Multiple Regulation of Rad51-Mediated Homologous Recombination by Fission Yeast Fbh1

Summary

Homologous recombination is required for repairing DNA double-strand breaks (DSBs), which are induced by exogenous factors such as DNA damaging agents or by endogenous factors such as collapse of DNA replication fork in mitotic cells. If improperly processed, DSBs could lead to chromosome rearrangement, cell death, or tumorigenesis in mammals, and thus HR is strictly controlled at several steps, including Rad51 recombinase-driven DNA strand exchange reaction. Specifically, DNA helicases have been shown to be important for suppression of inappropriate recombination events. In this study, we analyzed one such DNA helicase, fission yeast Fbh1. We used an in vivo single-DSB repair assay to show that Fbh1 suppresses crossover formation between homologous chromosomes. Next, we obtained in vitro evidence that Fbh1 acts as an inhibitor of the strand-exchange reaction in the absence of Swi5-Sfr1, but stimulates the reaction after it starts. Furthermore, we found that SCFFbh1 has ubiquitin-ligase activity toward Rad51 in vitro and that Fbh1 regulates the protein level of Rad51 in the stationary phase. These results suggest Fbh1 regulates Rad51-mediated homologous recombination by its seemingly-unrelated two activities, DNA helicase/translocase and ubiquitin ligase.

Introduction

Homologous recombination (HR), a fundamental biological process in all organisms, involves the exchange of sequence between two homologous DNA molecules. In eukaryotes, HR plays an essential role in generating genetic diversity by exchanging paternal and maternal genomic information during meiosis, and also helps form the physical connections between homologous chromosomes that ensure faithful segregation in meiosis I. On the other hand, during mitotic cell growth, HR is involved in repair of DNA damage such as double-strand breaks (DSBs), or upon collapse of replication forks.

At a very early step in homologous recombination repair (HRR), the ends of a DSB are nucleolytically processed to produce recombinogenic DNA with 3′ single-strand overhangs. Eukaryotic recombinase Rad51 binds the resulting single-stranded DNA (ssDNA) region to form a nucleoprotein filament, and then catalyzes a strand-exchange reaction between the broken end and the homologous sequence, forming a D-loop structure. Auxiliary factors are required to form and activate the presynaptic filament of Rad51 recombinase. One such auxiliary factor is Rad52 (formerly called Rad22 in fission yeast), first identified in the budding yeast Saccharomyces cerevisiae (Sc) and humans; this protein is termed a recombination mediator. Rad52 facilitates Rad51-mediated strand exchange between replication protein A (RPA)–pre-coated ssDNA and homologous double-stranded DNA (dsDNA) [1]–[4]. Several other recombination mediators have been identified, including the Rad51 paralogs Rad55 and Rad57, which form a heterodimeric complex [5], and BRCA2, the product of human breast-cancer susceptibility gene 2 [6].

The Swi5-Sfr1 complex from the fission yeast Schizosaccharomyces pombe (Sp) represents a novel class of auxiliary factor. Both Swi5 and Sfr1 are widely conserved from yeast to humans [7]–[9]. The budding yeast Sae3-Mei5 complex, a homolog of Swi5-Sfr1 that is specifically expressed in early meiosis, has also been proposed to act as a mediator for the meiotic-specific recombinase Dmc1 [10], [11]. Genetic studies in fission yeast have shown that the Rad55-Rad57 and Swi5-Sfr1 complexes act in Rad51 sub-pathways that are independent of each other [7]. In vitro, the Swi5-Sfr1 complex stimulates Rad51 strand-exchange activity [12].

In addition to these auxiliary factors, Rad51-mediated HR is regulated by several DNA helicases such as Fbh1, Srs2, and the RecQ family helicases. Srs2 helicase, a superfamily-1 helicase closely related to bacterial UvrD, has been identified in budding yeast as a suppressor of the DNA damage sensitivity of a rad6 mutants (suppressor of rad six) and a suppressor of hyper-recombination [13]–[15]. Several studies have suggested that Srs2 prevents HR during Rad6–Rad18 post-replication repair in budding yeast [reviewed in [16]]. In addition, Srs2 can disrupt Rad51 filaments and dissociate D-loop structures [17]–[19]. PARI has been identified as a human ortholog of yeast Srs2 [20].

The RecQ family helicases, which include ScSgs1, SpRqh1, HsBLM, HsWRN, and HsRecQL5, play a role in a late step of HR in which the double-Holliday junction is formed; this mature intermediate is dissolved by ScSgs1/HsBLM and topoisomerase III, yielding only non-crossover-type recombinants [21], [22]. Furthermore, BLM and RecQL5 dissociate human Rad51-ssDNA filaments in an ATPase-dependent manner [23], [24].

Fbh1 (F-box DNA helicase-1) was originally identified biochemically as a 3′ to 5′ DNA helicase in fission yeast by Seo and colleagues [25]. Subsequently, we independently cloned the fbh1⁺ gene encoding this protein, which revealed it to be one of the slr genes (slr5), in which mutations are synthetically lethal with the rad2Δ mutation [26]. Whitby and colleagues also identified the same gene as a suppressor of a rad52 mutation [27]. Mutations in either the DNA helicase or F-box motif of Fbh1 cause defects in HRR, suggesting that both the DNA helicase and ubiquitin-ligase activities of Fbh1 are involved in normal HRR [27], [28]. Further genetic studies have revealed that Fbh1 functions in a Rad51-dependent recombination pathway, and that fbh1 mutations are synthetically lethal with srs2Δ or rqh1Δ mutations [26], [27]. Importantly, the lethality of the double mutants is suppressed by deletion of Rad51 or Rad57, implying that toxic HR intermediates produced in a Rad51- and Rad57-dependent manner are resolved by one of these three DNA helicases [26].

Interestingly, Fbh1 does not have a homolog in budding yeast, but homologs exist in multicellular eukaryotes. Genetic studies have implicated Fbh1 as a novel conserved regulator of recombination: Fbh1 suppresses sister chromatid exchange (SCE) and Rad51-mediated recombination at stalled replication forks during mitosis in several species [29]–[34].

The human homolog hFbh1 (originally named Fdh1) exhibits both DNA helicase activity and ubiquitin-ligase activity in vitro [35], [36]. However, it remains unclear how its DNA helicase activity is involved in HR and HRR. In addition, although the hSCF^Fbh1 complex is required in vivo for degradation of the transcription factor Atf1 [37], a lack of Atf1 degradation cannot fully explain the phenotype of fbh1 mutants carrying mutations in the F-box motif, strongly suggesting that Fbh1 ubiquitinates other physiologically important target protein(s).

In this study, we characterized SpFbh1 both in vivo and in vitro to reveal how this protein modulates HR though its helicase/translocase and ubiquitin-ligase activities. First, we showed that Fbh1 suppresses crossover (CO) formation, as revealed by analyses of repair of single DSBs. Second, we purified Fbh1, which could only be recovered as a heterodimer in complex with Skp1, and demonstrated that this complex plays two opposing roles in the DNA strand-exchange reaction: a negative role via disruption of Rad51 filament, and a positive role, via stimulation of the strand-exchange reaction. Finally, we reconstituted an in vitro ubiquitination reaction and showed that SCF^Fbh1 E3 ligase efficiently promotes ubiquitination of Rad51.

Results

Fbh1 suppresses crossover during homologous recombination repair

We first investigated the functional differences among Fbh1, Srs2, and Rqh1 helicases using a site-specific DSBR assay system [38]. In this system, a single DSB is created by HO endonuclease at a 112 bp target site integrated into a nonessential minichromosome, Ch¹⁶-MG, which carries the ade6-M216 allele. This single HO-induced DSB can be repaired by the non-homologous end-joining (NHEJ) pathway or by HRR involving Ch¹⁶-MG and Chromosome III. The various outcomes of induced DSBs can be inferred from the status of selectable markers: HRR yields a cell that is Ade⁺ G418^s or Ade⁻ G418^s (the latter of which can also result from minichromosome loss), whereas NHEJ and sister chromatid conversion (SCC) yields a cell that is Ade⁺ G418^r. Pulsed-field gel electrophoresis (PFGE) analysis of independent Ade⁺ G418^s and Ade⁻ G418^s colonies from each assay can reveal whether HRR-mediated survivors arise by gene conversion (GC), crossover (CO), non-reciprocal exchange (BIR), or long-tract gene conversion (LTGC) (Figure S1) [8], [38]. Note that this assay cannot discriminate between Ade⁺ G418^r segregants arising from NHEJ and SCC [39].

We quantitated the outcomes of single-DSB induction by monitoring G418^r and Ade⁺ marker loss in a colony assay (Table S1). Based on the results, three categories of outcomes (NHEJ/SCC, HRR, and minichromosome loss) are displayed in Table 1. HRR, accounting for 72.9% of the outcomes in the wild-type strain, is a main repair pathway for single DSBs in this assay, as reported previously [8], [38]. HRR was reduced in all deletion mutants of individual helicases (rqh1Δ, srs2Δ, and fbh1Δ), indicating that these helicases are involved in DSB repair mediated by HRR: the rqh1Δ mutation caused the most drastic effect (12.9%), whereas srs2Δ and fbh1Δ reduced HRR more modestly (43.0% and 52.5%, respectively). By contrast, the levels of NHEJ/SCC in the three helicase mutants were significantly elevated, especially in the case of rqh1Δ (70.4% vs. 10.3% in the wild type). Previously, Hope et al. reported similar results: in the rqh1Δ mutant, most segregants were Ade⁺ G418^r (the products of NHEJ and SCC), whereas GC was drastically decreased. Given that HO endonuclease efficiently cuts Ch¹⁶-MG even in the rqh1Δ background, and that Ade⁺ G418^r segregants are independent of Ku, Hope et al. concluded that most Ch¹⁶-MG molecules cut by HO endonuclease are repaired by SCC in the rqh1Δ background [39]. In the srs2Δ and fbh1Δ mutants, the rates of NHEJ/SCC segregants were 42.7% and 43.4%, respectively.

We then investigated the possibility that SCC is elevated in these mutants, as in the case of the rqh1Δ mutant [39], by measuring the efficiency of HO digestion (Figure S2). First, we determined the relative copy numbers of the act1 and ade6 genes (the ade6/act1 ratio). Because the ade6 gene is carried by both Chromosome III and minichromosome Ch16-MG, the ade6/act1 ratio before HO induction should be ∼2; after Ch16-MG is lost, the ratio should be ∼1. As shown in Figure S2B, the ade6/act1 ratios in the three helicase mutants were ∼2, similar to the ratio in the wild-type strain, indicating that very little reduction occurred after HO induction; thus the minichromosome was retained in most mutant cells, even after HO induction. Next, we determined the HOcs/act1 ratios in the helicase mutants (Figure S2C). We determined that the digestion efficiency was 71.8% in wild type, 55.0% in fbh1Δ, 58.8% in srs2Δ, and 56.4% in rqh1Δ, as determined by the formula %efficiency = (1-[HOcs/act1 with HO induction]/[HOcs/act1 without HO induction])×100 (see [39]), indicating that DSBs were formed very efficiently upon HO induction. Therefore, we concluded that the elevated rates of SCC/NHEJ in the three helicase mutants were not primarily due to increases in the undigested population. Sequence analysis of the HOcs region in 48 independent Ade⁺Kan^r clones revealed that fewer than 4.2% of clones in each strain were repaired by NHEJ (Figure S2D). Therefore, these colonies most likely represent products of SCC rather than NHEJ. The elevation of SCC in the fbh1Δ mutant was consistent with previous reports [32], [40]. On the other hand, minichromosome loss was drastically reduced in the fbh1Δ single mutant (2.4% in fbh1Δ vs. 13.8% in the wild type), but drastically increased by the rad51Δ mutation (77.3%) (Table 1), suggesting that Rad51 plays an important role in maintenance of DSB-introduced minichromosomes and that Fbh1 suppresses Rad51 function(s).

Evaluation of the outcomes of HRR by PFGE revealed that GC was reduced to about 50% of the wild-type level in the fbh1Δ mutant (28.7% in fbh1Δ vs. 56.6% in the wild type), whereas CO was markedly higher (21.8% in fbh1Δ vs. 5.1% in the wild type) (Table 2). To investigate the genetic interactions between Fbh1 and other HRR factors, we introduced rad51Δ, swi5Δ, and rad57Δ mutations into the fbh1Δ mutant background. The rad51Δ fbh1Δ mutant completely abolished CO, indicating that the CO observed in the fbh1Δ mutant was dependent on rad51⁺. In fission yeast, the Rad51 pathway diverges into two genetically independent sub-pathways, Rad55-Rad57 and Swi5-Sfr1 [7]. The CO percentage in the rad57Δ fbh1Δ mutant (7.8%) was only marginally higher than that in the wild-type strain, and was significantly lower than the corresponding rate in the swi5Δ fbh1Δ mutant (14.2%) and the sfr1Δ fbh1Δ mutant (15.7%), suggesting that the elevated CO rate in the fbh1Δ mutant depends primarily on the Rad55-Rad57 sub-pathway.

Although both budding yeast and fission yeast Srs2 suppress CO formation, as demonstrated by multiple assays [13], [22], [41], [42], the srs2Δ mutation resulted in only a slight increase in CO in our assay (7.5%). This finding indicates that Srs2 is less important than Fbh1 for suppression of CO production from DSBRs, at least in this site-specific DSBR assay. The rqh1Δ mutation also had a very slight effect on CO production (6.0%).

Purification of Fbh1-Skp1 complex

To examine the function of Fbh1 biochemically, we purified recombinant proteins using a baculovirus system. Because we could not purify Fbh1 alone, we purified Fbh1 and Skp1 as a protein complex (Figure S3A). We also purified (in complex with Skp1) Fbh1^K301A, an Fbh1 mutant containing a substitution in an amino acid in the Walker A box that is critically important for ATPase activity, as well as Skp1 alone. To assess whether the Fbh1-Skp1 complex is functional in vitro, we measured its ATPase activity in the presence or absence of DNA (Figure S3B). The Fbh1-Skp1 heterodimer exhibited a robust, ssDNA-dependent ATPase activity. Because neither Fbh1^K301A-Skp1 nor Skp1 alone exhibited ATPase activity, we concluded that the observed ATPase activity was due to wild-type Fbh1 (Figure S3C). Next, we investigated the DNA-binding activity of Fbh1 by performing gel mobility-shift assays using ssDNA or double-stranded DNA (dsDNA); the results revealed that Fbh1 preferentially binds ssDNA (Figure S3D). Because Fbh1 has 3′ to 5′ DNA helicase activity [25], we subjected the purified Fbh1-Skp1 complex to a DNA helicase assay. Fbh1 unwound heteroduplex DNA with a 3′ overhang, but not a duplex or a heteroduplex with a 5′ overhang. Thus, as expected, the Fbh1-Skp1 complex exhibited helicase activity with 3′ to 5′ directionality (Figure S3E).

Fbh1 disrupts Rad51 filaments

Srs2 and Fbh1 are predicted to have similar biochemical activity, based on their structural relatedness to bacterial UvrD helicase. ScSrs2 disrupts ScRad51-ssDNA nucleoprotein filaments [17], [18]. Fbh1 has also been proposed to disrupt Rad51-ssDNA filaments based on its relationship to Srs2 and on the results of in vivo analyses in both fission yeast and humans [29], [33], [43]. Thus, we first investigated whether Fbh1 affects the stability of Rad51-ssDNA nucleoprotein filaments in vitro by preparing Rad51-ssDNA filaments using biotinylated ssDNA-coated beads (Figure 1A) and exposing them or not to Fbh1. In the absence of Fbh1-Skp1, Rad51 was found mostly in the bound fraction, indicating that it bound stably to the ssDNA beads (Figure 1B, lanes 1 and 9). However, in the presence of Fbh1-Skp1, Rad51 was found in the unbound fraction, indicating that Fbh1-Skp1 disrupted the Rad51-ssDNA filaments. The effect of Fbh1-Skp1 was dose-dependent (Figure 1B). The disruption of Rad51-ssDNA filaments by Fbh1-Skp1 was dependent on Fbh1 helicase/translocase activity, because Rad51 remained bound to the ssDNA beads in the presence of a Walker A mutant of Fbh1 (Fbh1^K301A-Skp1) or Skp1 alone (Figure 1C). Thus, we conclude that Fbh1 can disrupt Rad51 filaments via its helicase/translocase activity.

Swi5-Sfr1, an activator protein complex of Rad51, protects Rad51 filaments against Fbh1-mediated disassembly

Because the Swi5-Sfr1 complex activates Rad51 filaments [44], we considered the possibility that the Swi5-Sfr1 complex confers resistance to Rad51 displacement by Fbh1. To address this, we investigated whether Fbh1 disrupts Rad51-ssDNA nucleoprotein filament in the presence of the Swi5-Sfr1 complex. Indeed, Fbh1 disrupted Rad51-ssDNA nucleoprotein filaments in the absence, but not the presence, of Swi5-Sfr1 (Figure 2). In this assay, we used 5 µM Rad51, the same concentration used in the DNA strand-exchange assay that we established previously [12]. The DNA strand-exchange assay revealed that 0.5 µM Swi5-Sfr1 is sufficient for stimulation. Consistent with this, a similar concentration of Swi5-Sfr1 (0.25–1 µM) confers resistance to Rad51 displacement by Fbh1, probably via the activation of Rad51-ssDNA nucleoprotein filaments. During the preparation of this manuscript, another group reported that hFbh1 forms stable complexes with active hRad51 nucleoprotein filaments in the presence of Ca²⁺ [45]. To determine whether a similar interaction occurs between the fission yeast homologs of these proteins, we investigated whether Fbh1 binds active Rad51 filaments in the presence of the Swi5-Sfr1 complex (Figure 2). No significant increase in the amount of bead-bound Fbh1 was observed, suggesting either that SpFbh1 does not form a stable complex with SpRad51 nucleoprotein filaments, or that the state of SpRad51 filaments in the presence of Swi5-Sfr1 complex is different from that of hRad51 filaments activated by Ca²⁺.

Impacts of Fbh1 on the Rad51-Swi5-Sfr1-driven strand-exchange reaction

Next, we investigated whether Fbh1 inhibits the three-strand DNA exchange reaction mediated by Rad51, using a previously developed assay that allowed us to monitor homology search and strand exchange between ssDNA and dsDNA catalyzed by Rad51 recombinase [12]. As expected, both the reaction intermediates (joint molecules, JMs), and the final products (P, also referred to as the nicked circle, NC, and single-stranded linear DNA) were almost completely abolished if Fbh1-Skp1 was added at early steps (i) or (ii) when the Swi5-Sfr1 complex was absent (Figure 3B, lanes W1 and W2). Fbh1^K301A-Skp1 had very little effect (Figure 3B, lane K2); therefore, inhibition of the three-strand DNA exchange reaction was dependent on the helicase/translocase activity of Fbh1. By contrast, this inhibition was largely alleviated if Fbh1-Skp1 was added after step (iii) (Figure 3B, lanes W3 and W4). These results are consistent with the idea that Fbh1 disrupts Rad51-ssDNA filaments in the absence of the Swi5-Sfr1 complex, although full restoration of the strand-exchange reaction was not achieved by the addition of Swi5-Sfr1. One possible explanation for this finding is that short incubation time limited the activation of Rad51 filament by Swi5-Sfr1. To test this idea, we allowed Swi5-Sfr1 to activate Rad51 filament for various incubation times (5–30 min), and then added Fbh1 at step (iii) (Figure 3D). As shown in Figure 3E, the yield of three-strand exchange increased upon longer incubation. We also evaluated the amounts of bead-bound or free Rad51 protein resulting from addition of Fbh1 at different times, using ssDNA beads (times [I] and [II] in Figure S4A). In this experiment, we used almost the same conditions as in the strand-exchange reaction, but incubated for 60 min before collecting the beads. Addition of Fbh1 after incubation with Swi5-Sfr1 (i.e., time [II]) slightly increased the amount of bead-bound Rad51 relative to addition of Fbh1 time [I]. Taken together, the result indicated that Swi5-Sfr1 confers resistance to the helicase/translocase activity of Fbh1 in the strand-exchange reaction.

Surprisingly, the level of NC increased when Fbh1-Skp1 was added at step (v) or later (Figure 3B, lanes W5–W8), whereas the level of JMs decreased. These results indicate that Fbh1-Skp1 promotes the strand-exchange reaction of already formed JMs. This promotion also requires the helicase/translocase activity of Fbh1, because Fbh1^K301A-Skp1 was not effective in this respect (Figure 3B, lanes K5, K6, and K8). The stimulatory effect was not observed in the absence of Swi5-Sfr1 (Figure S5).

One possible explanation for the observed stimulation is that the 3′ end of the displaced strand accessible to Fbh1 may unwind the linear dsDNA via its 3′ to 5′ DNA helicase activity, allowing the NC to form by simple annealing. To address this possibility, we investigated whether Fbh1 stimulates the strand-exchange reaction mediated by RecA (Figure S6). However, Fbh1 inhibited the three-strand exchange rather than stimulating it (Figure S6B lanes 3–5), indicating that the formation of the accessible 3′ end of the displaced strand is not sufficient for stimulation.

Based on these results, we propose that Fbh1 plays both inhibitory and stimulatory roles in the Rad51-mediated strand-exchange reaction.

Fbh1 ubiquitinates Rad51

A previous genetic study revealed that both the helicase and F-box motifs are required for full Fbh1 functionality [28], suggesting that Fbh1 has ubiquitin-ligase (E3) activity in addition to helicase/translocase activity. In general, F-box proteins form SCF E3 complexes including Cullin1, Skp1, and Rbx1 proteins [46]. The human ortholog (HsFbh1) forms the HsSCF^Fbh1 complex, which has ubiquitin-ligase activity in vitro, although its target proteins remain unknown [35], [36]. Because the Fbh1-Skp1 complex physically and functionally interacts with Rad51 in vitro (Figures 1–3 and S7A), we suspected that Rad51 might be also a target of the E3 complex.

To obtain the SpSCF^Fbh1 complex, we separately purified Fbh1-Skp1 and Pcu1 (fission yeast Cullin1)-Rbx1 complexes, mixed them to form the SpSCF^Fbh1 complex, and used these recombinant proteins in an in vitro ubiquitination assay. Several SCF complexes have ubiquitin E3 ligase activity that requires either Ubc4 or Cdc34 as the E2 enzyme [47]. In fission yeast, Ubc15 is a candidate functional homolog of Ccd34. Thus, we tested both Ubc4 and Ubc15 as candidate E2 enzymes in a ubiquitination assay with the SCF^Fbh1 complex. As shown in Figure 4A, Rad51 was ubiquitinated in an Ubc4- and SCF^Fbh1-dependent manner.

We also tested commercially available human E2 enzymes. Rad51 was ubiquitinated efficiently in reactions containing three UbcH5 variants, but was not ubiquitinated in reactions containing UbcH13/Cdc34 (Figures S7B and S7C). This result is consistent with the results obtained in the S. pombe ubiquitination assay, because SpUbc4 and SpUbc15 are considered to be functional counterparts for UbcH5 proteins and UbcH13/Cdc34, respectively (Figure S8). Therefore, we conclude that Ubc4 is the functionally cognate E2 for the SpSCF^Fbh1 E3, at least for the in vitro ubiquitination of Rad51.

The SCF^Fbh1-K301A complex exhibited activity similar to that of SCF^Fbh1 (Figure 4B), indicating that SCF^Fbh1 E3 activity towards Rad51 is not dependent on its translocase activity. Therefore, we investigated whether Rad51 is ubiquitinated in the presence of ssDNA. However, the ubiquitination of Rad51 was inhibited by ssDNA, suggesting that Rad51-filament might not be the cognate substrate for the ubiquitination reaction (Figure 4B).

Swi5-Sfr1 inhibits ubiquitination of Rad51

In vitro ubiquitination of Rad51 was inhibited by the Swi5-Sfr1 complex in a dose-dependent manner (Figure 4C). Because Fbh1 appears not to interact with Swi5-Sfr1 (Figure S7A), Swi5-Sfr1 might occlude the ubiquitination site and/or induce a structural change in Rad51 that prevents ubiquitination by SCF^Fbh1. Taken together with the observation that Swi5-Sfr1 inhibited the disruption of Rad51 filaments by the helicase/translocase activity of Fbh1 (Figure 3), this finding indicates that Swi5-Sfr1 protects Rad51 against both of the inhibitory activities of Fbh1 described above.

Fbh1 affects Rad51 stability in stationary phase

Based on our observation that the SCF^Fbh1 complex ubiquitinates Rad51 in vitro, we next investigated whether Rad51 is ubiquitinated in vivo. However, we could not detect ubiquitinated Rad51 in cells treated with several DNA-damaging agents (Unpublished observation), possibly because ubiquitination of Rad51 is transient and/or inefficient. In the course of this analysis, we noticed that, in stationary phase, the Rad51 protein level decreased drastically in wild-type cells (Figure 4D), but increased in several fbh1 mutants. In addition, we found that the Rad51 stability in an F-box mutant, fbh1-fb, was similar to that in the fbh1Δ mutant, whereas the Rad51 stabilities in a helicase-dead mutant, fbh1-hl (fbh1^K301A), and a double mutant, fbh1-fb/hl, were lower. These results suggest that Fbh1 regulates the level of Rad51 protein in stationary phase, which is dependent on its F-box motif. Conversely, Rad52 is more stable than Rad51, even during stationary phase, in both the wild-type and fbh1 mutants (Figure 4D).

Discussion

In this study, we characterized the in vivo and in vitro roles of fission yeast Fbh1. Comparisons of the activities of rqh1Δ, srs2Δ, and fbh1Δ mutants in a site-specific DSBR assay revealed that Fbh1, but not Srs2, is important for the suppression of CO formation. Biochemical analysis showed that Fbh1 disrupts Rad51-ssDNA filaments in the absence, but not in the presence, of the Swi5-Sfr1 complex. Consistent with this, Fbh1 negatively regulated the Rad51-catalyzed strand exchange before the start of the reaction, especially when the Rad51 filament was not activated by the Swi5-Sfr1 complex. However, once the reaction started, Fbh1 stimulated the strand-exchange reaction. Furthermore, the SCF^Fbh1 complex ubiquitinated Rad51 in vitro. Based on these observations, we suggest that Fbh1 performs an anti-recombinase role via its helicase/translocase activity and ubiquitin ligase activity. Furthermore, we suspect that Fbh1 might also promote the strand exchange reaction under similar conditions.

Fbh1 suppresses CO formation during interchromosomal recombination

Using the same single-DSBR analysis employed in this study, we previously showed that Rad55-Rad57 is essential for CO formation in the fbh1⁺ background, whereas the Swi5-Sfr1 pathway is not [8]. In this study, we demonstrated that Fbh1 is important for the suppression of CO (Table 2). Elevated CO formation in the fbh1Δ mutant largely depended on the Rad55-Rad57 sub-pathway, rather than on the Swi5-Sfr1 sub-pathway (Table 2). Moreover, Whitby and colleagues showed that deletion of fbh1 has no effect on spontaneous intrachromosomal recombination [27]. Taken together, these findings suggest that Fbh1 negatively regulates the Rad55-Rad57 sub-pathway of Rad51-dependent HR to suppress CO formation during interchromosomal recombination.

Fission yeast has three functionally interdependent DNA helicases, Fbh1, Srs2, and the RecQ helicase Rqh1. By contrast, budding yeast has Srs2 and the RecQ helicase Sgs1, but no apparent Fbh1 homolog; however, some functions of Fbh1 may be served by Srs2, which suppresses CO in budding yeast [13], [22], [42]. Metazoans such as human and mouse have Fbh1, the Srs2 homolog PARI [20], and several RecQ homologs, including WRN, BLM, and RecQ5. HsFBH1 partially complements the phenotype of the budding yeast srs2Δ mutant [48], suggesting that Fbh1 and Srs2 are functionally redundant. In fission yeast, fbh1Δ and srs2Δ mutations cause a severe growth defect when combined [26], consistent with the idea that both helicases play overlapping roles in HR required for mitotic growth.

Widely conserved FANCM orthologs also suppress crossover during mitosis and/or meiosis in budding yeast, fission yeast, and plants [49]–[51]. ScMph1 and SpFml1 dissociate D-loop structures in vitro [50], [52]. Future work should address how cells efficiently utilize these DNA helicases to regulate HR.

Protection of Rad51 filaments from the anti-recombinase activity of Fbh1

Our in vitro analyses indicated that, in the absence of the Swi5-Sfr1 complex, Fbh1 inhibits the DNA strand-exchange reaction via disruption of the Rad51 filament, but not when the Rad51 filament has been activated by the Swi5-Sfr1 complex (Figures 2 and 3). Protection of Rad51 by Swi5-Sfr1 from Fbh1-mediated displacement is very efficient (Figure 2). However, Fbh1-mediated inhibition of DNA strand exchange was not completely restored by Swi5-Sfr1 (Figure 3). Our time-course experiment revealed that protection of Rad51 by Swi5-Sfr1 requires a long incubation time (Figure 3), but the mechanistic details underlying this observation remain unclear.

Heyer and colleagues showed that Rad55-Rad57 stabilizes Rad51-ssDNA filaments against disruption by Srs2 in budding yeast [53]. Therefore, the stabilization of auxiliary factors might be a conserved mechanism for quality control of Rad51 nucleoprotein filaments. In the case of Swi5-Sfr1, other unknown factor(s) might be required in vivo for efficient Rad51-mediated strand exchange and for protecting against inhibition by Fbh1.

Fbh1 stimulates branch migration in the strand-exchange reaction in vitro

In this study, we showed that Fbh1 could stimulate the strand-exchange reaction only after the reaction has already started (Figure 3). Although the molecular mechanism remains unclear, it is suggested that Fbh1-Skp1 promotes the strand-exchange reaction of already formed JMs, dependently of its helicase/translocase activity. Fbh1 does not promote the strand-exchange reaction mediated by RecA (Figure S6), indicating that the 3′ end of the displaced strand accessible to Fbh1 is not sufficient for the NC promotion. However, it is still possible that the 3′ end of the displaced strand aids in unwinding of linear dsDNA by Fbh1 only when Rad51 is present. In budding yeast, Rad51 stimulates Srs2 helicase activity [19]; similarly, in fission yeast, Rad51 might also stimulate the Fbh1 helicase. Although there is no direct evidence to support Fbh1 pro-recombinase activity in vivo, it is possible that variations in Rad51 filaments specific to the HRR sub-pathway exist, and Fbh1 might promote only recombination on a filament that is competent for the SDSA pathway. Further studies will be needed to address this hypothesis.

Because we could not purify the Rad55-Rad57 complex, we were unable to investigate the effect of Fbh1 on the Rad55-Rad57 recombination reaction in vitro. However, the single-DSBR assay revealed that Fbh1 suppresses Rad55-Rad57–mediated CO formation in vivo. Based on these observations, we speculate that Fbh1 reduces CO formation by stimulating the Swi5-Sfr1 pathway while simultaneously suppressing the Rad55-Rad57 pathway. In this context, it will be important to determine whether Rad51 filaments are resistant to Fbh1 in the presence of Rad55-Rad57.

Role of Fbh1 ubiquitin-ligase activity

Rad51 is ubiquitinated by SCF^Fbh1 in vitro (Figure 4). ssDNA prevented ubiquitination of Rad51, implying that Rad51 is not ubiquitinated during HRR repair, when Rad51 forms filaments on ssDNA. Although no currently available evidence directly supports this idea, Rad51 may be ubiquitinated after Rad51 is unloaded from ssDNA either after DNA damage is repaired or when unnecessary Rad51 filaments are formed.

Furthermore, the stability of Rad51 protein in the stationary phase is regulated by Fbh1 (Figure 4D). Previously, we showed that the fbh1Δ mutant loses viability in stationary phase, and that deletion of rad51 or rad57 suppresses this loss of viability [26]. High levels of Rad51 cause abnormal nuclear division [54], possibly by causing inappropriate recombination. Therefore, we propose that Fbh1 controls the level of Rad51 protein to suppress inappropriate recombination events, and that this interaction might be significant even in the late steps of HR.

Rad51 was mono-ubiquitinated rather than poly-ubiquitinated, raising several related possibilities: (i) ubiquitination of Rad51 is not a signal for protein degradation; (ii) other E3 and/or E4 enzymes are required for polyubiquitination of Rad51 [55]; or (iii) appropriate ubiquitination requires other unknown factor(s). Because Rad51 is phosphorylated in S. cerevisiae and human [56]–[60], we favor the third possibility, i.e., that phosphorylation of Rad51 is required for its efficient ubiquitination. In this regard, since the F-box of Fbh1 is essential for mitotic HRR [28], Rad51 ubiquitination by Fbh1 must play an active rather than a passive role, such as one limited to the degradation of Rad51. We attempted to identify the ubiquitination site by mass spectrometry, but the attempt was unsuccessful. The identification of the true ubiquitination site and analysis of the ubiquitination site mutant(s) would provide insight into the biological role(s) of Rad51 ubiquitination.

Two recent studies showed that HsFbh1 is ubiquitinated in vivo [43], [45]. This ubiquitination, which depends on PCNA and CRL4^Cdt2, leads to degradation of HsFbh1 [43]. Therefore, regulation of Fbh1 itself might also be important for genome integrity. Furthermore, HsFbh1 is deregulated in melanocytes, and depletion of HsFbh1 promotes UV-mediated transformation of these cells [61]. Further analysis of Fbh1 function in human cancer cells should increase our understanding of the role this protein plays during tumorigenesis.

Taken together, the results of this study demonstrate that Fbh1 plays multiple roles in regulation of recombination (Figure 5). By negatively regulating Rad51 association with ssDNA, Fbh1 would suppress recombination events. Once Swi5-Sfr1 has activated a Rad51 filament, Fbh1 is prevented from exerting its anti-recombinase activity. Once a Rad51 filament is thereby “committed”, Fbh1 is likely to accelerate the strand-exchange reaction in vivo. Future studies should address how the Swi5-Sfr1 interaction with Rad51 filaments prevents disruption by Fbh1, as well as the mechanism underlying the strand exchange stimulation by Fbh1. In addition, our analyses also suggest that Fbh1 contributes to regulation of homologous recombination by down-regulating Rad51 levels during stationary phase. Future work should seek to determine why cells require this multi-functional DNA helicase for regulation of homologous recombination.

Materials and Methods

Strains, media and growth conditions

The S. pombe strains used in this study are shown in Table S4. Standard procedures were used for culture and genetic manipulations [62].

Site-specific DSBR assay

The assay system and procedures were previously described [38]. Experiments were carried out three to five times for each strain. Detailed PFGE procedures are also described in [38]. The average frequencies of NHEJ/SCC, HRR, and minichromosome loss were calculated as (%Ade⁺Kan^r), {(%Ade⁺Kan^s)×[(%GC)+(%CO)+(%BIR type1)]+(%Ade⁺Kan^s)×[(%LTGC)+(%BIR type2)+(%GC w/CO)]}, and [(%Ade⁺Kan^s)×(%Minichromosome loss)], respectively.

To determine the copy numbers relative to the parental wild-type strain by quantitative PCR (qPCR), the following primer sets were used: act1-f (5′-GATAATGGCTCTGGTATGTG-3′) and act1-r (5′-CTTTTGTCCCATACCTACCA-3′) for act1; ade6-f (5′-CGCATCGACTTCCACAACTCATGCG-3′) and ade6-r (5′-CCGGGAATGGACAGAGAACG-3′) for ade6; HOcs-f (5′-CCTAGTTCACAAACAGCCAAAGATTCTC-3′) and HOcs-r (5′-TGTACGGGCGACAGTCACATCATGC-3′) for HOcs.

For sequence analysis of the HOcs region, genomic DNA was isolated from each Ade⁺Kan^r clone and the HOcs region was amplified by PCR using rad21-F3435 (5′-AGCACCAACGTACTGATACCTCAAC-3′) and KanMX-R348 (5′-AAGAACCTCAGTGGCAAATCCTAAC-3′). The resultant PCR product was purified from an agarose gel and sequenced using the rad21-F3435 primer.

Recombinant baculovirus

A recombinant baculovirus expressing S. pombe 6His-Fbh1 was constructed using BaculoDirect (Invitrogen) and a pENTR4 derivative, pENTR41-6His-Fbh1. Recombinant baculoviruses expressing S. pombe 6His-Skp1, 6His-Pcu1, and 6His-Rbx1 were prepared using the Bac-to-Bac expression system (Invitrogen).

Expression and purification of Skp1

Insect cells were infected with the 6His-Skp1 baculovirus, and 2×10⁹ cells were harvested from 1 L culture after 72 h. The cells were resuspended in R buffer (20 mM Tris-HCl [pH 8.0], 1 mM EDTA, 1 mM dithiothreitol [DTT], 10% glycerol) containing 300 mM NaCl and homogenized, and the sample was centrifuged at 30,000× g for 30 min. Clarified lysate was directly loaded onto TALON Metal Affinity Resin (Clontech). Bead-bound proteins were eluted in R buffer containing 300 mM NaCl and 300 mM imidazole and lacking DTT and EDTA. The sample was diluted 3-fold with R buffer and loaded onto a HiTrap Heparin column (GE Healthcare). The pass-through fraction was loaded onto a HiTrap Q column (GE Healthcare), and 6His-Skp1 was eluted at ∼550 mM NaCl with a linear gradient of 0.1–1.0 M NaCl in R buffer. Peak fractions were collected and dialyzed against T buffer (20 mM Tris-HCl [pH 7.5], 50% glycerol, 1 mM DTT) containing 300 mM NaCl. The Protein Assay Kit (Bio-Rad), with bovine serum albumin as the standard protein, was used for determination of the protein concentration of Skp1.

Expression and purification of the Fbh1-Skp1 complex

To express the Fbh1-Skp1 complex, insect cells were co-infected with 6His-Fbh1 and 6His-Skp1 baculoviruses. The ratio of Fbh1 virus to Skp1 virus was determined by measuring the expression levels of these proteins in the host cells. After 72 h, 3.6×10⁹ cells were harvested. The cells were resuspended in R buffer containing 750 mM NaCl and homogenized, and the sample was centrifuged at 30,000× g for 1 h. Clarified lysate was directly loaded onto TALON Metal Affinity Resin. Bead-bound proteins were eluted in R buffer containing 750 mM NaCl and 300 mM imidazole and lacking DTT and EDTA. The sample was diluted 5-fold with R buffer and loaded onto a HiTrap Q column. 6His-Fbh1 and 6His-Skp1 were co-eluted at ∼500 mM NaCl with a linear gradient of 0.1–1.0 M NaCl in R buffer. Eluted fractions were diluted 5-fold with R buffer and loaded onto a HiTrap Heparin column. 6His-Fbh1 and 6His-Skp1 were co-eluted at ∼600 mM NaCl with a linear gradient of 0.1–1.0 M NaCl in R buffer. 6His-Fbh1 and 6His-Skp1 fractions were applied to a HiLoad 16/60 Superdex 200 pg column (GE Healthcare) and developed in R buffer containing 1 M NaCl. Peak fractions were collected, diluted with R buffer, and loaded onto a ResourceQ column (GE Healthcare). 6His-Fbh1 and 6His-Skp1 were co-eluted at ∼600 mM NaCl with a linear gradient of 0.1–1.0 M NaCl in R buffer. Peak fractions were collected and dialyzed against T buffer containing 300 mM NaCl. Concentration of the Fbh1-Skp1 complex was determined as for Skp1 (above), under the assumption that the proteins formed a 1∶1 stoichiometric complex. The complex of 3FLAG6His-Fbh1 and 6His-Skp1 was prepared similarly.

Purification of the Pcu1-Rbx1 complex

To express the Pcu1-Rbx1 complex, insect cells were co-infected with the 6His-Pcu1 and 6His-Rbx1 baculoviruses. After 72 h, 3.6×10⁹ cells were harvested. The cells were homogenized, and the sample was centrifuged at 30,000× g for 1 h. Clarified lysate was directly loaded onto TALON Metal Affinity Resin. Bead-bound proteins were eluted in R buffer containing 300 mM NaCl and 300 mM imidazole and lacking DTT and EDTA. The sample was diluted 3-fold with R buffer and loaded onto a HiTrap Q column. 6His-Pcu1 and 6His-Rbx1 were co-eluted at ∼500 mM NaCl with a linear gradient of 0.1–1.0 M NaCl in R buffer. Eluted fractions were diluted 5-fold with R buffer and loaded onto a HiTrap Heparin column. 6His-Pcu1 and 6His-Rbx1 were co-eluted at ∼600 mM NaCl with a linear gradient of 0.05–1.0 M NaCl in R buffer. Peak fractions were collected and dialyzed against T buffer containing 300 mM NaCl. Concentration of the Pcu1-Rbx1 complex was determined as for Skp1 (above), under the assumption that the proteins formed a 1∶1 stoichiometric complex.

Purification of 3HA-ubiquitin, E1, and E2 enzymes

Recombinant S. pombe ubiquitin protein was expressed in the E. coli BL21-CodonPlus(DE3)-RIPL strain carrying a 3HA-tagged expression plasmid derived from pET11b (Novagen). Expression of 3HA-ubiquitin was induced with 0.5 mM isopropyl-β-D-thiogalactopyranoside (IPTG) at 30°C for 5 h. The cells were collected by centrifugation, resuspended in R buffer containing 300 mM NaCl, and disrupted by sonication; the lysate was clarified by ultracentrifugation. Proteins in the lysate were precipitated by ammonium sulfate fractionation at 40% saturation and centrifuged at 35,000× g for 30 min. The pellet was resuspended in R buffer containing ammonium sulfate at 20% saturation and directly loaded onto a HiTrap Phenyl FF (high sub) column (GE Healthcare). 3HA-ubiquitin was eluted at nearly 0% ammonium sulfate with a linear gradient of 20–0% ammonium sulfate in R buffer. Eluted fractions were dialyzed against R buffer containing 20 mM NaCl. The dialyzed sample was applied to a HiTrap Q column. Eluted 3HA-Ubiquitin was eluted at ∼300 mM NaCl with a linear gradient of 20–600 mM NaCl in R buffer. 3HA-ubiquitin fractions were applied to a HiLoad 16/60 Superdex 200 pg column and developed in R buffer containing 500 mM NaCl. Peak fractions were collected and concentrated using an Amicon Ultra-4 centrifugal device (Millipore) and dialyzed against R buffer containing 100 mM NaCl.

Expression of S. pombe 6His-Uba1 was induced with 0.5 mM IPTG at 18°C for 5 h. Harvested cells were disrupted as described above, and clarified lysate was directly loaded on Ni-NTA agarose. Bead-bound proteins were eluted in R buffer containing 300 mM NaCl and 200 mM imidazole and lacking DTT and EDTA. The sample was diluted 3-fold with R buffer and loaded onto a HiTrap Heparin column. The pass-through fraction was loaded directly onto a HiTrap SP column. The subsequent pass-through fraction was loaded onto a HiTrap Q column, and 6His-Uba1 was eluted at ∼300 mM NaCl with a linear gradient of 50–500 mM NaCl in R buffer. Peak fractions were applied to a HiLoad 16/60 Superdex 200 pg column and developed in R buffer containing 1 M NaCl. Peak fractions were collected and dialyzed against R buffer containing 200 mM NaCl.

Expression of S. pombe 6His-Ubc4 and 6His-Ubc15 was induced with 0.5 mM IPTG at 30°C for 3 h, respectively. Purification proceeded as described for 6His-Uba1, through the step in which the sample was loaded onto a HiTrap Heparin column. At that stage, 6His-Ubc4 was eluted from the HiTrap Heparin column at ∼300 mM NaCl with a linear gradient of 50–800 mM NaCl in R buffer. Peak fractions were diluted and loaded onto a HiTrap SP column, eluted at ∼200 mM NaCl with a linear gradient of 50–600 mM NaCl in R buffer. 6His-Ubc15 was eluted from the HiTrap Heparin column at ∼200 mM NaCl with a linear gradient of 50–600 mM NaCl in R buffer. Peak fractions were diluted and loaded onto a HiTrap SP column in R buffer containing 50 mM NaCl. The pass-through fraction was loaded directly onto a HiTrap Q column, and 6His-Ubc15 was eluted at ∼250 mM NaCl with a linear gradient of 50–600 mM NaCl in R buffer.

Protein concentrations were determined by measuring absorbance at 280 nm. The following extinction coefficients (ε280) were used: 1.49×10⁴ M⁻¹ cm⁻¹ for 3HA-Ubiquitin (Ub), 7.61×10⁴ M⁻¹ cm⁻¹ for 6His-Uba1 (E1), 2.58×10⁴ M⁻¹ cm⁻¹ for 6His-Ubc4 (E2), and 2.26×10⁴ M⁻¹ cm⁻¹ for 6His-Ubc15 (E2).

Purification of Rad51, Swi5-Sfr1, and RPA

Expression and purification of Fbh1-Skp1, Pcu1-Rbx1, Rad51, ubiquitin, Uba1, Ubc4, and Ubc15 are described in Supplemental Experimental Procedures. Rad51, Swi5-Sfr1, and RPA were bacterially expressed and purified as described previously [12], [44].

Human ubiquitin, E1, and E2 enzymes

Human biotin-ubiquitin, E1, E2 enzymes were purchased from Enzo Life Sciences Inc.

DNA substrates

DNA substrates used in three-strand exchange reactions were prepared as described previously [12]. A cccDNA of pBluescript SKII, which was used for D-loop analysis, was purified essentially according to the detergent lysis protocol described previously [63]. Synthetic oligonucleotides were purchased from Operon, Ltd. The sequences of the ssDNA oligonucleotides were as follows: F3-d47 (47-mer for ssDNA, dsDNA binding and helicase assay), 5′-AGCTATGACCATGATTACGAATTGCTTGGAATCCTGACGAACTGTAG-3′; F3-d47R (47-mer for dsDNA binding and helicase assay), 5′-CTACAGTTCGTCAGGATTCCAAGCAATTCGTAATCATGGTCATAGCT-3′; d20 (20-mer for helicase assay), 5′-CTACAGTTCGTCAGGATTCC-3′; d22, 5′- AATTCGTGCAGGCATGGTAGCT-3′; 49N2 (49-mer for helicase assay), 5′-AGCTACCATGCCTGCACGAATTCGTATCAGCGTAATCATGGTCATAGCT-3′.

ATPase assay

These procedures were essentially conducted as described previously [44]. Reaction mixtures (13.5 µl) contained 25 mM Tris-acetate (pH 7.5), 1 mM DTT, 5% glycerol, 3 mM Mg-acetate, 100 mM KCl, and 30 nM Fbh1-Skp1, Fbh1^K301A-Skp1, or Skp1 alone. In some assays, 10 µM øX174 ssDNA or 10 µM ApaLI-linearized øX174 dsDNA were added, as indicated. The reactions were started by adding 1.5 µl of a mixture of [γ-³²P]ATP and cold ATP (final concentration, 2 mM) at 30°C. Aliquots (2 µl) were taken at various time points and immediately mixed with 4 µl of stop solution (0.5 M EDTA). Samples (1 µl) were subjected to thin-layer chromatography, as described previously [12]. The amounts of ³²P_i and [γ-³²P]ATP in each spot were determined using a phosphoimager (Fuji BAS2500).

Gel-shift assay for DNA binding

DNA substrates for dsDNA (F3-d47R+³²P-labeled F3-d47) and ssDNA (³²P-labeled F3-d47) binding were as described above. Reaction mixtures contained 10 nM substrate DNA (ssDNA or dsDNA), the indicated concentration of Fbh1-Skp1 proteins, 25 mM Tris-acetate (pH 8.0), 1 mM DTT, 3 mM Mg-acetate, 5% glycerol, and 100 mM KCl. Reactions were incubated at 30°C for 10 min. Products were resolved by electrophoresis on 6% PAGE in TBE buffer. Gels were dried onto DE81 paper, and radiolabeled bands were detected using a Fuji BAS2500 image analyzer.

Helicase assay

Preparation of 5′-³²P-labeled substrates with a blunt end, 5′-overhang, or 3′-overhang were previously described [44], [64]. All DNA concentrations are expressed in moles of substrates.

Reaction mixtures (50 µl) containing Fbh1-Skp1 (30 nM), substrate DNA (2 nM), 2 mM ATP, 25 mM Tris-acetate (pH 8.0), 1 mM DTT, 3 mM Mg-acetate, 5% glycerol, and an ATP regeneration system (8 mM creatine phosphate and 8 U ml⁻¹ creatine kinase) were incubated at 30°C. At the indicated times, 10 µl of each reaction was collected, stopped with 6× stop buffer containing SDS and proteinase, and incubated for 10 min. Products were resolved by electrophoresis on 12% PAGE in TBE buffer. Gels were dried onto DE81 paper, and radiolabeled bands were detected using a Fuji BAS2500 image analyzer.

Assays for protein-protein interaction

In vitro co-immunoprecipitation assays were performed as follows. Each protein (0.5 µg) as indicated was mixed in 10 µl buffer (25 mM Tris-OAc [pH 7.5], 100 mM KCl, 0.5% NP40, 3 mM Mg-acetate) for 10 min at room temperature followed 20 min at 4°C. To these samples were added M2 FLAG tag antibodies in 90 µl buffer, and the mixtures were incubated for 1 h at 4°C. Dynabeads Protein G (Invitrogen) were then added, and the samples were incubated for 1 h incubation at 4°C. Immunocomplexes were washed three times with 200 µl buffer, and bead-bound proteins were eluted with SDS loading buffer and subjected to 10% SDS-PAGE. Protein complexes were detected by western blotting using anti-Rad51, anti-Sfr1, or anti-M2 antibody (Sigma).

ssDNA beads assay

ssDNA beads bound to a 608 ntd ssDNA sequence from phiX174 were prepared as described in [65]. The amount of ssDNA attached to the beads was quantified by qPCR. For pull-down experiments, the beads were incubated with Rad51 for 5 min at 37°C, followed by incubation with the Swi5-Sfr1 complex for 5 min at 37°C if required. Beads were washed once, and the resultant Rad51-ssDNA beads were challenged with the Fbh1-Skp1 complex at the indicated times. The buffer used in this assay was 30 mM Tris-HCl (pH 7.5), 1 mM DTT, 100 mM NaCl, 3.5 mM MgCl₂, 5% glycerol, and 0.25% Tween 20, and an ATP regeneration system (8 mM creatine phosphate and 8 U ml⁻¹ creatine kinase). The supernatant and bead fractions were analyzed by SDS-PAGE, and separated proteins were visualized with Coomassie G-250. The quantification of the amount of Rad51 was performed on an LAS-4000 mini (GE Healthcare).

Three-strand DNA exchange reaction

Three-strand DNA exchange reactions were performed as described in [12]. Fbh1-Skp1 complex was added at the indicated times. Reactions were incubated for 120 min and stopped by addition of a mixture containing 0.9 µl 10% (w/v) SDS, 0.3 µl 0.5 M EDTA, and 0.6 µl 20 mg/ml proteinase K, with a final incubation for 30 min at 37°C. Aliquots were mixed with 6× loading buffer, loaded onto a 1% (w/v) agarose gel, and electrophoresed at 50 V for 2.5 h at room temperature. To visualize DNA bands, gels were stained with SYBR-Gold (Molecular Probes), gel images were captured on an LAS-4000mini, and the intensities of DNA bands were quantified using Multi Gauge (GE healthcare). The percentage of final product was defined as [NC]/([JM]/1.5+[NC]+[ldsDNA])×100, and the percentage of intermediates was defined as ([JM]/1.5)/([JM]/1.5+[NC]+[ldsDNA])×100. In these expressions, the values in square brackets are the intensities of each type of DNA molecule: NC denotes nicked circular dsDNA, and JM denotes joint molecules.

Ubiquitination assay

For reconstitution of SCF^Fbh1, 100 nM of Fbh1-Skp1 and Pcu1-Rbx1 were mixed in buffer U (25 mM TrisOAc [pH 7.5], 5 mM Mg/ATP, 1 mM DTT) for 10 min at 37°C. In vitro ubiquitination was carried out in buffer U containing 0.1 µM Uba1, 2.5 µM E2, 0.1 µM SCF^Fbh1, 2.5 µM 3HA-Ub WT, and 1 µM Rad51. After incubation for 30 min at 37°C, the reaction was stopped by addition of 6× SDS-PAGE loading buffer and boiling for 5 min at 95°C. Samples were analyzed by western blotting.

Analysis of Rad51 and Rad52 protein levels in vivo

For investigations of Rad51 and Rad52 protein levels, cells were grown in YES media. To obtain log-phase samples, cells were collected at 0.5×10⁷ cells/ml and treated with 20% of trichloroacetic acid (TCA). For the stationary-phase samples, cells were grown to saturation. After incubation for a further 48 hours, cells were collected and treated with 20% of TCA. Cell lysates were prepared by disruption with glass beads as described in [66], and then analyzed by western blotting.

Supporting Information

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