Cargando…

The nuclear hormone receptor NHR-86 controls anti-pathogen responses in C. elegans

Nuclear hormone receptors (NHRs) are ligand-gated transcription factors that control adaptive host responses following recognition of specific endogenous or exogenous ligands. Although NHRs have expanded dramatically in C. elegans compared to other metazoans, the biological function of only a few of...

Descripción completa

Detalles Bibliográficos
Autores principales: Peterson, Nicholas D., Cheesman, Hilary K., Liu, Pengpeng, Anderson, Sarah M., Foster, Kyle J., Chhaya, Richa, Perrat, Paola, Thekkiniath, Jose, Yang, Qiyuan, Haynes, Cole M., Pukkila-Worley, Read
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6358101/
https://www.ncbi.nlm.nih.gov/pubmed/30668573
http://dx.doi.org/10.1371/journal.pgen.1007935
_version_ 1783391950176518144
author Peterson, Nicholas D.
Cheesman, Hilary K.
Liu, Pengpeng
Anderson, Sarah M.
Foster, Kyle J.
Chhaya, Richa
Perrat, Paola
Thekkiniath, Jose
Yang, Qiyuan
Haynes, Cole M.
Pukkila-Worley, Read
author_facet Peterson, Nicholas D.
Cheesman, Hilary K.
Liu, Pengpeng
Anderson, Sarah M.
Foster, Kyle J.
Chhaya, Richa
Perrat, Paola
Thekkiniath, Jose
Yang, Qiyuan
Haynes, Cole M.
Pukkila-Worley, Read
author_sort Peterson, Nicholas D.
collection PubMed
description Nuclear hormone receptors (NHRs) are ligand-gated transcription factors that control adaptive host responses following recognition of specific endogenous or exogenous ligands. Although NHRs have expanded dramatically in C. elegans compared to other metazoans, the biological function of only a few of these genes has been characterized in detail. Here, we demonstrate that an NHR can activate an anti-pathogen transcriptional program. Using genetic epistasis experiments, transcriptome profiling analyses and chromatin immunoprecipitation-sequencing, we show that, in the presence of an immunostimulatory small molecule, NHR-86 binds to the promoters of immune effectors to activate their transcription. NHR-86 is not required for resistance to the bacterial pathogen Pseudomonas aeruginosa at baseline, but activation of NHR-86 by this compound drives a transcriptional program that provides protection against this pathogen. Interestingly, NHR-86 targets immune effectors whose basal regulation requires the canonical p38 MAPK PMK-1 immune pathway. However, NHR-86 functions independently of PMK-1 and modulates the transcription of these infection response genes directly. These findings characterize a new transcriptional regulator in C. elegans that can induce a protective host response towards a bacterial pathogen.
format Online
Article
Text
id pubmed-6358101
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-63581012019-02-15 The nuclear hormone receptor NHR-86 controls anti-pathogen responses in C. elegans Peterson, Nicholas D. Cheesman, Hilary K. Liu, Pengpeng Anderson, Sarah M. Foster, Kyle J. Chhaya, Richa Perrat, Paola Thekkiniath, Jose Yang, Qiyuan Haynes, Cole M. Pukkila-Worley, Read PLoS Genet Research Article Nuclear hormone receptors (NHRs) are ligand-gated transcription factors that control adaptive host responses following recognition of specific endogenous or exogenous ligands. Although NHRs have expanded dramatically in C. elegans compared to other metazoans, the biological function of only a few of these genes has been characterized in detail. Here, we demonstrate that an NHR can activate an anti-pathogen transcriptional program. Using genetic epistasis experiments, transcriptome profiling analyses and chromatin immunoprecipitation-sequencing, we show that, in the presence of an immunostimulatory small molecule, NHR-86 binds to the promoters of immune effectors to activate their transcription. NHR-86 is not required for resistance to the bacterial pathogen Pseudomonas aeruginosa at baseline, but activation of NHR-86 by this compound drives a transcriptional program that provides protection against this pathogen. Interestingly, NHR-86 targets immune effectors whose basal regulation requires the canonical p38 MAPK PMK-1 immune pathway. However, NHR-86 functions independently of PMK-1 and modulates the transcription of these infection response genes directly. These findings characterize a new transcriptional regulator in C. elegans that can induce a protective host response towards a bacterial pathogen. Public Library of Science 2019-01-22 /pmc/articles/PMC6358101/ /pubmed/30668573 http://dx.doi.org/10.1371/journal.pgen.1007935 Text en © 2019 Peterson et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Peterson, Nicholas D.
Cheesman, Hilary K.
Liu, Pengpeng
Anderson, Sarah M.
Foster, Kyle J.
Chhaya, Richa
Perrat, Paola
Thekkiniath, Jose
Yang, Qiyuan
Haynes, Cole M.
Pukkila-Worley, Read
The nuclear hormone receptor NHR-86 controls anti-pathogen responses in C. elegans
title The nuclear hormone receptor NHR-86 controls anti-pathogen responses in C. elegans
title_full The nuclear hormone receptor NHR-86 controls anti-pathogen responses in C. elegans
title_fullStr The nuclear hormone receptor NHR-86 controls anti-pathogen responses in C. elegans
title_full_unstemmed The nuclear hormone receptor NHR-86 controls anti-pathogen responses in C. elegans
title_short The nuclear hormone receptor NHR-86 controls anti-pathogen responses in C. elegans
title_sort nuclear hormone receptor nhr-86 controls anti-pathogen responses in c. elegans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6358101/
https://www.ncbi.nlm.nih.gov/pubmed/30668573
http://dx.doi.org/10.1371/journal.pgen.1007935
work_keys_str_mv AT petersonnicholasd thenuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT cheesmanhilaryk thenuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT liupengpeng thenuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT andersonsarahm thenuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT fosterkylej thenuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT chhayaricha thenuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT perratpaola thenuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT thekkiniathjose thenuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT yangqiyuan thenuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT haynescolem thenuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT pukkilaworleyread thenuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT petersonnicholasd nuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT cheesmanhilaryk nuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT liupengpeng nuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT andersonsarahm nuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT fosterkylej nuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT chhayaricha nuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT perratpaola nuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT thekkiniathjose nuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT yangqiyuan nuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT haynescolem nuclearhormonereceptornhr86controlsantipathogenresponsesincelegans
AT pukkilaworleyread nuclearhormonereceptornhr86controlsantipathogenresponsesincelegans