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大鼠cMG1/TIS11b基因5'-侧翼区域功能性启动子元件的鉴定。

Identification of a functional promoter element in the 5'-flanking region of the rat cMG1/TIS11b gene.

作者信息

Corps A N, Pascall J C, Hadfield K M, Brown K D

机构信息

Department of Cellular Physiology, Babraham Institute, Cambridge, U.K.

出版信息

Biochem J. 1995 Oct 1;311 ( Pt 1)(Pt 1):251-8. doi: 10.1042/bj3110251.

Abstract

The cMG1 gene was originally identified as a mitogen-stimulated primary response gene. However, in contrast to genes such as c-fos and TIS11, cMG1 is also expressed at significant levels before and after the transient elevation induced by agonists. We have sequenced a 1.3 kb rat genomic cMG1 clone, which includes 931 bp upstream of the transcription start site identified by primer-extension analysis. A 1033 bp fragment, including this 5'-flanking sequence, directed the expression of the reporter gene chloramphenicol acetyltransferase (CAT) in transfected NIH-3T3 cells. Progressive 5'-to-3' deletion indicated that an element located between -138 and -114 was responsible for most of this basal CAT expression. DNA mobility-shift assays showed that the sequence between -143 and -105 contained binding sites for cellular proteins, the principal complexes involving nucleotides between -119 and -105. We conclude that these complexes may represent the transcription factor-DNA element interactions that determine basal cMG1 expression.

摘要

cMG1基因最初被鉴定为一种有丝分裂原刺激的初级反应基因。然而,与c-fos和TIS11等基因不同的是,cMG1在激动剂诱导的短暂升高之前和之后也有显著水平的表达。我们对一个1.3 kb的大鼠基因组cMG1克隆进行了测序,该克隆包括通过引物延伸分析确定的转录起始位点上游931 bp。一个1033 bp的片段,包括这个5'侧翼序列,在转染的NIH-3T3细胞中指导报告基因氯霉素乙酰转移酶(CAT)的表达。5'到3'的逐步缺失表明,位于-138和-114之间的一个元件负责大部分这种基础CAT表达。DNA迁移率变动分析表明,-143和-105之间的序列包含细胞蛋白的结合位点,主要复合物涉及-119和-105之间的核苷酸。我们得出结论,这些复合物可能代表决定基础cMG1表达的转录因子-DNA元件相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/884e/1136146/25c0810028ff/biochemj00054-0247-a.jpg

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