A mutant form of Dmc1 that bypasses the requirement for accessory protein Mei5-Sae3 reveals independent activities of Mei5-Sae3 and Rad51 in Dmc1 filament stability

Summary

During meiosis, homologous recombination repairs programmed DNA double-stranded breaks. Meiotic recombination physically links the homologous chromosomes (“homologs”), creating the tension between them that is required for their segregation. The central recombinase in this process is Dmc1. Dmc1’s activity is regulated by its accessory factors including the heterodimeric protein Mei5-Sae3 and Rad51. We use a gain-of-function dmc1 mutant, dmc1-E157D, that bypasses Mei5-Sae3 to gain insight into the role of this accessory factor and its relationship to mitotic recombinase Rad51, which also functions as a Dmc1 accessory protein during meiosis. We find that Mei5-Sae3 has a role in filament formation and stability, but not in the bias of recombination partner choice that favors homolog over sister chromatids. Analysis of meiotic recombination intermediates suggests that Mei5-Sae3 and Rad51 function independently in promoting filament stability. In spite of its ability to load onto single-stranded DNA and carry out recombination in the absence of Mei5-Sae3, recombination promoted by the Dmc1 mutant is abnormal in that it forms foci in the absence of DNA breaks, displays unusually high levels of multi-chromatid and intersister joint molecule intermediates, as well as high levels of ectopic recombination products. We use super-resolution microscopy to show that the mutant protein forms longer foci than those formed by wild-type Dmc1. Our data support a model in which longer filaments are more prone to engage in aberrant recombination events, suggesting that filament lengths are normally limited by a regulatory mechanism that functions to prevent recombination-mediated genome rearrangements.

Keywords:

DNA-binding proteins – Saccharomyces cerevisiae – Meiosis – Recombinant proteins – DNA repair – Homologous recombination – Recombinase polymerase amplification – DNA recombination

Introduction

Homologous recombination (HR) is a high-fidelity mechanism of repair of DNA double strand breaks (DSBs), interstrand cross-links, and stalled or collapsed replication forks in mitotically dividing cells. In addition, during meiosis, most eukaryotes rely on reciprocal crossover recombination (CO) to physically link the maternal and paternal chromosomes via chiasmata, thereby making it possible for the meiosis I (MI) spindle to create the tension between homolog pairs that is required for their reductional segregation [1]. The RecA homolog Dmc1 is specifically expressed in meiotic cells and plays the central catalytic role in meiotic recombination in budding yeast [2,3]. A second RecA homolog, Rad51, plays the central catalytic role in mitotic recombination [4,5], but is converted to an accessory protein that regulates Dmc1’s catalytic activity in meiotic cells [3].

Meiotic recombination is initiated by programmed DSBs formed by the activity of the transesterase Spo11 [6]. Following meiotic DSB formation and end resection, Dmc1 forms a helical nucleoprotein filament on the single-stranded DNA (ssDNA) tracts created by the resection machinery [7]. The nucleoprotein filament then searches the genome for a sequence of duplex DNA that is homologous to the ssDNA onto which it is loaded [8]. This region of homology can be an allelic site on one of the two homologous chromatids or on the sister chromatid. In addition, if a DSB is in a region that is repeated at more than one chromosomal locus, this can result in ectopic recombination between the two chromosomal loci [9–12]. Meiotic recombination normally favors the use of the homologous chromosome rather than the sister chromatid, consistent with the biological requirement for interhomolog (IH) COs for reductional segregation; this phenomenon is known as “IH bias” [13,14]. Once a homologous region of double-stranded DNA (dsDNA) is found, strand exchange occurs to form a tract of hybrid DNA, pairing the ssDNA with the complementary strand of the duplex. Hybrid DNA formation displaces the opposite strand of the donor dsDNA, forming a displacement loop (D-loop) [15]. The repair process then uses the intact donor duplex DNA as a template to direct recombination-associated DNA synthesis [16]. Processing of extended D-loops by helicases gives rise to non-crossover recombinants by a pathway referred to as synthesis-dependent strand annealing [17–19]. The subset of D-loops destined to become COs are stabilized to form a joint molecule (JM) species that can be detected on two-dimensional (2D) gels as a so-called single-end invasion (SEI) [20]. SEIs are then converted to double Holliday Junction intermediates (dHJs) by the capture of the second end of the DSB and further repair synthesis to generate full length dsDNA [21]. Finally dHJs are resolved by Exo1 and the MutLγ complex to give rise to COs [22].

HR is highly regulated to ensure its accuracy and avoid potentially deleterious consequences of the process. Two key steps in HR, nucleoprotein filament formation and the initial invasion event, are reversible and therefore subject to this regulation [23]. Nucleoprotein filament formation, or nucleation, involves the recruitment of the strand exchange protein to sites of ssDNA tracts, followed by displacement of the high affinity ssDNA binding protein RPA. Next, filaments elongate in a process that is driven by cooperative interactions between strand exchange protomers. A class of accessory proteins collectively referred to as “mediator” proteins can act to promote the displacement of RPA and/or to stabilize nascent filaments, allowing them to elongate [24,25]. Mutants lacking one of these assembly proteins display defects in formation of filaments on ssDNA, which can be detected by immunostaining or other cytological methods following DNA damaging treatment, or during the normal meiotic program. UvrD family helicases, including UvrD in prokaryotes and Srs2 in budding yeast, antagonize recombination at this step by disassembling ssDNA nucleoprotein filaments [26–29]. Though the strippase function of Srs2 with respect to Rad51 filaments has been well documented, Srs2 does not disassemble Dmc1 filaments, and in fact Dmc1 may inhibit Srs2 activity on ssDNA [30,31]. It is currently unknown whether there exists an ssDNA “strippase” that acts on Dmc1.

Under normal circumstances in vivo, RecA family proteins form nucleoprotein filaments that are shorter than the resolution limit of conventional light microscopy (~200 nanometers). This is true for RecA, and for both eukaryotic RecA homologs, Rad51 and Dmc1 [32–35]. Super-resolution microscopy imaging of Dmc1 filaments formed during meiosis indicates that Dmc1 filaments are typically about 120 nanometers (nm) long, a length that corresponds to roughly 100 nucleotides when taking into account the fact that RecA family proteins stretch the DNA ~1.5 fold when assembled into a filament [36,37]. Furthermore, in the exo1-D173A mutant, in which DNA end resection is impaired during meiosis, JMs are formed at a level that is equivalent to wild-type, implying that short ssDNA tracts support normal meiotic recombination [38]. In contrast, longer than normal Dmc1 filaments accumulate in the absence of Mnd1, a Dmc1 accessory protein that is required for Dmc1 activity after the filament formation stage [36]. Taken together, these results suggest that while RecA family proteins are competent to form long filaments, they are regulated such that they form relatively short filaments in vivo. The significance of this regulation and the factors that influence filament length are presently not well understood.

RecA family recombinases are DNA-dependent ATPases, but their ATPase activity is not required for filament formation or for stand exchange [39–42]. Instead, ATP binding changes the conformation of the protein to a form that has high affinity for DNA, and is thus the active form [39,43]. The ADP bound form of the protein has lower affinity for DNA than the ATP-bound form, and is inactive in homology search and strand exchange. In prokaryotes, RecA ATP hydrolysis is required for filament disassembly following strand exchange, or when the protein inappropriately assembles on dsDNA [35,42]. In contrast to RecA, the eukaryotic recombinases Rad51 and Dmc1 display relatively weak intrinsic ATPase activity and rely on Rad54 family ATP-dependent dsDNA translocases to promote their dissociation [44–48]. Translocase driven dissociation is required to clear strand exchange proteins from D-loops to allow completion of recombination events [49]. Translocases also prevent accumulation of off-pathway complexes formed by filament nucleation on unbroken dsDNA [47,49–53]. A previous study of human Rad51 used in vitro single-molecule fluorescence imaging to show that Rad51-ADP dissociation from dsDNA is inefficient and incomplete, suggesting that the activity of the translocases is required even when Rad51 is in the ADP-bound form [54]. Moreover, Rad54 overexpression was observed to suppress the defects associated with Rad51-K191R, a rad51 mutant that is completely defective in ATP hydrolysis, implying that the ATPase activity of Rad51 is not required for it to be removed from dsDNA by Rad54 [55–57]. Finally, in the context of the nucleoprotein filament, the ATPase domain of one protomer directly contacts the N-terminal binding domain of the adjacent protomer; this observation is believed to be the structural basis for the finding that ATP-binding promotes protomer-protomer cooperativity [58,59].

We are interested in understanding how accessory proteins regulate the activity of the meiotic RecA homolog Dmc1. In Saccharomyces cerevisiae, Dmc1’s activity is regulated by at least five key accessory proteins including RPA, Mei5-Sae3, Hop2-Mnd1, Rad51, and the translocase Rdh54 (a.k.a. Tid1). RPA rapidly binds to tracts of ssDNA and serves to coordinate the interactions between Dmc1’s other accessory proteins and ssDNA [60]. In vivo, Mei5-Sae3 and Rad51 are required for normal Dmc1 filament formation at tracts of RPA coated ssDNA, suggesting that these factors are involved in nucleation and/or filament elongation [61–63]. Conversely, Hop2-Mnd1 is required for strand exchange, but not for filament nucleation or stability [64,65]. Rdh54 is a Rad54 family translocase implicated in promoting dissociation of Dmc1 from dsDNA, as discussed above.

Budding yeast Mei5-Sae3 is a homolog of Schizosaccharomyces pombe and mammalian Sfr1-Swi5/MEI5-SWI5, with no known homolog in plants [66]. In budding yeast, Mei5-Sae3 is Dmc1-specific, whereas in fission yeast Sfr1-Swi5 is an accessory factor to both Dmc1 and Rad51 [67]. In mammals, MEI5-SWI5 protein is reported to function with RAD51, but there is no known interaction with DMC1, and an effort to detect DMC1 stimulatory activity in vitro yielded negative results [68,69]. Biochemical studies have suggested several functions for Mei5-Sae3. First, studies using fission yeast proteins have shown that Sfr1-Swi5 stimulates fission yeast Rad51 (referred to as Rhp51) and Dmc1 in three-stranded DNA exchange reactions, and it helps Rhp51 overcome the inhibitory effect of RPA [67]. Studies using purified budding yeast Mei5-Sae3 and Dmc1 similarly concluded that Mei5-Sae3 promotes Dmc1 loading onto RPA-coated ssDNA, and that it enhances Dmc1-mediated D-loop formation when used alone, or in combination with Rad51 [3,60,70]. In addition to this mediator activity, Haruta et al. also reported that Sfr1-Swi5 enhances Rhp51’s ATPase activity; this result was subsequently confirmed and extended by work from Su et al. using purified Mus musculus proteins [67,69]. Su et al. showed that SWI5-MEI5 stimulates RAD51 by promoting ADP release, the step in ATP hydrolysis that is believed to be the slowest and thus rate-limiting [69,71]. Enhancement of ADP release is thought to have a stabilizing effect on Rad51 filaments by maintaining them in the ATP-bound state. In addition, later studies using single-molecule fluorescence resonance energy transfer, concluded that mouse SWI5-MEI5 promotes RAD51 nucleation by preventing dissociation, effectively reducing the number of protomers required for a nucleation event from three to two [72]. The same study also found that fission yeast Sfr1-Swi5 prevents Rhp51 disassembly, suggesting a conserved role for this complex in stabilizing Rad51 filaments.

In vivo, Saccharomyces cerevisiae Dmc1 and Mei5-Sae3 are interdependent for focus formation, and the foci formed by the two proteins co-localize with one another, and with other DSB-dependent proteins such as Rad51 [62,63]. Moreover, Dmc1 and Mei5-Sae3 both depend on Rad51 for normal meiotic focus formation; average focus staining intensity is lower in rad51 mutants than in wild-type [61,62]. Consistent with it being necessary for Dmc1 focus formation, Mei5-Sae3 is also required for Dmc1-mediated recombination. In vivo, DSBs form normally in mei5 or sae3 mutants, but these intermediates are not converted to D-loops [62,63,73]. Fission yeast Rhp51 differs from Dmc1 in its dependency on Sfr1-Swi5; while loss of Sfr1-Swi5 reduces recombination, recombination is only eliminated when both Sfr1-Swi5 and Rhp55-Rhp57, a heterodimeric accessory protein homologous to budding yeast Rad55-Rad57, are deleted [74]. Similarly, knockdown of MEI5-SWI5 in human cells impairs RAD51 focus formation in response to ionizing radiation and also reduces recombination [68]. In contrast, deletion of mouse Swi5 and Sfr1 does not reduce the level of recombination when assayed with a direct-repeat reporter construct, but it does make cells more sensitive to DNA damaging agents that require HR for repair, including ionizing radiation, camptothecin, and poly(ADP-ribose) polymerase (PARP) inhibitor [75]. It is not known whether these differences in the requirement of SWI5-MEI5 by RAD51 in humans and mouse are due to differences in the cell types used or true biological differences in the human and mouse RAD51 recombinases [68].

Rad51, the RecA homolog that catalyzes homology search and strand exchange during mitotic recombination, is the second accessory protein that plays a role in forming wild-type Dmc1 filaments during meiosis [61]. Although Rad51 is required for normal meiotic recombination, its strand exchange activity is dispensable [3]. In fact, Rad51 strand exchange activity is inhibited during MI by the meiosis-specific protein Hed1 [76,77]. In the absence of Rad51, Dmc1 foci have reduced staining intensity, suggesting that filaments are defective [61,78]. Recombination still occurs in rad51 mutants, but it is mis-regulated such that D-loop formation occurs predominantly between sister chromatids, instead of between homologous chromosomes [79]. In addition, CO formation is reduced, only a sub-population progresses through meiotic divisions, and the spores formed are not viable [4]. In biochemical reconstitution experiments, Rad51 alone can stimulate Dmc1-mediated D-loop formation, although optimal levels of D-loop formation require both Rad51 and Mei5-Sae3 [3]. In spite of its importance as a Dmc1 accessory factor, very little is known about the molecular mechanisms involved in Rad51’s non-catalytic role in meiotic recombination.

One approach to studying the role of accessory proteins is to assume that the activity of the enzyme has evolved to depend on that accessory factor. In this view, beneficial regulation of an enzyme’s activity is selected for at the expense of the enzyme’s intrinsic activity. If such an evolutionary process is responsible for a particular regulatory mechanism, it should be possible to mutate the core enzyme to eliminate the “built-in” defect, rendering the mutant protein capable of catalyzing its reaction in the absence of the accessory protein. Comparison of the activities of the mutant and wild-type proteins with and without the accessory protein can then provide mechanistic insight into the processes that accessory protein normally regulates.

We applied this approach to Dmc1 in an attempt to further elucidate the mechanisms through which Mei5-Sae3 influences Dmc1’s activity. We identified a gain-of-function dmc1 mutant whose activity is independent of Mei5-Sae3. Characterization of this Dmc1 mutant provides new insight into the mechanism of action of Mei5-Sae3 in vivo, and also sheds light on the functional relationship between Mei5-Sae3 and Rad51. Furthermore, characterization of this gain-of-function version of Dmc1 reveals that it forms longer than normal filaments and displays higher than normal levels of IS, ectopic, and multi-chromatid recombination. We interpret these observations in the context of recent studies showing that a single strand exchange filament can simultaneously engage more than one dsDNA molecule.

Results

In order to better understand the function of Mei5-Sae3 and Rad51 in Dmc1-mediated HR, we sought to identify a DMC1 allele that would bypass the requirement for one of these accessory factors. Analysis of Dmc1-mediated recombination in the absence of an accessory factor would then allow us to identify regulatory features that depend on the accessory protein by comparison to the wild-type process. To this end, we constructed two dmc1 mutants based on previously characterized gain-of-function mutations in Dmc1 homologs, RecA-E96D and Rad51-I345T [42,80,81]. Sequence alignments indicated that the amino acid residues altered in RecA-E96 and Rad54-I145T mutants are conserved allowing us to construct corresponding mutant forms of Dmc1; for RecA-E96D the corresponding mutant is Dmc1-E157D and for Rad51-I134T the corresponding mutant is Dmc1-I282T. The RecA-E96D mutation shortens the length of a critical amino acid side chain in the ATPase active site, increasing the distance between the water molecule that acts as the nucleophile for hydrolysis and the activating carboxylate [80]. The mutation dramatically reduces the rate of ATP hydrolysis thereby maintaining RecA in the ATP-bound form, which is active for DNA binding, homology search, and strand exchange. Due to the high sequence conservation of this site, Dmc1-E157D is very likely to be defective in ATPase activity, like RecA-E96D. The Rad51-I345T mutation suppresses defects conferred by the heterodimeric accessory protein Rad55-Rad57, which stabilizes Rad51 filaments [81]; we reasoned that the corresponding mutation in Dmc1 might suppress the requirement for Mei5-Sae3 as biochemical studies on Swi5-Sfr1, which is homologous to Mei5-Sae3, indicated Swi5-Sfr1 also acts by stabilizing strand exchange filaments [67,74].

To assess whether either of these Dmc1 mutants would bypass Mei5-Sae3 and/or Rad51, we constructed diploid yeast lacking either Mei5 or Rad51 with the corresponding Dmc1 mutation, and assessed sporulation efficiency and spore viability alongside DMC1⁺ mei5 and DMC1⁺ rad51 controls. In a mei5 strain, tetrads are formed very inefficiently, whereas in a rad51 mutant, tetrads are formed, but almost all spores within them are dead [4,62,63]. We found that dmc1-E157D bypasses Mei5-Sae3 with respect to sporulation and spore viability (Table 1). The spore viabilities of dmc1-E157D, dmc1-E157D mei5, and dmc1-E157D sae3 are nearly identical to one another (57.6%, 50.3%, and 57.0% respectively), suggesting that Dmc1-E157D function is largely independent of Mei5-Sae3. In contrast, dmc1-E157D does not bypass the requirement for rad51 with respect to spore viability (<0.6% in rad51 versus 0.7% in dmc1-E157D rad51).

Spore viability data from a dmc1-E157D/DMC1⁺ mei5/mei5 heterozygote indicates that Dmc1-E157D is dominant to wild-type Dmc1 (Dmc1-WT) with respect to formation of viable spores in a mei5 mutant background (58.8% in dmc1-E157D/DMC1⁺ mei5/mei5, vs. 50.3% in dmc1-E157D/dmc1-E157D mei5/mei5). In contrast, Dmc1-E157D causes only a minor reduction in spore viability when both Dmc1-WT and Mei5 proteins are present (91.2% in dmc1-E157D/DMC1+ MEI5+/MEI5+ vs. 98.4% in WT). In contrast to dmc1-E157D, we did not detect phenotypic suppression in dmc1-I282T mutants, either with respect to prophase arrest in a mei5 mutant background, or with respect to spore viability in a rad51 background. Importantly, the Dmc1-E157D mutation does not result in increased expression or stability of the protein as assayed by Western blotting of meiotic yeast whole cell extracts, thus ruling out a trivial explanation for Dmc1-E157D’s bypass of the mei5 and sae3 mutations (S1 Fig).

Dmc1-E157D forms meiotic immunostaining foci in the absence of Mei5 and Rad51

We next performed immunofluorescence staining of spread meiotic nuclei to examine Dmc1 focus formation in the dmc1-E157D and dmc1-E157D mei5 strains. As shown previously, meiotic Dmc1-WT focus formation is severely defective in mei5 mutant cells, but Dmc1-E157D forms bright foci in the mei5 mutant background (Fig 1A) [62,63]. Notably, Dmc1 foci accumulate to higher levels and persist for longer in dmc1-E157D and dmc1-E157D mei5 when compared to wild-type (Fig 1B).

One model suggests that Mei5-Sae3 and Rad51 cooperate to promote Dmc1 filament formation [14]. Because dmc1-E157D bypasses mei5, we reasoned that if this model is correct, dmc1-E157D might also bypass the defect seen for formation of brightly-staining Dmc1 foci in rad51 cells, even though it does not suppress the spore viability defect observed in these cells. To test this, we constructed dmc1-E157D rad51 and dmc1-E157D mei5 rad51 strains, and looked for Dmc1 focus formation in spread meiotic nuclei. In contrast to a rad51 single mutant, in which Dmc1-WT staining intensity is reduced, the Dmc1 foci observed in dmc1-E157D rad51 and dmc1-E157D mei5 rad51 nuclei were brighter and more numerous than those in wild-type (Fig 1C and 1D) [61,78]. We conclude that dmc1-E157D appears to bypass the role of Rad51 with respect to Dmc1 focus formation.

dmc1-E157D forms immunostaining foci in the absence of DSBs

Because the Dmc1-E157D mutant is modeled after RecA-E96D, which has been shown to form foci on undamaged DNA, we wanted to ask whether the same was true of the corresponding Dmc1 mutant [35]. To determine whether any of the foci that we observed in the dmc1-E157D background resulted from binding to chromosomes independent of DSBs, we introduced the spo11 mutation into our dmc1-E157D strains to block DSB formation. Spo11 is the catalytic subunit of a meiosis-specific complex that induces DSBs at the outset of meiosis [6]. Immunostaining of spread meiotic nuclei for Dmc1 and RPA revealed that in contrast to the spo11 single mutant, which typically forms few if any Dmc1 foci, nearly all spo11 dmc1-E157D nuclei contained numerous Dmc1 foci (Fig 1C and 1E) [51]. RPA serves as a marker for DSB-associated tracts of ssDNA in mid-to-late prophase I. RPA foci are detected early in prophase in spo11 mutants owing to the role of RPA in pre-meiotic DNA replication, but then disappear 4 hours after induction of meiosis [83]. We found that at 4 hours, the majority of nuclei lacking RPA foci contained Dmc1 foci in spo11 dmc1-E157D and spo11 dmc1-E157D mei5 (100% and 96% of nuclei lacking RPA had Dmc1 foci, respectively) (Fig 1E) indicating that Dmc1-E157D forms DSB-independent foci. It is thus likely that a substantial fraction of the foci observed in SPO11⁺ dmc1-E157D cells represent off-pathway structures formed by binding unbroken chromosomal loci. However, an increase in the total number of DSBs formed or an increase in DSB lifespan could also partially account for the increased number of Dmc1 foci and their persistence in the dmc1-E157D background relative to wild-type.

dmc1-E157D bypasses Mei5, but not Rad51, with respect to meiotic CO formation

To examine whether Dmc1-E157D is competent to carry out recombination in the absence of Mei5, we performed one-dimensional (1D) gel electrophoresis, followed by Southern blotting, to examine DSBs and CO products at the well-characterized recombination hotspot HIS4::LEU2 [84]. XhoI digestion of genomic DNA from meiotic time course experiments followed by 1D gel electrophoresis and Southern blotting to detect the HIS4::LEU2 hotspot can be used to detect DSB intermediates and IH CO products, as well as products that result from ectopic recombination between the HIS4::LEU2 locus and the native LEU2 locus, which are separated by ~23 kilobases on chromosome III [12,84]. As shown previously, DSBs accumulate and CO formation is very limited in DMC1⁺ mei5 (Fig 2A and 2B) [62,63]. In contrast, although dmc1-E157D and dmc1-E157D mei5 cells initially accumulate DSBs (Fig 2A and 2B, S2 Fig), those breaks are resolved by 24 hours, at which point CO formation is equivalent to wild-type. Further examination of DSB formation in wild-type and dmc1-E157D cells using PstI digestion of genomic DNA from meiotic samples to look at DSB resection status revealed that although DSBs accumulate to somewhat higher levels in dmc1-E157D relative to wild-type, there are little or no differences in resection status between the two strains (S2 Fig). Interestingly, ectopic recombination is elevated ~3.5-fold in dmc1-E157D and dmc1-E157D mei5 relative to wild-type. In addition, whereas only 8.7% of DMC1⁺ mei5 cells progress through a meiotic division, 50.0% of dmc1-E157D mei5 cells progress, a level nearly equivalent to dmc1-E157D (58.4%) (Fig 2B). These results show that Dmc1-E157D bypasses the normal requirement for Mei5 during meiotic recombination.

Because Dmc1-E157D also bypasses Rad51 with respect to forming brightly staining Dmc1 foci, we wanted to ask whether it similarly bypasses Rad51 for CO formation and DSB resolution at HIS4::LEU2. Previous studies of rad51 mutants showed that DSBs accumulate and undergo more extensive resection than wild-type [4]. In addition, the final level of COs that form in rad51 was reported to be 5-fold lower than wild-type, and ectopic recombination is ~1.6-fold higher at 10 hours in sporulation medium [4,85]. We confirmed these phenotypes for the rad51 single mutant (Fig 2A and 2B). Consistent with the failure of dmc1-E157D to rescue the low spore viability phenotype of rad51 (Table 1), we found that dmc1-E157D rad51 accumulates hyper-resected DSBs (Fig 2A). Surprisingly, dmc1-E157D rad51 makes fewer COs than rad51, implying that the dmc1-E157D rad51 double mutant is more defective than either the dmc1-E157D or the rad51 single mutants. Meiotic progression data similarly indicate that dmc1-E157D rad51 is more defective than both dmc1-E157D and rad51; only 24.8% of dmc1-E157D rad51 cells execute at least one meiotic division, compared to 58.4% and 54.5% of dmc1-E157D and rad51 cells, respectively (Fig 2B). Additionally, very little ectopic recombination is detected in dmc1-E157D rad51, possibly reflecting the fact that there is less recombination overall, or indicating that there is a change in the pattern of JM formation or their resolution. Overall our results indicate that dmc1-E157D does not bypass rad51 with respect to resolution of meiotic DSBs.

The dmc1-E157D mei5 rad51 triple mutant was similar to the dmc1-E157D rad51 double mutant, with the triple mutant displaying slightly more pronounced defects in final CO levels (Fig 2A and 2B). We also found that the efficiency of the first meiotic division is somewhat reduced in the dmc1-E157D mei5 rad51 mutant (11.3%) compared to the dmc1-E157D rad51 (24.8%) mutant (Fig 2B). These results indicate that recombination in dmc1-E157D displays a strong dependence on Rad51, but very limited dependence on Mei5 unless Rad51 is absent.

spo11 rescues the meiotic progression and segregation defects associated with dmc1-E157D

In contrast to the typical MI segregation that is observed in wild-type cells, in which there are two well-defined and equally-sized DAPI staining bodies, MI segregation in dmc1-E157D often appears to be abnormal, and can include defects such as a single elongated DAPI staining body rather than two separated bodies, as well as separated DAPI staining bodies of dramatically different sizes (S3 Fig). Introduction of the spo11 mutation into the dmc1-E157D background largely rescued these deficiencies. In addition, the spo11 mutation suppressed the MI division delay that occurs in dmc1-E157D cells (S3 Fig). Thus the meiotic segregation and progression defects observed in the dmc1-E157D background are DSB-dependent. This finding suggests that although there are likely numerous DSB-independent Dmc1 foci in these strains, these Dmc1-dsDNA complexes do not dramatically interfere with chromosome segregation.

Dmc1-mediated meiotic recombination is independent of Mei5-Sae3 in dmc1-E157D

We next sought to further characterize Dmc1-E157D-mediated recombination in the absence of Mei5 by 2D gel electrophoresis and Southern blotting. Using this method, an array of JM recombination intermediates can be detected at the HIS4::LEU2 locus, including SEIs, intersister-dHJs (IS-dHJs), IH-dHJs, and multi-chromatid JMs (mcJMs) (Fig 3A) [86]. As expected, JM formation is severely compromised in mei5 (Fig 3B and 3C). In contrast, in dmc1-E157D mei5, JM formation is efficient, with IH-dHJ levels equivalent to those in wild-type. IS-dHJs, however, are increased ~3-fold, reducing the IH-dHJ/IS-dHJ ratio from 5.0 in wild-type to ~1.5 in dmc1-E157D (Fig 3C). dmc1-E157D mei5 phenocopies dmc1-E157D, also having increased IS-dHJs and a reduced IH/IS ratio of ~1.6. SEIs form at the similar levels in the dmc1-E157D and dmc1-E157D mei5 mutants as in wild-type (Fig 3C). Like IS-dHJs, mcJMs are increased relative to wild-type in both dmc1-E157D and dmc1-E157D mei5 (3.0-fold and 2.7-fold respectively). The similar array of JMs observed in dmc1-E157D and dmc1-E157D mei5 cells further indicates that Dmc1-E157D-mediated recombination occurs independent of Mei5-Sae3. Although a decrease in the IH/IS ratio can be interpreted as a defect in the mechanism of IH bias, this case is unusual in that the decreased ratio results from increased IS-dHJs, with no reciprocal decrease in IH-dHJs. The fact that the level of IH-dHJs in dmc1-E157D mei5 cells is equivalent to that in wild-type suggests that the mechanism of homolog bias is intact in this mutant, and reveals that Mei5-Sae3 is not required for IH bias. The data also suggest that the dmc1-E157D mutant is hyper-recombinant, displaying higher than normal levels of IS-dHJs and mcJMs (Fig 3C), as well as increased ectopic COs (Fig 2B).

The ndt80 mutation increases total JMs, but does not change their distribution

To rule out the possibility that certain JM species have longer lifespans in the dmc1-E157D background, we introduced the ndt80 mutation. Deletion of NDT80⁺ prevents recombination intermediate processing, and JMs accumulate to high levels in this background (S4 Fig) [19]. Importantly, we found that IS-dHJs and mcJMs are also elevated in ndt80 dmc1-E157D relative to ndt80, with no appreciable differences in SEIs and IH-dHJs (S4 Fig). These findings support a model in which the elevated levels of IS-dHJS and mcJMs are a result of increased formation of these species by Dmc1-E157D, as opposed these species being less efficiently resolved in dmc1-E157D and dmc1-E157D mei5 cells.

dmc1-E157D rad51 exhibits a profound IH bias defect and a reduction in JM formation

We next examined Dmc1-E157D-mediated recombination in the absence of Rad51 using 2D gel electrophoresis. In a rad51 mutant, Dmc1 carries out recombination, but there is a profound IH bias defect, and most recombination occurs between sisters [79]. The IH-dHJ/IS-dHJ ratio in rad51 is 0.4 and the same ratio is observed for dmc1-E157D rad51 (Fig 3D and 3E, S5 Fig). This defect in the IH/IS ratio is the result of increased IS-dHJs and at the expense of IH-dHJs. The profound defect in IH bias in dmc1-E157D rad51 contrasts with the dmc1-E157D single mutant, in which the IH-dHJ/IS-dHJ ratio is ~1.6. We conclude that rad51 is epistatic to dmc1-E157D with respect to its impact on partner choice. The impact of a rad51 mutation on the IH/IS ratio in dmc1-E157D cells further supports the view that the mechanism of IH bias is intact in dmc1-E157D mei5 cells and therefore the conclusion that Mei5-Sae3 is not required for IH bias. The levels of IS-dHJs, IH-dHJs, SEIs, and mcJMs are all reduced approximately 2-fold in dmc1-E157D rad51 relative to rad51 (Fig 3E); thus, the hyper-recombinant phenotype of dmc1-E157D cells is Rad51-dependent. These findings are also consistent with the observation that CO levels in dmc1-E157D are reduced about 2-fold by the rad51 mutation (Fig 2B).

JM formation is absent in triple mutant dmc1-E157D mei5 rad51

We also analyzed the dmc1-E157D mei5 rad51 triple mutant by 2D gel electrophoresis. Surprisingly, while both dmc1-E157D mei5 and dmc1-E157D rad51 formed readily-detectable levels of JMs (Fig 3B and 3D), and Dmc1 foci were detected in dmc1-E157D mei5 rad51 spread meiotic nuclei (Fig 1C and 1D), no JMs were detected in the triple mutant (Fig 3D and 3E). Because rad51 strains are genetically unstable, we constructed an independent dmc1-E157D mei5 rad51 diploid and repeated this experiment to ensure that our original strain had not picked up an additional mutation that suppressed the formation of JMs. Meiotic JMs were also undetectable in the duplicate dmc1-E157D mei5 rad51 strain (S5 Fig). Given that resected and unrepaired DSBs trigger delays in meiotic progression, the 2D gel analyses are consistent with our finding that only ~10% of cells progress through a meiotic division in dmc1-E157D mei5 rad51, and that there is hyper-resection and limited CO formation in this strain (Fig 2A and 2B). We conclude that recombination is further compromised in the triple mutant dmc1-E157D mei5 rad51 when compared to either double mutant. These results provide additional evidence that although Dmc1-E157D’s activity is essentially Mei5-Sae3 independent in RAD51⁺ cells, Mei5-Sae3 can promote limited Dmc1-E157D activity when Rad51 is absent.

The defects associated with dmc1-E157D and dmc1-E157D mei5 are independent of Rad51’s catalytic activity

One possible explanation for the results we obtained from our JM analysis in Fig 3 is that the dmc1-E157D mutation changes the behavior of Dmc1 in a manner that activates the strand exchange activity of Rad51. This possibility is emphasized by previous results suggesting that Dmc1 itself inhibits Rad51’s strand exchange activity [87,88]. Normally, Rad51’s strand exchange activity is repressed by Dmc1 and by the meiosis-specific Rad51 inhibitor Hed1 [3,76]. However, it was important to determine if Rad51’s strand exchange activity plays a greater role in promoting recombination in dmc1-E157D cells than in wild-type [88]. To test this, we crossed the rad51-II3A mutation into our dmc1-E157D strains. The three alanine substitutions coded by rad51-II3A eliminate DNA binding site II, the secondary, low affinity DNA binding site required for homology searching. Rad51-II3A forms filaments, but lacks the ability to catalyze D-loop formation [3].

Our results indicate that the rad51-II3A mutation does not alter the efficiency and pattern of JM formation in the dmc1-E157D mutant (S6 Fig). This observation indicates that Dmc1, not Rad51, promotes the majority of homology search and strand exchange in dmc1-E157D cells, as is the case in wild-type cells. Thus, the hyper-recombinant phenotype observed in dmc1-E157D results from increased Dmc1 activity rather than activation of Rad51’s activity. On the other hand, rad51-II3A causes a greater reduction in spore viability in a dmc1-E157D background than in a wild-type background (Table 1; from 57.6% to 17.0% for dmc1-E157D compared to 98.6% to 82.9% for DMC1⁺, p < 0.01). The modest reduction in viability seen in rad51-II3A single mutants was previously interpreted to suggest that Rad51’s strand exchange activity is only required at a small subset of the roughly 200 DSB sites where Dmc1-dependent DSB repair fails [3]. In the context of this interpretation, the data presented here can be explained if the fraction of attempted recombination events that require Rad51’s strand exchange activity, although still small, is higher in dmc1-E157D than in wild-type.

Meiotic two-hybrid analysis indicates that direct Rad51-Dmc1 interaction is independent of Mei5

The results presented in Fig 3 show that Rad51 can impact Dmc1’s activity in the absence of Mei5-Sae3. To determine if Rad51’s influence on Dmc1 can be explained by direct interaction of the two proteins, we carried out meiotic two-hybrid analysis. A previous two-hybrid study in budding yeast using the conventional mitotic method detected a low level of direct interaction between Rad51 and Dmc1, although the authors of that study did not ascribe significance to the interaction because it was much weaker than that observed for homotypic Rad51-Rad51 and Dmc1-Dmc1 interactions [89]. We wished to determine if Mei5-Sae3 enhanced the interaction between the two proteins and therefore used the meiotic two-hybrid method to test the interaction in a cell type that expresses the accessory protein. As in the previous study, the level of interaction observed for Rad51-Dmc1 was much lower than that in the Rad51-Rad51 and Dmc1-Dmc1 homotypic controls, but nonetheless reproducibly higher than the background level observed in empty vector controls (S7 Fig). Importantly, an equivalent two-hybrid signal was detected in a mei5 background as in a wild-type background (p = 0.5 using a Wilcoxon signed-rank test) indicating that, in this system, Rad51-Dmc1 interaction is independent of Mei5-Sae3.

Super-resolution imaging of dmc1-E157D mutants reveals abnormalities in Dmc1 and RPA foci

Because Dmc1-E157D forms foci at high density, we expected that the wide-field microscopy method was not resolving closely spaced foci. Therefore, in order to obtain more accurate focus measurements, we re-examined chromosome spreads using stimulated emission depletion (STED) microscopy, which improves the resolution limit from around 200 nanometers (nm) to under 50 nm (see Methods Section, S8 Fig). For each strain, we imaged at least 13 randomly selected RPA-positive nuclei (Fig 4A). The average number of RPA foci detected was lowest in wild-type (70.0 ± 22.2 foci) (Fig 4B). All other strains displayed higher average RPA focus counts including rad51 (140.5 ± 44.9 foci), dmc1-E157D (111.5 ± 28.8 foci), dmc1-E157D mei5 (130.8 ± 21.2 foci), dmc1-E157D rad51 (132.0 ± 21.7 foci), and dmc1-E157D mei5 rad51 (131.3 ± 38.6 foci). We also measured focus lengths, and found that wild-type RPA foci are the shortest (76.8 ± 27.0 nm), while rad51, dmc1-E157D rad51, and dmc1-E157D mei5 rad51 foci are all significantly longer (134.0 ± 70.4 nm, 136.0 ± 77.8 nm, 130.8 ± 63.8 nm respectively; p < 0.01, Wilcoxon test), but not significantly different from one another (pairwise p = 0.53, 0.60, and 0.94, respectively) (Fig 4C). The fact that RPA foci are longer in these strains is unsurprising given that we observed hyper-resection in these strains by 1D gel electrophoresis (Fig 2A). dmc1-E157D and dmc1-E157D mei5 mutant RPA foci are significantly different from both wild-type and rad51 mutants (107.4 ± 49.5 nm, 97.7 ± 39.6 nm respectively; p < 0.01), being an intermediate average length between the two. This finding contrasts with our Southern blotting analysis of DSBs (Fig 2A and S2 Fig), in which little to no difference between these two mutants and wild-type was detected with respect to resection tract lengths (see Discussion).

The average number of Dmc1 foci per nucleus was similar in wild-type and rad51 single mutants (26.9 ± 17.7 foci and 23.3 ± 12.8 foci, respectively, Fig 4A and 4B). All dmc1-E157D strains displayed higher than normal focus counts including dmc1-E157D (114.0 ± 21.0 foci), dmc1-E157D mei5 (119.2 ± 25.6 foci), dmc1-E157D rad51 (105.3 ± 27.0 foci), and dmc1-E157D mei5 rad51 (106.8 ± 23.8 foci) (Fig 4B). This result can be explained by the mutant’s ability to form DSB-independent foci, by a longer lifespan of DSB-dependent foci, and/or by an increase in the total number of DSBs formed (Fig 1E, S2 Fig). We also measured the lengths of these Dmc1 foci, and found that Dmc1 foci are significantly shorter in rad51 (82.5 ± 30.0 nm, p < 0.01, Wilcoxon test) than wild-type (97.1 ± 38.8 nm) (Fig 4C), consistent with previous wide-field microscopy analyses [78]. Dmc1 foci are longer in all dmc1-E157D strains, including dmc1-E157D (134.1 ± 61.5 nm, p < 0.01), dmc1-E157D mei5 (147.1 ± 66.4 nm, p < 0.01), dmc1-E157D rad51 (161.9 ± 78.9, p < 0.01), and dmc1-E157D mei5 rad51 (143.3 ± 64.7 nm, p < 0.01) relative to wild-type (Fig 4C).

Although measurements of Dmc1 focus lengths shows that Dmc1-E157D makes longer than normal filaments overall, the fact that the protein likely forms high levels of off-pathway foci in addition to forming foci at sites of recombination raises the possibility that the long filaments observed might only be off-pathway forms, with no appreciable change in the average length of recombinogenic filaments. Furthermore, the fraction of recombinogenic foci could differ in different strains. For example, off-pathway Dmc1 foci may make up a larger fraction of the total Dmc1 foci in dmc1-E157D strains than in wild-type and rad51. To provide evidence that recombinogenic foci are longer on average, we examined the lengths of Dmc1 foci that colocalized with RPA. Given that all of the mutants have more RPA foci and some have more Dmc1 foci (Fig 4B), the level of fortuitous colocalization is expected to be higher in the mutants than in wild-type. We therefore estimated the frequency of fortuitous colocalization in all strains by a previously described method [83]. This method may yield an overestimate of fortuitous colocalization because the most focus dense region of each nucleus was used in the analysis. Only nuclei in which the level of observed colocalization exceeded the estimated fortuitous colocalization in the same image by more than 5% were considered informative for analysis. A total of 10/13 wild-type nuclei (35.5% experimental and 18.8% fortuitous), 10/13 dmc1-E157D nuclei (70.1% experimental and 58.6% fortuitous colocalization), and 6/13 dmc1-E157D mei5 nuclei (69.1% experimental and 57.1% fortuitous colocalization) met our criterion for analysis, indicating that RPA-colocalization provides a meaningful criterion to identify a subset of Dmc1 foci enriched for recombinogenic as opposed to off-pathway structures in these cells. Because of higher focus density and average focus size, none of the dmc1-E157D rad51 and dmc1-E157D mei5 rad51 nuclei met our criterion for detection of true co-localization. The average contour length of Dmc1 filaments that colocalized with RPA was 118.9 ± 40.0 nm in wild-type, or ~100 nucleotides, similar to the corresponding value obtained using direct stochastic optical reconstruction microscopy (dSTORM), a different super-resolution light microscopy method (Fig 4D) [36]. The average focus length for RPA colocalizing Dmc1 foci in dmc1-E157D was significantly longer than wild-type (149.5 ± 66.8 nm, or ~ 160 nucleotides, p<0.01, Wilcoxon test), and also different from the total population of unselected Dmc1 foci in dmc1-E157D cells (134.1 ± 61.5 nm). The average focus length for RPA colocalizing Dmc1 foci in dmc1-E157D mei5 was also significantly longer than in wild-type (168.0 ± 66.4 nm, or ~190 nucleotides, p <0.01), and different from the total Dmc1 foci lengths in that background (147.1 ± 66.4 nm). Thus, Dmc1-E157D not only makes longer foci overall, but Dmc1-E157D foci associated with RPA-marked recombination sites are also distinctly longer under conditions of hyper-recombination (i.e. in dmc1-E157D and dmc1-E157D mei5) compared to wild-type.

Rhd54 promotes meiotic progression in dmc1-E157D cells

The cytological results presented above suggest that Dmc1-E157D is more likely than Dmc1-WT to form off-pathway filaments on dsDNA. DSB-independent foci are only easily detected for Dmc1-WT when Rdh54, the key translocase involved in disassembling them, is absent [51]. This observation suggested that Dmc1-E157D might be more resistant to dsDNA dissociation by Rdh54. To determine whether Rdh54 was active in dmc1-E157D mutants, we constructed the dmc1-E157D rdh54 double mutant. If Rdh54 is inefficient at promoting Dmc1-E157D dissociation from dsDNA, loss of Rdh54 in the dmc1-E157D background should be inconsequential. Instead, we find that although both dmc1-E157D and rdh54 single mutants progress through meiosis to form tetrads in which roughly 50% or more of spores are viable, the dmc1-E157D rdh54 double mutant arrested in prophase and failed to form spores (Table 1; S9 Fig). Thus, Rdh54 is active in dmc1-E157D cells.

Mei5-Sae3 is not required for the DSB-independent foci formed by Dmc1-WT protein in the absence of Rdh54

Dmc1-E157D differs from Dmc1-WT in that it forms high levels of off-pathway foci and does so independently of Mei5-Sae3. This suggests that although the mutant bypasses the requirement for Mei5-Sae3 with respect to forming recombinogenic foci, it might not fully recapitulate Mei5-Sae3 function because Mei5-Sae3’s activity has only been shown to display DSB-dependent foci. It was not known if Mei5-Sae3 is also required for the off-pathway Dmc1 foci that accumulate when disassembly of dsDNA bound structures is blocked by RDH54⁺ deletion. Therefore, to determine if Mei5-Sae3 is normally required for Dmc1 to form off-pathway complexes on dsDNA in vivo, we compared Dmc1 focus formation in spo11 rdh54 mei5 to that in the spo11 rdh54 double mutant; a spo11 single mutant served as the negative control. The controls generated the expected results with spo11 rdh54 nuclei displaying an average of 37 ± 14 Dmc1 foci per nucleus and spo11 nuclei an average of only 3 ± 4 foci per nucleus (S10 Fig). The spo11 rdh54 mei5 triple mutant displayed an average of 37 ± 13 foci, like the positive control, indicating that off-pathway focus formation by Dmc1-WT protein occurs independently of Mei5. Thus, Mei5-Sae3’s function is dispensable for nucleation of Dmc1 complexes on dsDNA that are substrates for Rdh54-mediated disassembly. The implications of this finding are discussed below.

Discussion

The mechanism of Mei5-Sae3-mediated Dmc1 filament formation

Dmc1-E157D was designed to mimic the activity of the previously characterized bacterial protein RecA-E96D. Assuming this prediction is correct and Dmc1-E157D has reduced ATPase activity, our results provide in vivo support for the conclusion of Chi and colleagues that Swi5-Sfr1 acts to stabilize Rad51 filaments by promoting ADP release, thereby maintaining the filament in the active, ATP-bound form [69], given that a mutation designed to favor the ATP bound form of Dmc1 bypasses the normal requirement for Mei5-Sae3. On the other hand, the regulatory defects observed in Dmc1-E157D suggest that the function of Mei5-Sae3-mediated regulation may involve more than overall enhancement of Dmc1 filament stability, because the Dmc1-E157D mutant displays abnormally high levels of spo11-independent Dmc1-E157D binding to chromosomes (Fig 1E). We also find that although Mei5-Sae3 is required for cytologically detectable Dmc1 focus formation at sites of DSBs in wild-type cells, it is not required to observe the off-pathway dsDNA-bound foci formed by Dmc1-WT in rdh54 cells (S10 Fig). These findings raise the possibility that stabilizing the ATP-bound form of Dmc1 alone may not fully explain Mei5-Sae3 function; it is possible that Mei5-Sae3 also confers ssDNA specificity to Dmc1-DNA interaction in vivo. The proposal that Mei5-Sae3 recruits Dmc1 to ssDNA is consistent with prior observations that Mei5-Sae3 preferentially binds ssDNA, and that it directly interacts with the ssDNA-specific protein RPA [60,67,70]. Thus, Mei5-Sae3 may combine the ability to enhance Dmc1 filament stability with the ability to specifically promote filament formation on ssDNA rather than dsDNA. An alternative explanation, which we cannot rule out at present, is that Mei5-Sae3 enhances the affinity of Dmc1 for both ssDNA and dsDNA equally, but that the concentration of available dsDNA exceeds the K_D for Dmc1 binding in the absence of Mei5-Sae3, while the concentration of ssDNA does not. Further studies are required to determine if either the ssDNA or the RPA binding activities of Mei5-Sae3 recruit Dmc1 to ssDNA tracts.

The ability of Dmc1-E157D to form functional filaments on ssDNA in vivo in the absence of Mei5-Sae3, and to do so by a mechanism involving filament stabilization, raises the possibility that Dmc1 recruitment to and nucleation on RPA coated ssDNA in wild-type cells is not reliant on Mei5-Sae3. Given that Mei5-Sae3 binds directly to both Dmc1 and RPA [62,63,70], we continue to favor models in which Mei5-Sae3 plays a role in recruitment/nucleation of Dmc1 filaments. We note, however, that Dmc1 could be recruited to sites of DSBs through its interactions with RPA [60], and that nucleation, but not filament elongation, could be Mei5-Sae3 independent. Dmc1 nucleation events might be undetected in the absence of Mei5-Sae3 because the resulting filaments never elongate to lengths sufficient to reach the threshold of cytological detection. It is also possible that Rad51 is normally partially responsible for Dmc1 recruitment/nucleation, in addition to its roles in filament stabilization and IH bias. These considerations highlight the need for further studies on the mechanism of Dmc1 recruitment/nucleation on RPA coated ssDNA tracts in vivo.

The role of Rad51 in Dmc1 filament dynamics

The absence of foci observed in mei5, sae3, and mei5 sae3 mutants, and the dimmer foci observed in rad51 mutants, indicate that normal Dmc1 focus formation involves both proteins [61,62,78]. The fact that recombination and DSB-dependent focus formation in rad51 yeast depends on Mei5-Sae3 suggests that Mei5-Sae3 is epistatic to Rad51. Furthermore, the formation of brightly staining Mei5-Sae3 foci depends on Rad51, as does the formation of brightly staining Dmc1 foci [62,78]. These dependency relationships raised the possibility that Rad51’s ability to influence Dmc1 filaments might require a direct interaction between Rad51 and Mei5-Sae3 [90]. However, the data presented here indicate that Rad51 promotes formation of functional Dmc1 filaments on ssDNA independently of Mei5-Sae3, thus Rad51’s normal influence on Dmc1 filament dynamics does not require, and may not involve, Mei5-Sae3 binding to Rad51.

Our data provide critical evidence that Mei5-Sae3 and Rad51 function independently with respect to enhancing the formation of functional Dmc1 filaments. Whereas dmc1-E157D mei5 forms COs at a level nearly equivalent to wild-type, dmc1-E157D rad51 suffers a dramatic reduction in CO formation, and experiences hyper-resection (Fig 2A and 2B). In addition, 2D gel electrophoresis shows that JM formation in dmc1-E157D mei5 is equivalent to dmc1-E157D, while the JMs formed in the dmc1-E157D rad51 background are significantly reduced relative to dmc1-E157D, and show an IH bias defect like the rad51 single mutant (Fig 3D and 3E). Thus, a mutation that alleviates Dmc1’s need for Mei5-Sae3, retains full dependency on Rad51. If the functions of Mei5-Sae3 and Rad51 were interdependent, a mutation that bypasses the requirement for Mei5-Sae3 would also bypass the requirement for Rad51. Under this model for independent function of the two accessory proteins, the partial dependency of Mei5-Sae3 foci on Rad51 can be explained if Mei5-Sae3 binds Dmc1 filaments along their entire contour, because Dmc1 forms shorter filaments in the absence of Rad51.

Rad51 is likely to impact Dmc1 filament dynamics by direct interaction. Although a previous study did not ascribe significance to the low level of interaction detected between budding yeast Rad51 and Dmc1 [89], two-hybrid studies in other organisms detected significant levels of Rad51-Dmc1 interaction, albeit at low levels compared to the homotypic interactions [91–93]. Budding yeast Rad51 binds Dmc1 directly when pure proteins are mixed [60], consistent with similar observations in other organisms [91–93]. Using the meiotic two-hybrid method, we were able to detect Rad51-Dmc1 interaction during meiotic prophase of budding yeast, and to show that this interaction does not require Mei5-Sae3 (S7 Fig). These findings provide additional evidence that Rad51 and Mei5-Sae3 influence Dmc1 DNA binding dynamics independently. The finding that Rad51-Dmc1 interaction occurs, but is weaker than homotypic interactions, is consistent with a single molecule study that showed mixtures of Rad51 and Dmc1 form predominantly homo-filaments on DNA [31], and with prior cytological studies that showed the foci formed by Rad51 and Dmc1 lie adjacent to one another rather than being perfectly colocalized [61,89,94]. Finally, we note that direct interaction between the two proteins can account for the observation that Rad51 can stimulate Dmc1-mediated D-loop formation in the absence of other proteins [3].

How might Mei5-Sae3 and Rad51 promote Dmc1 filament stability by independent mechanisms? There are at least two basic mechanisms that could contribute to filament stability. First, an accessory protein could promote the high-affinity ssDNA binding form. Second, if a strand exchange protein is normally subject to enzymatically-driven disassembly, an accessory protein might act by specifically blocking the activity of that enzyme. Mei5-Sae3’s role in filament stabilization in vivo almost certainly involves direct enhancement of DNA binding activity during nucleation and/or elongation, as is the case for Mei5-Sae3 homolog Sfr1-Swi5 [72]. Rad51 might also enhance binding directly, by reducing the off-rate of protomers from filaments. For example, a Rad51 monomer bound to the end of a Dmc1 filament might drastically reduce the off-rate of the adjacent Dmc1 protomer with a strong overall effect on filament stability, given that disassembly of filaments is expected to occur from filament ends [95].

Alternatively, or in addition, Rad51 may block a mechanism that actively dissociates Dmc1 filaments. Although no active disassembly mechanism has been identified for Dmc1 filaments, active disassembly could involve a helicase mechanism, similar to that mediated by UvrD and Srs2 [26–29]. One observation that appears to be at odds with the idea that Rad51 functions to promote Dmc1 filament formation by blocking an Srs2-like mechanism is that Rad51 stimulates Dmc1’s D-loop activity in a purified system that does not include an ssDNA-specific helicase. However, it is possible that the in vitro activity of Rad51 in stimulating Dmc1 does not fully recapitulate the in vivo function of the protein. This possibility is emphasized by previous work on the Rad51 accessory protein Rad55-Rad57. Both subunits of the Rad55-Rad57 heterodimer are structurally similar to Rad51. Rad55-Rad57 stimulates Rad51 activity in vitro, but in vivo it additionally functions to limit the Rad51 strippase activity of Srs2 [96,97]. Thus, Rad51’s impact on Dmc1 activity in vitro might similarly not fully represent its in vivo role in promoting stable Dmc1 filaments.

A model invoking inhibition of Dmc1-ssDNA filament disassembly can account for the fact that dmc1-E157D rad51 forms fewer JMs relative to DMC1⁺ rad51 (Fig 3E). Like Dmc1-E157D, the Rad51 ATPase mutant Rad51-K191R is defective in recruitment to DSB-associated tracts of ssDNA in vivo. The DNA binding defect of Rad51-K191R is partially suppressed by deletion of SRS2 or by overexpression of RAD54 [55,56]. These findings suggest that the recruitment defect displayed by Rad51-K191R results from a combination of the protein’s DNA binding defect, increased off-pathway dsDNA binding, and active disassembly of Rad51-K191R filaments that do form at DSB-associated tracts of ssDNA [57]. If Dmc1-E157D filaments form more slowly than wild-type filaments as a result of increased off-pathway binding, which would result in a decreased pool of free Dmc1 protomers, Dmc1-E157D filaments may be acutely sensitive to disassembly and/or end dissociation, thus explaining Dmc1-E157D’s dependency on Rad51. In addition, these models can account for the more severe phenotype of the dmc1-E157D mei5 rad51 triple mutant compared to the dmc1-E157D rad51 double mutant as a consequence of Mei5-Sae3 having a limited ability to block dissociation, or being able to promote fast reassembly. Such an activity of Mei5-Sae3 might be inconsequential for Dmc1-E157D DNA binding dynamics in vivo when Rad51 is present, explaining why the phenotypes of dmc1-E157D and dmc1-E157D mei5 are nearly identical.

Mei5-Sae3 is not required for IH bias

The results presented here also reveal for the first time that although both Rad51 and Mei5-Sae3 promote the formation of stable Dmc1 filaments, Mei5-Sae3 differs from Rad51 in that Mei5-Sae3 is not required for IH bias while Rad51 is. This conclusion could not have been arrived at based on earlier observations because recombination is blocked prior to formation of JMs in DMC1⁺ mei5 and DMC1⁺ sae3 cells; bypass of the requirement for Mei5-Sae3 for formation of functional filaments allowed us to assess the role of Mei5-Sae3 in recombination partner choice at the strand invasion stage. Previous work showed that Rad51 and Dmc1 are both required for IH bias [79,88]. The results here show that the cooperation between Rad51 and Dmc1 required for IH bias involves a Rad51-dependent mechanism that is independent of Mei5-Sae3. This interpretation is consistent with the fact that, in other species, homologs of Mei5-Sae3 regulate Rad51 activity, suggesting that the Mei5-Sae3 family of accessory proteins solves a problem common to both Rad51 and Dmc1 that is not unique to meiotic recombination.

Chromatin immunoprecipitation experiments have shown that cells lacking both Rdh54 and Rad54 fail to recruit Dmc1 to DSB hotspots as a consequence of sequestration caused by off pathway DNA binding. The failure to recruit Dmc1 to tracts of ssDNA accounts for the hyper-resection seen in rad54 rdh54 double mutants [51,98]. Given that Dmc1-E157D forms foci in the absence of DSBs, and that it is modeled on RecA-E96D, which displays a lower than normal off-rate for dsDNA binding, one might expect that Dmc1-E157D is less efficiently removed from dsDNA by Rdh54 (and Rad54). Surprisingly, we find no evidence for a decrease in CO formation or for hyper-resection in dmc1-E157D (Fig 2A and 2B, S2 Fig). Moreover, dHJ formation is increased, suggesting that Dmc1-E157D is efficiently removed from the 3’ end of the heteroduplex DNA to allow for recombination-associated DNA synthesis (Fig 3C and 3E). This function is likely carried out by Rdh54 given the corresponding activity of Rad54 on Rad51 and on the evidence that Rdh54 acts to remove off-pathway Dmc1 complexes from dsDNA [49,51]. We also find that the meiotic progression and spore formation observed in dmc1-E157D mutants is strongly dependent on Rdh54, indicating that Rdh54 is active in dmc1-E157D mutants (Table 1, S9 Fig). Thus, although Dmc1-E157D likely forms more off-pathway foci than Dmc1-WT, Rdh54 is apparently able to have some effect on Dmc1-E157D, which we presume involves dissociating the mutant Dmc1 protein from tracts of dsDNA.

Dmc1-E157D forms abnormally long filaments and is hyper-recombinant for certain JMs and recombination products

Although levels of IH CO intermediates and products are similar to those in wild-type, dmc1-E157D and dmc1-E157D mei5 display higher than normal levels of certain types of recombination intermediates and products including IS-dHJs, mcJMs, and ectopic COs. For simplicity, we will refer to these unusual types of recombination events collectively as “aberrant,” but we emphasize that all three types are observed at low levels in wild-type cells. IS-dHJs, mcJMs, and ectopic COs are all elevated about 3-fold in dmc1-E157D and dmc1-E157D mei5 cells (Figs 2B, 3C and 3E, S4 Fig). The combination of aberrant recombination phenotypes observed in dmc1-E157D cells is reminiscent of that reported for sgs1, top3, and rmi1 mutants during meiosis [99–101]. Sgs1, Top3, and Rmi1 have been shown to form a complex, STR, that disassembles D-loops [102–104]. In addition, during mitotic recombination, STR was shown to have a role in disassembling aberrant invasion events in which a single Rad51 filament invades two or more donor molecules (“multi-invasions”) [105]. This role of STR in multi-invasion disassembly was proposed to account for at least some of the phenotypes observed in the absence of Sgs1, Top3, or Rmi1 during meiosis [101]. In this context, maturation of a multi-invasion into a mcJM, followed by resolution of the multi-invasion, can account for the increase in mcJMs, IS-dHJs, and ectopic recombination observed in these mutants [106]. Further evidence that multi-invasions account for the meiotic STR mutant phenotypes is the fact that both multi-invasions and JMs in the sgs1, top3, or rmi1 mutant backgrounds are highly dependent on structure-selective nucleases Mus81-Mms4, Slx1-Slx4, and Yen1 [100,101,105,107–109].

Several possibilities account for why dmc1-E157D and dmc1-E157D mei5 are phenotypically similar to the sgs1, top3, and rmi1 mutants. Dmc1-E157D may form the same number of aberrant intermediates as wild-type, but STR-mediated disassembly could be rendered less efficient as a consequence of enhanced binding activity of Dmc1-E157D compared to Dmc1-WT. Alternatively, as a consequence of the fact that Dmc1-E157D forms longer filaments, it may also form longer D-loops. Piazza et al. have recently shown that two D-loop disassembly pathways function in somatic cells, one that relies on the activities of STR and Mph1, and another that relies on Srs2 [104]. Interestingly, Srs2-dependent D-loops may be longer than those processed by the STR and Mph1 pathway [104,110]. Thus, if Dmc1-E157D forms longer D-loops, it may perturb the balance between these two D-loop editing pathways, resulting in the phenotypes observed. Arguing against the notion that D-loop disassembly is impaired by the dmc1-E157D mutation is the fact that there is no appreciable increase in SEIs in dmc1-E157D and dmc1-E157D mei5 cells as compared to wild-type (Fig 3B and 3D), which might be expected if the mutant protein prevented D-loop disruption.

Our preferred model to account for the defects associated with dmc1-E157D and dmc1-E157D mei5 is that Dmc1-E157D makes more aberrant D-loops than Dmc1-WT. In this model, STR, and possibly other helicases, disassemble aberrant D-loops normally, but the mutant protein generates more multi-invasions than Dmc1-WT. The two regions of homology engaged in such multi-invasion events could be on one sister and one homolog, or on both of the homologs, likely engaging one template at the allelic site, and one at the ectopic site. The formation of the multi-invasions can account for the increased mcJMs, while processing of multi-invasions to yield fully repaired chromatids can explain the increases in IS-dHJs and ectopic COs [106]. Drawing on the “intersegmental contact sampling” model of homology search [111], we propose Dmc1-E157D makes more multi-invasions as a consequence of making longer filaments (Fig 5). The intersegmental contact sampling model maintains that a filament has a polyvalent interaction surface capable of simultaneously searching multiple, non-contiguous dsDNA regions for homology [111]. Longer filaments are able to search duplex DNA more efficiently, as a consequence of being able to engage in a greater number of simultaneous interactions. We have demonstrated that Dmc1-E157D forms longer filaments in vivo (Fig 4C and 4D). We posit that because filaments are longer, Dmc1-E157D engages in a higher number of simultaneous searching interactions that results in more frequent homology-dependent engagement of two different regions of homology by a single filament. Given that multi-invasion recombination is thought to generate secondary DSBs [105,106], this interpretation explains not only the defects that we see by 2D gel electrophoresis (Fig 3B–3E) but also why DSBs accumulate to higher levels in dmc1-E157D relative to wild-type (S2 Fig) and persist longer (Fig 2A and 2B).

Though these aberrant recombination events are increased in dmc1-E157D, they also make up a substantial fraction of the recombination events observed in wild-type cells [99,105]. Consistent with this finding, 14% of wild-type Dmc1 foci that colocalized with RPA were longer than 149 nm in length, the average length of Dmc1-E157D foci that colocalize with RPA in dmc1-E157D (Fig 4D). This finding suggests that although most foci are much shorter than 149 nm in wild-type cells, long filaments do occasionally form. The proposal that longer than normal filaments are responsible for higher than normal levels of multi-invasions is supported by previous work showed that (1) if longer ssDNA substrates are used, there is a higher incidence of multi-invasions [112]; (2) Rad55-Rad57 promotes both longer Rad51 filaments and the formation of multi-invasions [97,106]; and (3) multi-invasions increased more than linearly as a consequence of increasing homology between the broken molecule and one of the two donors sequences [105].

The aberrant event hyper-recombinant phenotype displayed by Dmc1-E157D is Rad51-dependent. The mechanism responsible for Rad51’s role in promoting the aberrant hyper-recombinant activity of Dmc1-E157D remains to be determined. Analysis of RPA co-localized foci provided evidence that Dmc1-E157D forms longer filaments on ssDNA in otherwise wild-type cells and in mei5 single mutants. The mutant protein also forms long filaments on dsDNA, given that long filaments are also observed in spo11 mutants (S8 Fig). Because both RPA and Dmc1 focus counts are increased in dmc1-E157D rad51 and dmc1-E157D mei5 rad51 mutants (Fig 4B), and because both RPA and Dmc1 foci are also longer in these mutants (Fig 4C), it was not possible to identify a sub-population that we could be confident was enriched for ssDNA bound structures in these mutants. As a result, it is unclear if the dependency of Dmc1-E157D’s hyper-recombinant phenotype on Rad51 reflects a requirement for Rad51 in forming long Dmc1 filaments on ssDNA, or if Rad51 plays some other role in promoting the high level of aberrant recombination events observed in dmc1-E157D and dmc1-E157D mei5. It is clear, however, that Rad51’s homology search and strand exchange activities are not required for the aberrant hyper-recombinant phenotype observed in dmc1-E157D cells because IS-dHJs and mcJMs are increased in dmc1-E157D rad51-II3A cells, in a manner that is nearly indistinguishable from the dmc1-E157D single mutant (S6 Fig).

We speculate that the lengths of RecA-family strand exchange filaments are limited by regulatory mechanisms that evolved to prevent homology-dependent translocations and other genome rearrangements. Limiting filament lengths may limit the ability of filaments to simultaneously engage more than one homologous target sequence. In this regard, it is relevant that the single molecule study that provided evidence for intersegmental transfer did not detect any homology-dependent target engagement with the shortest ssDNA substrate examined, which was 162 nucleotides in length [111]. However, in vivo, Dmc1 filaments are typically ~100 nucleotides in wild-type cells (Fig 4C) [36]. Thus, it is possible that the cost of multi-invasions to genome stability has constrained the length of strand exchange filaments such that intersegmental searching is restricted or prevented in vivo.

Materials and methods

Yeast strains

The yeast strains used in this study are listed in S1 Table. All yeast strains are isogenic derivatives of strain SK-1.

To construct the dmc1 point mutants, DKB plasmid pNRB628 containing the DMC1 open reading frame, a 701 base pair upstream homology arm, the TEF1 promoter, the natMX4 open reading frame, the ADH1 terminator, and a 40 base pair downstream homology arm, was modified by Gibson assembly to include the desired point mutations. dmc1::LEU2-URA3-KAN haploid yeast (DKB129, DKB130) were transformed with a linear PCR fragment containing the homology arms, the mutated dmc1 open reading frame, and the natMX4 (for resistance to nourseothricin sulfate, or cloNAT) selectable marker. Yeast were outgrown in 5 milliliters liquid YPDA for 4.5 hours at 30°C in a culture rotator, then plated on selective media and allowed to grow at 30°C for 3 days. After 3 days, colonies were struck out on the selective media and on 5-fluoroorotic acid (5-FOA), which selects against URA3⁺ yeast and therefore identifies clones that have lost the dmc1::LEU2-URA3-KAN allele. Those colonies that grew on the cloNAT media and did not grow on the 5-FOA plates were tested to confirm proper targeting by polymerase chain reaction, and then confirmed via sequencing.

Meiotic time courses

Yeast cultures were induced to undergo synchronous meiosis as described previously [61]. Appropriate samples were collected at time points indicated in figures.

Spore viability

Spore viability was determined by tetrad dissection as the percent of spores that germinate and form a colony on a YPDA plate relative to the number expected if all dissected spores had lived.

Preparation and staining of spread yeast nuclei

Surface-spreading and immunostaining of meiotic yeast chromosomes on glass slides was performed as described previously [113]. Primary antibodies were used at the following dilutions: purified anti-goat Dmc1 bleed #4 DKB antibody #192 (1:800), anti-rabbit Rad51 bleed #2 DKB antibody #159 (1:1000), anti-rabbit RFA2 (1:1000), and anti-rabbit Hop2 bleed #3 DKB antibody #143 (1:1000). Secondary antibodies were used at a dilution of 1:1000 and included: Alexa Fluor 488 chicken anti-goat (Invitrogen by ThermoFisher Scientific), Alexa Fluor 594 donkey anti-rabbit (Invitrogen by ThermoFisher Scientific), Alexa Fluor 594 donkey anti-goat (Invitrogen by ThermoFisher Scientific) and Alexa Fluor 488 donkey anti-rabbit (Invitrogen by ThermoFisher Scientific). Images were collected on a Zeiss Axiovision 4.6 wide-field fluorescence microscope at 100X magnification. The same imaging parameters were used for all samples.

Wide-field microscopy analysis

For each strain, 50 or more adjacent and randomly selected nuclei were imaged. A field of nuclei was chosen for analysis based on the DAPI staining pattern. Nuclei were scored as focus positive if there were 3 or more immunostaining foci in a given nucleus. Due to focus crowding in wide-field images, it was not possible to generate reliable focus counts using automated methods. Therefore, focus counts were determined by eye for the experiments reported in S8 Fig.

One-dimensional gel electrophoresis

One-dimensional gel electrophoresis at the HIS4::LEU2 meiotic hotspot was performed as follows. 15 milliliter sporulation media samples were collected at time points indicated from meiotic cultures. Sodium azide was added to a final concentration of 0.1%. Cells were spun down at 3000 rpm in tabletop clinical centrifuges for 5 minutes, then the supernatant was removed and the pellet was frozen at -20°C. DNA was then purified as described previously [114]. Approximately 2 micrograms DNA per sample was then digested with XhoI or PstI (as indicated in figure legend) restriction enzyme (New England BioLabs) and processed as described previously [114]. Samples were then run on a 0.6% (XhoI) or 0.7% (PstI) agarose gel at 2V/cm for 24 (XhoI) or 18 (PstI) hours, followed by Southern blotting as described previously [86].

Two-dimensional gel electrophoresis

Two-dimensional gel electrophoresis at the HIS4:LEU2 meiotic hotspot was performed as previously described [3].

Meiotic two-hybrid analysis

Analysis of Rad51-Dmc1 interaction in meiotic cells was performed using the meiotic two-hybrid method [115]. DNA binding domain constructs were transformed into MATa haploid strains DKB6431 (MEI5⁺) and DKB6429 (mei5) and activation domain constructs were transformed into MATα haploid strains DKB6430 (MEI5⁺) and DKB6428 (mei5). Independent transformants were mated to generate the diploid strains used for meiotic two hybrid experiments. 5 ml cultures were grown for 72 hours in synthetic tryptophan leucine dropout media to maintain 2μ plasmids and then transferred to YPD medium at OD600 = 0.2, and then grown for two generations before being transferred to SPS medium overnight, after which sporulation was induced on SPM-1/5COM medium. Recipes for media are as described previously [61]. Samples were prepared for β-galactosidase assays after 6 hours and 18 hours. The plasmids used for the two-hybrid studies were derived from pGAD-C1 [116] for activation domain fusions, and from pCA1 a gift from Scott Keeney [115] for DNA binding domain fusions. Note that this system uses E. coli lexA as DNA binding domain for hybrid constructs in combination with a lex-op::lacZ reporter construct [115]. Plasmid designations and the markers carried by the plasmids were as follows: Dmc1BD = pNRB729 2μ, TRP1, P_DMC1-DMC1-lexA, ampR, ori; Dmc1AD = pNRB271 2μ, LEU2, P_ADH-GAL4-AD::DMC1, ampR, ori; Rad51BD = pNRB727 2μ, TRP1, P_DMC1-lexA-Rad51, ampR, ori; Rad51AD = pNRB688 2μ, LEU2, P_ADH-GAL4-AD::RAD51, ampR, ori; ΔBD = pNRB728 2μ, TRP1, P_DMC1-lexA, ampR, ori; and ΔAD = pNRB267 2μ, LEU2, P_ADH-GAL4, ampR, ori. Plasmid sequences are available on request.

Immunofluorescence imaging by STED microscopy

Spreads were stained using a protocol described previously [113] with the following modifications. Spreads were dipped in 0.2% Photo-Flo (Kodak) for 30 seconds, the excess was tapped off, and then the slides were washed in 1X TBS for 5 minutes. Spreads were then blocked with 300μL 3% BSA in 1X TBS. Following blocking, spreads were incubated with anti-goat Dmc1 (1:800) and anti-Rabbit RPA (1:1000) for ≥16 hours at 4°C. Slides were then washed in 1X TBS + 0.05% Triton X-100 for 5 minutes with gentle rocking 7 times. Spreads were incubated with fluorochrome-conjugated secondary antibodies Alexa Fluor 594 donkey anti-goat and Alex Fluor 488 donkey anti-rabbit (1:1000) (ThermoFisher Scientific) for 2 hours at 4°C, followed by washes as described. Slides were allowed to dry completely in fume hood, then 35μL Vectashield (Vector Laboratories, Inc.) was added, a coverslip was placed atop the slide, and the coverslip was sealed with nail polish.

Imaging was conducted on a Leica SP8 3D, 3-color Stimulated Emission Depletion (STED) Laser Scanning Confocal Microscope at the University of Chicago Integrated Light Microscopy Core Facility. The same imaging parameters were used for all strains. Images were deconvolved using Huygens software and applying the same settings for each image. Resolution is reported based on measurements taken from deconvolved images.

STED microscopy analysis

To quantitate the number of foci in each nucleus, the image channels were separated, and each channel image was converted to a binary image in ImageJ. The “Analyze Particles” function was used to obtain information regarding the number of foci in an image, the coordinates of the center of each focus, and the major length of each focus. The same settings were used to analyze all images. Colocalization between Dmc1 and RPA was scored in R using the coordinates given by ImageJ to calculate the distance between a given Dmc1 focus and all RPA foci in the nucleus. A Dmc1 focus was scored as colocalizing with a RPA focus if the nearest RPA focus was less than the length of that Dmc1 focus plus a preset RPA value that was calculated for each strain. The RPA value was calculated based on one half of the average length of all RPA foci in that sample plus one half of two standard deviations of that RPA length. This means that if a given Dmc1 focus is sitting side-by-side with an RPA focus, the distance between it and the center of the nearest RPA focus can be the length of that Dmc1 focus plus one half the average length of all RPA foci in that strain background, plus one half of two standard deviations of the RPA focus lengths. This calculation attempts to take into account the fact that both RPA foci and Dmc1 focus lengths vary from sample to sample. Plots and statistical tests were carried out in R using the ggplot and ggpubr packages.

Meiotic whole cell lysate, SDS-PAGE, and Western blotting

4 milliliters of meiotic culture was collected at the appropriate time point. Tricholoroacetic acid was added to a final concentration of 10% weight/volume. Samples were placed in a 60°C water bath for 5 minutes, then placed on ice for 5 minutes. Next, samples were spun down at 3000 rotations per minute in a low-speed centrifuge, the supernatant removed by aspiration, and pellet then washed in ddH₂O. The pellet was then re-suspended in 1X-SDS-PAGE (60 mM TrisHCl pH 6.8, 0.05% SDS, 100 mM DTT, 5% glycerol) buffer supplemented with 50 mM sodium PIPES pH 7.5 to the appropriate concentration according to the optical density of cells in the sample. The samples were then boiled for 10 minutes, spun down, and pellets stored at -20°C.

A 12% SDS-polyacrylamide gel was prepared, and 30 microliters of each sample was run at 120V for 1.5 hours alongside 20 nanograms purified Dmc1 protein. Samples were then transferred to Merck Millipore Limited Immobilon-P Transfer Membrane for 16 hours at 50V at 4°C. The membrane was then blotted using anti-goat Dmc1 (1:1000) primary antibody and an anti-goat HRP-conjugated secondary antibody (1:1000).

Meiotic progression and MI segregation imaging

Differential interference contrast (DIC) and epifluorescence images were collected on an IX-81 microscope (Olympus, Tokyo, Japan) controlled by MetaMorph software (Molecular Devices, Sunnyvale, CA) and fitted with an Orca-ER camera (Hamamatsu, Bridgewater, NJ) and a 60X, 1.4 NA Plan Apo objective. Nuclear divisions were monitored by DAPI staining. Cells with two DAPI-staining bodies or a single DAPI-staining body that was stretched were scored as having initiated MI; cells with three or more DAPI bodies or an “X” shape were scored as undergoing meiosis II division.

Supporting information

S1 Fig [pdf]
expression for wild-type, .

S2 Fig [a]
Additional Southern blot analysis at the :: hotspot.

S3 Fig [a]
suppresses the meiotic progression defect associated with .

S4 Fig [a]
JMs accumulate at the :: recombination hotspot in the absence of .

S5 Fig [a]
Duplicate meiotic time course experiments for and .

S6 Fig [a]
The defects associated with are independent of Rad51’s catalytic activity.

S7 Fig [a]
Meiotic two-hybrid analysis detects a weak interaction between Rad51 and Dmc1 that is independent of Mei5.

S8 Fig [a]
Super-resolution imaging resolves closely spaced foci, but elongated Dmc1 foci still form in .

S9 Fig [pdf]
is more defective in meiotic progression than either of the single mutants, and .

S10 Fig [pdf]
DSB-independent Dmc1-WT focus formation does not require Mei5.

S1 Table [pdf]
Yeast strains used in this study.

S1 Data [xlsx]
Spreadsheets with numerical data used to generate all Figures.