Cargando…
Salicylic acid-induced transcriptional reprogramming by the HAC–NPR1–TGA histone acetyltransferase complex in Arabidopsis
Plant immunity depends on massive expression of pathogenesis-related genes (PRs) whose transcription is de-repressed by pathogen-induced signals. Salicylic acid (SA) acts as a major signaling molecule in plant immunity and systemic acquired resistance triggered by bacterial or viral pathogens. SA si...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6294559/ https://www.ncbi.nlm.nih.gov/pubmed/30239885 http://dx.doi.org/10.1093/nar/gky847 |
_version_ | 1783380751411052544 |
---|---|
author | Jin, Hongshi Choi, Sun-Mee Kang, Min-Jeong Yun, Se-Hun Kwon, Dong-Jin Noh, Yoo-Sun Noh, Bosl |
author_facet | Jin, Hongshi Choi, Sun-Mee Kang, Min-Jeong Yun, Se-Hun Kwon, Dong-Jin Noh, Yoo-Sun Noh, Bosl |
author_sort | Jin, Hongshi |
collection | PubMed |
description | Plant immunity depends on massive expression of pathogenesis-related genes (PRs) whose transcription is de-repressed by pathogen-induced signals. Salicylic acid (SA) acts as a major signaling molecule in plant immunity and systemic acquired resistance triggered by bacterial or viral pathogens. SA signal results in the activation of the master immune regulator, Nonexpressor of pathogenesis-related genes 1 (NPR1), which is thought to be recruited by transcription factors such as TGAs to numerous downstream PRs. Despite its key role in SA-triggered immunity, the biochemical nature of the transcriptional coactivator function of NPR1 and the massive transcriptional reprogramming induced by it remain obscure. Here we demonstrate that the CBP/p300-family histone acetyltransferases, HACs and NPR1 are both essential to develop SA-triggered immunity and PR induction. Indeed HACs and NPR1 form a coactivator complex and are recruited to PR chromatin through TGAs upon SA signal, and finally the HAC−NPR1−TGA complex activates PR transcription by histone acetylation-mediated epigenetic reprogramming. Thus, our study reveals a molecular mechanism of NPR1-mediated transcriptional reprogramming and a key epigenetic aspect of the central immune system in plants. |
format | Online Article Text |
id | pubmed-6294559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62945592018-12-21 Salicylic acid-induced transcriptional reprogramming by the HAC–NPR1–TGA histone acetyltransferase complex in Arabidopsis Jin, Hongshi Choi, Sun-Mee Kang, Min-Jeong Yun, Se-Hun Kwon, Dong-Jin Noh, Yoo-Sun Noh, Bosl Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Plant immunity depends on massive expression of pathogenesis-related genes (PRs) whose transcription is de-repressed by pathogen-induced signals. Salicylic acid (SA) acts as a major signaling molecule in plant immunity and systemic acquired resistance triggered by bacterial or viral pathogens. SA signal results in the activation of the master immune regulator, Nonexpressor of pathogenesis-related genes 1 (NPR1), which is thought to be recruited by transcription factors such as TGAs to numerous downstream PRs. Despite its key role in SA-triggered immunity, the biochemical nature of the transcriptional coactivator function of NPR1 and the massive transcriptional reprogramming induced by it remain obscure. Here we demonstrate that the CBP/p300-family histone acetyltransferases, HACs and NPR1 are both essential to develop SA-triggered immunity and PR induction. Indeed HACs and NPR1 form a coactivator complex and are recruited to PR chromatin through TGAs upon SA signal, and finally the HAC−NPR1−TGA complex activates PR transcription by histone acetylation-mediated epigenetic reprogramming. Thus, our study reveals a molecular mechanism of NPR1-mediated transcriptional reprogramming and a key epigenetic aspect of the central immune system in plants. Oxford University Press 2018-12-14 2018-09-17 /pmc/articles/PMC6294559/ /pubmed/30239885 http://dx.doi.org/10.1093/nar/gky847 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gene regulation, Chromatin and Epigenetics Jin, Hongshi Choi, Sun-Mee Kang, Min-Jeong Yun, Se-Hun Kwon, Dong-Jin Noh, Yoo-Sun Noh, Bosl Salicylic acid-induced transcriptional reprogramming by the HAC–NPR1–TGA histone acetyltransferase complex in Arabidopsis |
title | Salicylic acid-induced transcriptional reprogramming by the HAC–NPR1–TGA histone acetyltransferase complex in Arabidopsis |
title_full | Salicylic acid-induced transcriptional reprogramming by the HAC–NPR1–TGA histone acetyltransferase complex in Arabidopsis |
title_fullStr | Salicylic acid-induced transcriptional reprogramming by the HAC–NPR1–TGA histone acetyltransferase complex in Arabidopsis |
title_full_unstemmed | Salicylic acid-induced transcriptional reprogramming by the HAC–NPR1–TGA histone acetyltransferase complex in Arabidopsis |
title_short | Salicylic acid-induced transcriptional reprogramming by the HAC–NPR1–TGA histone acetyltransferase complex in Arabidopsis |
title_sort | salicylic acid-induced transcriptional reprogramming by the hac–npr1–tga histone acetyltransferase complex in arabidopsis |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6294559/ https://www.ncbi.nlm.nih.gov/pubmed/30239885 http://dx.doi.org/10.1093/nar/gky847 |
work_keys_str_mv | AT jinhongshi salicylicacidinducedtranscriptionalreprogrammingbythehacnpr1tgahistoneacetyltransferasecomplexinarabidopsis AT choisunmee salicylicacidinducedtranscriptionalreprogrammingbythehacnpr1tgahistoneacetyltransferasecomplexinarabidopsis AT kangminjeong salicylicacidinducedtranscriptionalreprogrammingbythehacnpr1tgahistoneacetyltransferasecomplexinarabidopsis AT yunsehun salicylicacidinducedtranscriptionalreprogrammingbythehacnpr1tgahistoneacetyltransferasecomplexinarabidopsis AT kwondongjin salicylicacidinducedtranscriptionalreprogrammingbythehacnpr1tgahistoneacetyltransferasecomplexinarabidopsis AT nohyoosun salicylicacidinducedtranscriptionalreprogrammingbythehacnpr1tgahistoneacetyltransferasecomplexinarabidopsis AT nohbosl salicylicacidinducedtranscriptionalreprogrammingbythehacnpr1tgahistoneacetyltransferasecomplexinarabidopsis |