Splicing Mutation in DNALI1 Causes Male Infertility with Severe Oligoasthenoteratozoospermia in Humans

被引:1
|
作者
Zhang, Fengbin [1 ]
Li, Jingping [1 ]
Liang, Zhongyan [1 ]
Chen, Xiaopan [2 ]
Zheng, Huimei [3 ]
Wu, Jinggen [1 ]
Chen, Weikang [1 ]
Li, Lejun [1 ]
机构
[1] Zhejiang Univ, Womens Hosp, Reprod Med Ctr, Dept Reprod Endocrinol,Sch Med, Hangzhou 310006, Zhejiang, Peoples R China
[2] Zhejiang Prov Peoples Hosp, Affiliated Peoples Hosp, Hangzhou Med Coll, Dept Genet & Genom Med, Hangzhou 310058, Peoples R China
[3] Zhejiang Univ, Womens Hosp, Zhejiang Prov Key Lab Precis Diag & Therapy Major, Sch Med,Div Human Reprod & Dev Genet,Reprod Med Ct, Hangzhou 310006, Zhejiang, Peoples R China
关键词
Male infertility; Oligo-astheno-teratozoospermia; DNALI1; Gene mutation; DYNEIN;
D O I
10.1007/s43032-023-01451-1
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Oligo-astheno-teratozoospermia (OAT), which is a common cause of male infertility, can be caused by genetic factors. This study reports on a case of a male patient suffering from infertility concomitant with OAT. Whole-exome sequencing (WES) confirmed the presence of a homozygous variant (NM_003462: c.464-1G > A) in the DNALI1 gene via Sanger sequencing. Immunofluorescence staining demonstrated that the DNALI1 signal was nearly undetectable in the patient's sperm. Bioinformatics analysis revealed that this mutation could reverse the splicing of the exon 4 acceptor splice site. A minigene experiment was performed to verify the mutation and the results confirmed that the mutation disrupted the splicing. Our findings show that this rare mutation in DNALI1 contributes to male infertility and OAT in humans, thereby expanding our understanding of the causes and pathogenesis of male infertility. This knowledge facilitates genetic counseling, clinical diagnosis, and therapeutic development of male infertility.
引用
收藏
页码:1610 / 1616
页数:7
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