNA (30 µM nucleotides), dsDNA (30 µM nucleotides), RPA (2 µM), Rad51 (10 µM), and with no Rad52 (lanes 1 and 2), 1.3 µM Rad52 (lanes 3 and 4), or 3 µM Rad52 (lanes 5 and 6) were incubated at 37 °C for 2 min and then centrifuged at 12,000 × g for 2 min at 25 °C. After centrifugation, 20 µl of the supernatant (S) was mixed with an equal volume of 1% SDS, whereas the material that remained in the tubes was mixed with 35 µl of 0.5% SDS and designated the pellet fraction (P). Portions of these fractions were analyzed by agarose gel electrophoresis for their DNA contents (I) and by SDS-PAGE for their protein contents (II), as shown. C, Rad52-mediated aggregation is DNA-dependent. Reactions containing Rad51 (10 µM), Rad52 (3 µM), RPA (2 µM), and with or without ssDNA (30 µM nucleotides) were assayed for aggregation. The supernatant (S) and pellet (P) fractions were analyzed for their protein contents. D, aggregation occurs with Rad52 alone and is DNA-dependent. Reaction mixtures containing 3 µM Rad52 protein and ssDNA (30 µM nucleotides) were assayed for aggregation. Symbols are the same as in C. E, aggregation does not occur with an oligonucleotide. Rad51 (10 µM), Rad52 (3 µM), and RPA (2 µM) were incubated with or without Oligo 2 (30 µM nucleotides), centrifuged, and the supernatant (S) and pellet (P) fractions were analyzed for their protein contents. B, C, and E, only the largest subunit of RPA is shown.

As expected, purified Rad51-Rad52 complex was completely inactive in the strand exchange system that employs X DNAs, with or without RPA (data not shown). Thus, it appears that the inhibitory effect of Rad52 on strand exchange is specific for long DNA molecules, as we did not observe strand exchange inhibition with short oligonucleotide substrates (Fig. 6A). Because of this observation, we considered the possibility that perhaps multimers of Rad52 have a tendency to interact with one another, thereby sequestering Rad51 and ssDNA through intramolecular aggregation. Indeed, when reaction mixtures containing increasing amounts of Rad52 were spun for a brief time in a bench top centrifuge, we found a Rad52 concentration-dependent aggregation of Rad51, Rad52, and ssDNA in a form recoverable in the bottom of the Eppendorf tubes (Fig. 6B). At 3 µM Rad52 (10 nucleotides per Rad52 monomer), where complete inhibition of strand exchange occurs, essentially all of the ssDNA and Rad51 co-aggregated with Rad52, whereas the expected amount of the duplex DNA remained in the supernatant (Fig. 6B, lanes 5 and 6). The amount of RPA that co-aggregated with the other reaction components varied between experiments but in general was much less than the amount of co-aggregating Rad51, Rad52, and ssDNA. The aggregation seen was induced by binding of Rad52 to the ssDNA because (i) in the absence of ssDNA the protein components remained in the supernatant after centrifugation (lanes 1 and 2 in Fig. 6, C and D), (ii) Rad52 by itself underwent DNA-dependent aggregation (lanes 3 and 4 in Fig. 6D), and (iii) Rad51, with or without RPA, did not undergo aggregation (lanes 1 and 2 in Fig. 6B, data not shown).

We have also examined whether relatively high amounts of Rad52 would inhibit strand exchange when the concentrations of the reactants were one-third those used in Fig. 6B. In these experiments, Rad52 again inhibited strand exchange when its concentration exceeded a ratio of 15 nucleotides per protein monomer, resulting in Rad51-Rad52-ssDNA aggregates that were readily pelleted by a brief spin in a microcentrifuge (data not shown). As expected, incubation of concentrations of Rad52 protein and the oligonucleotide used in strand exchange experiments did not result in aggregate formation (Fig. 6E), confirming that Rad52-mediated co-aggregation of Rad51 and ssDNA occurs efficiently only with long DNA molecules and that this aggregation results in inactivation of strand exchange.

Rad51-Rad52 Complex Can Utilize a Template Coated with RPA for Homologous Pairing-- The fact that Rad51-Rad52 complex is active in DNA strand exchange on oligonucleotide-based DNA substrates allows us to test whether or not it has the ability to utilize a template that is already saturated with RPA for pairing with the homologous duplex. For this purpose, we first carried out a titration experiment in which a fixed amount of ss oligonucleotide had been incubated with increasing concentrations of RPA before being mixed with Rad51 and the homologous duplex. The results from this experiment indicated that at a ratio of 20 nucleotides per RPA monomer, inhibition of homologous DNA pairing occurred (Fig. 7A), which is consistent with the result obtained using full-length X DNA (Fig. 1). As shown in Fig. 7B, when the Rad51-Rad52 protein complex was added to the oligonucleotide template precoated with RPA, a pairing reaction as robust as the ones that used either Rad51 or Rad51-Rad52 complex without RPA was seen. Since Rad51 alone is incapable of utilizing RPA-coated oligonucleotide for strand exchange, these results suggest that the Rad51-Rad52 complex has the ability to displace bound RPA off the DNA template.

View larger version (15K): [in this window] [in a new window]   Fig. 7.   Rad51-Rad52, but not Rad51, can utilize an RPA-coated ssDNA template for homologous pairing. A, homologous pairing reactions that used oligonucleotides (3 µM ss and 6 µM homologous duplex) with Rad51 protein (1 µM), in which increasing concentrations of RPA (0.07, 0.14, 0.28, and 0.56 µM) were either preincubated with the ss oligonucleotide (), added with Rad51 to the ss oligonucleotide (), or added after the ss oligonucleotide had been preincubated with Rad51 (). B, Rad51-Rad52 complex (1 µM) and oligonucleotide substrates (3 µM ss and 6 µM homologous duplex) were used in the strand exchange reactions. In these reactions, increasing concentrations of RPA (0.07, 0.14, 0.28, and 0.56 µM) were either preincubated with the ss oligonucleotide (), added with Rad51-Rad52 complex to the ss oligonucleotide (), or added after the ss oligonucleotide had been preincubated with Rad51-Rad52 complex (). After the addition of the 32P-labeled duplex, reaction mixtures were further incubated at 37 °C for 15 min. The reaction mixtures were resolved in 10% polyacrylamide gels, and the reaction products were quantified in the PhosphorImager.

Co-incubation of Rad51 and RPA also resulted in inhibition of the pairing reaction mediated by Rad51, although not to the same extent as when RPA was preincubated with the ssDNA substrate (Fig. 7A). As expected, RPA did not inhibit homologous pairing when added together with the Rad51-Rad52 complex to the ssDNA substrate (Fig. 7B) or added after Rad51 has already nucleated onto the oligonucleotide (Fig. 7A).

Rad52 Does Not Replace RPA nor Does It Lower the Dependence of Strand Exchange on RPA and Rad51-- Human Rad52 enhances the efficiency of homologous DNA pairing when human RPA is absent and human Rad51 is limiting relative to the ssDNA (26). To examine whether yeast Rad52 would exert a similar stimulatory effect on yeast Rad51, we fixed the quantity of the ssDNA and used a wide range of Rad51 concentrations from ratios of 7.5 nucleotides/protein monomer to 1.9 nucleotides/protein monomer, with or without Rad52 at below the optimal level to above the optimal level for its mediator function. As shown previously (6), elevating the level of Rad51 up until three nucleotides per Rad51 monomer results in increasing extent of pairing and strand exchange, whereas exceeding this amount of Rad51 results in progressive inhibition (Fig. 8, A and B). Unexpectedly, at and above Rad52 levels optimal for its mediator function, a highly significant depression of pairing and strand exchange occurred at the lower concentrations of Rad51 (Fig. 8A, panels III and IV). Thus, Rad52 actually suppresses the strand exchange reaction at low concentrations of Rad51, a result opposite to that observed for human RAD51 and RAD52 (26).

View larger version (24K): [in this window] [in a new window]   Fig. 8.   Effects of Rad52 on the dependence of strand exchange on Rad51. A, panel I shows strand exchange reactions in which increasing concentrations of Rad51 protein (4, 6, 8, 10, 12, and 16 µM in lanes 2-7, respectively) were preincubated with ssDNA (30 µM nucleotides) before the incorporation of RPA (1.5 µM), followed by dsDNA (30 µM nucleotides). The reactions in panels II-IV were set up exactly as described for panel I, except that 0.8, 1.2, and 1.8 µM Rad52 was added with Rad51 to the ssDNA in II-IV, respectively. The reaction time for these strand exchange experiments was 60 min. jm, joint molecules; nc, nicked circular duplex; ds, input linear duplex; ss, viral (+) strand and displaced linear (+) strand. B, the results shown in A are plotted: , results in I; , results in II; , results in III; , results in IV.

In the absence of RPA, the level of joint molecules increased from ~5% after 90 min of reaction with Rad51 alone to ~11% in the presence of 1.2 µM Rad52, and the amount of nicked circular duplex also increased from less than 1 to 3% at this amount of Rad52 (Fig. 9, A and B). The stimulation of Rad51 strand exchange activity by Rad52 is insignificant compared with that afforded by RPA. Interestingly, in the absence of RPA, concentrations of Rad52 at 2 µM and above also resulted in progressive inhibition of the reaction, such that at 3.2 µM Rad52, little reaction product was seen (Fig. 9, A and B). As shown earlier (Fig. 6), the inhibition of strand exchange is due to intramolecular aggregation mediated by Rad52. We have also investigated whether Rad52 would lessen the dependence of the pairing and strand exchange reaction on RPA (Fig. 9, C and D), but we have found that Rad52 at a level optimal for its mediator function has no measurable effect on the RPA requirement (Fig. 9C, panel II), and higher Rad52 amounts progressively inhibit strand exchange at all concentrations of RPA tested (Fig. 9C, panel III; data not shown).

View larger version (25K): [in this window] [in a new window]   Fig. 9.   Rad52 and RPA serve distinct roles in strand exchange. A, Rad52 does not replace RPA. Rad51 protein (10 µM) and increasing concentrations of Rad52 protein (0, 0.8, 1.2, 1.6, 2.0, 2.4, 2.8, and 3.2 µM in lanes 2-9, respectively) were used in strand exchange reactions without RPA. The Rad51 and Rad52 proteins were preincubated on ice for 45 min before the ssDNA was incorporated. The incubation time for this experiment was 90 min. The 60-min time point from a standard reaction in which Rad51 was preincubated with ssDNA without Rad52 followed by the addition of RPA is shown in lane 10 for comparison. jm, joint molecules; nc, nicked circular duplex; ds, input linear duplex; ss, viral (+) strand and displaced linear (+) strand. B, the results in lanes 2-9 of A are plotted. C, Rad52 does not lower dependence of strand exchange on RPA. Panel I, Rad51 protein (10 µM) was preincubated with ssDNA (30 µM nucleotides) before the incorporation of increasing concentrations of RPA (0.2, 0.4, 0.6, 0.8, 1, and 1.2 µM in lanes 2-7, respectively), followed by dsDNA (30 µM nucleotides). The reactions in panels II and III were set up exactly as described for panel I, except that 1.2 and 1.8 µM Rad52 protein was added with Rad51 to the ssDNA in II and III, respectively. The reaction time for these strand exchange experiments was 45 min. jm, joint molecules; nc, nicked circular duplex; ds, input linear duplex; ss, viral (+) strand and displaced linear (+) strand. D, the results shown in C are plotted: , results in I of C; , results in II of C; and , results in III of C.

	DISCUSSION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Rad52 as Mediator of Strand Exchange-- Since the RAD52 gene is indispensable for recombination and the Rad52 protein interacts with Rad51 in a two-hybrid system (27) and in vitro (Refs. 4 and 15 and this work), it seems possible that Rad52 protein may help overcome the competition posed by RPA for binding to ssDNA. Consistent with this idea, the inclusion of Rad52 protein in a pairing and strand exchange reaction neutralizes the inhibitory effect of RPA (12, 13, 15). New et al. (12) have also demonstrated that a RecA-mediated strand exchange reaction is in fact inhibited by the inclusion of Rad52 protein. Taken together, the biochemical studies have indicated that Rad52 protein fulfills the role of a molecular mediator, functionally linking the Rad51 recombinase and the ssDNA binding factor RPA (15, 16).

The results from our immunoprecipitation studies have revealed that (i) Rad52 is of lower abundance than Rad51 protein, (ii) the majority or maybe all of the cellular Rad52 protein is associated with Rad51, and (iii) the majority of cellular Rad51 is in fact free from Rad52 (15). In apparent congruence with the immunoprecipitation data, we have demonstrated that in mediating the reversal of inhibition by RPA, amounts of Rad52 protein substoichiometric to that of Rad51 are already sufficient for the full restoration of pairing and strand exchange. We have presented results from sizing experiments that indicate a multimeric nature of Rad52 protein and that the Rad52 multimer forms a stable, approximately equimolar complex with Rad51 protein. Since maximal mediator activity is seen at Rad52 amounts about one-seventh to one-tenth that of Rad51, we deduce that perhaps only a small fraction of Rad51 is stably associated with Rad52 protein under conditions of maximal restoration of DNA strand exchange.

Rad52 binds both ssDNA and dsDNA but shows higher affinity for ssDNA (Refs. 22 and 24, Fig. 3A). Whereas free Rad51 protein by itself requires ATP to bind to DNA, with apparently an equal affinity for ssDNA and dsDNA, the Rad51-Rad52 complex does not need ATP to bind DNA and appears to show a much higher affinity for ssDNA than dsDNA. It is apparent that in the presence of ATP, Rad51 is in contact with the DNA, as indicated by a normal level of ATPase activity (Fig. 4C). However, we do not yet know whether actual loading of Rad51 present in the Rad51-Rad52 complex to the ssDNA requires ATP binding and hydrolysis and whether upon binding of Rad51 to the ssDNA, Rad52 is displaced off the DNA substrate.

Although Rad52 protein enhances the level of pairing and strand exchange reaction products in the absence of RPA, even the maximally stimulated level is rather insignificant compared with what can be achieved with RPA (Fig. 9). The results from other related experiments have also indicated that the presence of Rad52 protein does not alter the amount of RPA required for maximal pairing and strand exchange (Fig. 9, C and D), thus eliminating the possibility Rad52 might have acted synergistically with RPA in the removal of secondary structure in the ssDNA substrate. We also considered the possibility that Rad52 protein may in fact lessen the reliance of the DNA strand exchange reaction on the Rad51 protein, especially that such an effect of human Rad52 on the equivalent reaction mediated by the human RAD51 protein has recently been reported by Benson et al. (26). In contrast to what has been observed with the equivalent human recombination factors, not only that yeast Rad52 does not lower the dependence of strand exchange on Rad51, it in fact suppresses this reaction significantly at suboptimal concentrations of Rad51 protein (Fig. 8, A and B). At suboptimal levels of Rad51 and without Rad52, we suspect that Rad51 could bind cooperatively to some of the ssDNA molecules and thus assemble into a limited number of functional presynaptic filaments. In the presence of Rad52 protein, however, the Rad51-Rad52 complex may nucleate randomly onto all of the ssDNA molecules and prime the assembly of partial Rad51 filaments that have only a limited ability to mediate pairing and strand exchange.

Recently, an inverse DNA strand exchange reaction mediated by a RecA-dsDNA complex was reported (34). We have examined the possibility that Rad52 protein bound to a ss oligonucleotide may function with a Rad51-ds oligonucleotide complex in a similar inverse strand exchange reaction. The results indicate that the nucleoprotein complex of Rad51 with ds oligonucleotide has at most a low level of strand exchange activity. More importantly, Rad52 prebound to ssDNA in fact suppresses this already negligible level of strand exchange further.² Although the results do not eliminate the possibility that Rad51 could promote limited inverse strand exchange, they indicate that Rad52 bound to ssDNA does not enhance a possible inverse strand exchange reaction. We have also tested whether Rad52 prebound to a ds oligonucleotide would enhance strand exchange with the Rad51-ss oligonucleotide complex. The results indicate that Rad52 suppresses strand exchange when bound to duplex oligonucleotide.²

How May Rad52 Work?-- Thus, Rad52 and RPA fulfill highly specialized functions in Rad51-mediated strand exchange, with RPA acting primarily to melt secondary structure in the ssDNA template and Rad52 functioning to facilitate Rad51-ssDNA nucleoprotein filament assembly when RPA is competing for binding sites on the template. Collectively, the results suggest that a preassembled, multimeric complex consisting of Rad51 and Rad52 binds to available sites on the ssDNA substrate, and we speculate that the DNA-bound Rad51-Rad52 complex could play two distinct roles to maximize the likelihood of assembling a functional presynaptic filament. First, the Rad51-Rad52 complex could displace RPA from the ssDNA within the vicinity of its initial loading site(s). Second, the stably bound Rad51-Rad52 complex could provide a priming effect for the recruitment of free Rad51 molecules. The growing chain of Rad51 protein filament then gradually displaces the bound RPA molecules in its path without additional assistance from Rad52 protein. It seems reasonable to suggest that the multimeric structure of Rad52 protein is relevant for its mediator function. Possibly, the oligomeric structure noted enables Rad52 protein and the Rad51-Rad52 complex to make multiple contacts with the DNA, resulting in a higher affinity of these protein species for DNA and enhanced stability of the nucleoprotein complexes that form. In addition, it is conceivable that the oligomeric structure helps ensure that one single nucleation event will lead to the loading of multiple Rad51 molecules onto the ssDNA, thus maximizing the chance for the assembly of a nascent Rad51 filament.

Interestingly, the mediator function of Rad52 described here is very familiar to those of UvsY in bacteriophage T4 and RecO-RecR complex in E. coli. These prokaryotic recombination factors promote the assembly of the recombinase-ssDNA nucleoprotein filament by overcoming the inhibition of an ssDNA-binding protein. The conservation of function of these mediators across divergent species is consistent with their importance in recombination (28).

Our studies have indicated that the complex of Rad55 and Rad57 proteins also functions as a mediator during the presynaptic phase of the pairing and strand exchange reaction. Whereas Rad52 is multimeric and associates stably with Rad51, Rad55-Rad57 is heterodimeric and interacts only weakly with Rad51 (14). Rad55-Rad57 heterodimer may act via a different mechanism or it may assist Rad51 at a stage in the assembly of the presynaptic filament temporally distinct from the reaction step that is dependent on Rad52.

RAD52-specific Recombination-- In addition to functioning as a mediator in Rad51-mediated homologous DNA pairing and strand exchange, Rad52 protein also mediates the annealing of complementary single strands (22) in a reaction that is accelerated by RPA (24, 25). The DNA strand annealing activity of Rad52 is likely to be relevant for its involvement in the single-strand annealing pathway of deletion-associated recombination between direct DNA repeats (see Ref. 29 for a discussion). Rad52 is also involved in a long tract gene conversion pathway known as break-induced replication or BIR (30, 31). In BIR, a heteroduplex DNA joint is formed between an initiating single-strand and a duplex donor molecule at a region of homology, to prime DNA synthesis for copying the genetic information in the donor DNA molecule. Whether or not the ssDNA annealing activity of Rad52 is utilized for making the heteroduplex joint in BIR remains to be determined. Recently, Van Dyck et al. (32) reported that human RAD52 protein binds specifically to the ssDNA tail portion of a partially duplex DNA molecule, consistent with the postulated role of Rad52 in promoting the utilization of the ssDNA tail arising from the end-processing reaction for recombination events in vivo.

	ACKNOWLEDGEMENTS

Michael Cox and Aimee Eggler are gratefully acknowledged for their critical reading of the manuscript and suggestions. We are thankful to Richard Kolodner for the yeast-based RPA overexpression system, to Rodney Rothstein for the plasmid that expresses histidine-tagged Rad52 protein, and to Sabrina Stratton for excellent assistance.

	FOOTNOTES

^* This work was supported by United States Public Health Service Grant ES07061 from the NIEHS and by NIGMS Grant GM57814 from the National Institutes of Health.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: Dept. of Molecular Medicine/Inst. of Biotechnology, University of Texas Health Science Center, 15355 Lambda Dr., San Antonio, TX 78245-3207. Tel.: 210-567-7216; Fax: 210-567-7277; E-mail: sung@uthscsa.edu.

Published, JBC Papers in Press, March 19, 2000, DOI 10.1074/jbc.M910244199

² B. W. Song and P. Sung, unpublished observations.

	ABBREVIATIONS

The abbreviations used are: ssDNA, single-stranded DNA; dsDNA, double-stranded DNA; DTT, dithiothreitol; BSA, bovine serum albumin; MOPS, 4-morpholinepropanesulfonic acid; BIR, break-induced replication; NTA, nitrilotriacetic acid; RPA, replication protein A.

	REFERENCES

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES