Modulation of Prdm9-controlled meiotic chromosome asynapsis overrides hybrid sterility in mice

Hybrid sterility is one of the reproductive isolation mechanisms leading to speciation. Prdm9, the only known vertebrate hybrid-sterility gene, causes failure of meiotic chromosome synapsis and infertility in male hybrids that are the offspring of two mouse subspecies. Within species, Prdm9 determines the sites of programmed DNA double-strand breaks (DSBs) and meiotic recombination hotspots. To investigate the relation between Prdm9-controlled meiotic arrest and asynapsis, we inserted random stretches of consubspecific homology on several autosomal pairs in sterile hybrids, and analyzed their ability to form synaptonemal complexes and to rescue male fertility. Twenty-seven or more megabases of consubspecific (belonging to the same subspecies) homology fully restored synapsis in a given autosomal pair, and we predicted that two or more DSBs within symmetric hotspots per chromosome are necessary for successful meiosis. We hypothesize that impaired recombination between evolutionarily diverged chromosomes could function as one of the mechanisms of hybrid sterility occurring in various sexually reproducing species

Data from: Hybrid sterility locus on Chromosome X controls meiotic recombination rate in mouse

Meiotic recombination safeguards proper segregation of homologous chromosomes into gametes, affects genetic variation within species, and contributes to meiotic chromosome recognition, pairing and synapsis. The Prdm9 gene has a dual role, it controls meiotic recombination by determining the genomic position of crossover hotspots and, in infertile hybrids of house mouse subspecies Mus m. musculus (Mmm) and Mus m. domesticus (Mmd), it further functions as the major hybrid sterility gene. In the latter role Prdm9 interacts with the hybrid sterility X 2 (Hstx2) genomic locus on Chromosome X (Chr X) by a still unknown mechanism. Here we investigated the meiotic recombination rate at the genome-wide level and its possible relation to hybrid sterility. Using immunofluorescence microscopy we quantified the foci of MLH1 DNA mismatch repair protein, the cytological counterparts of reciprocal crossovers, in a panel of inter-subspecific chromosome substitution strains. Two autosomes, Chr 7 and Chr 11, significantly modified the meiotic recombination rate, yet the strongest modifier, designated meiotic recombination 1, Meir1, emerged in the 4.7 Mb Hstx2 genomic locus on Chr X. The male-limited transgressive effect of Meir1 on recombination rate parallels the male-limited transgressive role of Hstx2 in hybrid male sterility. Thus, both genetic factors, the Prdm9 gene and the Hstx2/Meir1 genomic locus, indicate a link between meiotic recombination and hybrid sterility. A strong female-specific modifier of meiotic recombination rate with the effect opposite to Meir1 was localized on Chr X, distally to Meir1. Mapping Meir1 to a narrow candidate interval on Chr X is an important first step towards positional cloning of the respective gene(s) responsible for variation in the global recombination rate between closely related mouse subspecies

Data from: Hybrid sterility locus on Chromosome X controls meiotic recombination rate in mouse

Meiotic recombination safeguards proper segregation of homologous chromosomes into gametes, affects genetic variation within species, and contributes to meiotic chromosome recognition, pairing and synapsis. The Prdm9 gene has a dual role, it controls meiotic recombination by determining the genomic position of crossover hotspots and, in infertile hybrids of house mouse subspecies Mus m. musculus (Mmm) and Mus m. domesticus (Mmd), it further functions as the major hybrid sterility gene. In the latter role Prdm9 interacts with the hybrid sterility X 2 (Hstx2) genomic locus on Chromosome X (Chr X) by a still unknown mechanism. Here we investigated the meiotic recombination rate at the genome-wide level and its possible relation to hybrid sterility. Using immunofluorescence microscopy we quantified the foci of MLH1 DNA mismatch repair protein, the cytological counterparts of reciprocal crossovers, in a panel of inter-subspecific chromosome substitution strains. Two autosomes, Chr 7 and Chr 11, significantly modified the meiotic recombination rate, yet the strongest modifier, designated meiotic recombination 1, Meir1, emerged in the 4.7 Mb Hstx2 genomic locus on Chr X. The male-limited transgressive effect of Meir1 on recombination rate parallels the male-limited transgressive role of Hstx2 in hybrid male sterility. Thus, both genetic factors, the Prdm9 gene and the Hstx2/Meir1 genomic locus, indicate a link between meiotic recombination and hybrid sterility. A strong female-specific modifier of meiotic recombination rate with the effect opposite to Meir1 was localized on Chr X, distally to Meir1. Mapping Meir1 to a narrow candidate interval on Chr X is an important first step towards positional cloning of the respective gene(s) responsible for variation in the global recombination rate between closely related mouse subspecies

Balcova - raw data

The file structure is the same for all of .csv files. Each column represents one individiual mouse of the genotype stated in the header. Each cell of the column represents MLH1 or RAD51/DMC1 (according to the file name) count of analyzed cell of the given mouse. Strain abbreviation: D# is B6.PWD-Chr#; D7F1 is B6.PWD-Chr7 x B6 F1 The data were analyzed in R 3.2.2 and using its packages as is declared in Materials and Methods of the published paper

Fine mapping of meiotic recombination 1, <i>Meir1</i>, on Chr X^PWD using subconsomic strains.

<p>(<b>A</b>) The 4.7 Mb interval of the proximal part of Chr X shared by B6.PWD-Chr X.1s and B6.PWD-Chr X.2, but absent in B6.PWD-Chr X.1 and B6.PWD-Chr X.3, harbors a transgressive modifier of meiotic recombination rate <i>Meir1</i>. The Y axis shows the distance from the centromere in megabases (GRCm38). Chromosome intervals carrying the B6 DNA sequence are depicted in orange, the PWD sequence in blue. (<b>B</b>) The B6.PWD-Chr X.# subconsomics are abbreviated DX.# in column scatters. The significance of differences between strains (excluding PWD) is marked only when p<0.05. See <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1005906#pgen.1005906.g002" target="_blank">Fig 2</a> for legend.</p

Variation in recombination rate of B6 and PWD male mice.

<p>(<b>A</b>) Pachytene spread of a B6 male meiosis shows central elements of synaptonemal complexes of 19 autosomes immunostained for SYCP1 (green), 22 MLH1 foci (red) and foci of centromeric proteins (violet). The number of MLH1 foci per nucleus was used as an equivalent of number of crossovers. The pseudoautosomal region (PAR) of Chr X and Chr Y carries an additional CO mark. (<b>B</b>) Variation of the number of MLH1 foci per pachytene nucleus of PWD and B6 males. The PAR-associated MLH1 foci were not counted. Each dot represents the MLH1 count of one pachytene spermatocyte. Vertical bars designate SD of individual males, horizontal bars represent the mean number of MLH1 foci per analyzed animal. Average MLH1 counts significantly differ between both strains.</p

Meiotic recombination rate in males heterozygous for null mutation or carrying extra copies of <i>Prdm9</i>.

<p>The mean number of MLH1 foci depends on the genetic background of B6 and PWD males but does not reflect differences in the <i>Prdm9</i> copy number. See <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1005906#pgen.1005906.g002" target="_blank">Fig 2</a> for legend.</p

Mean MLH1 counts in female meiosis of Chr X subconsomic strains.

<p>The PWD genomic sequence present in B6.PWD-Chr X.2 carries the strongest female-specific modifier of meiotic recombination rate. For strain abbreviations see <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1005906#pgen.1005906.g004" target="_blank">Fig 4</a>. For detailed analysis of differences between individual subconsomics, see <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1005906#pgen.1005906.s010" target="_blank">S7 Table</a>. See <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1005906#pgen.1005906.g002" target="_blank">Fig 2</a> for legend.</p