Kataruka Shubhangini, Malla Aushaq B, Rainsford Shannon R, Lesch Bluma J
Department of Genetics, Yale School of Medicine, New Haven CT USA 06510.
Department of Obstetrics, Gynecology & Reproductive Sciences, Yale School of Medicine, New Haven CT USA 06510.
bioRxiv. 2024 Oct 17:2024.10.14.618292. doi: 10.1101/2024.10.14.618292.
Regulation of the transcriptome to promote meiosis is important for sperm development and fertility. However, how chromatin remodeling directs the transcriptome during meiosis in male germ cells is largely unknown. Here, we demonstrate that the ISWI family ATP-dependent chromatin remodeling factor SMARCA5 (SNF2H) plays a critical role in regulating meiotic prophase progression during spermatogenesis. Males with germ cell-specific depletion of SMARCA5 are infertile and unable to form sperm. Loss of results in failure of meiotic progression with abnormal spermatocytes beginning at the pachytene stage and an aberrant global increase in chromatin accessibility, especially at genes important for meiotic prophase.
转录组调控以促进减数分裂对精子发育和生育能力很重要。然而,在雄性生殖细胞减数分裂过程中,染色质重塑如何指导转录组在很大程度上尚不清楚。在这里,我们证明ISWI家族ATP依赖的染色质重塑因子SMARCA5(SNF2H)在精子发生过程中调节减数分裂前期进程中起关键作用。生殖细胞特异性缺失SMARCA5的雄性不育且无法形成精子。SMARCA5的缺失导致减数分裂进程失败,从粗线期开始精母细胞异常,染色质可及性全局异常增加,尤其是在减数分裂前期重要的基因处。