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
Abstract
AbstractMammalian 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.
Funder
Instituto de Salud Carlos III
Centro de Investigación Biomédica en Red de Cáncer
Agència de Gestió d'Ajuts Universitaris i de Recerca
Ministerio de Economía, Industria y Competitividad, Gobierno de España
Publisher
Springer Science and Business Media LLC
Cited by
12 articles.
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