کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2035492 1072178 2014 16 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Enhancer Activation Requires trans-Recruitment of a Mega Transcription Factor Complex
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیوشیمی، ژنتیک و زیست شناسی مولکولی (عمومی)
پیش نمایش صفحه اول مقاله
Enhancer Activation Requires trans-Recruitment of a Mega Transcription Factor Complex
چکیده انگلیسی


• ERα-regulated enhancers exhibit trans-recruitment of a DNA-binding factor complex
• These DNA-binding transcription factors are assembled in a 1–2 MDa complex by ERα
• The MegaTrans complex recruits specific, required enzymatic machinery to enhancers
• The MegaTrans complex serves as a functional signature of most regulated enhancers

SummaryEnhancers provide critical information directing cell-type-specific transcriptional programs, regulated by binding of signal-dependent transcription factors and their associated cofactors. Here, we report that the most strongly activated estrogen (E2)-responsive enhancers are characterized by trans-recruitment and in situ assembly of a large 1–2 MDa complex of diverse DNA-binding transcription factors by ERα at ERE-containing enhancers. We refer to enhancers recruiting these factors as mega transcription factor-bound in trans (MegaTrans) enhancers. The MegaTrans complex is a signature of the most potent functional enhancers and is required for activation of enhancer RNA transcription and recruitment of coactivators, including p300 and Med1. The MegaTrans complex functions, in part, by recruiting specific enzymatic machinery, exemplified by DNA-dependent protein kinase. Thus, MegaTrans-containing enhancers represent a cohort of functional enhancers that mediate a broad and important transcriptional program and provide a molecular explanation for transcription factor clustering and hotspots noted in the genome.

Graphical AbstractFigure optionsDownload high-quality image (154 K)Download as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: - Volume 159, Issue 2, 9 October 2014, Pages 358–373
نویسندگان
, , , , , , , , , , , ,