Nucleosome-level 3D organization of the genome

被引:12
|
作者
Ohno, Masae [1 ]
Priest, David G. [1 ]
Taniguchi, Yuichi [1 ,2 ]
机构
[1] RIKEN, Quantitat Biol Ctr, Lab Single Cell Gene Dynam, 6-2-3 Furuedai, Suita, Osaka 5650874, Japan
[2] Japan Sci & Technol Agcy, PRESTO, 4-1-8 Honcho, Kawaguchi, Saitama 3320012, Japan
基金
日本科学技术振兴机构; 日本学术振兴会;
关键词
HIGHER-ORDER STRUCTURE; 30-NM CHROMATIN FIBERS; H3 TAIL DOMAIN; IN-VIVO; LINKER HISTONES; REPEATING UNIT; CHROMOSOME CONFORMATION; ANGSTROM RESOLUTION; H4-K16; ACETYLATION; SELF-ASSOCIATION;
D O I
10.1042/BST20170388
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
Nucleosomes are the unitary structures of chromosome folding, and their arrangements are intimately coupled to the regulation of genome activities. Conventionally, structural analyses using electron microscopy and X-ray crystallography have been used to study such spatial nucleosome arrangements. In contrast, recent improvements in the resolution of sequencing-based methods allowed investigation of nucleosome arrangements separately at each genomic locus, enabling exploration of gene-dependent regulation mechanisms. Here, we review recent studies on nucleosome folding in chromosomes from these two methodological perspectives: conventional structural analyses and DNA sequencing, and discuss their implications for future research.
引用
收藏
页码:491 / 501
页数:11
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