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Two Waves of Nuclear Factor κb Recruitment to Target Promoters

Proinflammatory stimuli induce the rapid and transient translocation of nuclear factor (NF)-κB to the nucleus, where it activates transcription from several genes, including those encoding inflammatory cytokines and chemokines, adhesion molecules, and cytoprotective proteins. Using chromatin immunop...

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Detalles Bibliográficos
Autores principales: Saccani, Simona, Pantano, Serafino, Natoli, Gioacchino
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193297/
https://www.ncbi.nlm.nih.gov/pubmed/11413190
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author Saccani, Simona
Pantano, Serafino
Natoli, Gioacchino
author_facet Saccani, Simona
Pantano, Serafino
Natoli, Gioacchino
author_sort Saccani, Simona
collection PubMed
description Proinflammatory stimuli induce the rapid and transient translocation of nuclear factor (NF)-κB to the nucleus, where it activates transcription from several genes, including those encoding inflammatory cytokines and chemokines, adhesion molecules, and cytoprotective proteins. Using chromatin immunoprecipitation, we show that after an acute stimulation two distinct waves of NF-κB recruitment to target promoters occur: a fast recruitment to constitutively and immediately accessible (CIA) promoters and a late recruitment to promoters requiring stimulus-dependent modifications in chromatin structure to make NF-κB sites accessible (promoters with regulated and late accessibility [RLA]). Our results suggest that a mechanism of specificity in NF-κB–dependent transcriptional responses relies on the ability of individual stimuli to make RLA promoters accessible to NF-κB before its rapid extrusion from the nucleus.
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spelling pubmed-21932972008-04-14 Two Waves of Nuclear Factor κb Recruitment to Target Promoters Saccani, Simona Pantano, Serafino Natoli, Gioacchino J Exp Med Original Article Proinflammatory stimuli induce the rapid and transient translocation of nuclear factor (NF)-κB to the nucleus, where it activates transcription from several genes, including those encoding inflammatory cytokines and chemokines, adhesion molecules, and cytoprotective proteins. Using chromatin immunoprecipitation, we show that after an acute stimulation two distinct waves of NF-κB recruitment to target promoters occur: a fast recruitment to constitutively and immediately accessible (CIA) promoters and a late recruitment to promoters requiring stimulus-dependent modifications in chromatin structure to make NF-κB sites accessible (promoters with regulated and late accessibility [RLA]). Our results suggest that a mechanism of specificity in NF-κB–dependent transcriptional responses relies on the ability of individual stimuli to make RLA promoters accessible to NF-κB before its rapid extrusion from the nucleus. The Rockefeller University Press 2001-06-18 /pmc/articles/PMC2193297/ /pubmed/11413190 Text en © 2001 The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Original Article
Saccani, Simona
Pantano, Serafino
Natoli, Gioacchino
Two Waves of Nuclear Factor κb Recruitment to Target Promoters
title Two Waves of Nuclear Factor κb Recruitment to Target Promoters
title_full Two Waves of Nuclear Factor κb Recruitment to Target Promoters
title_fullStr Two Waves of Nuclear Factor κb Recruitment to Target Promoters
title_full_unstemmed Two Waves of Nuclear Factor κb Recruitment to Target Promoters
title_short Two Waves of Nuclear Factor κb Recruitment to Target Promoters
title_sort two waves of nuclear factor κb recruitment to target promoters
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193297/
https://www.ncbi.nlm.nih.gov/pubmed/11413190
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