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Selenoprotein TXNRD3 supports male fertility via the redox regulation of spermatogenesis.


ABSTRACT: Thioredoxin/glutathione reductase (TXNRD3) is a selenoprotein composed of thioredoxin reductase and glutaredoxin domains. This NADPH-dependent thiol oxidoreductase evolved through gene duplication within the Txnrd family, is expressed in the testes, and can reduce both thioredoxin and glutathione in vitro; however, the function of this enzyme remains unknown. To characterize the function of TXNRD3 in vivo, we generated a strain of mice bearing deletion of Txnrd3 gene. We show that these Txnrd3 knockout mice are viable and without discernable gross phenotypes, and also that TXNRD3 deficiency leads to fertility impairment in male mice. We found that Txnrd3 knockout animals exhibited a lower fertilization rate in vitro, a sperm movement phenotype, and an altered thiol redox status in sperm cells. Proteomic analyses further revealed a broad range of substrates reduced by TXNRD3 during sperm maturation, presumably as a part of sperm quality control. Taken together, these results show that TXNRD3 plays a critical role in male reproduction via the thiol redox control of spermatogenesis.

SUBMITTER: Dou Q 

PROVIDER: S-EPMC9352919 | biostudies-literature | 2022 Aug

REPOSITORIES: biostudies-literature

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Selenoprotein TXNRD3 supports male fertility via the redox regulation of spermatogenesis.

Dou Qianhui Q   Turanov Anton A AA   Mariotti Marco M   Hwang Jae Yeon JY   Wang Huafeng H   Lee Sang-Goo SG   Paulo Joao A JA   Yim Sun Hee SH   Gygi Stephen P SP   Chung Jean-Ju JJ   Gladyshev Vadim N VN  

The Journal of biological chemistry 20220623 8


Thioredoxin/glutathione reductase (TXNRD3) is a selenoprotein composed of thioredoxin reductase and glutaredoxin domains. This NADPH-dependent thiol oxidoreductase evolved through gene duplication within the Txnrd family, is expressed in the testes, and can reduce both thioredoxin and glutathione in vitro; however, the function of this enzyme remains unknown. To characterize the function of TXNRD3 in vivo, we generated a strain of mice bearing deletion of Txnrd3 gene. We show that these Txnrd3 k  ...[more]

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