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.
Original language | English (US) |
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Pages (from-to) | 647-661 |
Number of pages | 15 |
Journal | Molecular cell |
Volume | 63 |
Issue number | 4 |
DOIs | |
State | Published - Aug 18 2016 |
Externally published | Yes |
Keywords
- Cdx1
- Hoxb1
- Oct4
- RAR:RXR
- Wnt/β-catenin
- embryonic stem cell
- retinoic acid
ASJC Scopus subject areas
- Molecular Biology
- Cell Biology