Perry A C, Jones R, Niang L S, Jackson R M, Hall L
Department of Biochemistry, University of Bristol, School of Medical Sciences, U.K.
Biochem J. 1992 Aug 1;285 ( Pt 3)(Pt 3):863-70. doi: 10.1042/bj2850863.
Epididymal glutathione peroxidase (GPX) has been suggested as a major factor in combating loss of fertility of spermatozoa due to lipid peroxidation. We report here the isolation and sequence of putative GPX cDNAs from rat (Rattus rattus) and cynomolgus-monkey (Macaca fascicularis) epididymis, which exhibit marked sequence identity with known GPXs. In both species the cDNAs encode predicted preproteins containing 221 amino acid residues. Unlike other characterized GPX sequences, epididymal GPX mRNA does not contain a selenocysteine codon (UGA). However, sequence comparison and molecular-modelling studies suggest a high degree of structural conservation between epididymal and other GPXs. Transcripts corresponding to epididymal GPX are not detected in a variety of other tissues (liver, spleen, kidney and testis) and appear to be androgen-regulated in the epididymis.
附睾谷胱甘肽过氧化物酶(GPX)被认为是对抗因脂质过氧化导致的精子生育能力丧失的主要因素。我们在此报告从大鼠(褐家鼠)和食蟹猴(猕猴)附睾中分离出的假定GPX cDNA及其序列,它们与已知的GPX具有显著的序列同一性。在这两个物种中,cDNA编码预测的含221个氨基酸残基的前体蛋白。与其他已鉴定的GPX序列不同,附睾GPX mRNA不含硒代半胱氨酸密码子(UGA)。然而,序列比较和分子建模研究表明,附睾GPX与其他GPX之间存在高度的结构保守性。在多种其他组织(肝脏、脾脏、肾脏和睾丸)中未检测到与附睾GPX相对应的转录本,且附睾中的转录本似乎受雄激素调节。