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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |