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Extensive promoter-centered chromatin interactions provide a topological basis for transcription regulation
Li G.9; Ruan X.9; Auerbach R.K.6; Sandhu K.S.9; Zheng M.9; Wang P.9; Poh H.M.9; Goh Y.9; Lim J.9; Zhang J.9; Sim H.S.9; Peh S.Q.9; Mulawadi F.H.9; Ong C.T.9; Orlov Y.L.9; Hong S.9; Zhang Z.4; Landt S.2; Raha D.2; Euskirchen G.2; Wei C.-L.9; Ge W.7; Wang H.1; Davis C.1; Fisher-Aylor K.I.5; Mortazavi A.5; Gerstein M.6; Gingeras T.1; Wold B.5; Sun Y.7; Fullwood M.J.9; Cheung E.9; Liu E.9; Sung W.-K.9; Snyder M.2; Ruan Y.9
2012-01-20
Source PublicationCell
ISSN00928674 10974172
Volume148Issue:1-2Pages:84-98
Abstract

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 intragenic, extragenic, and intergenic 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 noncoding elements were found to be spatially engaged with corresponding genes through long-range interactions. Overall, our study provides insights into transcription regulation by three-dimensional chromatin interactions for both housekeeping and cell-specific genes in human cells. © 2012 Elsevier Inc.

DOI10.1016/j.cell.2011.12.014
URLView the original
Indexed BySCIE
WOS Research AreaBiochemistry & Molecular Biology ; Cell Biology
WOS SubjectBiochemistry & Molecular Biology ; Cell Biology
WOS IDWOS:000299540700016
Scopus ID2-s2.0-84862908850
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Document TypeJournal article
CollectionFaculty of Health Sciences
Affiliation1.Cold Spring Harbor Laboratory
2.Stanford University
3.Nanyang Technological University
4.National University of Singapore
5.California Institute of Technology
6.Yale University
7.University of California, Los Angeles
8.Huazhong Agricultural University
9.A-Star, Genome Institute of Singapore
Recommended Citation
GB/T 7714
Li G.,Ruan X.,Auerbach R.K.,et al. Extensive promoter-centered chromatin interactions provide a topological basis for transcription regulation[J]. Cell, 2012, 148(1-2), 84-98.
APA Li G.., Ruan X.., Auerbach R.K.., Sandhu K.S.., Zheng M.., Wang P.., Poh H.M.., Goh Y.., Lim J.., Zhang J.., Sim H.S.., Peh S.Q.., Mulawadi F.H.., Ong C.T.., Orlov Y.L.., Hong S.., Zhang Z.., Landt S.., Raha D.., ...& Ruan Y. (2012). Extensive promoter-centered chromatin interactions provide a topological basis for transcription regulation. Cell, 148(1-2), 84-98.
MLA Li G.,et al."Extensive promoter-centered chromatin interactions provide a topological basis for transcription regulation".Cell 148.1-2(2012):84-98.
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