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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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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
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author 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.
author_facet 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.
author_sort Kitazawa, Taro
collection PubMed
description 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.
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spelling pubmed-76103962021-08-18 A Unique Bipartite Polycomb Signature Regulates Stimulus-Response Transcription during Development 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. Nat Genet Article 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. 2021-03-01 2021-02-18 /pmc/articles/PMC7610396/ /pubmed/33603234 http://dx.doi.org/10.1038/s41588-021-00789-z Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
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.
A Unique Bipartite Polycomb Signature Regulates Stimulus-Response Transcription during Development
title A Unique Bipartite Polycomb Signature Regulates Stimulus-Response Transcription during Development
title_full A Unique Bipartite Polycomb Signature Regulates Stimulus-Response Transcription during Development
title_fullStr A Unique Bipartite Polycomb Signature Regulates Stimulus-Response Transcription during Development
title_full_unstemmed A Unique Bipartite Polycomb Signature Regulates Stimulus-Response Transcription during Development
title_short A Unique Bipartite Polycomb Signature Regulates Stimulus-Response Transcription during Development
title_sort unique bipartite polycomb signature regulates stimulus-response transcription during development
topic Article
url 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
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