Precise nucleosome positioning and the TATA box dictate requirements for the histone H4 tail and the bromodomain factor Bdf1

被引:51
作者
Martinez-Campa, C
Politis, P
Moreau, JL
Kent, N
Goodall, J
Mellor, J
Goding, CR [1 ]
机构
[1] Marie Curie Res Inst, Signalling & Dev Lab, Surrey RH8 0TL, England
[2] Univ Oxford, Dept Biochem, Oxford OX1 3QU, England
[3] Edificio Santiaqgo Gascon, Dept Bioquim, Lab 3 3, Asturias 33007, Spain
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
D O I
10.1016/j.molcel.2004.05.022
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
Acetylation of histone tails plays a key role in chromatin dynamics and is associated with the potential for gene expression. We show here that a 2-3 bp mispositioning of the nucleosome covering the TATA box at PHO5 induces a dependency on the acetylatable lysine residues of the histone H4 N-terminal region and on the TFIID-associated bromodomain factor Bdf1. This dependency arises either through fusion of the PHO5 promoter to a lacZ reporter or by mutation of the TATA box in the natural gene. The results suggest that promoters in which the TATA box is either absent or poorly accessible on the surface of a nucleosome may compensate by using Bdf1 bromodomains and acetylated H4 tails to anchor TFIID to the promoter during the initial stages of transcription activation. We propose that nucleosome positioning at the nucleotide level provides a subtle, but highly effective, mechanism for gene regulation.
引用
收藏
页码:69 / 81
页数:13
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