Reduced dosage of the chromosome axis factor Red1 selectively disrupts the meiotic recombination checkpoint in Saccharomyces cerevisiae.

Meiotic chromosomes assemble characteristic "axial element" structures that are essential for fertility and provide the chromosomal context for meiotic recombination, synapsis and checkpoint signaling. Whether these meiotic processes are equally dependent on axial element integrity has remained unclear. Here, we investigated this question in S. cerevisiae using the putative condensin allele ycs4S. We show that the severe axial element assembly defects of this allele are explained by a linked mutation in the promoter of the major axial element gene RED1 that reduces Red1 protein levels to 20-25% of wild type. Intriguingly, the Red1 levels of ycs4S mutants support meiotic processes linked to axis integrity, including DNA double-strand break formation and deposition of the synapsis protein Zip1, at levels that permit 70% gamete survival. By contrast, the ability to elicit a meiotic checkpoint arrest is completely eliminated. This selective loss of checkpoint function is supported by a RED1 dosage series and is associated with the loss of most of the cytologically detectable Red1 from the axial element. Our results indicate separable roles for Red1 in building the structural axis of meiotic chromosomes and mounting a sustained recombination checkpoint response.

Introduction

Meiosis is a specialized developmental process, in which a diploid cell undergoes two chromosomal divisions without an intervening S phase to produce haploid gametes for sexual reproduction. The reduction in ploidy occurs during meiosis I, when homologous chromosomes are segregated. To enable this unique segregation pattern, meiotic cells must identify and physically link homologous chromosome pairs. In most sexually reproducing organisms, such linkages are achieved by meiotic recombination. In addition to increasing genetic variation in the progeny, recombination leads to crossover exchanges that, together with sister chromatid cohesion, stably connect homologous chromosomes [1].

Meiotic crossover formation relies on the controlled introduction and repair of a large number of programmed DNA double-strand breaks (DSBs). DSBs are formed in a non-random manner across the genome by the conserved topoisomerase-like enzyme Spo11 [2-7]. In the budding yeast Saccharomyces cerevisiae, 160 DSBs are estimated to occur on average per meiosis [8]. Following DSB formation, nucleolytic processing releases Spo11 from break ends along with short covalently-linked oligonucleotides [9]. Exonucleases resect the break ends to produce 3’ single-stranded DNA (ssDNA) tails [10] that are used by the recombinases Rad51 and Dmc1 to preferentially invade the homologous chromosomes [11,12]. Some of the resulting strand-invasion intermediates are stabilized and processed to produce crossovers [13-17].

Meiotic recombination occurs in the context of highly conserved chromosome architecture, characterized by linear arrays of chromatin loops anchored to a proteinaceous axis known as the axial element [18-20]. As meiotic prophase progresses, axial elements of homologous chromosomes in many organisms co-align with the help of transverse filament proteins, such as Zip1 in yeast and Sycp1 in mice [21]. The axial elements subsequently form the lateral elements of the synaptonemal complex (SC), a ladder-like structure connecting homologous chromosome pairs in the later stages of meiosis [21]. Like the rest of the SC, axial elements are defined cytologically; they appear as electron dense linear structures by electron microscopy and can be visualized by immunofluorescence analysis of proteins localizing to these structures [20,22-26]. The structural axes of meiotic chromosomes are also defined functionally, with mutants that lose axial integrity exhibiting numerous defects in meiotic recombination, including reduced DSB formation, aberrant DSB repair, and a loss of DSB surveillance [18,27,28]. These defects lead to inviable gametes in a variety of model organisms [20] and are associated with male infertility and premature ovarian failure in human patients [29,30].

The molecular structure of the axial elements is only beginning to be understood. In S. cerevisiae, the axial element comprises a specialized meiotic cohesin complex, containing the meiosis-specific subunit Rec8 [23], as well as the meiotic proteins Red1 and Hop1 [22,24]. Rec8-cohesin is thought to form the chromatin anchor that recruits Red1 and Hop1 to axis-attachment sites along chromosomes [31,32]. Moreover, electron microscopy studies indicate that only Rec8-cohesin is essential for axial element formation, as red1 and hop1 mutants still exhibit dark-staining linear structures [23,33,34]. These structures, however, appear fragmented and irregular, suggesting that RED1 and HOP1 contribute to axial element formation or stability.

RED1 and HOP1 exert essential regulatory functions in the context of the axial element. Deletion of RED1 or HOP1 reduces DSB levels to 10–30% of wild type [12,35-39], likely because of the role of these genes in recruiting essential DSB factors near DSB hotspots [31]. Moreover, the DSBs that do form in red1 and hop1 mutants are associated with unusually long resection tracts [40,41]. Loss of RED1 or HOP1 function also causes severe synapsis defects [33,34], although linear stretches of the central SC component Zip1 remain detectable in some red1 mutant cells [24]. Finally, red1 and hop1 mutants fail to activate the meiotic checkpoint network [42,43], which helps block repair from the sister chromatid to bias repair events toward the homologous chromosome [44,45], and acts to arrest cells in meiotic prophase in response to unrepaired DSBs [27,38,46,47].

Surprisingly, mutants lacking REC8 recapitulate only some of the phenotypes of red1 and hop1 mutants. Although rec8Δ mutants are unable to synapse [23] and exhibit excessive resection [41], their defects in DSB formation are more nuanced than in red1 and hop1 mutants, affecting some chromosomal regions while sparing others [32,48,49]. In addition, rec8Δ mutants are proficient in mounting a meiotic checkpoint response [23,50]. This disparity may be explained by the fact that Red1 and Hop1 are recruited to a limited number of chromosomal regions in the absence of Rec8 [31,32]. Although their distribution pattern is highly abnormal, Hop1- and Red1-rich regions exhibit close to wild-type DSB levels [32,48,49], implying that the axis-associated DSB and checkpoint activities remain functional in these regions.

Red1 and Hop1 recruitment to the axial element is affected in mutants of the condensin complex. The condensin complex is a conserved regulator of chromosome architecture that localizes to axial elements and functions in chromosome compaction and removing cohesin from chromosomes at the end of meiotic prophase [51,52]. The intensity of Red1 and Hop1 on chromosome spreads is decreased in temperature-sensitive condensin mutants [51], and nearly undetectable in the meiosis-specific condensin allele ycs4S, which is linked to a C-terminal 12xMYC tag on the condensin subunit Ycs4 [51]. The reason for the more severe meiotic defects of ycs4S has remained unclear, in particular as other condensin functions, including cell survival and chromosome compaction, appear unaffected by this allele [51].

Here, we show that the ycs4S allele is in linkage with a promoter mutation in the nearby RED1 gene that reduces RED1 expression to about 25% of wild-type levels and explains most, if not all, ycs4S phenotypes. Intriguingly, the reduced Red1 levels cause a differential loss of RED1 activities. Analysis of a Red1 dosage series including the ycs4S allele shows that DSB formation, deposition of the synapsis protein Zip1, and spore viability are all buffered against substantial reductions in Red1 levels. By contrast, the ability to maintain a checkpoint arrest in meiotic prophase is very sensitive to Red1 dosage and abolished in the ycs4S mutant. These data suggest separable activities of Red1 in regulating axis integrity and the maintenance of checkpoint activity, and imply that the majority of Red1 is primarily involved in the maintenance of meiotic checkpoint activity.

Results

RED1 expression is reduced in ycs4S mutants

The low Red1 and Hop1 signals localizing to meiotic chromosomes of ycs4S mutants [51] prompted us to test whether total axis protein levels are reduced by this allele. To this end, wild-type and ycs4S cells were harvested in a synchronous meiotic time course, and the levels of Red1 and Hop1 were analyzed by western blotting. We found that total Hop1 levels are similar in both strains, although we noted a reduction in the slower migrating, phosphorylated forms of Hop1 [53] in the ycs4S mutant (Fig 1A). By contrast, Red1 protein levels are strongly reduced in the ycs4S mutant relative to wild-type meiotic cells. Quantitative western analyses showed that ycs4S mutants express on average approximately 20% of the Red1 protein levels of wild type during meiotic prophase (Fig 1B). This decrease in Red1 protein levels differentiates the ycs4S mutant from the temperature-sensitive ycg1-2 and ycs4-2 condensin mutants, which do not exhibit a discernable reduction of Red1 levels at the restrictive temperature of 34°C (Fig 1C).

Fig 1

ycs4S mutants have decreased levels of Red1.

(A) Red1 and Hop1 protein levels of whole-cell extracts from wild type (H7797) and ycs4S (H7011) as determined by western blotting at the indicated time points after meiotic induction. Arrows indicate the two Red1 bands. Bracket indicates positions of phosphorylated Hop1. Nsp1 was used as loading control. (B) Fluorescence-based quantitative measurement of total Red1 protein levels in wild type and ycs4S relative to Nsp1 at 2h, 3h, and 4h, n = 3. Error bars: S.E.M. *: p-value < 0.05, **: p-value < 0.005, paired Student t-test. (C) Western analysis of Red1 and Hop1 protein levels in wild-type, ycg1-2 (H8632), ycs4S, and ycs4-2 (H8601) strains. Nsp1 was used as loading control. ycg1-2 and ycs4-2 cultures were shifted to 34°C 1 hour after meiotic induction. (D) RED1, HOP1, REC8, and ZIP1 mRNA levels at 2h were measured by RT-qPCR from both wild-type (grey) and ycs4S (cyan) extracts, and normalized against ACT1, n = 3. Error bars: S.D. *: p-value < 0.05, Student t-test.

Coincident with the decrease in Red1 protein in the ycs4S mutant is a reduction of the slower migrating band, which is the result of Red1 phosphorylation [54] (compare late time points in Fig 1A). The biased loss may be the result of preferential degradation of phosphorylated Red1 in the ycs4S mutant or reflect reduced phosphorylation of Red1 as a result of reduced Red1 levels.

To test if the loss of Red1 abundance occurs at the transcriptional or post-transcriptional level, we analyzed relative RED1 mRNA levels at the 3-hour time point by qRT-PCR. These measurements revealed that RED1 mRNA levels in ycs4S mutants are about 25% of wild-type levels (p < 0.05; Student t-test, Fig 1D). By contrast, no significant difference was observed for the mRNA levels of the axial element components HOP1 and REC8, or the transverse filament component ZIP1 (p = 0.79, p = 0.43, and p = 0.10, respectively). Together, these data indicate that the ycs4S allele is associated with a specific loss of RED1 mRNA expression.

Increasing Red1 levels rescues the spore inviability of ycs4S mutants

Because ycs4S differs from other condensin mutants, both in its ability to compact its chromosomes [51] and in its decreased concentrations of Red1 protein, we hypothesized that the meiotic phenotypes displayed by ycs4S mutants could be primarily caused by low Red1 expression levels as opposed to a direct effect of condensin malfunction. To test this possibility, we placed RED1 under the control of the HOP1 promoter, which is unaffected in the ycs4S mutant (Fig 1D). Western blot analysis indicated that the pHOP1-RED1 construct leads to an overexpression of Red1, although this effect was less obvious in the ycs4S mutant (Fig 2A). In addition, Hop1 levels were slightly higher, including an increase in Hop1 phosphorylation signal (Fig 2A, bracket). Importantly, the pHOP1-RED1 construct completely rescued the spore viability defect of ycs4S cells (Student t-test: p-value = 1.1 x 10−4, Fig 2B).

Fig 2

ycs4S mutants have a mutation in the promoter of RED1.

(A) Red1 and Hop1 protein levels in wild type (H7797), ycs4S (H7011), pHOP1-RED1 (H8849), and pHOP1-RED1 (H8850) strains. Phosphorylated Hop1 indicated by bracket. Fpr3 was used as loading control. (B) Spore viability of wild-type, ycs4S, pHOP1-RED1, pHOP1-RED1, and YCS4-13xMYC (H9077) strains, as well as red1-pG162A (H9048) mutant strain and a matched control carrying only a marker insertion at position +400 upstream of the RED1 ORF (H9049), n>100. Error bars: S.D. **: p-value: < 0.005, Student t-test. (C) Schematic of the introgressed region in the ycs4S mutant. The genetic background of three separate lines was determined across a 35kb region of chromosome XII, which includes the RED1 and YCS4 genes. This was compared to a wild type SK1 background. Regions were color-coded as SK1 (blue), YPH499 (yellow), S288C (green), and indeterminate (grey). Positions of the 12xMYC tag and the G162A SNP in the promoter of RED1 are indicated. (D) Red1 and Hop1 protein levels in wild type and a ycs4S mutant, as well as a red1-pG162A mutant strain and its matched control. Fpr3 was used as loading control.

The ability of the pHOP1-RED1 construct to rescue the ycs4S spore viability defect indicates that the RED1 promoter has a role in causing the ycs4S phenotypes. This initially puzzling result is explained by the fact that the YCS4 gene (YLR272C) is located in close proximity to RED1 (YLR263W), with the RED1 promoter being separated from the C-terminal 12xMYC tag of ycs4S by less than 14kb. Sequence analysis revealed approximately 100 SNPs across this region that differ from the SK1 strain background and reflect the fact that the YCS4-12xMYC construct was introgressed from YPH499 into SK1 (Fig 2C) [51]. The preservation of YPH499-derived SNPs throughout this region over multiple crosses indicates a close genetic linkage between RED1 and YCS4.

We identified a single SNP in the RED1 promoter of the ycs4S mutant, a change from G to A at position -162 from the RED1 open reading frame. This SNP overlaps a conserved residue of a URS1 consensus site for the transcriptional regulator Ume6 [55], which is required for wild-type levels of RED1 expression [56]. Disruption of the corresponding residue along with a second residue in the URS1 sequence of the meiotic SPO13 gene causes a 6-fold reduction in expression [57]. Introduction of the YPH499 SNP into an otherwise wild-type SK1 strain resulted in decreased Red1 protein levels (Fig 2D, S1A Fig) and spore viability defects (Student t-test: p-value = 1 x 10−3, Fig 2B) comparable to those of ycs4S mutants. Introduction of a 13xMYC tag at the C-terminus of YCS4 had no effect on spore viability (Student t-test: p-value = 0.104, Fig 2B). These findings together with the rescue mediated by the HOP1 promoter suggest that the ycs4S phenotypes are caused by a linked mutation in the RED1 promoter that causes low RED1 expression. We note that providing the YPH499 genome in trans in a SK1/YPH499 hybrid diploid did not improve the spore viability defects caused by the red1-pG162A mutation (S1B Fig), indicating that YPH499 has not adapted to this mutation. For the remainder of this paper, we will refer to the introgressed YPH499 genomic fragment containing the YCS4-12xMYC construct and the red1-pG162A mutation as red1.

Red1 and Hop1 are recruited to axis attachment sites in red1 mutants

If the low levels of Red1 protein in the red1 mutant are responsible for its axis assembly defect, chromosomal levels of Red1 and Hop1 should be diminished but still distributed at the expected sites along meiotic chromosomes. To test this prediction, we probed Red1 and Hop1 recruitment in red1 mutants using immunofluorescence and ChIP-seq analysis. Consistent with published results [51], we found that Red1 and Hop1 levels on chromosome spreads are greatly reduced and no cytological axis structures are observed in red1 mutants (Fig 3A and 3B). Notably, whereas Red1 signals are nearly undetectable, nuclei with discernible Hop1 foci still exist. However, the intensity of total Hop1 signal on chromosomes in these nuclei was two-fold lower than in wild-type nuclei (Wilcoxon Sign Rank Test: p-value = 3.9 x 10−10, Fig 3C). The incongruity in the amount of Hop1 versus Red1 foci detected in our studies may be the result of different antibody sensitivities. Alternatively, given that Red1 is required for Hop1 recruitment to chromosomes [24,32], it may indicate that multiple Hop1 proteins are recruited per Red1 protein. Importantly, although no axis structures were observed cytologically, ChIP-seq analysis indicated that Red1 and Hop1 are nevertheless recruited in a wild-type pattern to meiotic chromosomes (Fig 3D, S2A Fig, Spearman correlation: 0.87 and 0.66, respectively). We note that the apparently similar signal intensities of wild-type and red1 profiles are a consequence of the necessary internal normalization, which precludes comparison of absolute intensities between ChIP-seq datasets [58]. Accordingly, ChIP-qPCR analysis of several loci revealed a general decrease in Red1 binding in the red1 mutants (S3B Fig). Together, these analyses show that axis protein binding is reduced in red1 mutants, but that the low chromosomal amounts of Red1 and Hop1 are distributed normally to axis recruitment sites, suggesting that their chromosomal binding per se is unaffected.

Fig 3

Decreased deposition but normal distribution of axis proteins in red1 mutants.

(A) Red1 binding and (B) Hop1 binding was analyzed on chromosome spreads from wild-type (H7797) and red1 (H7011) strains, n = 100 per time point. Patterns were classified into four categories: “No foci”, “Few foci” (less than 20 detectable by eye over background), “Many foci”, or “Short Tracks” (indicative of chromosome axes). Scale bars are 5μm. (C) Hop1 intensity values of nuclei spread at 2h after meiotic induction. Focus intensity across an entire spread was normalized against background intensity of an area of identical size. Average intensity is indicated for wild-type (grey), red1 (cyan), rec8Δ (pink, H5187), and red1 rec8Δ (orange, H7661) strains, n = 20. Error bars: S.D. ***: p-value < 10−5, Wilcox test. (D) Red1 chromosomal localization at 3h determined by ChIP-seq in wild-type (black, H119), red1 (H7011), rec8Δ (H7660 & H7772), and red1 rec8Δ (H7661) strains on chromosomes III and VIII, n = 2. Large black circles indicate the positions of the centromeres. Triangles indicate positions analyzed by ChIP-qPCR in S3B Fig. (E) Percentage of spreads at 2h from time course in (C) exhibiting clumps of Hop1 (arrow in example image), n = 100.

To determine if reducing the Red1 levels in red1 mutants affects cohesin-independent recruitment of axis proteins, we introduced a rec8Δ mutation. ChIP-seq analysis revealed that the patterning of Red1 and Hop1 is highly concordant in red1 rec8Δ mutants, a characteristic also observed in rec8Δ mutants [32] (Fig 3D, S2A Fig, Spearman correlation: 0.94 and 0.93, respectively). However, in the red1 rec8Δ mutant, the genomic regions with relative enrichment of Hop1 and Red1 exhibited a substantial dampening relative to the other strains, even though Hop1 and Red1 protein levels are not substantially different from the red1 strain (S4A and S4B Fig). Quantification of total chromosome-associated Hop1 signal on chromosome spreads indicated no further loss of axis proteins in the red1 rec8Δ double mutant compared to the red1 mutant (Wilcoxon Sign Rank Test: p-value = 0.66, Fig 3C), but this result is likely caused by the already low signal in the red1 mutant. Indeed, ChIP-qPCR analysis revealed a further loss of Red1 enrichment in the double mutant (S3A and S3B Fig). Some binding of Hop1 and Red1 likely remains even in the red1 rec8Δ mutant, especially on chromosome III, as indicated by a general enrichment compared to a mock ChIP-seq experiment (S2B and S2C Fig) and supported by ChIP-qPCR analysis (S3B Fig). In addition, a few sites with strong Hop1 and Red1 enrichment persist in the double mutant (e.g. Chr VIII, open triangle, Fig 3D, S2A, S2B, S3A and S3B Figs), but their significance is unclear as they are not associated with any obvious chromosomal landmarks.

Analysis of Hop1 signal on chromosome spreads also indicated that the red1 allele rescues a characteristic axis defect of rec8Δ mutants. While rec8Δ mutants form distinctive clumps of Hop1 and Red1 on chromosomes spreads [23], red1 rec8Δ mutants do not (Fig 3E, S4C Fig). These data indicate that these clumps are dependent on Red1 protein abundance.

No checkpoint arrest in red1 mutants

During our analysis of the red1 rec8Δ mutant, we noticed that these cultures produce a substantial number of spores (Fig 4A). This behavior is in contrast to rec8Δ single mutants, which arrest in meiotic prophase and fail to sporulate due to defects in DSB repair [23,50], suggesting that red1 rec8Δ mutants are unable to mount a sustained checkpoint-mediated arrest response. Consistent with this notion, phosphorylation of Hop1, one of the earliest markers of recombination checkpoint activation [45], and phosphorylation of histone H3 threonine 11 (H3T11), a marker for activity of the downstream checkpoint kinase Mek1 [45,59,60], are reduced in red1 cells (Fig 4B).

Fig 4

red1 mutants lack a sustained meiotic DNA damage checkpoint arrest.

(A) Sporulation efficiency of red1 (H7011), rec8Δ (H5187), and red1 rec8Δ (H7661) mutants relative to wild type (H7797), n = 200. (B) Western analysis of phosphorylation levels of Hop1-T318 and H3-T11 from wild-type and red1 cells. Fpr3 was used as loading control. (C) Spindle pole separation in fixed cells measured by anti-tubulin immunofluorescence of wild type (black circle), red1 (cyan triangle), rec8Δ (pink square), and red1 rec8Δ (orange diamond), n = 200. Spindle pole separation is an indication of progression out of meiotic prophase. (D) Spindle pole separation in red1 (H7088), rec8Δ (H7161), and red1 rec8Δ (H6589) mutants and their control (H7076) in a repair-deficient dmc1Δ rad51Δ background, n = 200. (E) Spindle pole separation of wild type (black closed circle), red1 (cyan closed triangle), red1-pG162A (H9080, cyan open triangle) and its matched control (H9078, black open circle) strains in a dmc1Δ rad51Δ background to measure checkpoint activity, n = 200. (F) Spindle pole separation of wild type (black closed circle), red1 (cyan closed triangle), pHOP1-RED1 (H8851, black open circle), and pHOP1-RED1 (H8852, cyan open triangle) strains in a dmc1Δ rad51Δ background to measure checkpoint activity, n = 200.

To investigate the kinetics of this arrest bypass, we followed the rate of meiotic spindle pole separation, which initiates after cells exit meiotic prophase [61]. In a rec8Δ mutant, few cells produced separated spindle poles as seen previously [49], whereas red1 mutants formed spindles at the same rate as wild type (Fig 4C). Wild-type kinetics of spindle pole separation were also observed in red1 rec8Δ double mutants, indicating the reduced levels of Red1 in the red1 mutant allow a complete bypass of the rec8Δ checkpoint arrest (Fig 4C).

We considered two non-exclusive explanations for this bypass. First, red1 rec8Δ may be able to repair DSBs using an alternative pathway. This possibility is supported by the fact that the barrier to sister chromatid repair is weakened in red1 mutants [51,62]. Second, the signaling response triggering the arrest could be weakened by the red1 allele, either by reduced DSB initiation or poor signal transduction.

To investigate arrest signaling without the confounding effects of DSB repair, we analyzed spindle pole separation in a dmc1Δ rad51Δ background, which prevents essentially all homologous meiotic DNA repair [63]. We confirmed that red1 leads to a similar reduction in Red1 levels in the presence of these mutations (S5A and S5B Fig). Importantly, consistent with the model that the reduced Red1 levels interfere with checkpoint signaling, the dmc1Δ rad51Δ red1 mutant completely bypassed the checkpoint arrest and proceeded through meiosis at a rate similar to wild-type cells (Fig 4D). This defect is specifically caused by the red1-pG162A mutation, as introduction of the SNP is sufficient to cause a bypass (Fig 4E). Moreover, the bypass is partially rescued by increasing RED1 expression (pHOP1-RED1; Fig 4F), indicating that reduced RED1 levels are responsible for the checkpoint defects. We note that the pHOP1-RED1 construct itself caused a slight defect in arrest activity, possibly due to RED1 overexpression, which is known to affect exit from meiotic prophase [64]. Furthermore, because dmc1Δ rad51Δ mutants do not completely arrest like dmc1Δ mutants [63], we also confirmed that the red1-pG162A mutation was able to bypass the arrest of a dmc1Δ mutant (S5C Fig). These data indicate that arrest signaling is defective in red1 mutants.

red1 mutants produce sufficient DSBs and resection to arrest

Our analysis showed that deletion of REC8 also allowed a partial bypass of the arrest expected in the dmc1Δ rad51Δ mutants (Fig 4D), which has been attributed to a reduced number of DSBs [50]. To investigate if reduced DSBs might explain the bypass of the dmc1Δ rad51Δ arrest, we determined total DSB activity in red1 mutants by immunoprecipitating Spo11 and quantifying the amount of associated oligonucleotides as a measure of Spo11 activity [9,65]. This analysis revealed that maximal DSB levels in red1 mutants are reduced by approximately 20% compared to wild type (Fig 5A), in line with Southern measurements at individual hotspots [51,62]. To further support this measurement, we compared chromosome breakage in red1 mutants to a collection of three spo11 mutants with defined DSB activities [65,66]. Quantification of several full-length chromosomes after pulsed-field gel electrophoresis (PFGE) revealed that red1 mutants undergo meiotic chromosome breakage at levels significantly below the 100% of wild type but significantly above the ~70% of DSB activity of the spo11-HA allele (paired Student t-test: p-value = 3 x 10−4 and 6.8 x 10−5 respectively, Fig 5B). red1Δ mutants exhibited ~30% of wild-type breakage levels. These trends were also observed when measuring DSB levels on chromosome XVI by Southern blotting (S6A and S6B Fig).

Fig 5

Lack of checkpoint arrest in red1 is not caused by insufficient DSBs or a lack of sustained resection.

(A) Measurement of Spo11-oligonucleotide complexes as a measure of DSB level independent of resection or repair. Experiments were completed in wild-type (H9082), red1 (H9084), rec8Δ (H9083), and red1 rec8Δ (H9085) strains. Upper panel: Representative autoradiograph of Spo11-oligo complex and measure of total Spo11 protein by anti-Flag western. Plus sign indicates non-specific band. Lower panel: Quantification of Spo11-oligo complex bands (background normalized), n = 4 for 0, 3, and 4h, n = 3 for 5h. Error bars: S.E.M. *: p-value < 0.05, paired Student t-test. (B) Upper panel: Ethidium bromide staining showing the levels of seven intact chromosomes in a red1Δ (H8058), red1 (H8096), and control (H8099) in a rad50S background compared to strains with defined DSB levels: 100% (H9202), 70% (H9203), 30% (H9204), and 20% (H9205) [65,66], see S1 Table. Lower panel: Levels of chromosome breakage quantified from top three bands above, n = 2. Error bars: S.E.M. *: p-value < 0.05, **: p-value < 0.005, paired Student t-test. (C) Upper panel: Schematic of the CCT6 hotspot indicating uncut parental band (P), DSB fragment length (DSB), and resection products (Res1-4) when genomic DNA is cut with XhoI (X) and NsiI (N). Lower panel: DSB and resection products at the CCT6 hotspot formed after meiotic synchronization in red1 (H7088), rec8Δ (H7161), and red1 rec8Δ (H6589) mutants and their control (H7076) in a dmc1Δ rad51Δ background. Arrows 1 and 2 were used as anchors to measure signal accumulation in (E). (D) DSB levels as a percent of dmc1Δ rad51Δ at the CCT6 hotspot, n = 2 for dmc1Δ rad51Δ and dmc1Δ rad51Δ red1. Error bars: range. (E) Linescans of DSB band from gel in (C). Arrow indicates accumulation of faster migrating bands over time in dmc1Δ rad51Δ. (F) Rate of accumulation of signal at Res4 as a percent of lane total. Values have been normalized against signal of all bands in the lane and followed by subtraction of the value at 0h.

Importantly, Spo11-oligo analysis indicated that total DSB levels in the red1 mutant are at least as high as in rec8Δ mutants, which have a nearly intact checkpoint response (Fig 4D). Moreover, DSB formation was not further reduced in a red1 rec8Δ double mutant (Fig 5A). Accordingly, DSB levels of the double mutant remained considerably higher than in red1Δ mutants, as indicated by pulse-field gel analysis of chromosome VIII (S6C and S6D Fig).

It is possible that dmc1Δ rad51Δ red1 mutants fail to efficiently activate the checkpoint arrest because of a failure to produce sufficient ssDNA. ssDNA coated with the ssDNA-binding protein RPA is the major signal that activates the checkpoint kinase ATR/Mec1 [67]. To investigate the amount of ssDNA formed by hyper-resection in checkpoint-activated dmc1Δ rad51Δ mutants, we used Southern blotting to analyze the CCT6 hotspot, which exhibits approximately 70% of wild-type DSB levels in all three mutants (Fig 5C and 5D). Resection can be seen at this hotspot as a smearing of the DSB band that progressively shifts to faster migrating species, corresponding to resection less than 5kb from the DSB site (Fig 5C and 5E). Resection is also detectable as fragments that are larger than the parental band (Fig 5C, Res1-4). These larger fragments are caused by the inability of a restriction enzyme to digest ssDNA once resection tracts have passed the respective restriction sites [40].

At 3h after induction of meiosis, all three mutants exhibited more extensive smearing of the DSB band compared to dmc1Δ rad51Δ control (Fig 5E), indicating more extensive resection. Moreover, the signal of the DSB band diminished in the mutants at later time points, as slower migrating fragments became apparent. Resection product Res4 (Fig 5C), which is produced when resection results in an ssDNA tract of at least 8kb, became detectable in red1 dmc1Δ rad51Δ and rec8Δ dmc1Δ rad51Δ mutants 5h after induction of meiosis and increased in intensity over time (Fig 5F), suggesting that resection tracts persist in the red1 dmc1Δ rad51Δ mutants even though a large portion of these cells have progressed out of meiotic prophase (Fig 4D). The Res4 signal in the red1 rec8Δ dmc1Δ rad51Δ mutant appeared earlier and at a higher levels than either of the single mutants (Fig 5F), suggesting that hyper-resection is faster and more sustained. These experiments are consistent with previous analyses showing that loss or RED1 or REC8 function leads to more extensive resection [40,41], and argue that insufficient resection is not the cause of the observed bypass of the checkpoint arrest by red1.

Extended checkpoint arrest requires higher Red1 levels than faithful chromosome assortment

The phenotypes described above suggest that different meiotic processes are differentially affected by changes in Red1 dosage. Specifically, the Red1 levels associated with the red1 mutant strain support sufficient DSB formation and homolog-directed crossover repair to yield nearly 70% viable spores (Fig 2B), yet are unable to trigger any detectable prophase delay in response to unrepaired DSBs (Fig 4D). To test this differential sensitivity in a more systematic manner, we took advantage of the cis-encoded reduction of Red1 protein levels of the red1 strain to create a Red1 dosage series (Fig 6A). Quantitative western analysis indicated that red1/RED1 and red1Δ/RED1 mutants have approximately 50% Red1 protein compared to wild type (Fig 6B), an estimate supported by direct comparison with a titration series of wild-type protein extracts (Fig 6A). The homozygous mutant red1/red1 strain and the red1Δ/ red1 strain have approximately 25% and 15% of wild type Red1 protein, respectively. Consistent with the data shown in Fig 1A, increased Red1 protein levels correlated well with an increased proportion of the slower migrating phosphorylated form of Red1 (R2 = 0.762, Fig 6C), suggesting that Red1 phosphorylation is stimulated by Red1 abundance.

Fig 6

Checkpoint arrest and spore viability require different amounts of Red1 protein.

(A) Semiquantitative western blot of a Red1 dosage series. Red1 levels of 2h samples from red1/RED1 (ycs4S/+, H8218), red1Δ/RED1 (H8220, Δ/+), red1/red1 (ycs4S/ycs4S, H7011), and red1 /red1Δ (ycs4S/Δ, H8219) were compared to a 2-fold serial dilution of a whole-cell extract from wild type (+/+, H7797) from the same time course. Fpr3 was used as loading control. (B) Quantitative measurement of total Red1 protein levels in the dosage series relative to Nsp1 at 2h and 3h, n = 3 per time point. Error bars: S.E.M. *: p-value < 0.05, **: < 0.005, paired Student t-test. (C) Ratio of upper (modified) band to lower (unmodified) band correlates with Red1 protein levels. Red1 levels were normalized against Nsp1. Quantifications come from the gels used in the creation of Fig 1B and Fig 6B. Linear regression of the data is shown along with adjusted R2. Examples of two points are shown in the inset. (D) Spindle pole separation of dmc1Δ rad51Δ (closed circle, H7076), dmc1Δ rad51Δ red1/RED1 (open square, H8467), dmc1Δ rad51Δ red1Δ/RED1 (open upward-facing triangle, H8494), dmc1Δ rad51Δ red1/red1 (closed squared, H7088), dmc1Δ rad51Δ red1/red1Δ (open downward-facing triangle, H8504), and dmc1Δ rad51Δ red1Δ/red1Δ (closed upward-facing triangle, H6023), n = 200. (E) Spore viability of the Red1 dosage series and red1Δ/red1Δ (H8098), n>100. *: p-value < 0.05, **: < 0.005, ***: < e-5 Student t-test. Samples range in color from dark purple to pale orange as they transition from highest Red1 levels to lowest.

Analysis of this dosage series revealed that strains expressing at least 50% of wild type Red1 protein trigger a meiotic delay in a dmc1Δ rad51Δ background (Fig 6D). By contrast, no delay is observed in strains with equal or less than 25% Red1 protein. We note that a phosphorylation-deficient red1 mutant fully maintains a dmc1Δ arrest [54], indicating that the observed loss of arrest activity is not caused by the dosage-dependent loss of Red1 phosphorylation. Importantly, despite the loss of checkpoint-dependent arrest activity, spore viability of red1/red1 mutants remains around 70%, with only mild meiosis I non-disjunction (Fig 6E, S7A–S7C Fig), suggesting that the ability of the meiotic checkpoint network to promote homolog-directed crossover formation remains at least partially active at around 25% Red1 levels. This interpretation is consistent with analysis of the HIS4LEU2 locus, revealing a partial block to sister repair and only a limited reduction in crossover levels in this mutant [62]. Indeed, even 15% Red1 levels of wild type support substantial spore viability, unlike red1Δ or hop1Δ null mutants, which do not form viable spores [33,34] (Fig 6E), or homolog bias-defective hop1-scd mutants, which form less than 7% viable spores [45]. These data indicate that mounting a meiotic prophase delay requires substantially higher doses of Red1 than promoting largely faithful meiotic chromosome segregation.

In an attempt to investigate DSB formation and resection cytologically in this dosage series, we analyzed chromosome spreads of dmc1Δ rad51Δ mutants using an antibody against the RPA subunit Rfa2. Spread nuclei of all strains analyzed exhibited foci and short tracks of Rfa2 indicative of resected DSBs. However, cells expressing lower levels of Red1 had a higher probability of accumulating large clumps of Rfa2 in low-DAPI regions of the nucleus (S7D Fig). These Rfa2 aggregates do not co-localize with Zip1 aggregates and are also formed at high frequency in resection-defective rad50S mutants (S7E Fig), indicating that they are not representative of ssDNA exposed at Spo11-dependent DSB ends. RPA aggregates have been reported in other meiotic DSB repair mutants, including rad52Δ [68], but their significance remains unclear. We note, however, that their appearance correlated well with loss of spore viability in the RED1 dosage series.

Chromosome synapsis does not require abundant Red1 on lateral elements

Red1 is also an important regulator of chromosome synapsis, as red1Δ mutants form little to no SC, although occasional cells with more elaborate SC structures can be observed [24]. Therefore, we investigated the formation of lateral and central elements of the SC in the Red1 dosage series by immunofluorescence analysis. Red1 binding patterns on chromosomes reflect the reduced Red1 levels, with only the wild-type and red1/RED1 strains exhibiting at least partial Red1 tracks on chromosome spreads (Fig 7A). By contrast, Zip1 deposition along meiotic chromosomes is only mildly affected by decreased RED1 dosage. Linear Zip1 tracks formed even in red1/red1 cells at levels similar to wild type (Fig 7B). Spreads with Zip1 tracks in these mutants had almost no cytologically detectable Red1 (Fig 7C and 7D), indicating that the majority of Red1 along lateral elements is dispensable for Zip1 deposition. Moreover, Zip1 tracks co-localize with SUMO in all strains (Fig 7E), suggesting the formation of mature central elements of the SC [69]. We did note an increase in late leptotene/early zygotene nuclei, characterized by the co-existence of abundant Zip1 puncta (leptotene configuration) and short Zip1 stretches (zygotene configuration), in red1/red1 mutants (Fig 7B). This class is rarely observed at higher Red1 dosage, and suggests that Zip1 deposition along chromosomes may be delayed at low Red1 levels. Consistent with this notion, we also observed an increasing incidence of Zip1 aggregates (polycomplexes; Fig 7F) as Red1 levels were reduced, although we note that polycomplex formation did not strictly correlate with Red1 levels, possibly because of the Ycs4-12xMYC tag in the red1 background. These data suggest that abundant binding of Red1 to lateral elements is not required for the formation of cytologically normal SCs.

Fig 7

Chromosome synapsis occurs with minimal Red1 protein.

(A) Quantification of Red1 binding on spread chromosomes 4h after meiotic initiation from wild-type (+/+, H7797), red1/RED1 (ycs4S/+, H8218), red1Δ/RED1 (H8220, Δ/+), and red1/red1 (ycs4S/ycs4S, H7011) strains, n = 100. Only nuclei with detectable Zip1 staining were included. Red1 binding was classified into: “No Red1”, “Only Red1 foci”, and “Partial Red1 tracks”. Scale bars on spreads are 5μm. (B) Zip1 binding on chromosome spreads of wild-type, red1/RED1, red1Δ/RED1, and red1/red1 strains, n = 100. Zip1 pattern was classified into: “Puncta”, “Puncta + short stretches”, “Short stretches”, and “Tracks”. (C) Example images of Red1 binding patterns on spreads with Zip1 tracks from (B). Zip1 is colored red, while Red1 is colored green. Scale bars on spreads are 5μm. (D) Red1 intensity levels on chromosome spreads with Zip1 tracks, measured as described for Fig 3C, n>15. Error bars: S.D. *: p-value < 0.05, **: p-value < 0.005 Wilcox test. Samples range in color from dark purple to orange as they transition from highest Red1 level to lowest. (E) Representative images of SUMO binding patterns on spreads with Zip1 tracks from (B). Zip1 is colored green, DAPI is colored blue, and SUMO is colored red. Scale bars are 1μm. (F) Frequency of Zip1 polycomplex formation in the spreads from (B). Scale bars on spreads are 5μm.

Discussion

Here, we demonstrate that most of the phenotypes previously ascribed to the ycs4S allele are explained by a linked partial loss-of-function mutation in RED1. We took advantage of this allele to investigate the dependencies of meiotic prophase events on Red1 dosage. These experiments revealed substantial differences in the robustness of meiotic processes to reduced Red1 levels and indicate that at least some of the meiotic roles of Red1 are genetically separable.

The genetic basis of ycs4S phenotypes

Our analyses show that the majority of ycs4S phenotypes can be explained by a linked point mutation in the RED1 promoter that reduces RED1 expression to ~25% of wild type. Deletion of RED1 causes spore lethality because of numerous meiotic defects, including reduced DSB levels, hyper-resection, failure to block repair from the sister chromatid, defective chromosome synapsis, and an inability to arrest cells in response to persistent DSBs [33,38,40,41]. The ycs4S mutant recapitulates all of these phenotypes, albeit to varying extents (this study and [51,62]). Consistent with the RED1 promoter mutation being the cause of most ycs4S phenotypes, a strain carrying this point mutation without the 12xMYC tag on YCS4 phenocopies the spore viability and arrest defects of the ycs4S mutant, while boosting RED1 expression levels in ycs4S meiotic cells using a heterologous HOP1 promoter essentially rescues the meiotic defects exhibited by ycs4S mutants.

The YCS4-12xMYC construct itself likely causes only minor meiotic effects. We observed a slightly higher rate of polycomplex formation in the red1/RED1 mutant compared to the red1Δ/RED1 mutant, even though the red1/RED1 mutant appeared to have more Red1 protein on its chromosomes. This elevation in polycomplex formation may be attributable to the YCS4-12xMYC construct. In addition, Red1 protein expression is slightly reduced in the red1 background even when RED1 is placed under control of the HOP1 promoter. Tagging YCS4 de novo with a C-terminal MYC tag does not affect spore viability (Fig 2B), suggesting that this effect may be caused by one of the additional SNPs in close linkage with the red1 promoter mutation.

Separation of Red1 roles in meiotic prophase

Our analyses indicate that reduced RED1 levels impact some meiotic processes more severely than others. The ability to mount an arrest response to unrepaired breaks is abolished at a Red1 dosage of approximately 25% of wild-type levels. By contrast, DSB formation and SC assembly are only mildly affected, and sufficient inter-homolog crossovers form to support ~70% spore viability. The mild effect on axis-associated processes, such as DSB formation and SC assembly, indicates that the structural chromosome axis remains largely intact at these levels of Red1. This interpretation is consistent with the observation that red1 mutants exhibit wild-type levels of chromosomal compaction [51], and that establishment of the crossover interference pattern, which requires SUMOylated Red1, is unaffected in red1 mutants [70].

The roles of Red1 in chromosome axis formation and checkpoint maintenance

The differential sensitivity of meiotic processes to altered Red1 levels may reflect differences in how long the presence of Red1 is needed to execute a given process. In particular, mounting a checkpoint delay or arrest that lasts for several hours is expected to require substantially longer residence time of Red1 on chromosomes than the formation of DSBs, which would require Red1 only until a DSB has formed. It is more difficult to explain the ability of cells with reduced Red1 levels to form synapsis-competent chromosome axes in this model, as stable axes are likely needed to support chromosome synapsis. It is possible, however, that Red1 is primarily involved in the formation chromosome axes and less in their structural maintenance. This model is consistent with the formation of axial structures in the absence of Red1 [33] and may explain the coexistence of leptotene and zygotene configurations in the same nucleus when Red1 levels are reduced (Fig 7B).

It is also possible that the differential sensitivity to altered Red1 levels reflects functionally distinct populations of Red1 on meiotic chromosomes that act in the assembly of DSB- and synapsis-competent chromosome axes and in checkpoint arrest maintenance, respectively. Indeed, Red1 not only interacts with multiple chromosomal proteins, including Rec8 and Hop1, but also multimerizes and is modified by both phosphorylation and SUMOylation, which could create functionally distinct forms of Red1 [32,37,42,54].

Finally, it is also possible that checkpoint signaling requires increased amounts of Red1 because of the need for signal amplification. This model is appealing because meiotic DSB resection tracts are kept relatively short by meiotic axis proteins [40,41], such that even resection tracts of irreparable breaks are maintained at lengths of about 1kb for several hours. By contrast, irreparable breaks in mitotic yeast cells are continuously resected, which is necessary for maintaining checkpoint activity of the CHK2-like kinase Rad53 [71,72]. In meiotic cells, Rad53 is largely inactive, as Spo11-dependent DSBs do not lead to Rad53 phosphorylation [73]. Instead, checkpoint maintenance is linked to the continued activity of CHK2-like kinase Mek1, which requires Red1 and Hop1 for activation [45,46,53,74]. Thus, the abundant binding of Red1 along chromosomes may amplify the binding and recruitment sites for Hop1 and Mek1 activation to support a sustained checkpoint signal without the associated risks of extensive resection. We note that Red1 is likely the limiting factor in this context because deletion of one copy of HOP1 in a red1/RED1 strain background has no effect on spore viability (S7F Fig).

The notion that axial element-associated Red1 provides a means for signal amplification may also explain why rec8Δ mutants are able to mount a strong checkpoint arrest despite having little Red1 bound along chromosomes and showing no axial elements by electron microscopy [23]. Although DSB formation in rec8Δ mutants is largely restricted to genomic regions that are able to recruit Red1 independently of Rec8-cohesin [32], these mutants display large clumps of Red1 and Hop1 on chromosomes (Figs 3E, S3D). These clumps may support the checkpoint-dependent prophase arrest of these mutants despite the absence of detectable axial elements. Consistent with this interpretation, rec8Δ red1 mutants do not form Hop1 clumps on chromosomes and fail to arrest.

Methods

Yeast strains and growth conditions

All strains had an SK1 background unless indicated otherwise. A complete list is located in S1 Table. The original ycs4S strain was a gift from D. Koshland [51], SPO11-6HIS-3FLAG-loxP-KanMX-loxP was provided by K. Ohta [48], and YPH499 was a gift from A. Strunnikov [75]. Gene disruption and tagging were carried out using a PCR-based protocol [76]. For pHOP1-RED1 and pHOP1-RED1, the HOP1 promoter (-200 to -2) as defined by Vershon et al. [77] was placed in pFA6a-kanMX6-pCLB2, replacing pCLB2. It was inserted into the indicated genomes using Longtine F4 and RHop1 [AAT TCC TGA CCT TTC TGA AA] primers as described [76] replacing the 25bp immediately upstream of the RED1 start codon with the HOP1 promoter construct. To transfer the red1-pG162A mutation from the ycs4S background into a clean SK1 background, an HphMX4 cassette [78] was inserted at -400 relative to the RED1 start site. The entire promoter region (-600 to +90) was transferred into a wild-type SK1 background by PCR amplification and selection on hygromycin. Transfer of the mutation was confirmed by sequencing. An HphMX4 insertion without associated promoter mutation was constructed in SK1 to serve as a wild-type control. Synchronous meiosis was induced as previously described [32].

Western blotting

Whole cell extraction by trichloroacetic acid precipitation, SDS-polyacrylamide gel electrophoresis and western blotting were completed as described [79]. Hop1 and Red1 (Lot#16441) were detected using rabbit serum at 1:10,000 (kind gifts of N. Hollingsworth). Hop1 phosphorylation was detected using affinity-purified pT318-Hop1 antibody at 1:100 as described [80]. Phosphorylation of histone H3 threonine 11 (H3T11) was detected with MC83 rabbit antibody (Millipore) at 1:2000. Nsp1 was detected using 32D6 mouse antibody (ThermoFisher Scientific) at 1:2500. Pgk1 was detected using 22C5D8 mouse antibody (ThermoFisher Scientific) at 1:500. Fpr3 was detected with anti-rabbit serum (kind gift from J. Thorner) at 1:5000. For all westerns, the secondary antibody was either anti-mouse HRP or anti-rabbit HRP used at 1:5000 (GE Healthcare).

For quantitative westerns, Nsp1 was detected using 32D6 at 1:25,000 and Red1 was detected using an anti-Red1 antibody (Lot#16440; kind gift of N. Hollingsworth) at 1:4000. The secondary antibodies anti-rabbit IRDye800CW and anti-mouse IRDye680RD (Li-Cor Biosciences) were used at 1:10,000. Membranes were scanned on a Li-Cor Odyssey imager under non-saturating conditions. Data were quantified using pixel intensities with the Odyssey software according to the protocols of the manufacturer (Li-Cor Biosciences).

Chromosome spreads

Meiotic nuclear spreads were performed as described [80]. Hop1 was detected using anti-Hop1 rabbit serum at 1:200 in blocking buffer and Alexa Fluor anti-rabbit (Jackson ImmunoResearch) at 1:200. Zip1 was detected using Zip1 yC-19 goat antibody (Santa Cruz Biotechnology) at 1:200 and anti-goat Cy3 at 1:200 (Jackson ImmunoResearch). Red1 was detected using anti-Red1 rabbit serum (Lot#16441) at 1:100 and Alexa Fluor anti-rabbit at 1:100. Rfa2 was detected using anti-Rfa2 rabbit serum (kindly provided by S. Brill) at 1:1000 and Alexa Fluor anti-rabbit at 1:200. Images were obtained as described [80] and analyzed using softWoRx 5.0 software. Scatterplots were created using Prism 6. For Fig 7E, affinity purified rabbit anti-Zip1 (raised at YenZym Antibodies, LLC, against a C terminal fragment of Zip1 as described [81]) was used at 1:100. Affinity purified guinea pig anti-SUMO was used at 1:200 (gift from G.S. Roeder [82]). Secondary antibodies Alexa Fluor 488 and Alexa Fluor 594 were used at 1:200 (Jackson ImmunoResearch). Microscopy and image processing were carried out using a Deltavision RT or a Deltavision Elite imaging system (Applied Precision) adapted to an Olympus IX17 microscope.

Chromatin immunoprecipitation and Illumina sequencing

All cultures were collected at the 3-hr time point. Chromatin immunoprecipitation was performed as described [83]. Samples were immunoprecipitated with 2 μL of either anti-Red1 (Lot#16440) or anti-Hop1 serum per IP. For qPCR, input samples were diluted 50X more than ChIP samples. qPCR was completed as described previously [84]. Library preparation was completed as described [32]. Library quality was confirmed by Qubit HS assay kit and Agilent 2100 Bioanalyzer or 2200 TapeStation. 51-bp single-end sequencing was accomplished on an Illumina HiSeq 2500 instrument.

Processing Illumina data

Sequencing reads were mapped to SacCer3 (S288C) using Bowtie [85]. The one condition adjusted was to only collect information about reads that mapped to a single position in the genome. Reads were also mapped to the SK1 genome (only allowing perfect matches) with similar results. Reads were extended towards 3’ ends to a final length of 150 bp using MACS-2.1.0 (https://github.com/taoliu/MACS) [86]. Normalization of read tag density was completed as described [32]. Plots shown are an average of two replicates. Datasets are available at GEO, accession number GSE87060.

DSB and resection experiments

Genomic DNA for DSB hotspot analysis was purified as described [79]. For the CCT6 hotspot, samples were digested with NsiI and XhoI, and run on a 0.6% agarose gel for ~18 hr. The probe was created as described [8]. Pulse-field gel electrophoresis and Southern blotting were performed as described [3]. Hybridization signal was detected using a Typhoon FLA 9000. DSB levels on PFGE were estimated assuming a Poisson distribution as described [66]. Specifically, DSB levels were calculated as -ln(uncuttimepoint/uncut0h).

End-labeling of Spo11-oligonucleotide complexes

End-labeling of Spo11-oligonucleotide complexes was completed as described [65] with a few changes. In brief, 100mL SPO cultures were lysed with glass beads in 10% trichloroacetic acid. Lysed cells were centrifuged, and then resuspended in 1.5mL of 2% SDS, 0.5M Tris-HCl pH 8.0, 10mM EDTA, and 2% β-mercaptoethanol. After boiling the samples, soluble protein was diluted 2X in 2% Triton X100, 30mM Tris-HCl pH 8.0, 300mM NaCl, 2mM EDTA, and 0.02% SDS. Immunoprecipitation of the Spo11-oligo complexes was completed using 2.5μg of monoclonal mouse anti-Flag M2 antibody (Sigma). Precipitated complexes were end-labeled with 5μCi of [α-32P]dCTP and 5 units of terminal deoxynucleotidyl transferase (Enzymatics). End-labeled complexes were run on a Bolt 4–10% bis tris plus acrylamide gel (ThermoFisher Scientific), blotted onto a PVDF membrane using an iBlot2 gel transfer device (ThermoFisher Scientific), and visualized using a Typhoon FLA 9000 (GE Healthcare). Blots were also probed with mouse monoclonal anti-FLAG M2-HRP (Sigma).

Other techniques

Spindle formation was followed by anti-tubulin immunofluorescence as described previously [87]. For each time point, 200 cells were classified based on whether or not they had undergone spindle pole separation, indicative of exit from meiotic prophase. Spore viability was determined by dissection of tetrads into individual spores unless otherwise stated. RNA was extracted as described [88]. Reverse transcription and qPCR was performed as previously described, but using RiboLock RNase inhibitor (Thermo Scientific) to prevent RNA degradation [84]. Primers used in this study are listed in S2 Table.

(A) Fluorescence-based quantitative measurement of total Red1 protein levels in the red1-pG162A mutant strain (H9048) and its matched control (H9049) relative to Nsp1 at 2h, n = 3. Error bars: S.E.M. (B) Spore viability of hybrid diploid strains composed of YPH499 (H2389) and either SK1 red1-pG162A (H8919) or its matched SK1 wild-type control carrying only a marker insertion at position +400 upstream of the RED1 ORF (H8901), n>60. Error bars: S.D. *: p-value: < 0.05, Student t-test.

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(A) Hop1 chromosomal localization determined by ChIP-seq at 3h in wild-type (black, H119 & H6408), red1 (cyan, H7011), rec8Δ (pink, H7660 & H7772), and red1 rec8Δ (orange, H7661) strains on chromosomes III and VIII, n = 2. Large black circles indicate the positions of the centromeres. (B) Red1 and Hop1 distribution in the red1 rec8Δ mutant compared to a mock (IgG only) control. Triangles indicate positions analyzed by ChIP-qPCR in S3B Fig. (C) Scatter plots of genome-wide ChIP-seq data (5kb averages) directly comparing two experiments from red1 rec8Δ mutants. Left panel: biological replicates of Hop1 binding; middle panel: average Red1 and Hop1 binding as seen in (B); right panel: Hop1 binding and the mock control.

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(A) Red1 enrichment over input at 3h determined by ChIP-seq in wild-type (black, H119), red1 (H7011), rec8Δ (H7660 & H7772), and red1 rec8Δ (H7661) strains at six positions across the genome, n = 2. Peaks were defined as regions of Red1 and Hop1 binding in all four strains as identified by ChIP-seq. (B) qPCR analysis of Red1 binding at five peaks and one negative control shown in (A) in wild type (grey, H7797) and red1 (cyan, H7011), rec8Δ (pink, H5187), and red1 rec8Δ (orange, H7661) mutants, n = 3 biological replicates. Error bars: S.E.M. Peak 2, peak 5, and the negative control are marked in Fig 3D and S2B Fig using identifying triangles.

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(A) Western analysis of Red1 and Hop1 protein levels of whole-cell extracts from wild type (H7797) and red1 (H7011), rec8Δ (H5187), and red1 rec8Δ (H7661) mutants induced to undergo synchronous meiosis. Phosphorylated Hop1 indicated by bracket. Pgk1 was used as loading control. (B) Fluorescence-based quantitative measurements of Red1 protein levels in rec8Δ and red1 rec8Δ at 2h, n = 3. Total Red1 levels relative to loading control Nsp1. Error bars: S.E.M. (C) Representative images of the predominant cytological patterns of Red1 observed in rec8Δ and red1 rec8Δ strains. Arrow indicates a Red1 clump. Scale bars are 5μm.

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(A) Red1 protein levels of whole-cell extracts from dmc1Δ rad51Δ (H7076) and dmc1Δ rad51Δ ycs4S (H7088) as determined by western blotting at the indicated time points after meiotic induction. Fpr3 was used as loading control. (B) Fluorescence-based quantitative measurement of Red1 protein levels in dmc1Δ rad51Δ and dmc1Δ rad51Δ ycs4S relative to Nsp1 at 2h, 3h, and 4h, n = 3. Error bars: S.E.M. *: p-value < 0.05 paired Student t-test. (C) Spindle formation of dmc1Δ red1-pG162A (H9081, cyan open triangle) and its matched control (H9079, black open circle) strains to measure checkpoint activity, n = 200.

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(A) DSB levels and patterns of chromosome XVI from gel in Fig 5B. Arrowhead indicates full-length chromosomes. (B) Quantifications of DSB levels on chromosome XVI, n = 2. Error bars: range. (C) Southern of pulse-field gel showing DSB patterns of chromosome VIII in red1Δ, hop1Δ, rec8Δ, and red1 rec8Δ mutants relative to their controls in a dmc1Δ rad51Δ background. Arrowhead indicates full-length chromosomes. Strains (L-R) are H5594, H5995, H6023, H7076, H7161, and H6589. (D) DSB levels of gel in (C), calculated from the level of remaining full-length chromosomes (see Methods).

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(A) Sporulation efficiency of wild-type (H7797, +/+), red1/RED1 (ycs4S/+, H8218), red1Δ/RED1 (H8220, Δ/+), red1/red1 (ycs4S/ycs4S, H7011), red1 /red1Δ (ycs4S/Δ, H8219), and red1Δ/red1Δ (Δ/Δ, H8098) strains, n = 200. (B) Percentage of tetrads from the strains in (A) that yielded 4, 3, 2, 1, or 0 viable colonies, n>100 tetrads per strain. (C) Viability of random spores from wild-type and red1 strains. Equal numbers of spores from tetrads, dyads, and monads were assessed for viability, n = 80 spores per strain. (D) Quantification of Rfa2 clumps on spreads 4h after meiotic initiation in Red1 dosage series in dmc1Δ rad51Δ background, n = 100 (RED1/RED1: H7076, red1/RED1: H8467, red1Δ/RED1: H8494, red1/red1: H7088, red1/ red1Δ: H8504, and red1Δ/red1Δ: H6023). Only nuclei with detectable Zip1 staining were included. Arrow on example spread indicates: low-DAPI region, lack of Zip1 staining, and Rfa2 clump. Arrowhead points at Zip1 polycomplex. (E) Quantification of Rfa2 clumps on spread chromosomes from rad50S (H8099), and rad50S red1/red1 (H8096) strains, n = 200. (F) Spore viability in red1/RED1 and red1/RED1 hop1Δ/HOP1 mutants (H8866), n>100.

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Strain list.

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qPCR primer list.

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Data in figures.

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Data in supplemental figures.

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