Restraint-based three-dimensional modeling of genomes and genomic domains

被引:67
作者
Serra, Francois [1 ,2 ]
Di Stefano, Marco [1 ,2 ]
Spill, Yannick G. [1 ,2 ]
Cuartero, Yasmina [1 ,2 ]
Goodstadt, Michael [1 ,2 ]
Bau, Davide [1 ,2 ]
Marti-Renom, Marc A. [1 ,2 ,3 ]
机构
[1] CNAG, Genome Biol Grp, Barcelona, Spain
[2] Ctr Genom Regulat CRG, Gene Regulat Stem Cells & Canc Program, Barcelona, Spain
[3] ICREA, Barcelona, Spain
基金
欧洲研究理事会;
关键词
Genome architecture; 3D genome reconstruction; Chromosome Conformation Capture; Restraint-based modeling; CHROMOSOME CONFORMATION CAPTURE; 30-NM CHROMATIN FIBERS; HI-C DATA; HIGH-RESOLUTION; PROTEIN CONFORMATIONS; TOPOLOGICAL DOMAINS; GENE-EXPRESSION; BUDDING YEAST; DOUBLE HELIX; REVEALS;
D O I
10.1016/j.febslet.2015.05.012
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
Chromosomes are large polymer molecules composed of nucleotides. In some species, such as humans, this polymer can sum up to meters long and still be properly folded within the nuclear space of few microns in size. The exact mechanisms of how the meters long DNA is folded into the nucleus, as well as how the regulatory machinery can access it, is to a large extend still a mystery. However, and thanks to newly developed molecular, genomic and computational approaches based on the Chromosome Conformation Capture (3C) technology, we are now obtaining insight on how genomes are spatially organized. Here we review a new family of computational approaches that aim at using 3C-based data to obtain spatial restraints for modeling genomes and genomic domains. (C) 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2987 / 2995
页数:9
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