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人类谷胱甘肽S-转移酶的分子遗传学

Molecular genetics of the human glutathione S-transferase.

作者信息

Board P G, Johnston P N, Ross V L, Webb G C, Coggan M, Suzuki T

机构信息

Molecular Genetics Group, John Curtin School of Medical Research, Australian National University, Canberra.

出版信息

Princess Takamatsu Symp. 1990;21:199-211.

PMID:2134679
Abstract

Multiple human cytosolic glutathione transferases have been described. These enzymes are the products of multiple genes that can be classified into at least four evolutionary classes. The genes encoding each class appear to be clustered on distinct chromosomes. Over-expression of glutathione S-transferase (GST) isoenzymes has been implicated in drug resistance and, conversely, deficiency of GST isoenzymes has been implicated in susceptibility to carcinogens. Some GST genes are expressed at varying levels in different individuals, and there is a frequent deficiency of the Mu class GST1 isoenzyme in all the racial groups studied so far. This deficiency is due to a deletion of the GST 1 gene. The Alpha class genes are located on the short arm of chromosome 6 and are closely linked, with less than 2 kb separating some genes. There is evidence for the existence of several pseudogenes in this cluster. A complete Alpha class gene has 7 exons and extends over 13 kb. The 5' flanking region of the gene encoding the GST2 type 1 isoenzyme has been cloned and sequenced. This region contains a number of putative promoter and enhancer elements that are similar to those found in rat and mouse Alpha class genes.

摘要

已经描述了多种人细胞质谷胱甘肽转移酶。这些酶是多个基因的产物,可分为至少四个进化类别。编码每个类别的基因似乎聚集在不同的染色体上。谷胱甘肽S-转移酶(GST)同工酶的过表达与耐药性有关,相反,GST同工酶的缺乏与对致癌物的易感性有关。一些GST基因在不同个体中的表达水平不同,并且在迄今为止研究的所有种族群体中,Mu类GST1同工酶经常缺乏。这种缺乏是由于GST 1基因的缺失。Alpha类基因位于6号染色体的短臂上,紧密相连,一些基因之间的间隔不到2 kb。有证据表明该簇中存在几个假基因。一个完整的Alpha类基因有7个外显子,延伸超过13 kb。编码GST2 1型同工酶的基因的5'侧翼区域已被克隆和测序。该区域包含许多推定的启动子和增强子元件,这些元件与在大鼠和小鼠Alpha类基因中发现的元件相似。

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