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Isolation of a cDNA clone and localization of human glutathione S-transferase 2 genes to chromosome band 6p12.

机译:cDNA克隆的分离和人类谷胱甘肽S-转移酶2基因的定位在染色体带6p12。

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摘要

The glutathione S-transferases (GST) (glutathione transferase; EC 2.5.1.18) are a family of enzymes responsible for the metabolism of a broad range of xenobiotics and carcinogens. A cDNA clone containing the entire amino acid coding sequence of a human GST-2 subunit has been isolated using a lambda gt11 expression library. The complete nucleotide sequence and a partial restriction map are presented. The subunit is composed of 221 amino acids with a molecular weight of 25,425 before posttranslational modification. The deduced amino acid sequence is rich in lysine, which is consistent with the relatively high pI of GST-2. The human sequence shows considerable homology with the rat Ya and Yc GST sequences but little homology with the rat GSTp and Yb subunit sequences. Southern blots of restriction digests of human DNA indicate that there may be multiple GST-2 genes. In situ hybridization of the cloned cDNA to human chromosomes produces intense labeling only over band p12 on the short arm of chromosome 6 near the centromere. This indicates that the GST-2 gene(s) are located only at this site.
机译:谷胱甘肽S-转移酶(GST)(谷胱甘肽转移酶; EC 2.5.1.18)是负责广泛的异种生物和致癌物代谢的酶家族。使用λgt11表达文库已分离出包含人GST-2亚基完整氨基酸编码序列的cDNA克隆。给出了完整的核苷酸序列和部分限制性图谱。在翻译后修饰之前,该亚基由221个氨基酸组成,分子量为25,425。推导的氨基酸序列富含赖氨酸,这与GST-2相对较高的pI相符。人序列与大鼠Ya和Yc GST序列显示相当的同源性,但与大鼠GSTp和Yb亚基序列同源性很小。人类DNA限制性消化的DNA印迹表明可能存在多个GST-2基因。克隆的cDNA与人染色体的原位杂交仅在着丝粒附近的6号染色体短臂上的p12带上产生强烈标记。这表明GST-2基因仅位于该位点。

著录项

  • 作者

    Board, P G; Webb, G C;

  • 作者单位
  • 年度 1987
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  • 原文格式 PDF
  • 正文语种 en
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