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Mechanisms of Groucho-mediated repression revealed by genome-wide analysis of Groucho binding and activity

BACKGROUND: The transcriptional corepressor Groucho (Gro) is required for the function of many developmentally regulated DNA binding repressors, thus helping to define the gene expression profile of each cell during development. The ability of Gro to repress transcription at a distance together with...

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Autores principales: Chambers, Michael, Turki-Judeh, Wiam, Kim, Min Woo, Chen, Kenny, Gallaher, Sean D., Courey, Albert J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331681/
https://www.ncbi.nlm.nih.gov/pubmed/28245789
http://dx.doi.org/10.1186/s12864-017-3589-6
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author Chambers, Michael
Turki-Judeh, Wiam
Kim, Min Woo
Chen, Kenny
Gallaher, Sean D.
Courey, Albert J.
author_facet Chambers, Michael
Turki-Judeh, Wiam
Kim, Min Woo
Chen, Kenny
Gallaher, Sean D.
Courey, Albert J.
author_sort Chambers, Michael
collection PubMed
description BACKGROUND: The transcriptional corepressor Groucho (Gro) is required for the function of many developmentally regulated DNA binding repressors, thus helping to define the gene expression profile of each cell during development. The ability of Gro to repress transcription at a distance together with its ability to oligomerize and bind to histones has led to the suggestion that Gro may spread along chromatin. However, much is unknown about the mechanism of Gro-mediated repression and about the dynamics of Gro targeting. RESULTS: Our chromatin immunoprecipitation sequencing analysis of temporally staged Drosophila embryos shows that Gro binds in a highly dynamic manner primarily to clusters of discrete (<1 kb) segments. Consistent with the idea that Gro may facilitate communication between silencers and promoters, Gro binding is enriched at both cis-regulatory modules, as well as within the promotors of potential target genes. While this Gro-recruitment is required for repression, our data show that it is not sufficient for repression. Integration of Gro binding data with transcriptomic analysis suggests that, contrary to what has been observed for another Gro family member, Drosophila Gro is probably a dedicated repressor. This analysis also allows us to define a set of high confidence Gro repression targets. Using publically available data regarding the physical and genetic interactions between these targets, we are able to place them in the regulatory network controlling development. Through analysis of chromatin associated pre-mRNA levels at these targets, we find that genes regulated by Gro in the embryo are enriched for characteristics of promoter proximal paused RNA polymerase II. CONCLUSIONS: Our findings are inconsistent with a one-dimensional spreading model for long-range repression and suggest that Gro-mediated repression must be regulated at a post-recruitment step. They also show that Gro is likely a dedicated repressor that sits at a prominent highly interconnected regulatory hub in the developmental network. Furthermore, our findings suggest a role for RNA polymerase II pausing in Gro-mediated repression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3589-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-53316812017-03-06 Mechanisms of Groucho-mediated repression revealed by genome-wide analysis of Groucho binding and activity Chambers, Michael Turki-Judeh, Wiam Kim, Min Woo Chen, Kenny Gallaher, Sean D. Courey, Albert J. BMC Genomics Research Article BACKGROUND: The transcriptional corepressor Groucho (Gro) is required for the function of many developmentally regulated DNA binding repressors, thus helping to define the gene expression profile of each cell during development. The ability of Gro to repress transcription at a distance together with its ability to oligomerize and bind to histones has led to the suggestion that Gro may spread along chromatin. However, much is unknown about the mechanism of Gro-mediated repression and about the dynamics of Gro targeting. RESULTS: Our chromatin immunoprecipitation sequencing analysis of temporally staged Drosophila embryos shows that Gro binds in a highly dynamic manner primarily to clusters of discrete (<1 kb) segments. Consistent with the idea that Gro may facilitate communication between silencers and promoters, Gro binding is enriched at both cis-regulatory modules, as well as within the promotors of potential target genes. While this Gro-recruitment is required for repression, our data show that it is not sufficient for repression. Integration of Gro binding data with transcriptomic analysis suggests that, contrary to what has been observed for another Gro family member, Drosophila Gro is probably a dedicated repressor. This analysis also allows us to define a set of high confidence Gro repression targets. Using publically available data regarding the physical and genetic interactions between these targets, we are able to place them in the regulatory network controlling development. Through analysis of chromatin associated pre-mRNA levels at these targets, we find that genes regulated by Gro in the embryo are enriched for characteristics of promoter proximal paused RNA polymerase II. CONCLUSIONS: Our findings are inconsistent with a one-dimensional spreading model for long-range repression and suggest that Gro-mediated repression must be regulated at a post-recruitment step. They also show that Gro is likely a dedicated repressor that sits at a prominent highly interconnected regulatory hub in the developmental network. Furthermore, our findings suggest a role for RNA polymerase II pausing in Gro-mediated repression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3589-6) contains supplementary material, which is available to authorized users. BioMed Central 2017-02-28 /pmc/articles/PMC5331681/ /pubmed/28245789 http://dx.doi.org/10.1186/s12864-017-3589-6 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Chambers, Michael
Turki-Judeh, Wiam
Kim, Min Woo
Chen, Kenny
Gallaher, Sean D.
Courey, Albert J.
Mechanisms of Groucho-mediated repression revealed by genome-wide analysis of Groucho binding and activity
title Mechanisms of Groucho-mediated repression revealed by genome-wide analysis of Groucho binding and activity
title_full Mechanisms of Groucho-mediated repression revealed by genome-wide analysis of Groucho binding and activity
title_fullStr Mechanisms of Groucho-mediated repression revealed by genome-wide analysis of Groucho binding and activity
title_full_unstemmed Mechanisms of Groucho-mediated repression revealed by genome-wide analysis of Groucho binding and activity
title_short Mechanisms of Groucho-mediated repression revealed by genome-wide analysis of Groucho binding and activity
title_sort mechanisms of groucho-mediated repression revealed by genome-wide analysis of groucho binding and activity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331681/
https://www.ncbi.nlm.nih.gov/pubmed/28245789
http://dx.doi.org/10.1186/s12864-017-3589-6
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