scholarly journals Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility

2020 ◽  
Vol 107 (2) ◽  
pp. 330-341 ◽  
Author(s):  
Chunyu Liu ◽  
Haruhiko Miyata ◽  
Yang Gao ◽  
Yanwei Sha ◽  
Shuyan Tang ◽  
...  
Author(s):  
Jae Yeon Hwang ◽  
Shoaib Nawaz ◽  
Jungmin Choi ◽  
Huafeng Wang ◽  
Shabir Hussain ◽  
...  

Asthenozoospermia accounts for over 80% of primary male infertility cases. Reduced sperm motility in asthenozoospermic patients are often accompanied by teratozoospermia, or defective sperm morphology, with varying severity. Multiple morphological abnormalities of the flagella (MMAF) is one of the most severe forms of asthenoteratozoospermia, characterized by heterogeneous flagellar abnormalities. Among various genetic factors known to cause MMAF, multiple variants in the DNAH2 gene are reported to underlie MMAF in humans. However, the pathogenicity by DNAH2 mutations remains largely unknown. In this study, we identified a novel recessive variant (NM_020877:c.12720G > T;p.W4240C) in DNAH2 by whole-exome sequencing, which fully co-segregated with the infertile male members in a consanguineous Pakistani family diagnosed with asthenozoospermia. 80–90% of the sperm from the patients are morphologically abnormal, and in silico analysis models reveal that the non-synonymous variant substitutes a residue in dynein heavy chain domain and destabilizes DNAH2. To better understand the pathogenicity of various DNAH2 variants underlying MMAF in general, we functionally characterized Dnah2-mutant mice generated by CRISPR/Cas9 genome editing. Dnah2-null males, but not females, are infertile. Dnah2-null sperm cells display absent, short, bent, coiled, and/or irregular flagella consistent with the MMAF phenotype. We found misexpression of centriolar proteins and delocalization of annulus proteins in Dnah2-null spermatids and sperm, suggesting dysregulated flagella development in spermiogenesis. Scanning and transmission electron microscopy analyses revealed that flagella ultrastructure is severely disorganized in Dnah2-null sperm. Absence of DNAH2 compromises the expression of other axonemal components such as DNAH1 and RSPH3. Our results demonstrate that DNAH2 is essential for multiple steps in sperm flagella formation and provide insights into molecular and cellular mechanisms of MMAF pathogenesis.


PLoS Genetics ◽  
2020 ◽  
Vol 16 (9) ◽  
pp. e1009020
Author(s):  
Ya-Yun Wang ◽  
Chih-Chun Ke ◽  
Yen-Lin Chen ◽  
Yu-Hua Lin ◽  
I-Shing Yu ◽  
...  

Author(s):  
Chaofeng Tu ◽  
Jiangshan Cong ◽  
Qianjun Zhang ◽  
Xiaojin He ◽  
Rui Zheng ◽  
...  

2019 ◽  
Vol 38 (5) ◽  
pp. 769-778 ◽  
Author(s):  
Huan Wu ◽  
Weiyu Li ◽  
Xiaojin He ◽  
Chunyu Liu ◽  
Youyan Fang ◽  
...  

2019 ◽  
Vol 7 (1.2) ◽  
pp. 6166-6170
Author(s):  
Bhavin B. Kodiyatar ◽  
◽  
Brijesh M. Patel ◽  
Viren B. Kariya ◽  
◽  
...  

Author(s):  
Asmaa Nasr El‐din ◽  
Hadeer Sorour ◽  
Mona Fattouh ◽  
Mohammed Abu El‐Hamd

2018 ◽  
Vol 102 (4) ◽  
pp. 636-648 ◽  
Author(s):  
Frederick N. Dong ◽  
Amir Amiri-Yekta ◽  
Guillaume Martinez ◽  
Antoine Saut ◽  
Julie Tek ◽  
...  

2020 ◽  
Vol 57 (10) ◽  
pp. 708-716 ◽  
Author(s):  
Guillaume Martinez ◽  
Julie Beurois ◽  
Denis Dacheux ◽  
Caroline Cazin ◽  
Marie Bidart ◽  
...  

BackgroundMultiple morphological abnormalities of the flagella (MMAF) consistently lead to male infertility due to a reduced or absent sperm motility defined as asthenozoospermia. Despite numerous genes recently described to be recurrently associated with MMAF, more than half of the cases analysed remain unresolved, suggesting that many yet uncharacterised gene defects account for this phenotypeMethodsExome sequencing was performed on 167 infertile men with an MMAF phenotype. Immunostaining and transmission electron microscopy (TEM) in sperm cells from affected individuals were performed to characterise the ultrastructural sperm defects. Gene inactivation using RNA interference (RNAi) was subsequently performed in Trypanosoma.ResultsWe identified six unrelated affected patients carrying a homozygous deleterious variants in MAATS1, a gene encoding CFAP91, a calmodulin-associated and spoke-associated complex (CSC) protein. TEM and immunostaining experiments in sperm cells showed severe central pair complex (CPC) and radial spokes defects. Moreover, we confirmed that the WDR66 protein is a physical and functional partner of CFAP91 into the CSC. Study of Trypanosoma MAATS1’s orthologue (TbCFAP91) highlighted high sequence and structural analogies with the human protein and confirmed the axonemal localisation of the protein. Knockdown of TbCFAP91 using RNAi impaired flagellar movement led to CPC defects in Trypanosoma as observed in humans.ConclusionsWe showed that CFAP91 is essential for normal sperm flagellum structure and function in human and Trypanosoma and that biallelic variants in this gene lead to severe flagellum malformations resulting in astheno-teratozoospermia and primary male infertility.


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