The transcriptional activity of a muscle-specific promoter depends critically on the structure of the TATA element and its binding protein

被引:17
作者
Diagana, TT [1 ]
North, DL [1 ]
Jabet, C [1 ]
Fiszman, MY [1 ]
Takeda, S [1 ]
Whalen, RG [1 ]
机构
[1] INST PASTEUR,DEPT MOL BIOL,UNITE BIOCHEM,F-75724 PARIS 15,FRANCE
关键词
TATA-binding protein; TATA box; muscle-specific transcription; myosin heavy chain;
D O I
10.1006/jmbi.1996.0752
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have previously characterized the proximal promoter of the mouse IIB myosin heavy chain (MyHC) gene, which is expressed only in fast-contracting glycolytic skeletal muscle fibers. We show here that the substitution into this promoter of a non-canonical TATA sequence from the IgH gene results in inactivity in muscle cells, even though TATA-binding protein (TBP) can bind strongly to this mutated promoter. Chemical footprinting data show, however, that TBP makes different DNA contacts on this heterologous TATA sequence. The inactivity of such a non-canonical TATA motif in the IIB promoter context appears to be caused by a nonfunctional conformation of the bound TBP-DNA complex that is incapable of sustaining transcription. The conclusions imply that the precise sequence of the promoter TATA motif needs to be matched with the specific functional class of upstream activator proteins present in a given cell type in order for the gene to be transcriptionally active. (C) 1997 Academic Press Limited.
引用
收藏
页码:480 / 493
页数:14
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