Extensive promoter-centered chromatin interactions provide a topological basis for transcription regulation.
Extensive promoter-centered chromatin interactions provide a topological basis for transcription regulation.
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DOI:
10.1016/j.cell.2011.12.014
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发表时间:
2012-01-20
期刊:
影响因子:
64.5
通讯作者:
Ruan Y
中科院分区:
文献类型:
--
作者:
Li G;Ruan X;Auerbach RK;Sandhu KS;Zheng M;Wang P;Poh HM;Goh Y;Lim J;Zhang J;Sim HS;Peh SQ;Mulawadi FH;Ong CT;Orlov YL;Hong S;Zhang Z;Landt S;Raha D;Euskirchen G;Wei CL;Ge W;Wang H;Davis C;Fisher-Aylor KI;Mortazavi A;Gerstein M;Gingeras T;Wold B;Sun Y;Fullwood MJ;Cheung E;Liu E;Sung WK;Snyder M;Ruan Y
Higher-order chromosomal organization for transcription regulation is poorly understood in eukaryotes. Using genome-wide Chromatin Interaction Analysis with Paired-End-Tag sequencing (ChIA-PET), we mapped long-range chromatin interactions associated with RNA polymerase II in human cells and uncovered widespread promoter-centered intra-genic, extra-genic and inter-genic interactions. These interactions further aggregated into higher-order clusters, wherein proximal and distal genes were engaged through promoter-promoter interactions. Most genes with promoter-promoter interactions were active and transcribed cooperatively, and some interacting promoters could influence each other implying combinatorial complexity of transcriptional controls. Comparative analyses of different cell lines showed that cell-specific chromatin interactions could provide structural frameworks for cell-specific transcription, and suggested significant enrichment of enhancer-promoter interactions for cell-specific functions. Furthermore, genetically-identified disease-associated non-coding elements were found to be spatially engaged with corresponding genes through long-range interactions. Overall, our study provides insights into the transcription regulation by three-dimensional chromatin interactions for both housekeeping and cell-specific genes in human cells.
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影响因子:
12.3
作者:
Li G;Fullwood MJ;Xu H;Mulawadi FH;Velkov S;Vega V;Ariyaratne PN;Mohamed YB;Ooi HS;Tennakoon C;Wei CL;Ruan Y;Sung WK
通讯作者:
Sung WK
影响因子:
64.8
作者:
Heintzman, Nathaniel D.;Hon, Gary C.;Hawkins, R. David;Kheradpour, Pouya;Stark, Alexander;Harp, Lindsey F.;Ye, Zhen;Lee, Leonard K.;Stuart, Rhona K.;Ching, Christina W.;Ching, Keith A.;Antosiewicz-Bourget, Jessica E.;Liu, Hui;Zhang, Xinmin;Green, Roland D.;Lobanenkov, Victor V.;Stewart, Ron;Thomson, James A.;Crawford, Gregory E.;Kellis, Manolis;Ren, Bing
通讯作者:
Ren, Bing
影响因子:
16.8
作者:
通讯作者:
--
影响因子:
12.3
作者:
Cope NF;Fraser P;Eskiw CH
通讯作者:
Eskiw CH
影响因子:
64.5
作者:
Hah N;Danko CG;Core L;Waterfall JJ;Siepel A;Lis JT;Kraus WL
通讯作者:
Kraus WL