Separable Roles for a Caenorhabditis elegans RMI1 Homolog in Promoting and Antagonizing Meiotic Crossovers Ensure Faithful Chromosome Inheritance

During the first meiotic division, crossovers (COs) between homologous chromosomes ensure their correct segregation. COs are produced by homologous recombination (HR)-mediated repair of programmed DNA double strand breaks (DSBs). As more DSBs are induced than COs, mechanisms are required to establish a regulated number of COs and to repair remaining intermediates as non-crossovers (NCOs). We show that the Caenorhabditis elegans RMI1 homolog-1 (RMH-1) functions during meiosis to promote both CO and NCO HR at appropriate chromosomal sites. RMH-1 accumulates at CO sites, dependent on known pro-CO factors, and acts to promote CO designation and enforce the CO outcome of HR-intermediate resolution. RMH-1 also localizes at NCO sites and functions in parallel with SMC-5 to antagonize excess HR-based connections between chromosomes. Moreover, RMH-1 also has a major role in channeling DSBs into an NCO HR outcome near the centers of chromosomes, thereby ensuring that COs form predominantly at off-center positions.


Introduction
During meiosis, the accurate segregation of chromosomes relies on the formation of crossovers (COs) and sister chromatid cohesion [1]. COs are produced by homologous recombination (HR)-mediated repair of programmed DNA double strand breaks (DSBs). In Caenorhabditis elegans, the holocentric chromosome pairs usually undergo a single off-center CO, resulting in a cruciform and asymmetric bivalent [2,3]. This is important to define the organization of kinetochore proteins, motor proteins, protein kinases, and the domains of cohesion release, which is necessary for the accurate segregation of homologs during anaphase I [4].
During prophase I, several mechanisms guarantee the formation of COs as well as the repair of the additional recombination intermediates as non-crossovers (NCOs).
In yeast, the bulk of DSBs not destined to become COs are processed by synthesis-dependent strand annealing (SDSA) at an early stage [25]. In C. elegans, a similar activity is attributed to RTEL-1 by D-loop displacement after strand invasion [26,27]. NCOs can also be generated by the activity of the RTR complex, composed of a RecQ helicase (Bloom syndrome protein [BLM]), topoisomerase IIIα (TOP3), and the RecQ-mediated genome instability 1 and 2 (RMI1,2) scaffolding proteins [28][29][30]. This complex provides a major NCO activity during mitosis. Importantly, patients with mutated BLM helicase display genomic instability and a cancer predisposition, and they exhibit a cellular phenotype of elevated COs between sister chromatids, which potentially drives cancer by loss of heterozygosity [31,32]. In vitro studies have shown that the RTR complex dismantles double Holliday junctions (dHJs). A branch migration step mediated by the RecQ helicase brings the two dHJs in close proximity to allow the topoisomerase to unhook the two DNA strands by decatenation, stimulated by the scaffolding proteins RMI1/2 [33].
RMI1 was discovered as a protein associated with BLM containing protein complexes [34]. It colocalizes with recombination foci containing BLM helicase [35]. RMI1 depletion leads to In the jf92 allele, the coding sequence was disrupted after the START codon by the insertion of the unc-119 gene by the CRISPR technology. In the jf54 allele, the G-to-A transition affects the first nucleotide of intron 1 and therefore, destroys the splice donor site of the preceding exon 1. qRT-PCR revealed the presence of different splicing variants (see S1 Fig). In the tn309 allele, the G-to-A transition introduces a premature STOP codon at position aa 640, leading to the deletion of the OB2 domain (for more details, see the Experimental Procedures section). (B-E) Oocyte nuclei at the diakinesis stage of meiotic prophase. Each image shows the complete set of DAPI-stained chromosomes from a single nucleus. The wild-type (WT) and rmh-2(jf94) nuclei contain six bivalents (homolog pairs connected by chiasmata), whereas the rmh-1 mutant nuclei contain a mixture of bivalents and univalents. (F) Quantification of the average number of DAPI-positive structures in diakinesis oocytes in the -1 position. WT n = 25, rmh-1(jf92) n = 21, rmh-1(jf54) n = 36, rmh-1(tn309) n = 30, and rmh-2(jf94) n = 18. (G-I) Quantification of embryonic hatch rates (G). Frequencies of male offspring (H) and larval arrest (I) among the progeny of WT and rmh-1 and rmh-2 mutant worms (n = 35-45 hermaphrodites per genotype). Data for F-I are represented as mean +/-SD; ns stands for not significant, differences are highlighted with stars (* p < 0.05, ** p < 0.01, *** p < 0.001. and **** p < 0.0001). Scale bars, 2 μm.

RMH-1 (But Not RMH-2) Is Required for Robust Chiasma Formation and Chromosome Segregation in Meiosis
To establish the respective requirements of rmh-1 and rmh-2, we examined the mutants for embryonic lethality, larval arrest, and a high incidence of males (Him) phenotype among the progeny. An increased incidence of males in the progeny indicates X chromosome nondisjunction during meiosis, as C. elegans hermaphrodites have the genotype X/X and males X/O. The combination of increased embryonic lethality with a Him phenotype further suggests the occurrence of aneuploid eggs arising from meiotic missegregation of autosomes [63]. Increased larval arrest is indicative of somatic defects.
Analysis of rmh-1 mutants revealed the cohort of phenotypes characteristic of a defect in meiotic recombination, as described above (Fig 1G and 1H). Second, DAPI staining of oocytes at diakinesis, the last stage of meiotic prophase, revealed that a fraction of chromosome pairs was not connected by chiasmata in rmh-1 mutants. Whereas in the wild type, six bivalents (chromosome pairs connected by chiasmata) can be seen in diakinesis oocytes, rmh-1 mutant alleles showed an increase of DAPI-stained bodies, reflecting a mixture of bivalents and univalents (achiasmate chromosomes) (Fig 1B-1E). In the -1 oocyte (the most mature oocyte, next to the spermatheca, the oocyte prior to fertilization), we observed on average 8.9 ± 1.0 DAPI bodies in rmh-1(jf92) and 9.3 ± 1.4 in rmh-1(jf54) ( Fig 1F). As the jf54 allele behaved identically to the jf92 insertion allele with regards to the hatch rate and Him and diakinesis phenotypes, and as we were unable to detect GFP::RMH-1 containing the jf54 mutation (S2B Fig), we infer that rmh-1(jf54) behaves like a null allele. Interestingly, fewer univalents were observed in rmh-1(tn309) (7.4 ± 1.1 DAPI bodies), suggesting that RMH-1 function is differently affected by this allele (Fig 1F). To confirm the presence of univalents in rmh-1 mutants (and not fragments due to absence of DNA repair), we measured the average volumes of DAPI bodies in diakinesis (S3A and S3B Fig and S1 Text) and confirmed both the presence of univalents and the absence of DNA fragments.
To better understand which meiotic processes are impaired in rmh-1(jf54), we analyzed chromosome pairing, synapsis, and induction and repair of DSBs. No defects in pairing and synapsis were observed (S4 Fig). To study the induction and processing of DSBs, we assessed the appearance and disappearance of foci of the strand exchange protein RAD-51 (Fig 2) [ 64,65]. RAD-51 foci appeared with normal timing in the rmh-1(jf54) mutant, but accumulated at higher levels than in wild type and persisted at elevated levels through late pachytene. However, RAD-51 foci disappeared in diplotene, suggesting that repair of DSBs was delayed but did eventually occur. We also found that rmh-1-specific chromosomal defects depended on the induction of meiotic DSBs. In summary, meiotic recombination is aberrant in rmh-1 mutants.

Dynamic Localization of RMH-1 in Distinct Foci during Pachytene Progression
To assess RMH-1 localization in the gonad, we expressed GFP::RMH-1 using its endogenous regulatory elements as a functional fusion protein. Indeed, GFP::RMH-1 is capable of rescuing embryonic lethality and the Him phenotype when expressed in the null allele jf92 (S5A and S5B Fig). GFP::RMH-1 was found in foci throughout pachytene (Fig 3A-3C). In early pachytene, RMH-1 was first detected as a nucleoplasmic haze, and faint foci progressively appeared on chromosomes. During mid pachytene, RMH-1 foci increased in number and intensity. Mid pachytene nuclei contained, on average, 15.2 foci ± 3.6, ranging from ten to 25, and, in late pachytene, the number of RMH-1 foci drastically reduced to 5.9 ± 1.7 (Fig 3D). In late pachytene, the number of foci ranged from one to nine foci; however, the majority of nuclei contained six or seven foci ( Fig 3E). (This distribution is broader than the distribution of COSA-1 foci, visible as six signals in late pachytene. However, the mutant phenotype of cosa-1 already suggests that it acts before the protein can be observed in the six prominent foci. In addition, we believe RMH-1 marks a stage of recombination, through which all mature CO intermediates have to pass). For quantification, gonads were divided into six equal zones (A). In both WT and rmh-1(jf54), zones 1 and 2 correspond to the mitotic zone; zone 3 to transition zone and early pachytene; zones 4 to 5 to pachytene. Analysis of n = 124-231 nuclei per zone for each genotype. Distribution of RAD-51 foci is significantly different between WT and mutant for the zones 3 to 6 (Mann Whitney test, **** p < 0.0001). Scale bar = 20 μm for gonads and 5 μm for insets. Importantly, RMH-1 foci seem to increase in signal intensity (about 1.8-fold) between mid and late pachytene. This suggested that the protein might accumulate over time.
The mid pachytene number of RMH-1 foci, at least twice the number of eventual COs, is consistent with RMH-1 localizing both at CO sites and at sites that will ultimately become NCOs. This is consistent with our analysis of GFP::RMH-1 localization following induction of excessive DNA breaks by ionizing radiation (IR, 50Gy). We found that at 4 h post IR treatment, the number of RMH-1 foci in mid pachytene nuclei had risen significantly, suggesting that RMH-1 was loaded on many of the excess recombination intermediates produced by IR. To understand what would happen to those excess recombination intermediates positive for RMH-1, we analyzed gonads 8 h post IR treatment (after this time, the nuclei with the increased number of RMH-1 foci should have reached late pachytene). However, at this stage, the numbers were reduced to wild type numbers of foci in late pachytene nuclei (S7A- S7C  Fig). Thus, we conclude that RMH-1 marks recombination intermediates that can be increased transiently by irradiation but will be repaired as NCOs, as the final number of marked CO sites is not affected.  The robust accumulation of RMH-1 at CO sites, the dependence of its localization on pro-CO factors, and the presence of univalents in the rmh-1 mutants together suggest that RMH-1 likely functions in promoting the CO outcome of initiated recombination events. Several lines of evidence provide further support for pro-CO role(s) for RMH-1. First, we tested whether rmh-1 is required for normal localization of pro-CO factors by assessing the localization of GFP::COSA-1 in rmh-1 mutants. This analysis revealed that only 75% of nuclei in tn309 and 57% of nuclei in jf54 had six COSA-1 foci (compared to 88% in wild-type) (Fig 4E and 4F), indicating a deficit of CO-designated sites in rmh-1 mutants.
Furthermore, we observed several indications of a delay in pachytene progression in both rmh-1 mutants. First, we assessed localization of ZHP-3, which normally localizes along the full length of the synaptonemal complex (SC) during mid pachytene, then retracts during late pachytene to a short stretch and, finally, to a single focus at the CO site in diplotene [66]; we found that ZHP-3 retraction was delayed in rmh-1(jf54) (S8A- S8D Fig). Second, we evaluated a readout of a checkpoint-like feedback mechanism that operates during C. elegans meiosis to coordinate meiotic progression with generation of CO-eligible recombination intermediates. A single chromosome pair that lacks a CO-eligible recombination intermediate can be detected and elicit a prophase progression delay, visible by the persistence of markers such as phospho-SUN-1 S8 on the nuclear envelope [67]. SUN-1 S8Pi staining was prolonged in rmh-1 mutants, indicating a delay in prophase progression (S8E-S8H Fig), which is in line with delayed and/or impaired formation of CO-specific recombination intermediates. These data in combination with the observed reduction in COSA-1-marked CO-designated sites together indicate a role for RMH-1 in ensuring efficient CO designation.
Although the number of CO-designated sites is reduced in rmh-1 mutants, CO designation still occurs to a large extent, as 57% to 75% of nuclei contain six COSA-1 foci. Moreover, the reduction in number of COSA-1-marked CO sites is not sufficient to account for the number of univalents observed. To calculate the expected number of DAPI bodies in diakinesis nuclei based on our quantification of COSA-1 foci in rmh-1 mutants, we assumed that pachytene nuclei containing six COSA-1 foci would lead to diakinesis nuclei with six bivalents, pachytene nuclei containing five COSA-1 foci would lead to diakinesis nuclei with seven DAPI bodies (five bivalents and two univalents), and so on. This approach yields an expectation of 6.7 DAPI bodies at diakinesis for rmh-1(jf54) and 6.6 for rmh-1(tn309), values that are significantly lower than those observed in the -1 oocytes of these mutants (Fig 1B and 1F). Thus, the number of univalents present at the end of meiotic prophase is higher than would be expected if all COSA-1-marked sites had successfully matured into COs.
To understand this excess of univalents, we investigated the organization of chromosomes in diakinesis. In wild type, the presence of a CO precursor triggers domain restructuring of the ensuing bivalent such that the axial proteins HTP-1/2 and LAB-1 become concentrated along the long arm of the bivalent, and the synapsis protein SYP-1 and the Aurora B kinase (AIR-2) are found on the short arm [68][69][70]. In spo-11 or msh-5 mutants, short and long arm markers overlapped on the univalents. In rmh-1 mutants, however, we observed long and short arm markers localized to reciprocal domains on univalents ( Fig  4G), suggesting that a CO site had been designated but failed to mature to actually link the homologs. Furthermore, quantification of DAPI bodies during progression through the diakinesis stage (-3, -2, and -1 oocyte) showed that they increased significantly (Fig 4H-4J). We observed that in the -3 oocyte, the number of DAPI bodies in rmh-1 mutants (6.9 ± 0.7 DAPI bodies for jf54 and 6.8 ± 0.9 for tn309) was significantly increased compared to wild type. Interestingly, the observed number of DAPI bodies in -3 oocytes of the mutants corresponds to the calculated number of DAPI bodies based on COSA-1 foci analysis. However, in both mutants, the number of DAPI bodies strongly increased during oocyte maturation. In rmh-1(jf54), we observed 9.3 ± 1.4 DAPI bodies in the -1 oocytes, while the effect was milder but still significant in rmh-1(tn309) (7.4 ± 1.1 in -1 oocytes). We conclude that, in rmh-1 mutants, connections between homologs may sometimes be lost after CO designation.

Genetic Interactions with Mutations Affecting Structure-Specific Endonucleases
Dissociation of bivalents that appeared to have undergone CO designation suggested that RMH-1 might function to enforce CO bias in the resolution of recombination intermediates at CO sites. This hypothesis prompted us to examine double mutants carrying rmh-1(jf54) in combination with mutations in xpf-1, mus-81, or slx-1, which encode structure-specific endonucleases proposed to function in two separate and partially redundant meiotic resolution pathways [22][23][24], and him-18 (Slx4 ortholog), which encodes a nuclease scaffolding protein [71]. Dissociation of bivalents in rmh-1(jf54) was reduced by loss of xpf-1, mus-81, or slx-1 (Fig 4K), consistent with persistence of recombination intermediates; however, it is unclear whether such putative persistent intermediates are located at CO-designated sites and/or at other sites on the chromosomes. Furthermore, we observed an elevated incidence of unresolved bivalents linked by DNA bridges (Fig 4M and 4N) in these double mutants compared to the xpf-1, mus-81, or slx-1 single mutants. Together with previous work showing that such linkages observed in nuclease-defective mutants are spo-11-dependent [22], these results suggest that loss of RMH-1 function may result in the accumulation of excess and/or aberrant recombination intermediates that require these structure-specific endonucleases for their resolution.
We also observed the occurrence of DNA bridges in the double rmh-1(jf54); him-18 mutant, but, those linkages appeared with the same frequency as in the him-18 single mutant. Furthermore, loss of him-18 in rmh-1(jf54) did not appreciably suppress the dissociation of homologs (Fig 4K), in contrast to the outcomes with the single-nuclease mutants. We can reconcile these seemingly paradoxical observations by postulating (1) that unscaffolded nucleases may be able to act on recombination intermediates produced in rmh-1 mutants to remove excess connections between homologs, and (2) that the presence of multiple unresolved intermediates connecting homologs (in rmh-1; xpf-1, rmh-1 mus-81, or rmh-1 slx-1 mutants) might obscure detection of discrete bridges.

Interdependent and Separable Functions of RMH-1 and HIM-6 (BLM Helicase)
As RMI1 was first identified as a component of a complex containing the RecQ helicase BLM and the topoisomerase TOP3, we used the yeast-two-hybrid assay to confirm interactions between RMH-1 and HIM-6 (the C. elegans BLM ortholog) and between RMH-1 and TOP-3 (S9A Fig). Furthermore, as several phenotypes of the rmh-1 mutants resemble phenotypes seen in him-6 mutants (S9B and S9C Fig) [46,53], we investigated the cytological and functional inter-relationships between RMH-1 and HIM-6.
To examine colocalization of RMH-1 and HIM-6, we used the CRISPR method to tag the him-6 locus with a C-terminal human influenza hemagglutinin (HA) epitope. The tag did not compromise HIM-6 function, since neither an increase in embryonic inviability nor a Him phenotype was observed (S5 Fig). HIM-6 is found in few foci in early pachytene. The number of foci increases in mid pachytene and decreases again in late pachytene, reminiscent of the RMH-1 pattern. In mid pachytene, RMH-1 and HIM-6 substantially colocalized, and, in late pachytene, RMH-1 strictly colocalized with HIM-6; however, additional HIM-6 foci were also present (96.6 +/-4.1% RMH-1 foci colocalize with HIM-6 in mid pachytene and 96.3 +/-6.7% in late pachytene; Fig 5A-5C).
To investigate the interdependence of localization, we assayed localization of HIM-6::HA in rmh-1 mutants. In tn309, HIM-6 was completely absent in most of the gonads we imaged. In the rest, HIM-6 was barely detectable, and when foci were seen, they were not at CO sites in late pachytene (Fig 5D). In jf54, HIM-6 foci were present in all gonads but seemed smaller and fainter in mid and late pachytene, suggesting that RMH-1 is required to stabilize and enrich HIM-6 in foci (Fig 5E). Although HIM-6 is sometimes found in proximity to CO site markers, these do not exhibit robust colocalization in the absence of rmh-1 (Fig 5E).
Assessment of the localization of GFP::RMH-1 in the him-6(ok412) mutant revealed that him-6 is required for RMH-1 localization in mid pachytene but not in late pachytene (Fig 5H-5J). This finding is consistent with the idea that RMH-1 may be present in genetically distinguishable complexes in mid and late pachytene stages. However, him-6 is required for normal numbers of RMH-1 foci even in late pachytene (Fig 5K).
An important difference between rmh-1 and him-6 mutants is their impact on CO designation. A previous study showed that in the null allele of him-6, the abundance of COSA-1 foci was unaffected [46]; thus, the him-6 null mutant appears to be proficient for CO designation. On the other hand, both rmh-1 alleles impair CO designation, as evidenced by an elevated frequency of nuclei containing fewer than six COSA-1 foci (Fig 5F). Furthermore, the fact that CO designation is unaffected in a him-6 null mutant but is impaired in an rmh-1; him-6 double mutant implies that RMH-1 can assist in promoting CO designation in the absence of HIM-6.
A deficit of bivalent connections is a shared feature of rmh-1 and him-6 mutants. The phenotype is evident but less pronounced in him-6 or rmh-1(tn309) (p < 0.05), while it is more prominent in rmh-1(jf54) (p < 0.01). The number of DAPI bodies in rmh-1(tn309); him-6 (ok412) and the respective single mutants was not different. Interestingly, however, we found that the deficit of connections between homologs in rmh-1(jf54); him-6(ok412) oocytes was reduced compared to the rmh-1(jf54) single mutant (Fig 5G), despite the fact that COSA-1 foci were reduced in this double mutant. One possible explanation for this observation would be that the dissociation of bivalents observed in rmh-1(jf54) might be mediated by HIM-6. An alternative explanation is that the simultaneous loss of HIM-6 and RMH-1 may lead to persistence of unresolved recombination intermediates that maintain connections between the homologs. We investigated the foci structure of RMH-1 and HIM-6 foci using structured illumination microscopy (SIM). Both in mid pachytene and late pachytene, RMH-1 and HIM-6 signals were resolved into more complex structures (Fig 6). In mid pachytene, we observed foci that clearly exhibit a doublet structure and foci that show an elongated shape (Fig 6A and 6B). In late pachytene, RMH-1 and HIM-6 appear even more clearly as doublets (Fig 6C-6E). In both pachytene stages, we hypothesize that RMH-1 and HIM-6 foci mark similar recombination intermediates. The doublet structure is likely easier to observe in late foci as RMH-1 protein accumulates during pachytene progression, leading to larger foci in late pachytene. We measured the average distance between the foci peak in the three-dimensional stacks as an average of 227 +/-46 nm. Interestingly, in Drosophila, the size of a recombination nodule has been estimated to around 100 nm [72]. It has also been shown that 1 kb of B-form DNA is 340 nm in length. We conclude that the structure we describe here is on an appropriate scale for flanking dHJs. We also observed that the late pachytene HIM-6 doublet structures flank a COSA-1 focus in the wild type ( Fig 6F). Interestingly, in the rmh-1(jf54) mutant, HIM-6 appears as single foci and not as elongated or doublet structures in late pachytene (Fig 6G). This suggests that rmh-1 is required to concentrate HIM-6 at CO sites and also to organize a complex structure surrounding late recombination intermediates.

SMC-5 and RMH-1 Act Synergistically to Eliminate Illegitimate Interhomolog Connections
The mid pachytene localization of RMH-1 (and HIM-6) to numerous foci in excess of the eventual number of COs, together with the well-known role for the RTR complex in discouraging COs in other systems (see Introduction), led us to investigate the possibility that RMH-1 also functions at NCO sites during C. elegans meiosis. We focused on the possibility that RMH-1 might function in parallel with the SMC-5/6 complex, based on several considerations. First, several studies in budding yeast showed that in the absence of Smc5 or Smc6 during meiosis, COs form but joint molecules accumulate, leading to chromosome segregation defects [57][58][59]. Moreover, it was shown that Smc6 was required for the resolution of the joint molecules accumulating in absence of Sgs1, suggesting collaboration of pathways mediated through those two proteins [59]. Second, a prior study showed that the C. elegans SMC-5/6 complex is important for meiotic DSB repair under conditions in which interhomolog CO formation is abrogated and/or in mutant situations when intersister repair is the only option [73]. Moreover, the data of Bickel et al. are fully consistent with the SMC-5/6 complex participating in interhomolog NCO repair as well.
Several lines of evidence support the hypothesis that RMH-1 functions in parallel with the SMC-5/6 complex to antagonize accumulation of aberrant interhomolog connections. First, we small and faint (two gonads) or completely undetectable (three gonads). Inset: residual HIM-6 foci do not colocalize (white arrows) with ZHP-3. (E) In rmh-1 (jf54), HIM-6 is still present in foci. Insets for MP (1) and LP (2); in (2), HIM-6 foci can be found in proximity of ZHP-3 at some putative CO-designated sites; however, most do not colocalize. (F) Stacked bar graph showing the percentage of nuclei containing a defined number of COSA-1 foci either in WT (n = 428), rmh-1(jf54) (n = 291), rmh-1(tn309) (n = 329), him-6(ok412) (n = 204), or rmh-1(jf54); him-6 (n = 177). The data presented for WT, rmh-1(jf54), and rmh-1 (tn309) are the same as in Fig 4F. Difference in COSA-1 foci distribution was assessed by a Mann Whitney test: ns stands for not significant and **** p < 0.0001. (G) Quantification of the number of DAPI positive structures in the -1 oocyte for WT; single mutants (rmh-1(tn309)him-6(ok412)-rmh-1(jf54)) and the double rmh-1(tn309); him-6 and rmh-1(jf54); him-6 (n = 15-36 nuclei per genotype). Data are represented as mean +/-SEM with ns (not significant) and **** p < 0.001. (H) In him-6(ok412), RMH-1 is not detectable in MP (I,I 0 ), but bright RMH-1 foci are present in LP (J,J 0 ), albeit quantification (K) indicates that their numbers are reduced relative to WT (p < 0.001). Data are represented as mean +/-SD. Scale bar 20 μm for gonads, 5 μm for pachytene nuclei insets, and 2.5 μm for single nuclei.  RMH-1 in C. elegans meiosis observed a significant increase in RMH-1 foci in mid pachytene nuclei in the smc-5 mutant; 29.1% of nuclei contained more than 25 foci, never seen in wild type (Fig 7A and 7B). However, late pachytene nuclei in the smc-5 mutant had an average of six foci per nucleus, as in wild type (Fig 7C), suggesting that an excess of RMH-1-associated recombination intermediates accumulate in the smc-5 mutant, but they are ultimately taken care of in agreement with the wild type viability of the single mutant ( Fig 7D). Second, the rmh-1(jf54); smc-5(ok2421) double mutant showed both a synthetic decrease in embryonic hatch rates and increase in larval arrest (Fig 7D  and 7E), indicating a strong genetic interaction between rmh-1 and smc-5 in the soma but also likely during meiosis (a similar genetic interaction is reported between him-6 and smc-5 in [74]). Third, quantification of the number of DAPI bodies in diakinesis oocytes in the rmh-1; smc-5 double mutant revealed an average of 5.9 ± 0.3 DAPI bodies in the -1 oocyte (Fig 7F), consistent with the presence of connections between the homologs. However, cytological examination of chromosome organization revealed that these interhomolog connections were aberrant. Consistent with the low viability of this double mutant, bivalent organization was dramatically defective: both long arms (indicated by LAB-1 staining) were always found together, precluding the wild-type cross-shaped appearance of the bivalent (Fig 7G-7J). Such abnormal bivalents were already observed at a low frequency in each of the single mutants, but are now present in each diakinesis nucleus in the double mutant ( Fig 7K). This result strongly suggests that rmh-1 and smc-5 cooperate to eliminate and/or prevent accumulation of connections between homologs at NCO sites. Finally, we found that simultaneous loss of both RMH-1 and SMC-5 results in a high frequency of interhomolog connections even in the absence of the conserved meiotic CO factor ZHP-3. Whereas COs and chiasmata are eliminated in the zhp-3 single mutant [16], a small but significant reduction in DAPI bodies in -1 oocytes was observed in the zhp-3; smc-5 mutant (Fig 7L, 7M and 7O). This ability to create aberrant homolog connections in a zhp-3 mutant is consistent with the finding that a mutation affecting the budding yeast Smc5/6 complex has the ability to create connections between homologous chromosomes in a mutant lacking Zip3 (the ZHP-3 ortholog) [59]. Moreover, ectopic ZHP-3-independent connections occurred at very high frequency in a zhp-3; rmh-1; smc-5 triple mutant, in which we observed an average of 7.3 DAPI bodies at diakinesis (Fig 7N and 7O). Together, our data indicate that smc-5 and rmh-1 act in parallel to antagonize MutS gamma-independent interhomolog connections, supporting the conclusion that RMH-1 also functions at NCO sites.

RMH-1 Discourages COs in the Center of Chromosomes
To assess the role of RMH-1 at NCO sites in more detail, we analyzed the localization of COs along the chromosomes. We used deep sequencing to compare CO frequency and CO distribution between the wild type and rmh-1 mutants (jf54 and tn309). We took advantage of the C. elegans Hawaiian (Hw) strain, which contains a high frequency of SNPs compared to the Bristol strain (wild type). Thus, we generated strains containing rmh-1 mutants in combination with a subset of introgressed "Hawaii chromosomes": chromosomes II and V for rmh-1(jf54) and chromosomes X, IV, and V for rmh-1(tn309). (Introgression of all Hawaii chromosomes into the rmh-1 mutants led to sterility).
We sequenced all the parental strains (Bristol, Hw, and the "Hw introgressed rmh-1 mutants") and used them as references. Recombinants between the Bristol strain and Hw were generated as described in Fig 8A. We singled F2 animals and allowed them to self-fertilize for three to four generations and deep-sequenced DNA isolated from their progeny. Paired-end reads were mapped as described in the Experimental Procedures section. Bioinformatic analysis identified 166,928 homozygous unique SNPs in the Hw genome. To assess the chromosome composition in each recombinant, we used the homozygous unique SNPs of the Hw strain. We used SNPs located at least 400 bp apart to avoid having two or more SNPs per paired read. In the absence of recombination, two genotypes are expected in the offspring: fully homozygous (i.e., both homologous chromosomes come from the same parental strain) and fully heterozygous (each homolog comes from one parental strain). If recombination occurred, blocks of homozygosity and blocks of heterozygosity were detected. We identified the recombination break-points by analyzing the changes in heterozygosity along the chromosome (for more details, see the Experimental Procedures section).
DAPI bodies in diakinesis oocytes (F) for WT, rmh-1(jf54), smc-5(ok2421), and rmh-1(jf54); smc-5 (n = 35-45 hermaphrodites per genotype). Data are represented as mean +/-SD with ns (not significant) and * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. (G-J) Images of individual diakinesis bivalents stained for long arm and short arm markers. Both rmh-1(jf54) and smc-5 single mutants exhibit abnormally structured bivalents at low frequency (H, I). In rmh-1; smc-5, all diakinesis nuclei contain bivalents with abnormal structures; typical of these abnormalities is a side-by-side organization of the long arms of the bivalents (J 0 ), presumably reflecting the presence of persistent interhomolog associations at NCO sites. (K) Quantification of the frequencies of diakinesis nuclei (-2 and -1) containing at least one abnormal bivalent (n = 13-25 nuclei per genotype). Data are represented as percentage with ns (not significant) and ** p < 0.01, *** p < 0.001, and **** p < 0.0001 (Chi 2 test) (L-N) Images of chromosomes in diakinesis nuclei from zhp-3; smc-5 and rmh-1 (jf54) zhp-3; smc-5 worms. Despite the absence of the canonical meiotic CO machinery component ZHP-3, fewer than 12 DAPI structures are observed in some zhp-3; smc-5-1 oocytes, indicating the presence of ectopic connections (L,M). Such ectopic connections occur at high frequency in the rmh-1(jf54) zhp-3; smc-5 triple mutant (N-N 0 ). The quantification is presented in (O) with n = 13-36 oocytes per genotype. Data are represented as mean +/-SD with ns (not significant), * p < 0.05 and **** p < 0.0001.  We did not detect a significant difference between the mutants and wild-type control in the total frequencies of crossovers (Fig 8B). This observation contrasts with the reduction in COSA-1 foci observed in both mutants, and could potentially reflect sample size or the fact that viable progeny were used in the recombination assay; alternatively, it may reflect crossovers occurring at sites not marked by COSA-1 foci in the mutants. However, we found that the positions of the COs were shifted significantly toward the center of chromosomes in both mutants, in contrast to the preference observed in the wild type, in which the majority of COs occurred in the gene-sparse "arm" regions of the chromosomes (Fig 8C and 8D).
We conclude that rmh-1 is required to discourage COs in the center of chromosomes. A shift of COs toward chromosome centers in the rmh-1(jf54) mutant was confirmed by using a PCR-based assay to genotype four SNPs along chromosome IV (S10 Fig). A parallel study analyzed the recombination rate and CO position in the him-6 mutant. Here, the entire brood was used (dead and living progeny) to determine recombination; similarly, a shift toward the chromosome centers was observed [74].

Genetically Separable Roles for RMH-1 at CO and NCO Sites
Although protein complexes involving RMI1 and/or BLM helicase were initially recognized based on anti-CO activities, recent work in several systems has led to a growing realization that BLM and RMI1 play multiple roles during meiotic recombination, functioning both in antagonizing and promoting COs (for review, see [75] and Introduction). One current view for Saccharomyces cerevisiae is that the primary role of the RTR complex is as a "recombination intermediate chaperone" [41,44,45,55,56]. Under this model, RTR plays an indirect role in promoting COs during yeast meiosis, either by generating recombination intermediates recognized and processed by the Exo1-MutLγ pathway or by disassembling aberrant recombination intermediates, thereby helping to channel early recombination intermediates into either a MutSγ-dependent CO pathway or into the SDSA pathway for generating NCOs. Yeast Sgs1 has also been implicated in promoting resolution of CO intermediates under circumstances in which JM resolution is impaired [55]. A more prominent pro-CO role has been uncovered for HIM-6/BLM during C. elegans meiosis, in which loss of BLM function results in reduced COs [53,54]. It was proposed that HIM-6 functions to enforce a CO-biased outcome of resolution of CO intermediates; however, it was not clear whether this proposed pro-CO role for HIM-6 was direct or indirect [22,46]. Our combined genetic and cytological analysis provides a strong case that RMH-1 functions directly at both CO and NCO sites. For a summary, see Fig 9. First, RMH-1 and HIM-6 colocalize at CO designated sites (Figs 3G-3K, 5A-5C and 6F), and this late pachytene localization is dependent on conserved pro-CO factors (Fig 4A-4D). Conversely, pro-CO factors can concentrate at presumptive CO sites in the absence of HIM-6 or RMH-1 (albeit less reliably in rmh-1 mutants) consistent with RMH-1 and HIM-6 being recruited to CO designated sites to perform a late function in CO formation (Figs 4E, 4F and 5F). Moreover, SIM imaging of CO sites in late pachytene nuclei revealed that RMH-1 and HIM-6 colocalize in an elongated structure or closely juxtaposed doublets, potentially reflecting two separate populations of RTR complexes flanking the two junctions of a dHJ CO intermediate (Fig 6). The "doublet" organization leads us to suggest that RMH-1 and HIM-6 localized at CO sites may support the CO outcome of recombination intermediate resolution either by promoting an optimal geometry for endonucleases (resolvases) to position DNA cleavage, or by protecting the structure from unscheduled action of endonucleases. Our analysis with the truncation allele tn309 raises the possibility that HIM-6 itself may contribute to inappropriate resolution when RMH-1 is absent. Interestingly, RMH-1 and HIM-6 differ regarding the requirements for their recruitment at CO sites. Whereas RMH-1 is successfully recruited to most presumptive CO sites in him-6 mutants (Fig 5H-5K), HIM-6 does not stably concentrate at the sites of pro-CO factors in rmh-1 mutants (Fig 6G), raising the possibility that RMH-1 (or TOP-3 associated with RMH-1) may interact more directly with pro-CO factors at such sites. The absence of HIM-6 at CO sites in rmh-1 mutants suggests that RMH-1 might provide a structural support to ensure the final processing of a mature recombination intermediate by limiting branch migration or the collapse of a putative dHJ and, thereby, influencing the outcome of resolution.
We provide multiple lines of evidence that RMH-1 also localizes to NCO sites and that its function(s) in NCO repair events are distinct from its pro-CO role(s). First, localization of RMH-1 during early and mid pachytene has different genetic requirements than its late pachytene localization at CO-associated foci: Early/mid pachytene RMH-1 foci can still form (albeit at reduced levels) in mutants defective for pro-CO factors, but are strictly dependent on HIM-6, suggesting that the intermediates present at early and late foci differ in structure (Figs 4A-4D and 5H-5K). Furthermore, we show that such foci can occur at elevated levels when numbers of DSB are increased or when alternative pathways for DSB repair are abrogated (Fig 7A  and S7A-S7C Fig).
In mid pachytene, HIM-6 and RMH-1 proteins colocalize, but only a fraction colocalize with MSH-5 (Fig 3G-3I). We hypothesize that foci positive for all three proteins correspond to CO-eligible recombination sites, while those positive for only HIM-6 and RMH-1 may be processed as NCOs (perhaps by a decatenation reaction). The occurrence of chromosome bridges in rmh-1; resolvase double mutants could indicate either the accumulation of recombination intermediates due to defective dissolution or a more direct collaboration between RMH-1 and resolvases to produce COs and/or NCOs (Fig 4K-4M).
Together, our data suggest direct but distinct roles for RMH-1 in both CO and NCO repair during C. elegans meiosis.

Functions of RMH-1 at CO and NCO Sites Collaborate to Prepare Chromosomes for Segregation During the Meiotic Divisions
Another important concept emphasized by our work analyzing the functions of RMH-1 during C. elegans meiosis is that a successful outcome of meiosis requires proper execution of the prescribed recombination events at both CO and NCO repair sites. Whereas COs serve as the basis of chiasmata that connect homologous chromosomes to enable them to orient toward opposite poles of the meiosis I spindle, efficient homolog segregation also depends on elimination of other recombination-based interactions between homologs that might impede their timely separation.
Beyond ensuring CO formation, RMH-1 has (at least) two roles in preparing homologous chromosome for segregation at meiosis I. First, RMH-1 functions in parallel with SMC-5 in eliminating excess associations between homologs (Fig 7). Importantly, we also demonstrate another major role for RMH-1 in ensuring that COs usually form in positions that favor reliable homolog segregation. In the absence of localized centromeres (due to the holocentric nature of C. elegans chromosomes), the position of the CO dictates multiple features of bivalent organization that are crucial for correct alignment and behavior of chromosomes [69]. This defines distinct long arm and short arm domains where cohesion will be retained or released at Last row: pro CO functions: role of RMH-1 in CO designation, in assurance of chiasma formation and, finally, its potential function in supporting the geometry of recombination intermediates. We propose timing for the different functions based on our data and previous publications. However, the C. elegans gonad is a continuous production line of meiocytes, and we do not intend to imply sharper transitions between meiotic stages than exist.
doi:10.1371/journal.pbio.1002412.g009 RMH-1 in C. elegans meiosis the meiosis I division and delineates how kinetochore components, motor proteins, and celldivision protein kinases associate with the chromosomes. We found that, whereas COs usually occur at off-center positions during wild-type meiosis, COs occurred more frequently near the centers of the chromosomes in rmh-1 mutants (Fig 8 and S10 Fig). We speculate that an altered distribution of COs in an rmh-1 mutant may reflect impaired execution at both CO and NCO repair sites. On the one hand, an impaired ability to impose CO-biased resolution at CO-designated sites results in intermediates at some of those sites being resolved as NCOs. On the other hand, impairment of a mechanism that would normally help dissociate intermediates to promote repair via SDSA may result in accumulation of DNA structures that require structurespecific endonucleases for their resolution, resulting in CO repair products at some sites that should have been NCOs. We have not observed a significant frequency of double COs in the mutants, suggesting that the misplaced COs are still subjected to interference. Interestingly, the SLX-1 resolvase is also required to suppress CO formation in the chromosome center [24]. It is appealing to speculate that RMH-1 might cooperate with SLX-1 in a locally defined region to promote NCO resolution.
We note that while CO positioning may be especially important in organisms like C. elegans that use COs to trigger differentiation of the bivalent, CO position is also very important during Drosophila, yeast, and human meiosis. in Drosophila, centromere proximal recombination events have been correlated to metaphase II nondisjunction [76]. In yeast, centromere proximal COs have been shown to trigger premature separation of sister chromatids (PSSC). Interestingly, sgs1 mutants exhibit reduced spore viability, potentially due to an excess of COs near the centromere leading to PSSC [77]. In human meiosis, COs located very near to either telomeres or centromeres are associated with elevated risk of aneuploidies, e.g., [78][79][80][81][82].

Experimental Procedures
Cultivation of worms followed standard protocols [83]. All experiments were performed at 20°C. N2 Bristol was used as wild type. Experiments using GFP::RMH-1 always included the wild-type rmh-1 gene, if not indicated otherwise. Strains are listed in S1 Text. Raw data for the figures can be found in S1 Table. Cytological Preparations and Immunofluorescence Analysis Dissection and immunostaining was performed as described in [67] with modifications when using SYP-1, LAB-1, and S10 phospho-histone 3: dissection and fixation was performed in 1x EBT instead of PBS 1X [66]. Adults 24 h post L4 were dissected. Images are projections of stacks encompassing whole nuclei. For details on antibodies and microscopy, refer to S1 Text.
See also S1 Text for rmh-1 allele isolation and characterization, protein tagging (RMH-1, HIM-6::HA), generation of the rmh-2 knockout, irradiation conditions, yeast two hybrid assays, photoconversion experiments, and recombination assays. , with the DUF1767 domain (green frame) as described in [47] and the OB domains (orange frame) as described in [35]. (B) The mutation in rmh-1(jf54) affects the splice donor site of the first exon. Schematics of PCR primers used to analyze the structures of transcripts produced by the rmh-1 locus. The spliced version corresponds to the wild type. In the unspliced version, intron 1 is present. Two different guanidines (three base pairs apart), present in exon 1, were used as cryptic splicing donor sites to substitute the original G mutated site in rmh-1(jf54). Those versions led to deletions of intron 1 and a small portion of exon 1 (conserved amino acid in the DUF domain), as illustrated in (A). (C) Quantification of transcript abundance (four replicates). The percentage of transcripts represents the fraction of the total population of transcripts in one genotype (wild type or jf54). Data are represented as mean +/-SD ( ÃÃÃ p < 0.001 and ÃÃÃÃ p < 0.0001). (D) Schematics of the protein products predicted for the different mutant alleles of rmh-1: jf92, tn309, and jf54. Quantification of the average volume of a bivalent (assessed in the wild type) and a univalent (assessed in the msh-5 (me23) mutant in the -1 oocyte (n = 13 nuclei for both genotypes). Data are presented as mean +/-SD with p < 0.0001. (B) Classification of the DAPI structures found in rmh-1(jf54) and rmh-1(tn309). Classes (fragment < univalent < bivalent < chromatin masses) were defined by the volume of the structure (n = 13 nuclei for wild type, msh-5(me23), and rmh-1(tn309), and n = 12 nuclei for rmh-1(jf54)). Yeast two-hybrid assays for protein interactions between RMH-1, HIM-6, and TOP-3. Full-length RMH-1 interacts with TOP-3 (row 1) and with HIM-6 (row 2), respectively. A truncation protein of RMH-1 containing only the N-terminal part with the DUF and OB1 domains (reminiscent of tn309) interacts with TOP-3 (row 5). Auto-activation of both bait and prey vectors were tested in lanes 6 to 10. Interactions were scored by growth on SC-Leu-Trp-His plates (left panel) and growth on SC-Leu-Trp plates (right panel). Quantification of the percentage of hatch rate (B) and males in offspring (C) for wild type (n = 45 hermaphrodites), single mutants (rmh-1(tn309) (n = 45)-him-6(ok412) (n = 35)-rmh-1(jf54) (n = 45)), and the double mutants rmh-1(tn309); him-6 (n = 43) and rmh-1(jf54); him-6 (n = 45). Data are represented as mean +/-SD with ns (not significant) and Ã p < 0.05, ÃÃ p < 0.01, ÃÃÃ p < 0.001, ÃÃÃÃ p < 0.0001. the SNPs used during the recombination assay. SNP A is localized on the left arm, B is at the junction between left arm and the center, C is at the junction between the center and right arm, and D is on the right arm. (C) Recombination frequencies on chromosome IV left arm between SNP A and B for wild type (n = 94 individuals) and rmh-1(jf54) (n = 96 individuals). (D) Recombination frequencies on chromosome IV center between SNP B and C for wild type (n = 94 individuals) and rmh-1(jf54) (n = 96 individuals). COs were shifted to the centers of the chromosome in the mutant. (E) Recombination frequencies on chromosome IV right arm between SNPs C and D for wild type (n = 94 individuals) and rmh-1 (jf54) (n = 96 individuals). (C-E) The column "theoretical" corresponds to the expected recombination frequency based on the published genetic distance (http://www.wormbase.org). Data are represented as percentage with ns for not significant, Ã for p < 0.05, and ÃÃ for p < 0.01 (Chi 2 test on raw data). (F) Graph illustrating the percentage of CO events along chromosome IV for wild type and rmh-1(jf54). In the wild type, COs are concentrated to chromosome arms, whereas in the mutant, they are more concentrated at the center. (TIF) S1 Table. Raw data. (XLSX) S1 Text. Supporting information materials and methods. Detailed descriptions are provided for the strains used and generated in this study, antibodies and imaging methods, FISH procedure, identification of the rmh-1 alleles, generation of rmh-1, rmh-2 alleles and him6::HA strain by CRISPR method, the tagging of RMH-1, RT-PCR procedure, measurements of DAPI bodies in diakinesis, the Y2H assay, the recombination assays by PCR-based SNP mapping, and deep sequencing. (DOCX)