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Ancestral function of Inhibitors-of-kappaB regulates Caenorhabditis elegans development
Mammalian IκB proteins (IκBs) exert their main function as negative regulators of NF-κB, a central signaling pathway controlling immunity and inflammation. An alternative chromatin role for IκBs has been shown to affect stemness and cell differentiation. However, the involvement of NF-κB in this fun...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7527347/ https://www.ncbi.nlm.nih.gov/pubmed/32999373 http://dx.doi.org/10.1038/s41598-020-73146-5 |
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author | Brena, David Bertran, Joan Porta-de-la-Riva, Montserrat Guillén, Yolanda Cornes, Eric Kukhtar, Dmytro Campos-Vicens, Lluís Fernández, Lierni Pecharroman, Irene García-López, Albert Islam, Abul B. M. M. K. Marruecos, Laura Bigas, Anna Cerón, Julián Espinosa, Lluís |
author_facet | Brena, David Bertran, Joan Porta-de-la-Riva, Montserrat Guillén, Yolanda Cornes, Eric Kukhtar, Dmytro Campos-Vicens, Lluís Fernández, Lierni Pecharroman, Irene García-López, Albert Islam, Abul B. M. M. K. Marruecos, Laura Bigas, Anna Cerón, Julián Espinosa, Lluís |
author_sort | Brena, David |
collection | PubMed |
description | Mammalian IκB proteins (IκBs) exert their main function as negative regulators of NF-κB, a central signaling pathway controlling immunity and inflammation. An alternative chromatin role for IκBs has been shown to affect stemness and cell differentiation. However, the involvement of NF-κB in this function has not been excluded. NFKI-1 and IKB-1 are IκB homologs in Caenorhabditis elegans, which lacks NF-κB nuclear effectors. We found that nfki-1 and ikb-1 mutants display developmental defects that phenocopy mutations in Polycomb and UTX-1 histone demethylase, suggesting a role for C. elegans IκBs in chromatin regulation. Further supporting this possibility (1) we detected NFKI-1 in the nucleus of cells; (2) NFKI-1 and IKB-1 bind to histones and Polycomb proteins, (3) and associate with chromatin in vivo, and (4) mutations in nfki-1 and ikb-1 alter chromatin marks. Based on these results, we propose that ancestral IκB inhibitors modulate Polycomb activity at specific gene subsets with an impact on development. |
format | Online Article Text |
id | pubmed-7527347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75273472020-10-01 Ancestral function of Inhibitors-of-kappaB regulates Caenorhabditis elegans development Brena, David Bertran, Joan Porta-de-la-Riva, Montserrat Guillén, Yolanda Cornes, Eric Kukhtar, Dmytro Campos-Vicens, Lluís Fernández, Lierni Pecharroman, Irene García-López, Albert Islam, Abul B. M. M. K. Marruecos, Laura Bigas, Anna Cerón, Julián Espinosa, Lluís Sci Rep Article Mammalian IκB proteins (IκBs) exert their main function as negative regulators of NF-κB, a central signaling pathway controlling immunity and inflammation. An alternative chromatin role for IκBs has been shown to affect stemness and cell differentiation. However, the involvement of NF-κB in this function has not been excluded. NFKI-1 and IKB-1 are IκB homologs in Caenorhabditis elegans, which lacks NF-κB nuclear effectors. We found that nfki-1 and ikb-1 mutants display developmental defects that phenocopy mutations in Polycomb and UTX-1 histone demethylase, suggesting a role for C. elegans IκBs in chromatin regulation. Further supporting this possibility (1) we detected NFKI-1 in the nucleus of cells; (2) NFKI-1 and IKB-1 bind to histones and Polycomb proteins, (3) and associate with chromatin in vivo, and (4) mutations in nfki-1 and ikb-1 alter chromatin marks. Based on these results, we propose that ancestral IκB inhibitors modulate Polycomb activity at specific gene subsets with an impact on development. Nature Publishing Group UK 2020-09-30 /pmc/articles/PMC7527347/ /pubmed/32999373 http://dx.doi.org/10.1038/s41598-020-73146-5 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Brena, David Bertran, Joan Porta-de-la-Riva, Montserrat Guillén, Yolanda Cornes, Eric Kukhtar, Dmytro Campos-Vicens, Lluís Fernández, Lierni Pecharroman, Irene García-López, Albert Islam, Abul B. M. M. K. Marruecos, Laura Bigas, Anna Cerón, Julián Espinosa, Lluís Ancestral function of Inhibitors-of-kappaB regulates Caenorhabditis elegans development |
title | Ancestral function of Inhibitors-of-kappaB regulates Caenorhabditis elegans development |
title_full | Ancestral function of Inhibitors-of-kappaB regulates Caenorhabditis elegans development |
title_fullStr | Ancestral function of Inhibitors-of-kappaB regulates Caenorhabditis elegans development |
title_full_unstemmed | Ancestral function of Inhibitors-of-kappaB regulates Caenorhabditis elegans development |
title_short | Ancestral function of Inhibitors-of-kappaB regulates Caenorhabditis elegans development |
title_sort | ancestral function of inhibitors-of-kappab regulates caenorhabditis elegans development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7527347/ https://www.ncbi.nlm.nih.gov/pubmed/32999373 http://dx.doi.org/10.1038/s41598-020-73146-5 |
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