We have characterized a cDNA pGPX1211 encoding rat glutathione peroxidase I. The selenocysteine in the protein corresponded to a TGA codon in the coding region of the cDNA, similar to earlier findings in mouse and human genes, and a gene encoding the formate dehydrogenase from E. coli, another selenoenzyme. The rat GSH peroxidase I has a calculated subunit molecular weight of 22,155 daltons and shares 95% and 86% sequence homology with the mouse and human subunits, respectively. The 3'-noncoding sequence (greater than 930 bp) in pGPX1211 is much longer than that of the human sequences. We found that glutathione peroxidase I mRNA, but not the polypeptide, was expressed under nutritional stress of selenium deficiency where no glutathione peroxidase I activity can be detected. The failure of detecting any apoprotein for the glutathione peroxidase I under selenium deficiency and results published from other laboratories supports the proposal that selenium may be incorporated into the glutathione peroxidase I co-translationally.

译文

:我们已经表征了编码大鼠谷胱甘肽过氧化物酶I的cDNA pGPX1211。该蛋白中的硒代半胱氨酸对应于该cDNA编码区中的TGA密码子,类似于小鼠和人类基因中的早期发现,以及一个编码来自E的甲酸脱氢酶的基因大肠杆菌,另一种硒酶。大鼠GSH过氧化物酶I的计算亚单位分子量为22155道尔顿,分别与小鼠和人亚单位具有95%和86%的序列同源性。 pGPX1211中的3'非编码序列(大于930 bp)比人类序列长得多。我们发现,在缺乏硒的营养胁迫下谷胱甘肽过氧化物酶I mRNA而不是多肽被表达,在硒缺乏的情况下,谷胱甘肽过氧化物酶I的活性无法被检测到。在硒缺乏的情况下未能检测到谷胱甘肽过氧化物酶I的任何载脂蛋白,以及其他实验室发表的结果支持了将硒共翻译入谷胱甘肽过氧化物酶I的提议。

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