Cargando…
A high-resolution map of transcriptional repression
Turning genes on and off is essential for development and homeostasis, yet little is known about the sequence and causal role of chromatin state changes during the repression of active genes. This is surprising, as defective gene silencing underlies developmental abnormalities and disease. Here we d...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5373822/ https://www.ncbi.nlm.nih.gov/pubmed/28318487 http://dx.doi.org/10.7554/eLife.22767 |
_version_ | 1782518812726263808 |
---|---|
author | Liang, Ziwei Brown, Karen E Carroll, Thomas Taylor, Benjamin Vidal, Isabel Ferreirós Hendrich, Brian Rueda, David Fisher, Amanda G Merkenschlager, Matthias |
author_facet | Liang, Ziwei Brown, Karen E Carroll, Thomas Taylor, Benjamin Vidal, Isabel Ferreirós Hendrich, Brian Rueda, David Fisher, Amanda G Merkenschlager, Matthias |
author_sort | Liang, Ziwei |
collection | PubMed |
description | Turning genes on and off is essential for development and homeostasis, yet little is known about the sequence and causal role of chromatin state changes during the repression of active genes. This is surprising, as defective gene silencing underlies developmental abnormalities and disease. Here we delineate the sequence and functional contribution of transcriptional repression mechanisms at high temporal resolution. Inducible entry of the NuRD-interacting transcriptional regulator Ikaros into mouse pre-B cell nuclei triggered immediate binding to target gene promoters. Rapid RNAP2 eviction, transcriptional shutdown, nucleosome invasion, and reduced transcriptional activator binding required chromatin remodeling by NuRD-associated Mi2beta/CHD4, but were independent of HDAC activity. Histone deacetylation occurred after transcriptional repression. Nevertheless, HDAC activity contributed to stable gene silencing. Hence, high resolution mapping of transcriptional repression reveals complex and interdependent mechanisms that underpin rapid transitions between transcriptional states, and elucidates the temporal order, functional role and mechanistic separation of NuRD-associated enzymatic activities. DOI: http://dx.doi.org/10.7554/eLife.22767.001 |
format | Online Article Text |
id | pubmed-5373822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53738222017-03-31 A high-resolution map of transcriptional repression Liang, Ziwei Brown, Karen E Carroll, Thomas Taylor, Benjamin Vidal, Isabel Ferreirós Hendrich, Brian Rueda, David Fisher, Amanda G Merkenschlager, Matthias eLife Genes and Chromosomes Turning genes on and off is essential for development and homeostasis, yet little is known about the sequence and causal role of chromatin state changes during the repression of active genes. This is surprising, as defective gene silencing underlies developmental abnormalities and disease. Here we delineate the sequence and functional contribution of transcriptional repression mechanisms at high temporal resolution. Inducible entry of the NuRD-interacting transcriptional regulator Ikaros into mouse pre-B cell nuclei triggered immediate binding to target gene promoters. Rapid RNAP2 eviction, transcriptional shutdown, nucleosome invasion, and reduced transcriptional activator binding required chromatin remodeling by NuRD-associated Mi2beta/CHD4, but were independent of HDAC activity. Histone deacetylation occurred after transcriptional repression. Nevertheless, HDAC activity contributed to stable gene silencing. Hence, high resolution mapping of transcriptional repression reveals complex and interdependent mechanisms that underpin rapid transitions between transcriptional states, and elucidates the temporal order, functional role and mechanistic separation of NuRD-associated enzymatic activities. DOI: http://dx.doi.org/10.7554/eLife.22767.001 eLife Sciences Publications, Ltd 2017-03-20 /pmc/articles/PMC5373822/ /pubmed/28318487 http://dx.doi.org/10.7554/eLife.22767 Text en © 2017, Liang et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Genes and Chromosomes Liang, Ziwei Brown, Karen E Carroll, Thomas Taylor, Benjamin Vidal, Isabel Ferreirós Hendrich, Brian Rueda, David Fisher, Amanda G Merkenschlager, Matthias A high-resolution map of transcriptional repression |
title | A high-resolution map of transcriptional repression |
title_full | A high-resolution map of transcriptional repression |
title_fullStr | A high-resolution map of transcriptional repression |
title_full_unstemmed | A high-resolution map of transcriptional repression |
title_short | A high-resolution map of transcriptional repression |
title_sort | high-resolution map of transcriptional repression |
topic | Genes and Chromosomes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5373822/ https://www.ncbi.nlm.nih.gov/pubmed/28318487 http://dx.doi.org/10.7554/eLife.22767 |
work_keys_str_mv | AT liangziwei ahighresolutionmapoftranscriptionalrepression AT brownkarene ahighresolutionmapoftranscriptionalrepression AT carrollthomas ahighresolutionmapoftranscriptionalrepression AT taylorbenjamin ahighresolutionmapoftranscriptionalrepression AT vidalisabelferreiros ahighresolutionmapoftranscriptionalrepression AT hendrichbrian ahighresolutionmapoftranscriptionalrepression AT ruedadavid ahighresolutionmapoftranscriptionalrepression AT fisheramandag ahighresolutionmapoftranscriptionalrepression AT merkenschlagermatthias ahighresolutionmapoftranscriptionalrepression AT liangziwei highresolutionmapoftranscriptionalrepression AT brownkarene highresolutionmapoftranscriptionalrepression AT carrollthomas highresolutionmapoftranscriptionalrepression AT taylorbenjamin highresolutionmapoftranscriptionalrepression AT vidalisabelferreiros highresolutionmapoftranscriptionalrepression AT hendrichbrian highresolutionmapoftranscriptionalrepression AT ruedadavid highresolutionmapoftranscriptionalrepression AT fisheramandag highresolutionmapoftranscriptionalrepression AT merkenschlagermatthias highresolutionmapoftranscriptionalrepression |