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Signal Integration by the IκB Protein Pickle Shapes Drosophila Innate Host Defense
Pattern recognition receptors are activated following infection and trigger transcriptional programs important for host defense. Tight regulation of NF-κB activation is critical to avoid detrimental and misbalanced responses. We describe Pickle, a Drosophila nuclear IκB that integrates signaling inp...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026699/ https://www.ncbi.nlm.nih.gov/pubmed/27631699 http://dx.doi.org/10.1016/j.chom.2016.08.003 |
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author | Morris, Otto Liu, Xi Domingues, Celia Runchel, Christopher Chai, Andrea Basith, Shaherin Tenev, Tencho Chen, Haiyang Choi, Sangdun Pennetta, Giuseppa Buchon, Nicolas Meier, Pascal |
author_facet | Morris, Otto Liu, Xi Domingues, Celia Runchel, Christopher Chai, Andrea Basith, Shaherin Tenev, Tencho Chen, Haiyang Choi, Sangdun Pennetta, Giuseppa Buchon, Nicolas Meier, Pascal |
author_sort | Morris, Otto |
collection | PubMed |
description | Pattern recognition receptors are activated following infection and trigger transcriptional programs important for host defense. Tight regulation of NF-κB activation is critical to avoid detrimental and misbalanced responses. We describe Pickle, a Drosophila nuclear IκB that integrates signaling inputs from both the Imd and Toll pathways by skewing the transcriptional output of the NF-κB dimer repertoire. Pickle interacts with the NF-κB protein Relish and the histone deacetylase dHDAC1, selectively repressing Relish homodimers while leaving other NF-κB dimer combinations unscathed. Pickle’s ability to selectively inhibit Relish homodimer activity contributes to proper host immunity and organismal health. Although loss of pickle results in hyper-induction of Relish target genes and improved host resistance to pathogenic bacteria in the short term, chronic inactivation of pickle causes loss of immune tolerance and shortened lifespan. Pickle therefore allows balanced immune responses that protect from pathogenic microbes while permitting the establishment of beneficial commensal host-microbe relationships. |
format | Online Article Text |
id | pubmed-5026699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50266992016-09-23 Signal Integration by the IκB Protein Pickle Shapes Drosophila Innate Host Defense Morris, Otto Liu, Xi Domingues, Celia Runchel, Christopher Chai, Andrea Basith, Shaherin Tenev, Tencho Chen, Haiyang Choi, Sangdun Pennetta, Giuseppa Buchon, Nicolas Meier, Pascal Cell Host Microbe Article Pattern recognition receptors are activated following infection and trigger transcriptional programs important for host defense. Tight regulation of NF-κB activation is critical to avoid detrimental and misbalanced responses. We describe Pickle, a Drosophila nuclear IκB that integrates signaling inputs from both the Imd and Toll pathways by skewing the transcriptional output of the NF-κB dimer repertoire. Pickle interacts with the NF-κB protein Relish and the histone deacetylase dHDAC1, selectively repressing Relish homodimers while leaving other NF-κB dimer combinations unscathed. Pickle’s ability to selectively inhibit Relish homodimer activity contributes to proper host immunity and organismal health. Although loss of pickle results in hyper-induction of Relish target genes and improved host resistance to pathogenic bacteria in the short term, chronic inactivation of pickle causes loss of immune tolerance and shortened lifespan. Pickle therefore allows balanced immune responses that protect from pathogenic microbes while permitting the establishment of beneficial commensal host-microbe relationships. Cell Press 2016-09-14 /pmc/articles/PMC5026699/ /pubmed/27631699 http://dx.doi.org/10.1016/j.chom.2016.08.003 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Morris, Otto Liu, Xi Domingues, Celia Runchel, Christopher Chai, Andrea Basith, Shaherin Tenev, Tencho Chen, Haiyang Choi, Sangdun Pennetta, Giuseppa Buchon, Nicolas Meier, Pascal Signal Integration by the IκB Protein Pickle Shapes Drosophila Innate Host Defense |
title | Signal Integration by the IκB Protein Pickle Shapes Drosophila Innate Host Defense |
title_full | Signal Integration by the IκB Protein Pickle Shapes Drosophila Innate Host Defense |
title_fullStr | Signal Integration by the IκB Protein Pickle Shapes Drosophila Innate Host Defense |
title_full_unstemmed | Signal Integration by the IκB Protein Pickle Shapes Drosophila Innate Host Defense |
title_short | Signal Integration by the IκB Protein Pickle Shapes Drosophila Innate Host Defense |
title_sort | signal integration by the iκb protein pickle shapes drosophila innate host defense |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026699/ https://www.ncbi.nlm.nih.gov/pubmed/27631699 http://dx.doi.org/10.1016/j.chom.2016.08.003 |
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