The three-dimensional folding of the α-globin gene domain reveals formation of chromatin globules

被引:210
|
作者
Bau, Davide [2 ]
Sanyal, Amartya [1 ]
Lajoie, Bryan R. [1 ]
Capriotti, Emidio [2 ]
Byron, Meg [3 ]
Lawrence, Jeanne B. [3 ]
Dekker, Job [1 ]
Marti-Renom, Marc A. [2 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Biochem & Mol Pharmacol, Program Gene Funct & Express, Worcester, MA 01605 USA
[2] Ctr Invest Principe Felipe, Bioinformat & Genom Dept, Struct Genom Unit, Valencia, Spain
[3] Univ Massachusetts, Sch Med, Dept Cell Biol, Worcester, MA 01655 USA
基金
美国国家卫生研究院;
关键词
CHROMOSOME CONFORMATION CAPTURE; TRANSCRIPTION FACTORIES; INTERPHASE CHROMOSOMES; NUCLEAR-ORGANIZATION; HYPERSENSITIVE SITES; GENOME; EXPRESSION; PROMOTER; ELEMENTS; MODEL;
D O I
10.1038/nsmb.1936
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
We developed a general approach that combines chromosome conformation capture carbon copy (5C) with the Integrated Modeling Platform (IMP) to generate high-resolution three-dimensional models of chromatin at the megabase scale. We applied this approach to the ENm008 domain on human chromosome 16, containing the alpha-globin locus, which is expressed in K562 cells and silenced in lymphoblastoid cells (GM12878). The models accurately reproduce the known looping interactions between the alpha-globin genes and their distal regulatory elements. Further, we find using our approach that the domain folds into a single globular conformation in GM12878 cells, whereas two globules are formed in K562 cells. The central cores of these globules are enriched for transcribed genes, whereas nontranscribed chromatin is more peripheral. We propose that globule formation represents a higher-order folding state related to clustering of transcribed genes around shared transcription machineries, as previously observed by microscopy.
引用
收藏
页码:107 / +
页数:9
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