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Widespread transcription at neuronal activity-regulated enhancers
We used genome-wide sequencing methods to study stimulus-dependent enhancer function in neurons. We identified ∼12,000 neuronal activity-regulated enhancers that are bound by the general transcriptional co-activator CBP in an activity-dependent manner. A function of CBP at enhancers may be to recrui...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3020079/ https://www.ncbi.nlm.nih.gov/pubmed/20393465 http://dx.doi.org/10.1038/nature09033 |
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author | Kim, Tae-Kyung Hemberg, Martin Gray, Jesse M. Costa, Allen M. Bear, Daniel M. Wu, Jing Harmin, David A. Laptewicz, Mike Barbara-Haley, Kellie Kuersten, Scott Markenscoff-Papadimitriou, Eirene Kuhl, Dietmar Bito, Haruhiko Worley, Paul F. Kreiman, Gabriel Greenberg, Michael E. |
author_facet | Kim, Tae-Kyung Hemberg, Martin Gray, Jesse M. Costa, Allen M. Bear, Daniel M. Wu, Jing Harmin, David A. Laptewicz, Mike Barbara-Haley, Kellie Kuersten, Scott Markenscoff-Papadimitriou, Eirene Kuhl, Dietmar Bito, Haruhiko Worley, Paul F. Kreiman, Gabriel Greenberg, Michael E. |
author_sort | Kim, Tae-Kyung |
collection | PubMed |
description | We used genome-wide sequencing methods to study stimulus-dependent enhancer function in neurons. We identified ∼12,000 neuronal activity-regulated enhancers that are bound by the general transcriptional co-activator CBP in an activity-dependent manner. A function of CBP at enhancers may be to recruit RNA polymerase II (RNAPII), as we also observed activity-regulated RNAPII binding to thousands of enhancers. Remarkably, RNAPII at enhancers transcribes bi-directionally a novel class of enhancer RNAs (eRNAs) within enhancer domains defined by the presence of histone H3 that is mono-methylated at lysine 4 (H3K4me1). The level of eRNA expression at neuronal enhancers positively correlates with the level of mRNA synthesis at nearby genes, suggesting that eRNA synthesis occurs specifically at enhancers that are actively engaged in promoting mRNA synthesis. These findings reveal that a widespread mechanism of enhancer activation involves RNAPII binding and eRNA synthesis. |
format | Text |
id | pubmed-3020079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
record_format | MEDLINE/PubMed |
spelling | pubmed-30200792011-01-12 Widespread transcription at neuronal activity-regulated enhancers Kim, Tae-Kyung Hemberg, Martin Gray, Jesse M. Costa, Allen M. Bear, Daniel M. Wu, Jing Harmin, David A. Laptewicz, Mike Barbara-Haley, Kellie Kuersten, Scott Markenscoff-Papadimitriou, Eirene Kuhl, Dietmar Bito, Haruhiko Worley, Paul F. Kreiman, Gabriel Greenberg, Michael E. Nature Article We used genome-wide sequencing methods to study stimulus-dependent enhancer function in neurons. We identified ∼12,000 neuronal activity-regulated enhancers that are bound by the general transcriptional co-activator CBP in an activity-dependent manner. A function of CBP at enhancers may be to recruit RNA polymerase II (RNAPII), as we also observed activity-regulated RNAPII binding to thousands of enhancers. Remarkably, RNAPII at enhancers transcribes bi-directionally a novel class of enhancer RNAs (eRNAs) within enhancer domains defined by the presence of histone H3 that is mono-methylated at lysine 4 (H3K4me1). The level of eRNA expression at neuronal enhancers positively correlates with the level of mRNA synthesis at nearby genes, suggesting that eRNA synthesis occurs specifically at enhancers that are actively engaged in promoting mRNA synthesis. These findings reveal that a widespread mechanism of enhancer activation involves RNAPII binding and eRNA synthesis. 2010-04-14 2010-05-13 /pmc/articles/PMC3020079/ /pubmed/20393465 http://dx.doi.org/10.1038/nature09033 Text en http://www.nature.com/authors/editorial_policies/license.html#terms 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 Kim, Tae-Kyung Hemberg, Martin Gray, Jesse M. Costa, Allen M. Bear, Daniel M. Wu, Jing Harmin, David A. Laptewicz, Mike Barbara-Haley, Kellie Kuersten, Scott Markenscoff-Papadimitriou, Eirene Kuhl, Dietmar Bito, Haruhiko Worley, Paul F. Kreiman, Gabriel Greenberg, Michael E. Widespread transcription at neuronal activity-regulated enhancers |
title | Widespread transcription at neuronal activity-regulated enhancers |
title_full | Widespread transcription at neuronal activity-regulated enhancers |
title_fullStr | Widespread transcription at neuronal activity-regulated enhancers |
title_full_unstemmed | Widespread transcription at neuronal activity-regulated enhancers |
title_short | Widespread transcription at neuronal activity-regulated enhancers |
title_sort | widespread transcription at neuronal activity-regulated enhancers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3020079/ https://www.ncbi.nlm.nih.gov/pubmed/20393465 http://dx.doi.org/10.1038/nature09033 |
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