Novel Biallelic DNAH1 Variations Cause Multiple Morphological Abnormalities of the Sperm Flagella

生物 鞭毛 精子 遗传学 轴丝 桑格测序 基因 男性不育 精子活力 运动纤毛 不育 突变 怀孕
作者
Huaying Hu,Tianying Wei,Zhan‐Ke Feng,Song-jun Li,Rong Zhao,Xiao-ling Yi,Ti-ling Hu,Huan Zhao,Cunxi Li,Zuguo Liu
出处
期刊:DNA and Cell Biology [Mary Ann Liebert, Inc.]
卷期号:40 (6): 833-840 被引量:13
标识
DOI:10.1089/dna.2021.0097
摘要

Sperm motility is vital to human reproduction, and malformed sperm flagella can cause male infertility. Individuals with multiple morphological abnormalities of the flagella mostly have absent, short, coiled, bent, and/or irregular-caliber flagella. In this study, a patient with male infertility underwent a physical examination along with his wife. Genetic testing was performed by whole-exome sequencing of the couple, and Sanger sequencing was performed for validation. Novel biallelic variations in the DNAH1: (NM_015512.4) gene consisting of c.1336G>C (p.E446Q) and c.2912G>A (p.R971H) were identified. In silico structural analysis revealed that the amino acid residues affected by the variation were evolutionarily conserved, and the variant p.R971H influenced the stability of the DNAH1 protein. Morphological studies of the patient's sperm showed defects in its flagella. Results of Papanicolaou staining and scanning electron microscopy demonstrated coiled and short flagella with multiple anomalies. Transmission electron microscopy of the sperm flagella showed that the inner dynein arm and radial spoke were absent, and the dense fiber and microtubule doublets were displaced. Quantitative PCR of the mRNA of the patient's sperm showed that the expression of DNALI1 was dramatically reduced. Collectively, these findings elucidated the genetic cause of the family's infertility and provided insight into the functioning of the DNAH1 gene.
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