Cargando…

The E3 Ubiquitin Ligase ATL9 Affects Expression of Defense Related Genes, Cell Death and Callose Deposition in Response to Fungal Infection

Plants use diverse strategies to defend themselves from biotic stresses in nature, which include the activation of defense gene expression and a variety of signal transduction pathways. Previous studies have shown that protein ubiquitination plays a critical role in plant defense responses, however...

Descripción completa

Detalles Bibliográficos
Autores principales: Guo, Tingwei, Kong, Feng, Burton, Carter, Scaglione, Steven, Beagles, Blake, Ray, Justin, Ramonell, Katrina M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778023/
https://www.ncbi.nlm.nih.gov/pubmed/35056016
http://dx.doi.org/10.3390/pathogens11010068
_version_ 1784637216666943488
author Guo, Tingwei
Kong, Feng
Burton, Carter
Scaglione, Steven
Beagles, Blake
Ray, Justin
Ramonell, Katrina M.
author_facet Guo, Tingwei
Kong, Feng
Burton, Carter
Scaglione, Steven
Beagles, Blake
Ray, Justin
Ramonell, Katrina M.
author_sort Guo, Tingwei
collection PubMed
description Plants use diverse strategies to defend themselves from biotic stresses in nature, which include the activation of defense gene expression and a variety of signal transduction pathways. Previous studies have shown that protein ubiquitination plays a critical role in plant defense responses, however the details of its function remain unclear. Our previous work has shown that increasing expression levels of ATL9, an E3 ubiquitin ligase in Arabidopsis thaliana, increased resistance to infection by the fungal pathogen, Golovinomyces cichoracearum. In this study, we demonstrate that the defense-related proteins PDF1.2, PCC1 and FBS1 directly interact with ATL9 and are targeted for degradation to the proteasome by ATL9. The expression levels of PDF1.2, PCC1 and FBS1 are decreased in T-DNA insertional mutants of atl9 and T-DNA insertional mutants of pdf1.2, pcc1 and fbs1 are more susceptible to fungal infection. In addition, callose is more heavily deposited at infection sites in the mutants of atl9, fbs1, pcc1 and pdf1.2. Overexpression of ATL9 and of mutants in fbs1, pcc1 and pdf1.2 showed increased levels of cell death during infection. Together these results indicate that ubiquitination, cell death and callose deposition may work together to enhance defense responses to fungal pathogens.
format Online
Article
Text
id pubmed-8778023
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-87780232022-01-22 The E3 Ubiquitin Ligase ATL9 Affects Expression of Defense Related Genes, Cell Death and Callose Deposition in Response to Fungal Infection Guo, Tingwei Kong, Feng Burton, Carter Scaglione, Steven Beagles, Blake Ray, Justin Ramonell, Katrina M. Pathogens Article Plants use diverse strategies to defend themselves from biotic stresses in nature, which include the activation of defense gene expression and a variety of signal transduction pathways. Previous studies have shown that protein ubiquitination plays a critical role in plant defense responses, however the details of its function remain unclear. Our previous work has shown that increasing expression levels of ATL9, an E3 ubiquitin ligase in Arabidopsis thaliana, increased resistance to infection by the fungal pathogen, Golovinomyces cichoracearum. In this study, we demonstrate that the defense-related proteins PDF1.2, PCC1 and FBS1 directly interact with ATL9 and are targeted for degradation to the proteasome by ATL9. The expression levels of PDF1.2, PCC1 and FBS1 are decreased in T-DNA insertional mutants of atl9 and T-DNA insertional mutants of pdf1.2, pcc1 and fbs1 are more susceptible to fungal infection. In addition, callose is more heavily deposited at infection sites in the mutants of atl9, fbs1, pcc1 and pdf1.2. Overexpression of ATL9 and of mutants in fbs1, pcc1 and pdf1.2 showed increased levels of cell death during infection. Together these results indicate that ubiquitination, cell death and callose deposition may work together to enhance defense responses to fungal pathogens. MDPI 2022-01-05 /pmc/articles/PMC8778023/ /pubmed/35056016 http://dx.doi.org/10.3390/pathogens11010068 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Guo, Tingwei
Kong, Feng
Burton, Carter
Scaglione, Steven
Beagles, Blake
Ray, Justin
Ramonell, Katrina M.
The E3 Ubiquitin Ligase ATL9 Affects Expression of Defense Related Genes, Cell Death and Callose Deposition in Response to Fungal Infection
title The E3 Ubiquitin Ligase ATL9 Affects Expression of Defense Related Genes, Cell Death and Callose Deposition in Response to Fungal Infection
title_full The E3 Ubiquitin Ligase ATL9 Affects Expression of Defense Related Genes, Cell Death and Callose Deposition in Response to Fungal Infection
title_fullStr The E3 Ubiquitin Ligase ATL9 Affects Expression of Defense Related Genes, Cell Death and Callose Deposition in Response to Fungal Infection
title_full_unstemmed The E3 Ubiquitin Ligase ATL9 Affects Expression of Defense Related Genes, Cell Death and Callose Deposition in Response to Fungal Infection
title_short The E3 Ubiquitin Ligase ATL9 Affects Expression of Defense Related Genes, Cell Death and Callose Deposition in Response to Fungal Infection
title_sort e3 ubiquitin ligase atl9 affects expression of defense related genes, cell death and callose deposition in response to fungal infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778023/
https://www.ncbi.nlm.nih.gov/pubmed/35056016
http://dx.doi.org/10.3390/pathogens11010068
work_keys_str_mv AT guotingwei thee3ubiquitinligaseatl9affectsexpressionofdefenserelatedgenescelldeathandcallosedepositioninresponsetofungalinfection
AT kongfeng thee3ubiquitinligaseatl9affectsexpressionofdefenserelatedgenescelldeathandcallosedepositioninresponsetofungalinfection
AT burtoncarter thee3ubiquitinligaseatl9affectsexpressionofdefenserelatedgenescelldeathandcallosedepositioninresponsetofungalinfection
AT scaglionesteven thee3ubiquitinligaseatl9affectsexpressionofdefenserelatedgenescelldeathandcallosedepositioninresponsetofungalinfection
AT beaglesblake thee3ubiquitinligaseatl9affectsexpressionofdefenserelatedgenescelldeathandcallosedepositioninresponsetofungalinfection
AT rayjustin thee3ubiquitinligaseatl9affectsexpressionofdefenserelatedgenescelldeathandcallosedepositioninresponsetofungalinfection
AT ramonellkatrinam thee3ubiquitinligaseatl9affectsexpressionofdefenserelatedgenescelldeathandcallosedepositioninresponsetofungalinfection
AT guotingwei e3ubiquitinligaseatl9affectsexpressionofdefenserelatedgenescelldeathandcallosedepositioninresponsetofungalinfection
AT kongfeng e3ubiquitinligaseatl9affectsexpressionofdefenserelatedgenescelldeathandcallosedepositioninresponsetofungalinfection
AT burtoncarter e3ubiquitinligaseatl9affectsexpressionofdefenserelatedgenescelldeathandcallosedepositioninresponsetofungalinfection
AT scaglionesteven e3ubiquitinligaseatl9affectsexpressionofdefenserelatedgenescelldeathandcallosedepositioninresponsetofungalinfection
AT beaglesblake e3ubiquitinligaseatl9affectsexpressionofdefenserelatedgenescelldeathandcallosedepositioninresponsetofungalinfection
AT rayjustin e3ubiquitinligaseatl9affectsexpressionofdefenserelatedgenescelldeathandcallosedepositioninresponsetofungalinfection
AT ramonellkatrinam e3ubiquitinligaseatl9affectsexpressionofdefenserelatedgenescelldeathandcallosedepositioninresponsetofungalinfection