Novel variations in TENT5D lead to teratozoospermia in infertile patients

Author:

Zhang Ying‐Teng1ORCID,Shen Gan1,Zhuo Liang‐Chai1,Yang Xue1,Wang Su‐Yan1,Ruan Tie‐Chao12,Jiang Chuan1,Wang Xiang1,Wang Yan3ORCID,Yang Yi‐Hong3ORCID,Shen Ying14ORCID

Affiliation:

1. Department of Obstetrics/Gynecology Key Laboratory of Obstetric Gynecologic and Pediatric Diseases and Birth Defects of Ministry of Education, West China Second University Hospital, Sichuan University Chengdu China

2. Department of Pediatrics West China Second University Hospital, Sichuan University Chengdu China

3. Reproduction Medical Center of West China Second University Hospital, Key Laboratory of Obstetric, Gynecologic and Pediatric Diseases and Birth Defects of Ministry of Education, Sichuan University Chengdu China

4. NHC Key Laboratory of Chronobiology Sichuan University Chengdu China

Abstract

AbstractPurposeTeratozoospermia is the main pathogenic factor of male infertility. However, the genetic etiology of teratozoospermia is largely unknown. This study aims to clarify the relationship between novel variations in TENT5D and teratozoospermia in infertile patients.Materials and methodsTwo infertile patients were enrolled. Routine semen analysis of patients and normal controls was conducted with the WHO guidelines. Whole‐exome sequencing (WES) was conducted to identify pathogenic variants in the two patients. Morphology and ultrastructure analysis of spermatozoa in the two patients was determined by Papanicolaou staining, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The functional effect of the identified variants was analyzed by immunofluorescence staining and western blotting. The expression of TENT5D in different germ cells was detected by immunofluorescence staining.ResultsTwo new hemizygous variations, c.101C > T (p.P34L) and c.125A > T (p.D42V), in TENT5D were detected in two patients with male infertility. Morphology analysis showed abnormalities in spermatozoa morphology in the two patients, including multiple heads, headless, multiple tails, coiled, and/or bent flagella. Ultrastructure analysis showed that most of the spermatozoa exhibited missing or irregularly arranged ‘9+2’ structures. Further functional experiments confirmed the abrogated TENT5D protein expression in patients. In addition, both p.P34L and p.D42V substitutions resulted in a conformational change of the TENT5D protein. We precisely analyzed the subcellular localization of TENT5D in germ cells in humans and mice. And we found that TENT5D was predominantly detected in the head and flagellum of elongating spermatids and epididymal spermatozoa.ConclusionsOur results showed further evidence of a relationship between TENT5D mutation and human male infertility, providing new genetic insight for use in the diagnosis and treatment of male infertility.

Publisher

Wiley

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