生物
CTCF公司
基因组
染色质
增强子
遗传学
倍性
染色体构象捕获
组蛋白
计算生物学
基因
发起人
基因表达
作者
Suhas S.P. Rao,Miriam H. Huntley,Neva C. Durand,Elena K. Stamenova,Ivan D. Bochkov,James T. Robinson,Adrian L. Sanborn,Ido Machol,Arina D. Omer,Eric S. Lander,Erez Lieberman Aiden
出处
期刊:Cell
[Elsevier]
日期:2014-12-18
卷期号:159 (7): 1665-1680
被引量:4760
标识
DOI:10.1016/j.cell.2014.11.021
摘要
We use in situ Hi-C to probe the 3D architecture of genomes, constructing haploid and diploid maps of nine cell types. The densest, in human lymphoblastoid cells, contains 4.9 billion contacts, achieving 1 kb resolution. We find that genomes are partitioned into contact domains (median length, 185 kb), which are associated with distinct patterns of histone marks and segregate into six subcompartments. We identify ∼10,000 loops. These loops frequently link promoters and enhancers, correlate with gene activation, and show conservation across cell types and species. Loop anchors typically occur at domain boundaries and bind CTCF. CTCF sites at loop anchors occur predominantly (>90%) in a convergent orientation, with the asymmetric motifs "facing" one another. The inactive X chromosome splits into two massive domains and contains large loops anchored at CTCF-binding repeats.
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