Binding of the winged-helix transcription factor HNF3 to a linker histone site on the nucleosome

被引:307
作者
Cirillo, LA
McPherson, CE
Bossard, P
Stevens, K
Cherian, S
Shim, EY
Clark, KL
Burley, SK
Zaret, KS
机构
[1] Brown Univ, Dept Mol Biol Cell Biol & Biochem, Providence, RI 02912 USA
[2] Rockefeller Univ, Lab Mol Biophys, New York, NY 10021 USA
[3] Howard Hughes Med Inst, New York, NY 10021 USA
关键词
chromatin; HNF3; linker histone; nucleosome; transcription factor;
D O I
10.1093/emboj/17.1.244
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 transcription factor HNF3 and linker histones H1 and H5 possess winged-helix DNA-binding domains, yet HNF3 and other fork head-related proteins activate genes during development whereas linker histones compact DNA in chromatin and repress gene expression, We compared how the two classes of factors interact with chromatin templates and found that HNF3 binds DNA at the side of nucleosome cores, similarly to what has been reported for linker histone, A nucleosome structural binding site for HNF3 is occupied at the albumin transcriptional enhancer in active and potentially active chromatin, but not in inactive chromatin in vivo, while wild-type HNF3 protein does not compact DNA extending from the nucleosome, as does linker histone, site-directed mutants of HNF3 can compact nucleosomal DNA if they contain basic amino acids at positions previously shown to be essential for nucleosomal DNA compaction by linker histones, The results illustrate how transcription factors can possess special nucleosome-binding activities that are not predicted from studies of factor interactions with free DNA.
引用
收藏
页码:244 / 254
页数:11
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