Kelner M J, Montoya M A
Department of Pathology, University of California, San Diego 92103-8320, USA.
Biochem Biophys Res Commun. 1998 Aug 10;249(1):53-5. doi: 10.1006/bbrc.1998.9086.
The primary structure of human selenium-dependent phospholipid hydroperoxide glutathione peroxidase (GPX4) was determined by genomic cloning. The gene structure of GPX4 spans only 2.8 kb and consists of 7 exons. The coding sequence resides on all 7 exons, and the mitochondrial leader sequence is contained entirely within the first exon. The selenocysteine coding nucleotide resides on the third exon. The introns all commenced with the consensus nucleotide sequence GTR and ended with the consensus nucleotide sequence YAG. Analysis of the GPX4 gene sequence identified a potential alternative tissue-specific first exon. Chromosomal FISH studies placed the GPX4 gene at 19p13.3 location, and downstream of the 23 k-Da polypeptide DNA-directed RNA polymerase gene.
通过基因组克隆确定了人硒依赖性磷脂氢谷胱甘肽过氧化物酶(GPX4)的一级结构。GPX4的基因结构仅跨越2.8 kb,由7个外显子组成。编码序列位于所有7个外显子上,线粒体前导序列完全包含在第一个外显子内。硒代半胱氨酸编码核苷酸位于第三个外显子上。所有内含子均以共有核苷酸序列GTR开始,并以共有核苷酸序列YAG结束。对GPX4基因序列的分析确定了一个潜在的组织特异性可变第一外显子。染色体荧光原位杂交研究将GPX4基因定位在19p13.3位置,在23 kDa多肽DNA指导的RNA聚合酶基因的下游。