Managing the Steady State Chromatin Landscape by Nucleosome Dynamics

被引:15
作者
Ahmad, Kami [1 ]
Henikoff, Steven [1 ,2 ]
Ramachandran, Srinivas [3 ,4 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Basic Sci Div, 1124 Columbia St, Seattle, WA 98104 USA
[2] Fred Hutchinson Canc Res Ctr, Howard Hughes Med Inst, 1124 Columbia St, Seattle, WA 98104 USA
[3] Univ Colorado, Sch Med, Dept Biochem & Mol Genet, Aurora, CO USA
[4] Univ Colorado, Sch Med, RNA Biosci Initiat, Aurora, CO USA
基金
美国国家卫生研究院;
关键词
TRANSCRIPTION FACTORS; COOPERATIVE BINDING; REPLICATION; DNA; PRINCIPLES; GENOME; H3.3; DETERMINANTS; CONSTRAINTS; MECHANISMS;
D O I
10.1146/annurev-biochem-032620-104508
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
Gene regulation arises out of dynamic competition between nucleosomes, transcription factors, and other chromatin proteins for the opportunity to bind genomic DNA. The timescales of nucleosome assembly and binding of factors to DNA determine the outcomes of this competition at any given locus. Here, we review how these properties of chromatin proteins and the interplay between the dynamics of different factors are critical for gene regulation. We discuss how molecular structures of large chromatin-associated complexes, kinetic measurements, and high resolution mapping of protein-DNA complexes in vivo set the boundary conditions for chromatin dynamics, leading to models of how the steady state behaviors of regulatory elements arise.
引用
收藏
页码:183 / 195
页数:13
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