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人胰岛素受体基因启动子区域的序列与分析

Sequence and analysis of promoter region of human insulin-receptor gene.

作者信息

Mamula P W, Wong K Y, Maddux B A, McDonald A R, Goldfine I D

机构信息

Department of Medicine, Mount Zion Hospital and Medical Center, San Francisco, CA 94120.

出版信息

Diabetes. 1988 Sep;37(9):1241-6. doi: 10.2337/diab.37.9.1241.

Abstract

The promoter region of the human insulin-receptor (HINSR) gene was isolated from a human chromosome 19 bacteriophage library. With S1 nuclease mapping and primer-extension analysis, we identified multiple transcription-initiation sites. Dexamethasone, a known inducer of HINSR transcription, enhanced transcription of all major transcription-initiation sites. DNA sequence analysis indicated that the HINSR promoter has neither a TATA box nor a CAAT box. The HINSR promoter region contains six GGGCGG sequences that may be binding sites for the transcription factor Sp1. In addition, there were three TCCC sequences that were putative promoter regulatory regions. The HINSR gene promoter has structural similarity to the epidermal growth factor receptor gene promoter and has some features of the promoter of the meglutol (hydroxymethylglutaryl, HMG) CoA reductase gene and the early promoter of simian virus 40.

摘要

从人19号染色体噬菌体文库中分离出人类胰岛素受体(HINSR)基因的启动子区域。通过S1核酸酶图谱分析和引物延伸分析,我们确定了多个转录起始位点。地塞米松是已知的HINSR转录诱导剂,可增强所有主要转录起始位点的转录。DNA序列分析表明,HINSR启动子既没有TATA盒也没有CAAT盒。HINSR启动子区域包含六个GGGCGG序列,它们可能是转录因子Sp1的结合位点。此外,还有三个TCCC序列,它们是假定的启动子调控区域。HINSR基因启动子与表皮生长因子受体基因启动子具有结构相似性,并且具有甲戊二酰辅酶A(HMG)还原酶基因启动子和猿猴病毒40早期启动子的一些特征。

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