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人谷胱甘肽S-转移酶Ha1亚基基因的分离与鉴定

Isolation and characterization of a human glutathione S-transferase Ha1 subunit gene.

作者信息

Rozen F, Nguyen T, Pickett C B

机构信息

Merck Frosst Centre for Therapeutic Research, Pointe Claire-Dorval, Quebec, Canada.

出版信息

Arch Biochem Biophys. 1992 Feb 1;292(2):589-93. doi: 10.1016/0003-9861(92)90035-u.

Abstract

We have isolated and characterized a human liver glutathione S-transferase Ha1 subunit gene. The gene spans approximately 12 kilobases and comprises seven exons separated by six introns. The transcription initiation site has been determined by primer extension analysis. A TATA box is located 26 nucleotides upstream from the transcription initiation site, an adenine residue. RNA blot analysis reveals that the gene is expressed at significantly higher levels in human liver than in HepG2 cells. The isolation and characterization of a human glutathione S-transferase Ha1 subunit gene should facilitate a detailed analysis of its transcriptional regulation.

摘要

我们已经分离并鉴定了一个人类肝脏谷胱甘肽S-转移酶Ha1亚基基因。该基因跨度约12千碱基,由7个外显子和6个内含子分隔。转录起始位点已通过引物延伸分析确定。一个TATA框位于转录起始位点上游26个核苷酸处,即一个腺嘌呤残基处。RNA印迹分析表明,该基因在人类肝脏中的表达水平明显高于HepG2细胞。人类谷胱甘肽S-转移酶Ha1亚基基因的分离和鉴定应有助于对其转录调控进行详细分析。

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