Cargando…
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...
Autores principales: | , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783605185996652544 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7610396 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT kitazawataro auniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT machlabdania auniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT joshionkar auniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT maioranonicola auniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT kohlerhubertus auniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT ducretsebastien auniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT kesslersandra auniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT gezeliushenrik auniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT sonesoncharlotte auniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT papasaikaspanagiotis auniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT lopezbenditoguillermina auniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT stadlermichaelb auniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT rijlifilippom auniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT kitazawataro uniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT machlabdania uniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT joshionkar uniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT maioranonicola uniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT kohlerhubertus uniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT ducretsebastien uniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT kesslersandra uniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT gezeliushenrik uniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT sonesoncharlotte uniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT papasaikaspanagiotis uniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT lopezbenditoguillermina uniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT stadlermichaelb uniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment AT rijlifilippom uniquebipartitepolycombsignatureregulatesstimulusresponsetranscriptionduringdevelopment |