Novel bi-allelic variants in DNAH2 cause severe asthenoteratozoospermia with multiple morphological abnormalities of the flagella

被引:30
|
作者
Gao, Yang [1 ,2 ,3 ]
Tian, Shixiong [4 ,5 ,6 ]
Sha, Yanwei [7 ,8 ,9 ,10 ]
Zha, Xiaomin [1 ,2 ,3 ,11 ]
Cheng, Huiru [1 ,12 ,13 ]
Wang, Anyong [11 ]
Liu, Chunyu [4 ,5 ,6 ]
Lv, Mingrong [1 ,12 ,13 ]
Ni, Xiaoqing [1 ,2 ,3 ]
Li, Qiang [12 ,13 ]
Wu, Huan [1 ,2 ,3 ]
Tan, Qing [1 ,14 ]
Tang, Dongdong [1 ,2 ,3 ]
Song, Bing [1 ,2 ,3 ]
Ding, Ding [1 ,2 ,3 ]
Cong, Jiangshan [4 ,5 ,6 ]
Xu, Yuping [1 ,2 ,3 ]
Zhou, Ping [1 ,2 ,3 ]
Wei, Zhaolian [1 ,2 ,3 ]
Cao, Yunxia [1 ,2 ,3 ]
Xu, Yuanhong [11 ]
Zhang, Feng [4 ,5 ,6 ]
He, Xiaojin [1 ,2 ,3 ]
机构
[1] Anhui Med Univ, Reprod Med Ctr, Dept Obstet & Gynecol, Affiliated Hosp 1, Hefei 230022, Peoples R China
[2] Anhui Med Univ, NHC Key Lab Study Abnormal Gametes & Reprod Tract, Hefei 230032, Peoples R China
[3] Anhui Med Univ, Minist Educ Peoples Republ China, Key Lab Populat Hlth Life Cycle, Hefei 230032, Peoples R China
[4] Fudan Univ, State Key Lab Genet Engn, Obstet & Gynecol Hosp,Sch Life Sci, NHC Key Lab Reprod Regulat,Shanghai Inst Planned, Shanghai 200011, Peoples R China
[5] Shanghai Key Lab Female Reprod Endocrine Related, Shanghai 200011, Peoples R China
[6] Nanjing Med Univ, Ctr Global Hlth, Sch Publ Hlth, State Key Lab Reprod Med, Nanjing 211166, Peoples R China
[7] Xiamen Univ, Sch Publ Hlth, Xiamen 361005, Fujian, Peoples R China
[8] Xiamen Univ, Women & Childrens Hosp, Xiamen 361005, Fujian, Peoples R China
[9] Xiamen Univ, State Key Lab Mol Vaccinol & Mol Diagnost, Sch Publ Hlth, Xiamen 361102, Peoples R China
[10] Xiamen Univ, Ctr Mol Imaging & Translat Med, Sch Publ Hlth, Xiamen 361102, Peoples R China
[11] Anhui Med Univ, Dept Clin Lab, Affiliated Hosp 1, Hefei 230022, Peoples R China
[12] Anhui Med Univ, Anhui Prov Engn Res Ctr, Biopreservat & Artificial Organs, Hefei 230032, Peoples R China
[13] Anhui Prov Key Lab Reprod Hlth & Genet, Hefei 230032, Peoples R China
[14] Anhui Med Univ, Anhui Prov Human Sperm Bank, Affiliated Hosp 1, Hefei 230022, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
Asthenoteratozoospermia; Axonemal dyneins; DNAH2; Flagella; MMAF; SPERM FLAGELLA; DYNEIN; MUTATIONS; ORGANIZATION; DNAH1; LEAD;
D O I
10.1016/j.rbmo.2021.01.011
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Research question: Multiple morphological abnormalities of the flagella (MMAF) is characterized by excessive immotile spermatozoa with severe flagellar abnormalities in the ejaculate. Previous studies have reported a heterogeneous genetic profile associated with MMAF. What other genetic variants might explain the cause of MMAF? Design: Whole-exome sequencing was conducted in a cohort of 90 Chinese patients with MMAF. The pathogenicity of identified mutations was assessed through electron microscopy and immunofluorescent examinations. Results: Three unrelated men with bi-allelic DNAH2 variants were identified. Sanger sequencing verified that the six novel variants originated from every parent. All these variants were located at the conserved domains of DNAH2 and predicted to be deleterious by bioinformatic tools. Haematoxylin and eosin staining and scanning electron microscopy revealed that spermatozoa harbouring DNAH2 variants displayed severely aberrant morphology mainly with absent and short flagella (>= 78%). Moreover, transmission electron microscopy revealed the obvious absence of a central pair of microtubules and inner dynein arms in the spermatozoa with mutated DNAH2. Immunofluorescence data further validated these findings, showing reduced DNAH2 protein expression in the spermatozoa with DNAH2 variants, compared with normal spermatozoa. Intracytoplasmic sperm injection using spermatozoa from the three men with mutated DNAH2 resulted in blastocyst formation in all cases. Embryo transfer was carried out in two couples, both resulting in clinical pregnancy. Conclusions: These experimental and clinical data suggest that bi-allelic DNAH2 variants might induce MMAF-associated asthenoteratozoospermia, which can be overcome through intracytoplasmic sperm injection. These findings contribute to the knowledge of the genetic landscape of asthenoteratozoospermia and clinical counselling of male infertility.
引用
收藏
页码:963 / 972
页数:10
相关论文
共 50 条
  • [21] Novel bi-allelic CAD variants cause epileptic encephalopathy responsive to triacetyluridine supplementation
    Anderson, Katherine
    Wiltrout, Kimberly
    Giummo, Christine
    Wortmann, Saskia B.
    Freeze, Hudson
    del Cano Ochoa, Francisco
    Ramon, Santiago
    MOLECULAR GENETICS AND METABOLISM, 2024, 141 (04)
  • [22] Novel bi-allelic HPDL variants cause hereditary spastic paraplegia in a Chinese patient
    Yu, Hao
    Wei, Qiao
    Luo, Wen-Jiao
    Wu, Zhi-Ying
    CLINICAL GENETICS, 2021, 100 (06) : 777 - 778
  • [23] RBL2 bi-allelic truncating variants cause severe motor and cognitive impairment without evidence for abnormalities in DNA methylation or telomeric function
    Nadra Samra
    Shir Toubiana
    Hilde Yttervik
    Aya Tzur-Gilat
    Ilham Morani
    Chen Itzkovich
    Liran Giladi
    Kamal Abu Jabal
    John Z. Cao
    Lucy A. Godley
    Adi Mory
    Hagit Baris Feldman
    Kristian Tveten
    Sara Selig
    Karin Weiss
    Journal of Human Genetics, 2021, 66 : 1101 - 1112
  • [24] RBL2 bi-allelic truncating variants cause severe motor and cognitive impairment without evidence for abnormalities in DNA methylation or telomeric function
    Samra, Nadra
    Toubiana, Shir
    Yttervik, Hilde
    Tzur-Gilat, Aya
    Morani, Ilham
    Itzkovich, Chen
    Giladi, Liran
    Abu Jabal, Kamal
    Cao, John Z.
    Godley, Lucy A.
    Mory, Adi
    Baris Feldman, Hagit
    Tveten, Kristian
    Selig, Sara
    Weiss, Karin
    JOURNAL OF HUMAN GENETICS, 2021, 66 (11) : 1101 - 1112
  • [25] Novel compound heterozygous mutations in DNAH1 cause primary infertility in Han Chinese males with multiple morphological abnormalities of the sperm flagella
    Wang, Meng
    Yang, Qi-Yu
    Zhou, Jue-Pu
    Tan, Hui-Ping
    Hu, Juan
    Jin, Lei
    Zhu, Li-Xia
    ASIAN JOURNAL OF ANDROLOGY, 2023, 25 (04) : 512 - 519
  • [26] Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice
    He, Xiaojin
    Liu, Chunyu
    Yang, Xiaoyu
    Lv, Mingrong
    Ni, Xiaoqing
    Li, Qiang
    Cheng, Huiru
    Liu, Wangjie
    Tian, Shixiong
    Wu, Huan
    Gao, Yang
    Yang, Chenyu
    Tan, Qing
    Cong, Jiangshan
    Tang, Dongdong
    Zhang, Jingjing
    Song, Bing
    Zhong, Yading
    Li, Hang
    Zhi, Weiwei
    Mao, Xiaohong
    Fu, Feifei
    Ge, Lei
    Shen, Qunshan
    Zhang, Manyu
    Saiyin, Hexige
    Jin, Li
    Xu, Yuping
    Zhou, Ping
    Wei, Zhaolian
    Zhang, Feng
    Cao, Yunxia
    AMERICAN JOURNAL OF HUMAN GENETICS, 2020, 107 (03) : 514 - 526
  • [27] Two novel bi-allelic KDELR2 missense variants cause osteogenesis imperfecta with neurodevelopmental features
    Efthymiou, Stephanie
    Herman, Isabella
    Rahman, Fatima
    Anwar, Najwa
    Maroofian, Reza
    Yip, Janice
    Mitani, Tadahiro
    Calame, Daniel G.
    Hunter, Jill V.
    Sutton, V. Reid
    Yilmaz Gulec, Elif
    Duan, Ruizhi
    Fatih, Jawid M.
    Marafi, Dana
    Pehlivan, Davut
    Jhangiani, Shalini N.
    Gibbs, Richard A.
    Posey, Jennifer E.
    Maqbool, Shazia
    Lupski, James R.
    Houlden, Henry
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2021, 185 (07) : 2241 - 2249
  • [28] Bi-allelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia
    Hu, T.
    Meng, L.
    Tan, C.
    Luo, C.
    He, W. B.
    Tu, C.
    Zhang, H.
    Du, J.
    Nie, H.
    Lu, G. X.
    Lin, G.
    Tan, Y. Q.
    HUMAN REPRODUCTION, 2022, 37
  • [29] Novel DNAH1 Mutation Loci Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Literature Review
    Zhuang, Bao-Jun
    Xu, Su-Yun
    Dong, Liang
    Zhang, Pei-Hai
    Zhuang, Bao-Lin
    Huang, Xiao-Peng
    Li, Guang-Sen
    You, Yao-Dong
    Chen, Di'Ang
    Yu, Xu-Jun
    Chang, De-Gui
    WORLD JOURNAL OF MENS HEALTH, 2022, 40 (04): : 551 - 560
  • [30] Biallelic Variants in CFAP61 Cause Multiple Morphological Abnormalities of the Flagella and Male Infertility
    Ma, Ao
    Zeb, Aurang
    Ali, Imtiaz
    Zhao, Daren
    Khan, Asad
    Zhang, Beibei
    Zhou, Jianteng
    Khan, Ranjha
    Zhang, Huan
    Zhang, Yuanwei
    Khan, Ihsan
    Shah, Wasim
    Ali, Haider
    Javed, Abdul Rafay
    Ma, Hui
    Shi, Qinghua
    FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2022, 9