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NF-κB oscillations translate into functionally related patterns of gene expression

Several transcription factors (TFs) oscillate, periodically relocating between the cytoplasm and the nucleus. NF-κB, which plays key roles in inflammation and cancer, displays oscillations whose biological advantage remains unclear. Recent work indicated that NF-κB displays sustained oscillations th...

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Autores principales: Zambrano, Samuel, De Toma, Ilario, Piffer, Arianna, Bianchi, Marco E, Agresti, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4798970/
https://www.ncbi.nlm.nih.gov/pubmed/26765569
http://dx.doi.org/10.7554/eLife.09100
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author Zambrano, Samuel
De Toma, Ilario
Piffer, Arianna
Bianchi, Marco E
Agresti, Alessandra
author_facet Zambrano, Samuel
De Toma, Ilario
Piffer, Arianna
Bianchi, Marco E
Agresti, Alessandra
author_sort Zambrano, Samuel
collection PubMed
description Several transcription factors (TFs) oscillate, periodically relocating between the cytoplasm and the nucleus. NF-κB, which plays key roles in inflammation and cancer, displays oscillations whose biological advantage remains unclear. Recent work indicated that NF-κB displays sustained oscillations that can be entrained, that is, reach a persistent synchronized state through small periodic perturbations. We show here that for our GFP-p65 knock-in cells NF-κB behaves as a damped oscillator able to synchronize to a variety of periodic external perturbations with no memory. We imposed synchronous dynamics to prove that transcription of NF-κB-controlled genes also oscillates, but mature transcript levels follow three distinct patterns. Two sets of transcripts accumulate fast or slowly, respectively. Another set, comprising chemokine and chemokine receptor mRNAs, oscillates and resets at each new stimulus, with no memory of the past. We propose that TF oscillatory dynamics is a means of segmenting time to provide renewing opportunity windows for decision. DOI: http://dx.doi.org/10.7554/eLife.09100.001
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spelling pubmed-47989702016-03-21 NF-κB oscillations translate into functionally related patterns of gene expression Zambrano, Samuel De Toma, Ilario Piffer, Arianna Bianchi, Marco E Agresti, Alessandra eLife Computational and Systems Biology Several transcription factors (TFs) oscillate, periodically relocating between the cytoplasm and the nucleus. NF-κB, which plays key roles in inflammation and cancer, displays oscillations whose biological advantage remains unclear. Recent work indicated that NF-κB displays sustained oscillations that can be entrained, that is, reach a persistent synchronized state through small periodic perturbations. We show here that for our GFP-p65 knock-in cells NF-κB behaves as a damped oscillator able to synchronize to a variety of periodic external perturbations with no memory. We imposed synchronous dynamics to prove that transcription of NF-κB-controlled genes also oscillates, but mature transcript levels follow three distinct patterns. Two sets of transcripts accumulate fast or slowly, respectively. Another set, comprising chemokine and chemokine receptor mRNAs, oscillates and resets at each new stimulus, with no memory of the past. We propose that TF oscillatory dynamics is a means of segmenting time to provide renewing opportunity windows for decision. DOI: http://dx.doi.org/10.7554/eLife.09100.001 eLife Sciences Publications, Ltd 2016-01-14 /pmc/articles/PMC4798970/ /pubmed/26765569 http://dx.doi.org/10.7554/eLife.09100 Text en © 2016, Zambrano et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Computational and Systems Biology
Zambrano, Samuel
De Toma, Ilario
Piffer, Arianna
Bianchi, Marco E
Agresti, Alessandra
NF-κB oscillations translate into functionally related patterns of gene expression
title NF-κB oscillations translate into functionally related patterns of gene expression
title_full NF-κB oscillations translate into functionally related patterns of gene expression
title_fullStr NF-κB oscillations translate into functionally related patterns of gene expression
title_full_unstemmed NF-κB oscillations translate into functionally related patterns of gene expression
title_short NF-κB oscillations translate into functionally related patterns of gene expression
title_sort nf-κb oscillations translate into functionally related patterns of gene expression
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4798970/
https://www.ncbi.nlm.nih.gov/pubmed/26765569
http://dx.doi.org/10.7554/eLife.09100
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