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Regulation of the positive transcriptional effect of PLZF through a non-canonical EZH2 activity
The transcription factor PLZF (promyelocytic leukemia zinc finger protein) acts as an epigenetic regulator balancing self-renewal and differentiation of hematopoietic cells through binding to various chromatin-modifying factors. First described as a transcriptional repressor, PLZF is also associated...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909434/ https://www.ncbi.nlm.nih.gov/pubmed/29425303 http://dx.doi.org/10.1093/nar/gky080 |
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author | Koubi, Myriam Poplineau, Mathilde Vernerey, Julien N’Guyen, Lia Tiberi, Guillaume Garciaz, Sylvain El-Kaoutari, Abdessamad Maqbool, Muhammad A Andrau, Jean-Christophe Guillouf, Christel Saurin, Andrew J Duprez, Estelle |
author_facet | Koubi, Myriam Poplineau, Mathilde Vernerey, Julien N’Guyen, Lia Tiberi, Guillaume Garciaz, Sylvain El-Kaoutari, Abdessamad Maqbool, Muhammad A Andrau, Jean-Christophe Guillouf, Christel Saurin, Andrew J Duprez, Estelle |
author_sort | Koubi, Myriam |
collection | PubMed |
description | The transcription factor PLZF (promyelocytic leukemia zinc finger protein) acts as an epigenetic regulator balancing self-renewal and differentiation of hematopoietic cells through binding to various chromatin-modifying factors. First described as a transcriptional repressor, PLZF is also associated with active transcription, although the molecular bases underlying the differences are unknown. Here, we reveal that in a hematopoietic cell line, PLZF is predominantly associated with transcribed genes. Additionally, we identify a new association between PLZF and the histone methyltransferase, EZH2 at the genomic level. We find that co-occupancy of PLZF and EZH2 on chromatin at PLZF target genes is not associated with SUZ12 or trimethylated lysine 27 of histone H3 (H3K27me3) but with the active histone mark H3K4me3 and active transcription. Removal of EZH2 leads to an increase of PLZF binding and increased gene expression. Our results suggest a new role of EZH2 in restricting PLZF positive transcriptional activity independently of its canonical PRC2 activity. |
format | Online Article Text |
id | pubmed-5909434 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-59094342018-04-24 Regulation of the positive transcriptional effect of PLZF through a non-canonical EZH2 activity Koubi, Myriam Poplineau, Mathilde Vernerey, Julien N’Guyen, Lia Tiberi, Guillaume Garciaz, Sylvain El-Kaoutari, Abdessamad Maqbool, Muhammad A Andrau, Jean-Christophe Guillouf, Christel Saurin, Andrew J Duprez, Estelle Nucleic Acids Res Gene regulation, Chromatin and Epigenetics The transcription factor PLZF (promyelocytic leukemia zinc finger protein) acts as an epigenetic regulator balancing self-renewal and differentiation of hematopoietic cells through binding to various chromatin-modifying factors. First described as a transcriptional repressor, PLZF is also associated with active transcription, although the molecular bases underlying the differences are unknown. Here, we reveal that in a hematopoietic cell line, PLZF is predominantly associated with transcribed genes. Additionally, we identify a new association between PLZF and the histone methyltransferase, EZH2 at the genomic level. We find that co-occupancy of PLZF and EZH2 on chromatin at PLZF target genes is not associated with SUZ12 or trimethylated lysine 27 of histone H3 (H3K27me3) but with the active histone mark H3K4me3 and active transcription. Removal of EZH2 leads to an increase of PLZF binding and increased gene expression. Our results suggest a new role of EZH2 in restricting PLZF positive transcriptional activity independently of its canonical PRC2 activity. Oxford University Press 2018-04-20 2018-02-07 /pmc/articles/PMC5909434/ /pubmed/29425303 http://dx.doi.org/10.1093/nar/gky080 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Gene regulation, Chromatin and Epigenetics Koubi, Myriam Poplineau, Mathilde Vernerey, Julien N’Guyen, Lia Tiberi, Guillaume Garciaz, Sylvain El-Kaoutari, Abdessamad Maqbool, Muhammad A Andrau, Jean-Christophe Guillouf, Christel Saurin, Andrew J Duprez, Estelle Regulation of the positive transcriptional effect of PLZF through a non-canonical EZH2 activity |
title | Regulation of the positive transcriptional effect of PLZF through a non-canonical EZH2 activity |
title_full | Regulation of the positive transcriptional effect of PLZF through a non-canonical EZH2 activity |
title_fullStr | Regulation of the positive transcriptional effect of PLZF through a non-canonical EZH2 activity |
title_full_unstemmed | Regulation of the positive transcriptional effect of PLZF through a non-canonical EZH2 activity |
title_short | Regulation of the positive transcriptional effect of PLZF through a non-canonical EZH2 activity |
title_sort | regulation of the positive transcriptional effect of plzf through a non-canonical ezh2 activity |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909434/ https://www.ncbi.nlm.nih.gov/pubmed/29425303 http://dx.doi.org/10.1093/nar/gky080 |
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