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               <dc:title>Ancestral function ofInhibitors-of-kappaB regulates Caenorhabditis elegans development</dc:title>
               <dc:creator>Brena, David</dc:creator>
               <dc:creator>Bertran, Joan</dc:creator>
               <dc:creator>Porta de la Riva, Montserrat</dc:creator>
               <dc:creator>Guillen, Yolanda</dc:creator>
               <dc:creator>Cornes, Eric</dc:creator>
               <dc:creator>Kukhtar, Dmytro</dc:creator>
               <dc:creator>Campos Vicens, Lluís</dc:creator>
               <dc:creator>Fernández, Lierni</dc:creator>
               <dc:creator>Pecharroman, Irene</dc:creator>
               <dc:creator>García López, Albert</dc:creator>
               <dc:creator>Islam, Abul B. M. M. K.</dc:creator>
               <dc:creator>Marruecos, Laura</dc:creator>
               <dc:creator>Bigas Salvans, Anna</dc:creator>
               <dc:creator>Cerón Madrigal, Julián</dc:creator>
               <dc:creator>Espinosa, Lluís</dc:creator>
               <dc:subject>Anàlisi de proteïnes</dc:subject>
               <dc:subject>Nematodes</dc:subject>
               <dc:subject>Analysis of proteins</dc:subject>
               <dc:subject>Nematodes</dc:subject>
               <dc:description>Mammalian I kappa B proteins (I kappa Bs) exert their main function as negative regulators of NF-kappa B, a central signaling pathway controlling immunity and inflammation. An alternative chromatin role for I kappa Bs has been shown to affect stemness and cell differentiation. However, the involvement of NF-kappa B in this function has not been excluded. NFKI-1 and IKB-1 are I kappa B homologs in Caenorhabditis elegans, which lacks NF-kappa B 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 I kappa Bs 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 I kappa B inhibitors modulate Polycomb activity at specific gene subsets with an impact on development.</dc:description>
               <dc:date>2021-02-23T18:43:58Z</dc:date>
               <dc:date>2021-02-23T18:43:58Z</dc:date>
               <dc:date>2020-09-30</dc:date>
               <dc:date>2021-02-08T10:33:13Z</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:relation>Reproducció del document publicat a: https://doi.org/10.1038/s41598-020-73146-5</dc:relation>
               <dc:relation>Scientific Reports, 2020, vol. 10</dc:relation>
               <dc:relation>https://doi.org/10.1038/s41598-020-73146-5</dc:relation>
               <dc:rights>cc by (c) Brena et al., 2020</dc:rights>
               <dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Nature Research</dc:publisher>
               <dc:source>Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))</dc:source>
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