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Status |
Public on Jan 12, 2015 |
Title |
Retinoic acid induces Snai1 in stem cells of the preimplantation blastocyst to initiate differentiation |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
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Summary |
Although much is known about the pluripotency self-renewal circuitry, the molecular events that lead embryonic stem cells (ESCs) exit from pluripotency and begin differentiation are largely unknown. We found that the zinc finger transcription factor Snai1, involved in gastrulation and epithelial- mesenchymal transition (EMT) is already expressed in the inner cell mass of the preimplantation blastocysts. In ESCs Snai1 does not respond to TGFα or BMP4 signalling but it is induced by retinoic acid (RA) treatment, which induces the binding, on the Snai1 promoter, of the retinoid receptors RARγ and RXRα the dissociation of the Polycomb repressor compex 2 (PRC2) which results in the decrease of H3K27me3 and the increase of histone H3K4me3. Snai1 mediates the repression of pluripotency genes by binding directly to the promoters of Nanog, Nr5a2, Tcl1, c-Kit, and Tcfcp2l1. The transient activation of Snai1 in embryoid bodies induces the expression of the markers of all three germ layers. These results suggest that Snai1 is a key factor that triggers ESCs exit from the pluripotency state and initiate their differentiation processes.
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Overall design |
microarray analysis of embryonic stem cells (ESC) expressing Snail-ER at various time points of induction with 4-OHT
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Web link |
http://epigenetics.hugef-research.org/data/snail.php
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Contributor(s) |
Neri F, Oliviero S, Galvagni F |
Citation(s) |
25504116, 26484184 |
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Submission date |
May 21, 2014 |
Last update date |
Jan 16, 2019 |
Contact name |
Francesco Neri |
E-mail(s) |
francesco.neri@unito.it
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Organization name |
University of Torino
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Street address |
Via Nizza 52
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City |
Torino |
State/province |
Italy |
ZIP/Postal code |
10126 |
Country |
Italy |
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Platforms (1) |
GPL6887 |
Illumina MouseWG-6 v2.0 expression beadchip |
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Samples (6)
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Relations |
BioProject |
PRJNA248261 |