Suppr超能文献

人类凝血酶原基因:HepG2细胞中的转录调控

The human prothrombin gene: transcriptional regulation in HepG2 cells.

作者信息

Bancroft J D, McDowell S A, Degen S J

机构信息

Division of Basic Science Research, Children's Hospital Research Foundation, Cincinnati, Ohio 45229.

出版信息

Biochemistry. 1992 Dec 15;31(49):12469-76. doi: 10.1021/bi00164a025.

Abstract

The human prothrombin gene is expressed predominantly in hepatocytes. Previous work indicated that this tissue specificity is transcriptionally regulated. In order to identify the cis-acting regulatory elements in the 5' flanking region of the human prothrombin gene which may direct the expression of prothrombin in hepatocytes, a series of hybrid plasmids were constructed linking portions of the 5' flanking region of the human prothrombin gene to the bacterial chloramphenicol acetyltransferase gene. Expression of these hybrid plasmids was examined in calcium phosphate-mediated transient transfections of HepG2 cells, a human hepatoblastoma cell line which expresses prothrombin, and HeLa cells, an adenocarcinoma cell line which does not express detectable amounts of prothrombin. Both the prothrombin promoter and an upstream regulatory region containing sequence homologous to the hepatocyte nuclear factor 1 (HNF-1) binding site (nucleotides -919 to -790 relative to the prothrombin transcription initiation site) were required for expression in HepG2 cells. The upstream region also exhibited non-tissue-specific enhancer activity. Gel mobility shift assays confirmed cell-type-specific differences in the protein-DNA interactions between proteins in HepG2 or HeLa nuclear extracts and either the promoter region or the upstream regulatory region of the gene.

摘要

人凝血酶原基因主要在肝细胞中表达。先前的研究表明,这种组织特异性是由转录调控的。为了确定人凝血酶原基因5'侧翼区域中可能指导凝血酶原在肝细胞中表达的顺式作用调控元件,构建了一系列杂交质粒,将人凝血酶原基因5'侧翼区域的部分片段与细菌氯霉素乙酰转移酶基因连接起来。在人肝癌细胞系HepG2细胞(一种表达凝血酶原的细胞系)和HeLa细胞(一种不表达可检测量凝血酶原的腺癌细胞系)的磷酸钙介导的瞬时转染中检测了这些杂交质粒的表达。凝血酶原启动子和一个上游调控区域(该区域含有与肝细胞核因子1(HNF-1)结合位点同源的序列,相对于凝血酶原转录起始位点为核苷酸-919至-790)对于在HepG2细胞中的表达都是必需的。上游区域还表现出非组织特异性的增强子活性。凝胶迁移率变动分析证实了HepG2或HeLa细胞核提取物中的蛋白质与该基因的启动子区域或上游调控区域之间在蛋白质-DNA相互作用方面存在细胞类型特异性差异。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验