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Pho dynamically interacts with Spt5 to facilitate transcriptional switches at the hsp70 locus
BACKGROUND: Numerous target genes of the Polycomb group (PcG) are transiently activated by a stimulus and subsequently repressed. However, mechanisms by which PcG proteins regulate such target genes remain elusive. RESULTS: We employed the heat shock-responsive hsp70 locus in Drosophila to study the...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5718073/ https://www.ncbi.nlm.nih.gov/pubmed/29208012 http://dx.doi.org/10.1186/s13072-017-0166-9 |
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author | Pereira, Allwyn Paro, Renato |
author_facet | Pereira, Allwyn Paro, Renato |
author_sort | Pereira, Allwyn |
collection | PubMed |
description | BACKGROUND: Numerous target genes of the Polycomb group (PcG) are transiently activated by a stimulus and subsequently repressed. However, mechanisms by which PcG proteins regulate such target genes remain elusive. RESULTS: We employed the heat shock-responsive hsp70 locus in Drosophila to study the chromatin dynamics of PRC1 and its interplay with known regulators of the locus before, during and after heat shock. We detected mutually exclusive binding patterns for HSF and PRC1 at the hsp70 locus. We found that Pleiohomeotic (Pho), a DNA-binding PcG member, dynamically interacts with Spt5, an elongation factor. The dynamic interaction switch between Pho and Spt5 is triggered by the recruitment of HSF to chromatin. Mutation in the protein–protein interaction domain (REPO domain) of Pho interferes with the dynamics of its interaction with Spt5. The transcriptional kinetics of the heat shock response is negatively affected by a mutation in the REPO domain of Pho. CONCLUSIONS: We propose that a dynamic interaction switch between PcG proteins and an elongation factor enables stress-inducible genes to efficiently switch between ON/OFF states in the presence/absence of the activating stimulus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13072-017-0166-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5718073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57180732017-12-08 Pho dynamically interacts with Spt5 to facilitate transcriptional switches at the hsp70 locus Pereira, Allwyn Paro, Renato Epigenetics Chromatin Research BACKGROUND: Numerous target genes of the Polycomb group (PcG) are transiently activated by a stimulus and subsequently repressed. However, mechanisms by which PcG proteins regulate such target genes remain elusive. RESULTS: We employed the heat shock-responsive hsp70 locus in Drosophila to study the chromatin dynamics of PRC1 and its interplay with known regulators of the locus before, during and after heat shock. We detected mutually exclusive binding patterns for HSF and PRC1 at the hsp70 locus. We found that Pleiohomeotic (Pho), a DNA-binding PcG member, dynamically interacts with Spt5, an elongation factor. The dynamic interaction switch between Pho and Spt5 is triggered by the recruitment of HSF to chromatin. Mutation in the protein–protein interaction domain (REPO domain) of Pho interferes with the dynamics of its interaction with Spt5. The transcriptional kinetics of the heat shock response is negatively affected by a mutation in the REPO domain of Pho. CONCLUSIONS: We propose that a dynamic interaction switch between PcG proteins and an elongation factor enables stress-inducible genes to efficiently switch between ON/OFF states in the presence/absence of the activating stimulus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13072-017-0166-9) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-06 /pmc/articles/PMC5718073/ /pubmed/29208012 http://dx.doi.org/10.1186/s13072-017-0166-9 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 Pereira, Allwyn Paro, Renato Pho dynamically interacts with Spt5 to facilitate transcriptional switches at the hsp70 locus |
title | Pho dynamically interacts with Spt5 to facilitate transcriptional switches at the hsp70 locus |
title_full | Pho dynamically interacts with Spt5 to facilitate transcriptional switches at the hsp70 locus |
title_fullStr | Pho dynamically interacts with Spt5 to facilitate transcriptional switches at the hsp70 locus |
title_full_unstemmed | Pho dynamically interacts with Spt5 to facilitate transcriptional switches at the hsp70 locus |
title_short | Pho dynamically interacts with Spt5 to facilitate transcriptional switches at the hsp70 locus |
title_sort | pho dynamically interacts with spt5 to facilitate transcriptional switches at the hsp70 locus |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5718073/ https://www.ncbi.nlm.nih.gov/pubmed/29208012 http://dx.doi.org/10.1186/s13072-017-0166-9 |
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