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A bi-allelic REC114 loss-of-function variant causes meiotic arrest and nonobstructive azoospermia.

Shuai XuJingpeng ZhaoFeng GaoYuxiang ZhangJiaqiang LuoChenwang ZhangRuhui TianErlei ZhiJianxiong ZhangFurong BaiHongfang SunFujun ZhaoYuhua HuangPeng LiLiren JiangZheng LiChencheng YaoZhi Zhou
Published in: Clinical genetics (2023)
Nonobstructive azoospermia (NOA), the most severe manifestation of male infertility, lacks a comprehensive understanding of its genetic etiology. Here, a bi-allelic loss-of-function variant in REC114 (c.568C > T: p.Gln190*) were identified through whole exome sequencing (WES) in a Chinese NOA patient. Testicular histopathological analysis and meiotic chromosomal spread analysis were conducted to assess the stage of spermatogenesis arrested. Co-immunoprecipitation (Co-IP) and Western blot (WB) were used to investigate the influence of variant in vitro. In addition, our results revealed that the variant resulted in truncated REC114 protein and impaired interaction with MEI4, which was essential for meiotic DNA double-strand break (DSB) formation. As far as we know, this study presents the first report that identifies REC114 as the causative gene for male infertility. Furthermore, our study demonstrated indispensability of the REC114-MEI4 complex in maintaining DSB homoeostasis, and highlighted that the disruption of the complex due to the REC114 variant may underline the mechanism of NOA.
Keyphrases
  • genome wide
  • copy number
  • case report
  • south africa
  • single cell
  • early onset
  • polycystic ovary syndrome
  • cell cycle
  • single molecule
  • atrial fibrillation
  • cell free
  • nucleic acid
  • high throughput sequencing
  • germ cell