Promoter analysis of the human translation termination factor 1 gene

被引:8
作者
Dubourg, C [1 ]
Toutain, B [1 ]
Le Gall, JY [1 ]
Le Treut, A [1 ]
Guenet, L [1 ]
机构
[1] Fac Med, UMR 6061, Dept Biochim & Biol Mol, F-35043 Rennes, France
关键词
transcription regulation; TATA-less; Sp1/Sp3; gene expression;
D O I
10.1016/S0378-1119(03)00742-X
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The human translation termination factor 1 (ETF1) gene encodes a class-1 release factor, eRF1, which catalyses termination of protein synthesis at all three stop codons. In this report, we describe the functional organization of the 5'-region of the gene. Primer extension and ribonuclease protection mapping revealed three transcription start sites clustered within similar to 10 bp. DNase I-hypersensitive site analysis identified five hypersensitive sites, one of which was located downstream of the initiation start sites. We used transient expression assays to define the 5'-regulating regions and in vivo and in vitro footprinting analysis to identify potential cis-acting regulatory elements. A basal promoter, spanning nucleotides -210/+117, contained no TATA box but a putative initiator element (Inr) and multiple potential Sp1/Sp3 binding sites, and thus displayed some of the features of a housekeeping gene. An additional upstream promoter containing positive and negative regulatory elements also regulated ETF1 gene expression. Real-time quantitative RT-PCR analysis showed tissue-specific expression of ETF1 transcripts in mouse tissues. Our results are suggestive of a constitutive expression of the human ETF1 gene but with possible cell- and tissue-specific regulation. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:91 / 101
页数:11
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