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
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