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Nat Commun ; 12(1): 5136, 2021 08 26.
Artículo en Inglés | MEDLINE | ID: mdl-34446717

RESUMEN

One fundamental yet unresolved question in biology remains how cells interpret the same signalling cues in a context-dependent manner resulting in lineage specification. A key step for decoding signalling cues is the establishment of a permissive chromatin environment at lineage-specific genes triggering transcriptional responses to inductive signals. For instance, bipotent neuromesodermal progenitors (NMPs) are equipped with a WNT-decoding module, which relies on TCFs/LEF activity to sustain both NMP expansion and paraxial mesoderm differentiation. However, how WNT signalling activates lineage specific genes in a temporal manner remains unclear. Here, we demonstrate that paraxial mesoderm induction relies on the TALE/HOX combinatorial activity that simultaneously represses NMP genes and activates the differentiation program. We identify the BRACHYURY-TALE/HOX code that destabilizes the nucleosomes at WNT-responsive regions and establishes the permissive chromatin landscape for de novo recruitment of the WNT-effector LEF1, unlocking the WNT-mediated transcriptional program that drives NMPs towards the paraxial mesodermal fate.


Asunto(s)
Proteínas Fetales/metabolismo , Mesodermo/metabolismo , Familia de Multigenes , Células-Madre Neurales/metabolismo , Proteínas de Dominio T Box/metabolismo , Vía de Señalización Wnt , Animales , Diferenciación Celular , Linaje de la Célula , Proteínas Fetales/genética , Regulación del Desarrollo de la Expresión Génica , Proteínas de Homeodominio/genética , Proteínas de Homeodominio/metabolismo , Mesodermo/embriología , Ratones , Ratones Noqueados , Células-Madre Neurales/citología , Nucleosomas/genética , Nucleosomas/metabolismo , Proteínas de Dominio T Box/genética
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