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Flightless-I governs cell fate by recruiting the SUMO isopeptidase SENP3 to distinct HOX genes
BACKGROUND: Despite recent studies on the role of ubiquitin-related SUMO modifier in cell fate decisions, our understanding on precise molecular mechanisms of these processes is limited. Previously, we established that the SUMO isopeptidase SENP3 regulates chromatin assembly of the MLL1/2 histone me...
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/PMC5364561/ https://www.ncbi.nlm.nih.gov/pubmed/28344658 http://dx.doi.org/10.1186/s13072-017-0122-8 |
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author | Nayak, Arnab Reck, Anja Morsczeck, Christian Müller, Stefan |
author_facet | Nayak, Arnab Reck, Anja Morsczeck, Christian Müller, Stefan |
author_sort | Nayak, Arnab |
collection | PubMed |
description | BACKGROUND: Despite recent studies on the role of ubiquitin-related SUMO modifier in cell fate decisions, our understanding on precise molecular mechanisms of these processes is limited. Previously, we established that the SUMO isopeptidase SENP3 regulates chromatin assembly of the MLL1/2 histone methyltransferase complex at distinct HOX genes, including the osteogenic master regulator DLX3. A comprehensive mechanism that regulates SENP3 transcriptional function was not understood. RESULTS: Here, we identified flightless-I homolog (FLII), a member of the gelsolin family of actin-remodeling proteins, as a novel regulator of SENP3. We demonstrate that FLII is associated with SENP3 and the MLL1/2 complex. We further show that FLII determines SENP3 recruitment and MLL1/2 complex assembly on the DLX3 gene. Consequently, FLII is indispensible for H3K4 methylation and proper loading of active RNA polymerase II at this gene locus. Most importantly, FLII-mediated SENP3 regulation governs osteogenic differentiation of human mesenchymal stem cells. CONCLUSION: Altogether, these data reveal a crucial functional interconnection of FLII with the sumoylation machinery that converges on epigenetic regulation and cell fate determination. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13072-017-0122-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5364561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53645612017-03-24 Flightless-I governs cell fate by recruiting the SUMO isopeptidase SENP3 to distinct HOX genes Nayak, Arnab Reck, Anja Morsczeck, Christian Müller, Stefan Epigenetics Chromatin Research BACKGROUND: Despite recent studies on the role of ubiquitin-related SUMO modifier in cell fate decisions, our understanding on precise molecular mechanisms of these processes is limited. Previously, we established that the SUMO isopeptidase SENP3 regulates chromatin assembly of the MLL1/2 histone methyltransferase complex at distinct HOX genes, including the osteogenic master regulator DLX3. A comprehensive mechanism that regulates SENP3 transcriptional function was not understood. RESULTS: Here, we identified flightless-I homolog (FLII), a member of the gelsolin family of actin-remodeling proteins, as a novel regulator of SENP3. We demonstrate that FLII is associated with SENP3 and the MLL1/2 complex. We further show that FLII determines SENP3 recruitment and MLL1/2 complex assembly on the DLX3 gene. Consequently, FLII is indispensible for H3K4 methylation and proper loading of active RNA polymerase II at this gene locus. Most importantly, FLII-mediated SENP3 regulation governs osteogenic differentiation of human mesenchymal stem cells. CONCLUSION: Altogether, these data reveal a crucial functional interconnection of FLII with the sumoylation machinery that converges on epigenetic regulation and cell fate determination. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13072-017-0122-8) contains supplementary material, which is available to authorized users. BioMed Central 2017-03-23 /pmc/articles/PMC5364561/ /pubmed/28344658 http://dx.doi.org/10.1186/s13072-017-0122-8 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 Nayak, Arnab Reck, Anja Morsczeck, Christian Müller, Stefan Flightless-I governs cell fate by recruiting the SUMO isopeptidase SENP3 to distinct HOX genes |
title | Flightless-I governs cell fate by recruiting the SUMO isopeptidase SENP3 to distinct HOX genes |
title_full | Flightless-I governs cell fate by recruiting the SUMO isopeptidase SENP3 to distinct HOX genes |
title_fullStr | Flightless-I governs cell fate by recruiting the SUMO isopeptidase SENP3 to distinct HOX genes |
title_full_unstemmed | Flightless-I governs cell fate by recruiting the SUMO isopeptidase SENP3 to distinct HOX genes |
title_short | Flightless-I governs cell fate by recruiting the SUMO isopeptidase SENP3 to distinct HOX genes |
title_sort | flightless-i governs cell fate by recruiting the sumo isopeptidase senp3 to distinct hox genes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364561/ https://www.ncbi.nlm.nih.gov/pubmed/28344658 http://dx.doi.org/10.1186/s13072-017-0122-8 |
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