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TEAD and YAP regulate the enhancer network of human embryonic pancreatic progenitors

The genomic regulatory programs that underlie human organogenesis are poorly understood. Pancreas development, in particular, has pivotal implications for pancreatic regeneration, cancer, and diabetes. We have now characterized the regulatory landscape of embryonic multipotent progenitor cells that...

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Detalles Bibliográficos
Autores principales: Cebola, Inês, Rodríguez-Seguí, Santiago A., Cho, Candy H.-H., Bessa, José, Rovira, Meritxell, Luengo, Mario, Chhatriwala, Mariya, Berry, Andrew, Ponsa-Cobas, Joan, Maestro, Miguel Angel, Jennings, Rachel E., Pasquali, Lorenzo, Morán, Ignasi, Castro, Natalia, Hanley, Neil A., Gomez-Skarmeta, Jose Luis, Vallier, Ludovic, Ferrer, Jorge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4434585/
https://www.ncbi.nlm.nih.gov/pubmed/25915126
http://dx.doi.org/10.1038/ncb3160
Descripción
Sumario:The genomic regulatory programs that underlie human organogenesis are poorly understood. Pancreas development, in particular, has pivotal implications for pancreatic regeneration, cancer, and diabetes. We have now characterized the regulatory landscape of embryonic multipotent progenitor cells that give rise to all pancreatic epithelial lineages. Using human embryonic pancreas and embryonic stem cell-derived progenitors we identify stage-specific transcripts and associated enhancers, many of which are co-occupied by transcription factors that are essential for pancreas development. We further show that TEAD1, a Hippo signaling effector, is an integral component of the transcription factor combinatorial code of pancreatic progenitor enhancers. TEAD and its coactivator YAP activate key pancreatic signaling mediators and transcription factors, and regulate the expansion of pancreatic progenitors. This work therefore uncovers a central role of TEAD and YAP as signal-responsive regulators of multipotent pancreatic progenitors, and provides a resource for the study of embryonic development of the human pancreas.