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大鼠黄曲霉毒素B1醛还原酶基因AKR7A1的特性。AKR7A1的结构与染色体定位以及该基因启动子中抗氧化反应元件的鉴定。

Characterization of the rat aflatoxin B1 aldehyde reductase gene, AKR7A1. Structure and chromosomal localization of AKR7A1 as well as identification of antioxidant response elements in the gene promoter.

作者信息

Ellis Elizabeth M, Slattery Cara M, Hayes John D

机构信息

Department of Bioscience and Pharmaceutical Sciences, University of Strathclyde, Glasgow G1 1XW, UK.

出版信息

Carcinogenesis. 2003 Apr;24(4):727-37. doi: 10.1093/carcin/bgg016.

Abstract

Rat aflatoxin B(1) aldehyde reductase (called AFAR1 or AKR7A1) is a member of the aldo-keto reductase 7 family, which metabolizes the environmental carcinogen aflatoxin B(1). The expression of this enzyme is markedly increased in rat liver by cancer chemopreventive agents, many of which are believed to regulate gene expression through the antioxidant response element (ARE). In order to understand how this gene is regulated, two overlapping genomic clones have been isolated that contain most of the coding region for the enzyme; together they encompass 14.1 kb of DNA. Characterization of these clones has shown that rat AFAR1 is approximately 8 kb long and comprises seven exons and six introns. The seven exons are between 97 and 380 bp in size. The introns range in size from 194 bp to approximately 2.9 kb. Fluorescent in situ hybridization localized AFAR1 to rat chromosome 5q36.5, a region that is syntenic with human chromosome 1p35-1p36.1 where AKR7A2 resides. The transcriptional start site (TSS) was determined, using 5'-rapid amplification of cDNA ends, to be an A nucleotide 73 bp upstream from the ATG initiation codon. The 5'-flanking region of AFAR1 was isolated by polymerase chain reaction-based genome walking, and resulted in the isolation of approximately 900 bp of genomic DNA upstream from the TSS. Use of a gene expression reporter assay demonstrated that this cloned 5'-flanking region of AFAR1 could support transcription in the rat liver 34 (RL34) epithelial cell line. Within this upstream region of the promoter, a substantial number of sequences were found that are closely similar, but not identical, to the 'core' ARE consensus sequence. Between nucleotides -810 and -106 bp from the TSS 16 ARE-related sequences were identified. Four of these putative enhancers lay between -389 and -355 bp, and the motif 5'-GAGTGAG-3' was repeated three times within the 35 bp region.

摘要

大鼠黄曲霉毒素B(1)醛还原酶(称为AFAR1或AKR7A1)是醛酮还原酶7家族的成员,可代谢环境致癌物黄曲霉毒素B(1)。癌症化学预防剂可使该酶在大鼠肝脏中的表达显著增加,其中许多化学预防剂被认为是通过抗氧化反应元件(ARE)来调节基因表达的。为了了解该基因是如何被调控的,已分离出两个重叠的基因组克隆,它们包含该酶的大部分编码区;二者共包含14.1 kb的DNA。对这些克隆的特征分析表明,大鼠AFAR1约8 kb长,由7个外显子和6个内含子组成。7个外显子的大小在97至380 bp之间。内含子的大小范围从194 bp到约2.9 kb。荧光原位杂交将AFAR1定位到大鼠染色体5q36.5,该区域与人类染色体1p35 - 1p36.1同线,AKR7A2位于该区域。使用5'-cDNA末端快速扩增法确定转录起始位点(TSS)为ATG起始密码子上游73 bp处的一个A核苷酸。通过基于聚合酶链反应的基因组步移法分离出AFAR1的5'-侧翼区域,结果在TSS上游分离出约900 bp的基因组DNA。使用基因表达报告基因检测表明,AFAR1这个克隆的5'-侧翼区域可在大鼠肝脏34(RL34)上皮细胞系中支持转录。在启动子的这个上游区域,发现了大量与“核心”ARE共有序列密切相似但不完全相同的序列。在距TSS - 810至 - 106 bp的核苷酸之间鉴定出16个与ARE相关的序列。其中4个假定的增强子位于 - 389至 - 355 bp之间,基序5'-GAGTGAG-3'在35 bp区域内重复3次。

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