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The histone modification reader ZCWPW1 is required for meiosis prophase I in male but not in female mice

机译:雄性小鼠减数分裂I期需要组蛋白修饰阅读器ZCWPW1

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摘要

Meiosis is a specialized type of cell division that creates haploid germ cells and ensures their genetic diversity through homologous recombination. We show that the H3K4me3 reader ZCWPW1 is specifically required for meiosis prophase I progression in male but not in female germ cells in mice. Loss of Zcwpw1 in male mice caused a complete failure of synapsis, resulting in meiotic arrest at the zygotene to pachytene stage, accompanied by incomplete DNA double-strand break repair and lack of crossover formation, leading to male infertility. In oocytes, deletion of Zcwpw1 only somewhat slowed down meiosis prophase I progression; Zcwpw1−/− oocytes were able to complete meiosis, and Zcwpw1−/− female mice had normal fertility until mid-adulthood. We conclude that the H3K4me3 reader ZCWPW1 is indispensable for meiosis synapsis in males but is dispensable for females. Our results suggest that ZCWPW1 may represent a previously unknown, sex-dependent epigenetic regulator of germ cell meiosis in mammals.
机译:减数分裂是细胞分裂的一种特殊类型,其产生单倍体生殖细胞并通过同源重组确保其遗传多样性。我们显示H3K4me3阅读器ZCWPW1是雄性减数分裂前期I进程特别需要的,而小鼠的雌性生殖细胞则不需要。雄性小鼠中Zcwpw1的缺失导致突触的完全失败,导致减数分裂停滞在合子期至粗线期,伴有不完全的DNA双链断裂修复和缺乏交叉形成,从而导致雄性不育。在卵母细胞中,Zcwpw1的缺失仅在一定程度上减缓了减数分裂I阶段的进展。 Zcwpw1 -/-卵母细胞能够完成减数分裂,而Zcwpw1 -/-雌性小鼠的生育能力正常,直到成年中期。我们得出结论,H3K4me3阅读器ZCWPW1对于男性减数分裂突触是必不可少的,但对于女性则是必不可少的。我们的结果表明,ZCWPW1可能代表了哺乳动物生殖细胞减数分裂的未知,性别依赖性的表观遗传调控因子。

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