GAGA factor and the TFIID complex collaborate in generating an open chromatin structure at the Drosophila melanogaster hsp26 promoter

被引:50
作者
Leibovitch, BA
Lu, Q
Benjamin, LR
Liu, YY
Gilmour, DS
Elgin, SCR
机构
[1] Washington Univ, Dept Biol, St Louis, MO 63130 USA
[2] Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
关键词
D O I
10.1128/MCB.22.17.6148-6157.2002
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
The upstream regulatory region of the Drosophila melanogaster hsp26 genie includes two DNase I-hypersensitive sites (DH sites) that encompass the critical beat shock elements. This chromatin structure is required for heat shock-inducible expression and depends on two (CT)(n) . (GA)(n) elements bound by GAGA factor. To determine whether GAGA factor alone is sufficient to drive formation of the DH sites, we have created flies with an hsp26/lacZ transgene wherein the entire DNA segment known to interact with the TFIID complex has been replaced by a random sequence. The replacement results in a loss of heat shock-inducible hsp26 expression and drastically diminishes nuclease accessibility in the chromatin of the regulatory region. Chromatin immunoprecipitation experiments show that the decrease in TFIID binding does not reduce GAGA factor binding. In contrast, the loss of GAGA factor binding resulting from (CT)(n) mutations decreases TFIID binding. These data suggest that both GAGA factor and TFIID are necessary for formation of the appropriate chromatin structure at the hsp26 promoter and predict a regulatory mechanism in which GAGA factor binding precedes and contributes to the recruitment of TFIID.
引用
收藏
页码:6148 / 6157
页数:10
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