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STATs Shape the Active Enhancer Landscape of T Cell Populations
Author(s) -
Golnaz Vahedi,
Hayato Takahashi,
Shingo Nakayamada,
HongWei Sun,
Vittorio Sartorelli,
Yuka Kanno,
John J. O’Shea
Publication year - 2012
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2012.09.044
Subject(s) - enhancer , biology , chromatin , microbiology and biotechnology , enhancer rnas , transcriptome , regulation of gene expression , cell type , cellular differentiation , gene expression , signal transduction , gene , cell , computational biology , genetics
Signaling pathways are intimately involved in cellular differentiation, allowing cells to respond to their environment by regulating gene expression. Although enhancers are recognized as key elements that regulate selective gene expression, the interplay between signaling pathways and actively used enhancer elements is not clear. Here, we use CD4(+) T cells as a model of differentiation, mapping the activity of cell-type-specific enhancer elements in T helper 1 (Th1) and Th2 cells. Our data establish that STAT proteins have a major impact on the activation of lineage-specific enhancers and the suppression of enhancers associated with alternative cell fates. Transcriptome analysis further supports a functional role for enhancers regulated by STATs. Importantly, expression of lineage-defining master regulators in STAT-deficient cells fails to fully recover the chromatin signature of STAT-dependent enhancers. Thus, these findings point to a critical role of STATs as environmental sensors in dynamically molding the specialized enhancer architecture of differentiating cells.

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