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TDRD9 中的一种新的复合杂合突变导致少精子症。

A Novel Compound Heterozygous Mutation in TDRD9 Causes Oligozoospermia.

机构信息

Center of Reproductive Medicine, Affiliated Jinling Hospital, Nanjing Medical University, Nanjing, 210002, Jiangsu, China.

Center of Reproductive Medicine, Clinical School of Medical College, Nanjing Jinling Hospital, Nanjing University, Nanjing, 210002, Jiangsu, China.

出版信息

Reprod Sci. 2024 Nov;31(11):3413-3419. doi: 10.1007/s43032-024-01665-x. Epub 2024 Aug 22.

Abstract

Oligozoospermia is an important cause of male infertility for which treatment options are limited. Spermatogenesis is complex, and the causes of oligozoospermia remain largely unknown. Because genetic mutations are important factors of oligozoospermia pathogenesis, our study aimed to explore the genetic causes of oligozoospermia. Whole- exome sequencing (WES) was performed on one proband from a Chinese family who was diagnosed with oligozoospermia. The pathogenic mutations were confirmed by Sanger sequencing, and a minigene assay was used to determine the effect of the identified splicing mutation. We identified a novel compound heterozygous mutation in the TDRD9 gene, comprising a splicing mutation (c.1115 + 3A > G) and a frameshift mutation (c.958delC), in the proband; neither of these mutations were found in 50 unrelated healthy people. In addition, a minigene assay demonstrated that the frameshift produced partially truncated protein, and the splicing mutation led to a frameshift mutation and premature termination due to abnormal alternative splicing of TDRD9. These findings indicate that deleterious compound heterozygous mutation in TDRD9 could lead to oligozoospermia, highlighting the crucial role of TDRD9 in spermatogenesis and further clarifying the genetic causes of male infertility resulting from oligozoospermia. Our study expands the spectrum of TDRD9-related phenotypes and provides a new specific target for future genetic counseling.

摘要

少精子症是男性不育的一个重要原因,其治疗选择有限。精子发生过程复杂,少精子症的病因仍很大程度上未知。由于遗传突变是少精子症发病机制的重要因素,我们的研究旨在探索少精子症的遗传原因。对一个被诊断为少精子症的中国家庭的先证者进行了全外显子组测序 (WES)。通过 Sanger 测序证实了致病性突变,并进行了小基因检测以确定鉴定的剪接突变的影响。我们在该先证者中发现了 TDRD9 基因的一个新型复合杂合突变,包括一个剪接突变 (c.1115 + 3A > G) 和一个移码突变 (c.958delC);这两种突变在 50 名无关健康人中均未发现。此外,小基因检测表明移码突变产生了部分截断的蛋白,而剪接突变导致 TDRD9 的异常选择性剪接产生移码突变和提前终止。这些发现表明 TDRD9 中的有害复合杂合突变可导致少精子症,强调了 TDRD9 在精子发生中的关键作用,并进一步阐明了少精子症导致的男性不育的遗传原因。我们的研究扩展了 TDRD9 相关表型谱,并为未来的遗传咨询提供了新的特定靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f434/11527903/a10fe0462b6f/43032_2024_1665_Fig2_HTML.jpg

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