Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

Dataset Information

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Genome-wide mapping of REST-bound sites in human CD4+ T cells


ABSTRACT: We performed ChIP-seq to identify genome-wide REST (NRSF) binding in the human CD4+ T cells. The data were compared to REST occupancy in additional 15 human cell types analyzed by the ENCODE project (GSE32465) in order to study the dynamics and context-dependent functions of REST-chromatin interaction. Identification of REST binding by ChIP-seq in human CD4+ T cells.

ORGANISM(S): Homo sapiens

SUBMITTER: Shira Rockowitz 

PROVIDER: E-GEOD-49570 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Comparison of REST cistromes across human cell types reveals common and context-specific functions.

Rockowitz Shira S   Lien Wen-Hui WH   Pedrosa Erika E   Wei Gang G   Lin Mingyan M   Zhao Keji K   Lachman Herbert M HM   Fuchs Elaine E   Zheng Deyou D  

PLoS computational biology 20140612 6


Recent studies have shown that the transcriptional functions of REST are much broader than repressing neuronal genes in non-neuronal systems. Whether REST occupies similar chromatin regions in different cell types and how it interacts with other transcriptional regulators to execute its functions in a context-dependent manner has not been adequately investigated. We have applied ChIP-seq analysis to identify the REST cistrome in human CD4+ T cells and compared it with published data from 15 othe  ...[more]

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