A novel homozygous splicing mutation in AK7 causes multiple morphological abnormalities of sperm flagella in patients from consanguineous Pakistani families.

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Tác giả: Musavir Abbas, Tanveer Abbas, Nisar Ahmed, Imtiaz Ali, Ansar Hussain, Khalid Khan, Muzammil Ahmad Khan, Hui Ma, Ghulam Mustafa, Fazal Rahim, Yousaf Raza, Wasim Shah, Qing-Hua Shi, Meftah Uddin, Nadeem Ullah, Bo Yang, Aurang Zeb, Huan Zhang, Muhammad Zubair

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: China : Asian journal of andrology , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 735671

 Multiple morphological abnormalities of the flagella (MMAF) represent a severe form of sperm defects leading to asthenozoospermia and male infertility. In this study, we identified a novel homozygous splicing mutation (c.871-4 ACA>
 A) in the adenylate kinase 7 (AK7) gene by whole-exome sequencing in infertile individuals. Spermatozoa from affected individuals exhibited typical MMAF characteristics, including coiled, bent, short, absent, and irregular flagella. Transmission electron microscopy analysis showed disorganized axonemal structure and abnormal mitochondrial sheets in sperm flagella. Immunofluorescence staining confirmed the absence of AK7 protein from the patients' spermatozoa, validating the pathogenic nature of the mutation. This study provides direct evidence linking the AK7 gene to MMAF-associated asthenozoospermia in humans, expanding the mutational spectrum of AK7 and enhancing our understanding of the genetic basis of male infertility.
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