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硒蛋白TXNRD3通过对精子发生的氧化还原调节来维持雄性生育能力。

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

作者信息

Dou Qianhui, Turanov Anton A, Mariotti Marco, Hwang Jae Yeon, Wang Huafeng, Lee Sang-Goo, Paulo Joao A, Yim Sun Hee, Gygi Stephen P, Chung Jean-Ju, Gladyshev Vadim N

机构信息

Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA; Department of Genetics, Microbiology and Statistics, Universitat de Barcelona, Barcelona, Catalonia, Spain.

出版信息

J Biol Chem. 2022 Aug;298(8):102183. doi: 10.1016/j.jbc.2022.102183. Epub 2022 Jun 23.

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.

摘要

硫氧还蛋白/谷胱甘肽还原酶(TXNRD3)是一种由硫氧还蛋白还原酶和谷氧还蛋白结构域组成的硒蛋白。这种依赖烟酰胺腺嘌呤二核苷酸磷酸(NADPH)的硫醇氧化还原酶通过硫氧还蛋白还原酶(Txnrd)家族内的基因复制进化而来,在睾丸中表达,并且在体外能够还原硫氧还蛋白和谷胱甘肽;然而,这种酶的功能仍然未知。为了在体内表征TXNRD3的功能,我们构建了一种Txnrd3基因缺失的小鼠品系。我们发现这些Txnrd3基因敲除小鼠能够存活且没有明显的总体表型,并且TXNRD3缺乏会导致雄性小鼠生育能力受损。我们发现Txnrd3基因敲除动物在体外表现出较低的受精率、精子运动表型以及精子细胞中硫醇氧化还原状态的改变。蛋白质组学分析进一步揭示了TXNRD3在精子成熟过程中还原的广泛底物,推测这是精子质量控制的一部分。综上所述,这些结果表明TXNRD3通过对精子发生的硫醇氧化还原控制在雄性生殖中发挥关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f6/9352919/98264c6f69fe/gr1.jpg

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