Residential College | false |
Status | 已發表Published |
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 Publication | Cell |
ISSN | 00928674 10974172 |
Volume | 148Issue: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. |
DOI | 10.1016/j.cell.2011.12.014 |
URL | View the original |
Indexed By | SCIE |
WOS Research Area | Biochemistry & Molecular Biology ; Cell Biology |
WOS Subject | Biochemistry & Molecular Biology ; Cell Biology |
WOS ID | WOS:000299540700016 |
Scopus ID | 2-s2.0-84862908850 |
Fulltext Access | |
Citation statistics | |
Document Type | Journal article |
Collection | Faculty of Health Sciences |
Affiliation | 1.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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