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Extensive Promoter-Centered Chromatin Interactions Provide a Topological Basis for Transcription Regulation

  作者 Li, GL; Ruan, XA; Auerbach, RK; Sandhu, KS; Zheng, MZ; Wang, P; Poh, HM; Goh, Y; Lim, J; Zhang, JY; Sim, HS; Peh, SQ; Mulawadi, FH; Ong, CT; Orlov, YL; Hong, SZ; Zhang, ZZ; Landt, S; Raha, D; Euskirchen, G; Wei, CL; Ge, WH; Wang, HE; 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, YJ  
  选自 期刊  Cell;  卷期  2012年148-1-2;  页码  84-98  
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[摘要]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.

 
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