Beyond the Nucleosome: Nucleosome-Protein Interactions and Higher Order Chromatin Structure

被引:15
|
作者
Lobbia, Vincenzo R. [1 ]
Sanchez, Maria Cristina Trueba [1 ]
van Ingen, Hugo [1 ]
机构
[1] Univ Utrecht, Bijvoet Ctr Biomol Res, NMR Spect, Padualaan 8, NL-3584 CH Utrecht, Netherlands
关键词
Linker histone; HP1; Phase separation; Nucleosomal arrays; Oligonucleosomes; PHASE-SEPARATION; CRYOELECTRON MICROSCOPY; LINKER HISTONES; CRYO-EM; HETEROCHROMATIN; HP1; DOMAIN; MECHANISMS; DYNAMICS; BINDING;
D O I
10.1016/j.jmb.2021.166827
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 regulation of chromatin biology ultimately depends on the manipulation of its smallest subunit, the nucleosome. The proteins that bind and operate on the nucleosome do so, while their substrate is part of a polymer embedded in the dense nuclear environment. Their molecular interactions must in some way be tuned to deal with this complexity. Due to the rapid increase in the number of high-resolution structures of nucleosome-protein complexes and the increasing understanding of the cellular chromatin structure, it is starting to become clearer how chromatin factors operate in this complex environment. In this review, we analyze the current literature on the interplay between nucleosome-protein interactions and higher-order chromatin structure. We examine in what way nucleosomes-protein interactions can affect and can be affected by chromatin organization at the oligonucleosomal level. In addition, we review the characteristics of nucleosome-protein interactions that can cause phase separation of chromatin. Throughout, we hope to illustrate the exciting challenges in characterizing nucleosome-protein interactions beyond the nucleosome. (C) 2021 The Author(s). Published by Elsevier Ltd.
引用
收藏
页数:18
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