Department of Genetics & Genome Biology, University of Leicester, Leicester, United Kingdom.
Department of Forensic Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
PLoS Genet. 2018 Oct 8;14(10):e1007680. doi: 10.1371/journal.pgen.1007680. eCollection 2018 Oct.
The human X and Y chromosomes are heteromorphic but share a region of homology at the tips of their short arms, pseudoautosomal region 1 (PAR1), that supports obligate crossover in male meiosis. Although the boundary between pseudoautosomal and sex-specific DNA has traditionally been regarded as conserved among primates, it was recently discovered that the boundary position varies among human males, due to a translocation of ~110 kb from the X to the Y chromosome that creates an extended PAR1 (ePAR). This event has occurred at least twice in human evolution. So far, only limited evidence has been presented to suggest this extension is recombinationally active. Here, we sought direct proof by examining thousands of gametes from each of two ePAR-carrying men, for two subregions chosen on the basis of previously published male X-chromosomal meiotic double-strand break (DSB) maps. Crossover activity comparable to that seen at autosomal hotspots was observed between the X and the ePAR borne on the Y chromosome both at a distal and a proximal site within the 110-kb extension. Other hallmarks of classic recombination hotspots included evidence of transmission distortion and GC-biased gene conversion. We observed good correspondence between the male DSB clusters and historical recombination activity of this region in the X chromosomes of females, as ascertained from linkage disequilibrium analysis; this suggests that this region is similarly primed for crossover in both male and female germlines, although sex-specific differences may also exist. Extensive resequencing and inference of ePAR haplotypes, placed in the framework of the Y phylogeny as ascertained by both Y microsatellites and single nucleotide polymorphisms, allowed us to estimate a minimum rate of crossover over the entire ePAR region of 6-fold greater than genome average, comparable with pedigree estimates of PAR1 activity generally. We conclude ePAR very likely contributes to the critical crossover function of PAR1.
人类的 X 和 Y 染色体是异型的,但在它们短臂的末端共享一个同源区域,即假常染色体区 1(PAR1),该区域支持雄性减数分裂中的强制性交叉。尽管假常染色体和性别特异性 DNA 之间的边界传统上被认为在灵长类动物中是保守的,但最近发现由于 X 染色体到 Y 染色体的约 110kb 易位导致了扩展的 PAR1(ePAR),导致人类男性之间的边界位置发生了变化。这种事件在人类进化中至少发生了两次。到目前为止,只有有限的证据表明这种延伸是重组活跃的。在这里,我们通过检查来自两个携带 ePAR 的男性的数千个配子,为两个选择的亚区进行了直接证明,这些亚区是基于先前发表的雄性 X 染色体减数分裂双链断裂(DSB)图谱选择的。在 110kb 延伸的远端和近端位置,在 X 染色体和 Y 染色体上携带的 ePAR 之间观察到与常染色体热点相似的交叉活性。经典重组热点的其他标志包括证据表明存在传输扭曲和 GC 偏向性基因转换。我们观察到男性 DSB 簇与女性 X 染色体上该区域的历史重组活性之间的良好对应关系,这是通过连锁不平衡分析确定的;这表明该区域在雄性和雌性生殖细胞中同样适合交叉,尽管可能存在性别特异性差异。广泛的重新测序和推断 ePAR 单倍型,在 Y 微卫星和单核苷酸多态性确定的 Y 进化框架中确定,使我们能够估计整个 ePAR 区域的交叉率至少比基因组平均值高 6 倍,与一般 PAR1 活性的系谱估计相当。我们得出结论,ePAR 很可能有助于 PAR1 的关键交叉功能。