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缺乏 18 号染色体粗线期 piRNA 的小鼠精子顶体过度生长和不育。

Sperm acrosome overgrowth and infertility in mice lacking chromosome 18 pachytene piRNA.

机构信息

Laboratory of Cellular and Developmental Biology, NIDDK, National Institutes of Health, Bethesda, MD, United States of America.

出版信息

PLoS Genet. 2021 Apr 8;17(4):e1009485. doi: 10.1371/journal.pgen.1009485. eCollection 2021 Apr.

Abstract

piRNAs are small non-coding RNAs required to maintain genome integrity and preserve RNA homeostasis during male gametogenesis. In murine adult testes, the highest levels of piRNAs are present in the pachytene stage of meiosis, but their mode of action and function remain incompletely understood. We previously reported that BTBD18 binds to 50 pachytene piRNA-producing loci. Here we show that spermatozoa in gene-edited mice lacking a BTBD18 targeted pachytene piRNA cluster on Chr18 have severe sperm head dysmorphology, poor motility, impaired acrosome exocytosis, zona pellucida penetration and are sterile. The mutant phenotype arises from aberrant formation of proacrosomal vesicles, distortion of the trans-Golgi network, and up-regulation of GOLGA2 transcripts and protein associated with acrosome dysgenesis. Collectively, our findings reveal central role of pachytene piRNAs in controlling spermiogenesis and male fertility.

摘要

piRNAs 是在雄性配子发生过程中维持基因组完整性和保持 RNA 动态平衡所必需的小非编码 RNA。在成年小鼠的睾丸中,piRNAs 的水平在减数分裂的粗线期最高,但它们的作用方式和功能仍不完全清楚。我们之前报道过,BTBD18 与 50 个粗线期产生 piRNA 的基因座结合。在这里,我们发现缺乏靶向 Chr18 上粗线期 piRNA 簇的 BTBD18 的基因编辑小鼠的精子具有严重的头部畸形、运动能力差、顶体反应异常、透明带穿透能力受损和不育。突变表型是由于前顶体小泡的异常形成、高尔基体网络的扭曲以及与顶体发育不良相关的 GOLGA2 转录本和蛋白的上调引起的。总之,我们的研究结果揭示了粗线期 piRNAs 在控制精子发生和男性生育能力中的核心作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c8d/8057611/14bf2b2e0d3b/pgen.1009485.g001.jpg

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