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新型双等位基因MCMDC2变异与减数分裂停滞和非梗阻性无精子症相关。

Novel biallelic MCMDC2 variants were associated with meiotic arrest and nonobstructive azoospermia.

作者信息

Bai Hao-Wei, Li Na, Zhang Yu-Xiang, Luo Jia-Qiang, Tian Ru-Hui, Li Peng, Huang Yu-Hua, Bai Fu-Rong, Deng Cun-Zhong, Zhao Fu-Jun, Mo Ren, Chi Ning, Zhou Yu-Chuan, Li Zheng, Yao Chen-Cheng, Zhi Er-Lei

机构信息

Department of Andrology, The Center for Men's Health, Urologic Medical Center, Shanghai Key Laboratory of Reproductive Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200000, China.

Department of Urology, Inner Mongolia People's Hospital, Inner Mongolia Urological Institute, Hohhot 010017, China.

出版信息

Asian J Androl. 2025 Mar 1;27(2):268-275. doi: 10.4103/aja202495. Epub 2025 Jan 10.

Abstract

Nonobstructive azoospermia (NOA), one of the most severe types of male infertility, etiology often remains unclear in most cases. Therefore, this study aimed to detect four biallelic detrimental variants (0.5%) in the minichromosome maintenance domain containing 2 ( MCMDC2 ) genes in 768 NOA patients by whole-exome sequencing (WES). Hematoxylin and eosin (H&E) demonstrated that MCMDC2 deleterious variants caused meiotic arrest in three patients (c.1360G>T, c.1956G>T, and c.685C>T) and hypospermatogenesis in one patient (c.94G>T), as further confirmed through immunofluorescence (IF) staining. The single-cell RNA sequencing data indicated that MCMDC2 was substantially expressed during spermatogenesis. The variants were confirmed as deleterious and responsible for patient infertility through bioinformatics and in vitro experimental analyses. The results revealed four MCMDC2 variants related to NOA, which contributes to the current perception of the function of MCMDC2 in male fertility and presents new perspectives on the genetic etiology of NOA.

摘要

非梗阻性无精子症(NOA)是男性不育最严重的类型之一,在大多数情况下,其病因往往仍不明确。因此,本研究旨在通过全外显子测序(WES)检测768例NOA患者中微小染色体维持结构域包含蛋白2(MCMDC2)基因的4个双等位有害变异(0.5%)。苏木精-伊红(H&E)染色显示,MCMDC2有害变异导致3例患者减数分裂停滞(c.1360G>T、c.1956G>T和c.685C>T),1例患者精子发生减少(c.94G>T),免疫荧光(IF)染色进一步证实了这一点。单细胞RNA测序数据表明,MCMDC2在精子发生过程中大量表达。通过生物信息学和体外实验分析,这些变异被确认为有害变异且与患者不育有关。结果揭示了4个与NOA相关的MCMDC2变异,这有助于目前对MCMDC2在男性生育功能方面的认识,并为NOA的遗传病因提供了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b312/11949460/9c1dff7d75b7/AJA-27-268-g001.jpg

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