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 49 条
  • [41] Identification of novel homozygous asthenoteratospermia-causing ARMC2 mutations associated with multiple morphological abnormalities of the sperm flagella
    Zhao, Siyi
    Liu, Qiong
    Su, Lilan
    Meng, Lanlan
    Tan, Chen
    Wei, Chunjia
    Zhang, Huan
    Luo, Tao
    Zhang, Qianjun
    Tan, Yue-Qiu
    Tu, Chaofeng
    Chen, Houyang
    Gao, Xingcheng
    JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 2024, 41 (05) : 1297 - 1306
  • [42] Loss-of-function mutations in QRICH2 cause male infertility with multiple morphological abnormalities of the sperm flagella
    Shen, Ying
    Zhang, Feng
    Li, Fuping
    Jiang, Xiaohui
    Yang, Yihong
    Li, Xiaoliang
    Li, Weiyu
    Wang, Xiang
    Cheng, Juan
    Liu, Mohan
    Zhang, Xueguang
    Yuan, Guiping
    Pei, Xue
    Cai, Kailai
    Hu, Fengyun
    Sun, Jianfeng
    Yan, Lanzhen
    Tang, Li
    Jiang, Chuan
    Tu, Wenling
    Xu, Jinyan
    Wu, Haojuan
    Kong, Weiqi
    Li, Shuying
    Wang, Ke
    Sheng, Kai
    Zhao, Xudong
    Yue, Huanxun
    Yang, Xiaoyu
    Xu, Wenming
    NATURE COMMUNICATIONS, 2019, 10 (1)
  • [43] Bi-allelic Variants in DYNC1I2 Cause Syndromic Microcephaly with Intellectual Disability, Cerebral Malformations, and Dysmorphic Facial Features
    Ansar, Muhammad
    Ullah, Farid
    Paracha, Sohail A.
    Adams, Darius J.
    Lai, Abbe
    Pais, Lynn
    Iwaszkiewicz, Justyna
    Millan, Francisca
    Sarwar, Muhammad T.
    Agha, Zehra
    Shah, Sayyed Fahim
    Qaisar, Azhar Ali
    Falconnet, Emilie
    Zoete, Vincent
    Ranza, Emmanuelle
    Makrythanasis, Periklis
    Santoni, Federico A.
    Ahmed, Jawad
    Katsanis, Nicholas
    Walsh, Christopher
    Davis, Erica E.
    Antonarakis, Stylianos E.
    AMERICAN JOURNAL OF HUMAN GENETICS, 2019, 104 (06) : 1073 - 1087
  • [44] Novel mutations in FSIP2 lead to multiple morphological abnormalities of the sperm flagella and poor ICSI prognosis
    Liu, Mohan
    Sun, Yongkang
    Li, Yaqian
    Sun, Jianfeng
    Yang, Yihong
    Shen, Ying
    GENE, 2021, 781
  • [45] Bi-allelic LoF NRROS Variants Impairing Active TGF-β1 Delivery Cause a Severe Infantile-Onset Neuro degenerative Condition with Intracranial Calcification
    Dong, Xiaomin
    Tan, Natalie B.
    Howell, Katherine B.
    Barresi, Sabina
    Freeman, Jeremy L.
    Vecchio, Davide
    Piccione, Maria
    Radio, Francesca Clementina
    Calame, Daniel
    Zong, Shan
    Eggers, Stefanie
    Scheffer, Ingrid E.
    Tan, Tiong Y.
    Van Bergen, Nicole J.
    Tartaglia, Marco
    Christodoulou, John
    White, Susan M.
    AMERICAN JOURNAL OF HUMAN GENETICS, 2020, 106 (04) : 559 - 569
  • [46] Bi-allelic variants in CEP295 cause Seckel-like syndrome presenting with primary microcephaly, developmental delay, intellectual disability, short stature, craniofacial and digital abnormalities
    Li, Niu
    Xu, Yufei
    Chen, Hongzhu
    Lin, Jingqi
    Alabdi, Lama
    Bekheirnia, Mir Reza
    Li, Guoqiang
    Go, Yoel
    Bekheirnia, Nasim
    Faqeih, Eissa
    Chen, Lina
    Chang, Guoying
    Tang, Jie
    Yao, Ruen
    Yu, Tingting
    Wang, Xiumin
    Fu, Wei
    Fu, Qihua
    Shen, Yiping
    Alkuraya, Fowzan S.
    Machol, Keren
    Wang, Jian
    EBIOMEDICINE, 2024, 99
  • [47] Novel Compound Heterozygous Mutation in FSIP2 Causes Multiple Morphological Abnormalities of the Sperm Flagella (MMAF) and Male Infertility
    Meiqi Hou
    Qingsong Xi
    Lixia Zhu
    Weimin Jia
    Zhenxing Liu
    Cheng Wang
    Xiaopei Zhou
    Dazhi Zhang
    Chenxi Xing
    Xuejie Peng
    Yalin Luo
    Lei Jin
    Zhou Li
    Xianqin Zhang
    Reproductive Sciences, 2022, 29 : 2697 - 2702
  • [48] Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations
    Kherraf, Zine-Eddine
    Cazin, Caroline
    Coutton, Charles
    Amiri-Yekta, Amir
    Martinez, Guillaume
    Boguenet, Magalie
    Ben Mustapha, Selima Fourati
    Kharouf, Mahmoud
    Gourabi, Hamid
    Hosseini, Seyedeh Hanieh
    Daneshipour, Abbas
    Toure, Aminata
    Thierry-Mieg, Nicolas
    Zouari, Raoudha
    Arnoult, Christophe
    Ray, Pierre F.
    CLINICAL GENETICS, 2019, 96 (05) : 394 - 401
  • [49] Patient with multiple morphological abnormalities of sperm flagella caused by a novel ARMC2 mutation has a favorable pregnancy outcome from intracytoplasmic sperm injection
    Wang, Jiaxiong
    Liu, Xiaoran
    Zhang, Ce
    Xu, Yongle
    Wang, Weizhuo
    Li, Hong
    Yang, Shenmin
    Zhao, Jing
    JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 2022, 39 (07) : 1673 - 1681