TENT5D disruption causes oligoasthenoteratozoospermia and male infertility

Author:

Sha Yanwei123ORCID,Liu Wensheng4ORCID,Tang Songxi5,Zhang Xiaoya6,Xiao Ziyi7,Xiao Yuwei7,Deng Hongjing7,Zhou Huiliang5,Wei Xiaoli7ORCID

Affiliation:

1. Department of Andrology, Women and Children's Hospital, School of Medicine Xiamen University Xiamen Fujian China

2. Fujian Provincial Key Laboratory of Reproductive Health Research, School of Medicine Xiamen University Xiamen Fujian China

3. State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, School of Public Health Xiamen University Xiamen Fujian China

4. NHC Key Laboratory of Male Reproduction and Genetics Guangdong Provincial Reproductive Science Institute (Guangdong Provincial Fertility Hospital) Guangzhou Guangdong China

5. Department of Andrology First Affiliated Hospital of Fujian Medical University Fuzhou Fujian China

6. State Key Laboratory of Cellular Stress Biology, School of Pharmaceutical Sciences Xiamen University Xiamen Fujian China

7. School of Medicine Yunnan University Kunming Yunnan China

Abstract

AbstractBackgroundOligoasthenoteratozoospermia (OAT) is one of the most complex aggregators of male gametic problems. However, the genetic etiology of OAT is still largely unknown.ObjectivesTo reveal the new genetic factors responsible for male infertility owning to OAT and reveal the outcomes of the affected patients from intracytoplasmic sperm injection (ICSI).Materials and methodsTwo infertile men with typical OAT were recruited in 2018 and retrospected a cohort that included 47 patients with OAT from 2013 to 2021. Fifty healthy men with proven fertility served as control subjects. To identify the novel pathogenic variants, whole‐exome sequencing and Sanger sequencing were used. In silico analysis revealed the affecting of the variants. Field emission scanning electron microscopy was employed to observe the morphological defects of the spermatozoa. Immunofluorescence was used to analyze the expression and localization of the related protein. CRISPR/Cas9 was used to generate the mouse model. ICSI was used as a treatment for the patients and to assess the effects of the pathogenic variant on fertilization and embryo development.ResultsWe identified a loss‐of‐function mutation NM_001170574.2:c.823G > T (p.Glu275*) in X‐linked TENT5D from two patients with OAT. This variant is highly deleterious and has not been found in the human population. The count of patients’ spermatozoa is dramatically decreased and displays multiple morphologic abnormalities with poor motility. Tent5d knockout mice are infertile and exhibit parallel defects. ICSI could rescue the infertility of the Tent5d knockout male mice. Moreover, the proband was treated with ICSI and achieved a successful pregnancy outcome for the first time. Subsequent mutation screening identified no TENT5D mutations among 47 additional patients with OAT and 50 control subjects.ConclusionMutation in TENT5D results in OAT and male infertility, and this terrible situation could be rescued by ICSI.

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Medical Innovation Project of Fujian Province

Publisher

Wiley

Subject

Urology,Endocrinology,Reproductive Medicine,Endocrinology, Diabetes and Metabolism

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