| Literature DB >> 29272704 |
Thomas Vierbuchen1, Emi Ling2, Christopher J Cowley2, Cameron H Couch2, Xiaofeng Wang3, David A Harmin2, Charles W M Roberts4, Michael E Greenberg2.
Abstract
Enhancer elements are genomic regulatory sequences that direct the selective expression of genes so that genetically identical cells can differentiate and acquire the highly specialized forms and functions required to build a functioning animal. To differentiate, cells must select from among the ∼106 enhancers encoded in the genome the thousands of enhancers that drive the gene programs that impart their distinct features. We used a genetic approach to identify transcription factors (TFs) required for enhancer selection in fibroblasts. This revealed that the broadly expressed, growth-factor-inducible TFs FOS/JUN (AP-1) play a central role in enhancer selection. FOS/JUN selects enhancers together with cell-type-specific TFs by collaboratively binding to nucleosomal enhancers and recruiting the SWI/SNF (BAF) chromatin remodeling complex to establish accessible chromatin. These experiments demonstrate how environmental signals acting via FOS/JUN and BAF coordinate with cell-type-specific TFs to select enhancer repertoires that enable differentiation during development.Entities:
Keywords: Ras/MAPK signaling; chromatin remodeling complexes; enhancers; genetics; genomics; growth factor signaling; lineage specification; mSWI/SNF (BAF) complexes; transcription factors; transcriptional regulation
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Year: 2017 PMID: 29272704 PMCID: PMC5744881 DOI: 10.1016/j.molcel.2017.11.026
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970