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A Unique Bipartite Polycomb Signature Regulates Stimulus-Response Transcription during Development

Rapid cellular responses to environmental stimuli are fundamental for development and maturation. Immediate early genes (IEGs) can be transcriptionally induced within minutes in response to a variety of signals. How their induction levels are regulated and their untimely activation by spurious signa...

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Detalles Bibliográficos
Autores principales: Kitazawa, Taro, Machlab, Dania, Joshi, Onkar, Maiorano, Nicola, Kohler, Hubertus, Ducret, Sebastien, Kessler, Sandra, Gezelius, Henrik, Soneson, Charlotte, Papasaikas, Panagiotis, López-Bendito, Guillermina, Stadler, Michael B., Rijli, Filippo M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7610396/
https://www.ncbi.nlm.nih.gov/pubmed/33603234
http://dx.doi.org/10.1038/s41588-021-00789-z
Descripción
Sumario:Rapid cellular responses to environmental stimuli are fundamental for development and maturation. Immediate early genes (IEGs) can be transcriptionally induced within minutes in response to a variety of signals. How their induction levels are regulated and their untimely activation by spurious signals prevented during development is poorly understood. We found that in developing sensory neurons, prior to perinatal sensory activity-dependent induction, IEGs are embedded into a unique bipartite Polycomb chromatin signature, carrying active H3K27ac on promoters but repressive Ezh2-dependent H3K27me3 on gene bodies. This bipartite signature is widely present in developing cell types, including embryonic stem cells (ESCs). Polycomb marking of gene bodies inhibits mRNA elongation, dampening productive transcription, while still allowing for fast stimulus-dependent mark removal and bipartite gene induction. We reveal a developmental epigenetic mechanism regulating rapidity and amplitude of the transcriptional response to relevant stimuli, while preventing inappropriate activation of stimulus-response genes.