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Ligand-dependent dynamics of retinoic acid receptor binding during early neurogenesis

Author(s)
Mahony, Shaun; Mazzoni, Esteban O.; McCuine, Scott; Young, Richard A.; Wichterle, Hynek; Gifford, David K.; ... Show more Show less
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Abstract
Abstract Background Among its many roles in development, retinoic acid determines the anterior-posterior identity of differentiating motor neurons by activating retinoic acid receptor (RAR)-mediated transcription. RAR is thought to bind the genome constitutively, and only induce transcription in the presence of the retinoid ligand. However, little is known about where RAR binds to the genome or how it selects target sites. Results We tested the constitutive RAR binding model using the retinoic acid-driven differentiation of mouse embryonic stem cells into differentiated motor neurons. We find that retinoic acid treatment results in widespread changes in RAR genomic binding, including novel binding to genes directly responsible for anterior-posterior specification, as well as the subsequent recruitment of the basal polymerase machinery. Finally, we discovered that the binding of transcription factors at the embryonic stem cell stage can accurately predict where in the genome RAR binds after initial differentiation. Conclusions We have characterized a ligand-dependent shift in RAR genomic occupancy at the initiation of neurogenesis. Our data also suggest that enhancers active in pluripotent embryonic stem cells may be preselecting regions that will be activated by RAR during neuronal differentiation.
Date issued
2011-01
URI
http://hdl.handle.net/1721.1/65633
Department
Massachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory; Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science
Journal
Genome Biology
Publisher
BioMed Central Ltd.
Citation
Mahony, Shaun et al. “Ligand-dependent dynamics of retinoic acid receptor binding during early neurogenesis.” Genome Biology 12 (2011): R2.
Version: Final published version
ISSN
1474-7596
1474-760X

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