A novel missense mutation of CCDC34 causes male infertility with oligoasthenoteratozoospermia in a consanguineous Pakistani family.
- Author:
Nisar AHMAD
1
;
Meng-Lei YANG
;
Aurang ZEB
;
Jian-Teng ZHOU
;
Muhammad ZUBAIR
;
Tanveer ABBAS
;
Xiao-Hua JIANG
;
Yuan-Wei ZHANG
;
Huan ZHANG
;
Wasim SHAH
;
Qing-Hua SHI
Author Information
- Publication Type:Case Reports
- MeSH: Humans; Male; Mutation, Missense/genetics*; Pakistan; Consanguinity; Asthenozoospermia/genetics*; Pedigree; Infertility, Male/genetics*; Adult; Oligospermia/genetics*; Exome Sequencing; Axoneme/ultrastructure*; Spermatozoa/ultrastructure*
- From: Asian Journal of Andrology 2024;26(6):605-609
- CountryChina
- Language:English
- Abstract: Male infertility is a worldwide health issue, affecting 8%-12% of the global population. Oligoasthenoteratozoospermia (OAT) represents a severe type of male infertility, characterized by reduced sperm count and motility and an increased frequency of sperm with aberrant morphology. Using whole-exome sequencing, this study identified a novel missense mutation (c.848C>A, p.A283E) in the coiled-coil domain-containing 34 gene (CCDC34) in a consanguineous Pakistani family. This rare mutation was predicted to be deleterious and to affect the protein stability. Hematoxylin and eosin staining of spermatozoa from the patient with OAT revealed multiple morphological abnormalities of the flagella and transmission electron microscopy indicated axonemal ultrastructural defects with a lack of outer dynein arms. These findings indicated that CCDC34 plays a role in maintaining the axonemal ultrastructure and the assembly or stability of the outer dynein arms, thus expanding the phenotypic spectrum of CCDC34 missense mutations.
