| Literature DB >> 27499297 |
Zoltan Simandi1, Attila Horvath2, Lyndsey C Wright3, Ixchelt Cuaranta-Monroy2, Isabella De Luca4, Katalin Karolyi4, Sascha Sauer5, Jean-Francois Deleuze6, Lorraine J Gudas7, Shaun M Cowley3, Laszlo Nagy8.
Abstract
Cell type specification relies on the capacity of undifferentiated cells to properly respond to specific differentiation-inducing signals. Using genomic approaches along with loss- and gain-of-function genetic models, we identified OCT4-dependent mechanisms that provide embryonic stem cells with the means to customize their response to external cues. OCT4 binds a large set of low-accessible genomic regions. At these sites, OCT4 is required for proper enhancer and gene activation by recruiting co-regulators and RAR:RXR or β-catenin, suggesting an unexpected collaboration between the lineage-determining transcription factor and these differentiation-initiating, signal-dependent transcription factors. As a proof of concept, we demonstrate that overexpression of OCT4 in a kidney cell line is sufficient for signal-dependent activation of otherwise unresponsive genes in these cells. Our results uncover OCT4 as an integral and necessary component of signal-regulated transcriptional processes required for tissue-specific responses.Entities:
Keywords: Cdx1; Hoxb1; Oct4; RAR:RXR; Wnt/β-catenin; embryonic stem cell; retinoic acid
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Year: 2016 PMID: 27499297 DOI: 10.1016/j.molcel.2016.06.039
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970