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
相关论文
共 50 条
  • [21] A novel mutation of DRC1 gene causes multiple morphological abnormalities of the sperm flagella and male infertility in humans
    Fu, T.
    Liao, H.
    Long, S.
    Tang, X.
    Huang, G.
    Han, W.
    Liu, W.
    Lin, T.
    HUMAN REPRODUCTION, 2023, 38
  • [22] A homozygous nonsense variant in HENMT1 causes male infertility in humans and mice
    Li, Ming
    Abbas, Tanveer
    Wang, Yue
    Zhi, Aoran
    Zhou, Jianteng
    Ma, Ao
    Murtaza, Ghulam
    Wu, Yufan
    Shah, Wasim
    Zubair, Muhammad
    Khan, Muzammil Ahmad
    Iqbal, Furhan
    Jiang, Xiaohua
    Zhang, Huan
    Shi, Qinghua
    ANDROLOGY, 2024,
  • [23] A novel homozygous LRRC6 mutation causes male infertility with asthenozoospermia and primary ciliary dyskinesia in humans
    Shi, Shengjia
    Tang, Xiangrong
    Long, Shunhua
    Yang, Jie
    Wang, Tianwei
    Wang, Hongmei
    Hu, Tingwenyi
    Shi, Juanzi
    Huang, Guoning
    Qiao, Sen
    Lin, Tingting
    ANDROLOGY, 2025, 13 (03) : 459 - 472
  • [24] A novel homozygous CFAP65 mutation in humans causes male infertility with multiple morphological abnormalities of the sperm flagella
    Zhang, Xueguang
    Shen, Ying
    Wang, Xiang
    Yuan, Guiping
    Zhang, Chaoliang
    Yang, Yihong
    CLINICAL GENETICS, 2019, 96 (06) : 541 - 548
  • [25] A hemizygous loss-of-function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia
    Luo, Chen
    Chen, Zixu
    Meng, Lanlan
    Tan, Chen
    He, Wenbin
    Tu, Chaofeng
    Du, Juan
    Lu, Guang-Xiu
    Lin, Ge
    Tan, Yue-Qiu
    Hu, Tong-Yao
    CLINICAL GENETICS, 2024, 106 (01) : 27 - 36
  • [26] A gain-of-function mutation in the ITPR1 gating domain causes male infertility in mice
    Sun, Bo
    Ni, Mingke
    Tian, Shanshan
    Guo, Wenting
    Cai, Shitian
    Sondergaard, Mads T.
    Chen, Yongxiang
    Mu, Yongxin
    Estillore, John P.
    Wang, Ruiwu
    Chen, Ju
    Overgaard, Michael T.
    Fill, Michael
    Ramos-Franco, Josefina
    Nyegaard, Mette
    Wayne Chen, Sui Rong
    JOURNAL OF CELLULAR PHYSIOLOGY, 2022, 237 (08) : 3305 - 3316
  • [27] A mutation on mouse chromosome 15 causes sperm motility defects and male infertility
    Borg, Claire
    Adams, Victoria
    Sanchez-Partida, Luis
    de Kretser, David
    O'Bryan, Moira
    BIOLOGY OF REPRODUCTION, 2008, : 296 - 296
  • [28] TESTICULAR BIOPSY IN STUDY OF MALE INFERTILITY .1. TESTICULAR CAUSES OF INFERTILITY
    WONG, TW
    STRAUS, FH
    WARNER, NE
    ARCHIVES OF PATHOLOGY, 1973, 95 (03): : 151 - 159
  • [29] ZP1-Y262C mutation causes abnormal zona pellucida formation and female infertility in humans
    Cao, Guangyi
    Yu, Lina
    Fang, Junshun
    Shi, Ruixin
    Li, Huijun
    Lu, Feifei
    Shen, Xiaoyue
    Zhu, Xiangyu
    Wang, Shanshan
    Kong, Na
    FRONTIERS IN GENETICS, 2024, 15
  • [30] A homozygous frameshift mutation in ADAD2 causes male infertility with spermatogenic impairments
    Tian, Shixiong
    Wang, Ziqi
    Liu, Liting
    Zhou, Yiling
    Lv, Yue
    Tang, Dongdong
    Wang, Jiaxiong
    Jiang, Jing
    Wu, Huan
    Tang, Shuyan
    Wang, Guanxiong
    Geng, Hao
    Tao, Fangbiao
    Liu, Hongbin
    He, Xiaojin
    Zhang, Feng
    Li, Jinsong
    Jin, Li
    Huang, Tao
    Liu, Chunyu
    Cao, Yunxia
    JOURNAL OF GENETICS AND GENOMICS, 2023, 50 (04) : 284 - 288