Details

Autor(en) / Beteiligte

• Khan, Khalid
• Zhang, Xiangjun
• Dil, Sobia
• Khan, Ihsan
• Unar, Ahsanullah
• Ye, Jingwei
• Zeb, Aurang
• Zubair, Muhammad
• Shah, Wasim
• Zhang, Huan
• Khan, Muzammil Ahmad
• Wu, Limin
• Xu, Bo
• Ma, Hui
• Wen, Zina
• Shi, Qinghua

Titel

A novel homozygous TSGA10 missense variant causes acephalic spermatozoa syndrome in a Pakistani family

Ist Teil von

• Basic and clinical andrology, 2024-02, Vol.34 (1), p.4-4, Article 4

Ort / Verlag

England: BioMed Central

Erscheinungsjahr

2024

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• Acephalic spermatozoa syndrome is a rare type of teratozoospermia causing male infertility due to detachment of the sperm head and flagellum, which precludes fertilization potential. Although loss-of-function variations in several genes, including TSGA10, have been associated with acephalic spermatozoa syndrome, the genetic cause of many cases remains unclear. We recruited a Pakistani family with two infertile brothers who suffered from acephalic spermatozoa syndrome. Through whole-exome sequencing (WES) followed by Sanger sequencing, we identified a novel missense variant in TSGA10 (c.1112T > C, p. Leu371Pro), which recessively co-segregated with the acephalic spermatozoa syndrome within this family. Ultrastructural analyses of spermatozoa from the patient revealed that 98% of flagellar cross-sections displayed abnormal axonemal ultrastructure, in addition to the head-flagellum detachment. Real-time quantitative PCR analysis revealed almost no detectable TSAG10 mRNA and western blot analysis also failed to detect TSAG10 protein in patient's sperm samples while TSGA10 expression was clearly detected in control samples. Consistently, immunofluorescence analysis demonstrated the presence of TSGA10 signal in the midpiece of sperm from the control but a complete absence of TSGA10 signal in sperm from the patient. Altogether, our study identifies a novel TSGA10 pathogenic variant as a cause of acephalic spermatozoa syndrome in this family and provides information regarding the clinical manifestations associated with TSGA10 variants in human.