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The moss-specific transcription factor PpERF24 positively modulates immunity against fungal pathogens in Physcomitrium patens

APETALA2/ethylene response factors (AP2/ERFs) transcription factors (TFs) have greatly expanded in land plants compared to algae. In angiosperms, AP2/ERFs play important regulatory functions in plant defenses against pathogens and abiotic stress by controlling the expression of target genes. In the...

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Autores principales: Reboledo, Guillermo, Agorio, Astrid, Vignale, Lucía, Alvarez, Alfonso, Ponce De León, Inés
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520294/
https://www.ncbi.nlm.nih.gov/pubmed/36186018
http://dx.doi.org/10.3389/fpls.2022.908682
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author Reboledo, Guillermo
Agorio, Astrid
Vignale, Lucía
Alvarez, Alfonso
Ponce De León, Inés
author_facet Reboledo, Guillermo
Agorio, Astrid
Vignale, Lucía
Alvarez, Alfonso
Ponce De León, Inés
author_sort Reboledo, Guillermo
collection PubMed
description APETALA2/ethylene response factors (AP2/ERFs) transcription factors (TFs) have greatly expanded in land plants compared to algae. In angiosperms, AP2/ERFs play important regulatory functions in plant defenses against pathogens and abiotic stress by controlling the expression of target genes. In the moss Physcomitrium patens, a high number of members of the ERF family are induced during pathogen infection, suggesting that they are important regulators in bryophyte immunity. In the current study, we analyzed a P. patens pathogen-inducible ERF family member designated as PpERF24. Orthologs of PpERF24 were only found in other mosses, while they were absent in the bryophytes Marchantia polymorpha and Anthoceros agrestis, the vascular plant Selaginella moellendorffii, and angiosperms. We show that PpERF24 belongs to a moss-specific clade with distinctive amino acids features in the AP2 domain that binds to the DNA. Interestingly, all P. patens members of the PpERF24 subclade are induced by fungal pathogens. The function of PpERF24 during plant immunity was assessed by an overexpression approach and transcriptomic analysis. Overexpressing lines showed increased defenses to infection by the fungal pathogens Botrytis cinerea and Colletotrichum gloeosporioides evidenced by reduced cellular damage and fungal biomass compared to wild-type plants. Transcriptomic and RT-qPCR analysis revealed that PpERF24 positively regulates the expression levels of defense genes involved in transcriptional regulation, phenylpropanoid and jasmonate pathways, oxidative burst and pathogenesis-related (PR) genes. These findings give novel insights into potential mechanism by which PpERF24 increases plant defenses against several pathogens by regulating important players in plant immunity.
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spelling pubmed-95202942022-09-30 The moss-specific transcription factor PpERF24 positively modulates immunity against fungal pathogens in Physcomitrium patens Reboledo, Guillermo Agorio, Astrid Vignale, Lucía Alvarez, Alfonso Ponce De León, Inés Front Plant Sci Plant Science APETALA2/ethylene response factors (AP2/ERFs) transcription factors (TFs) have greatly expanded in land plants compared to algae. In angiosperms, AP2/ERFs play important regulatory functions in plant defenses against pathogens and abiotic stress by controlling the expression of target genes. In the moss Physcomitrium patens, a high number of members of the ERF family are induced during pathogen infection, suggesting that they are important regulators in bryophyte immunity. In the current study, we analyzed a P. patens pathogen-inducible ERF family member designated as PpERF24. Orthologs of PpERF24 were only found in other mosses, while they were absent in the bryophytes Marchantia polymorpha and Anthoceros agrestis, the vascular plant Selaginella moellendorffii, and angiosperms. We show that PpERF24 belongs to a moss-specific clade with distinctive amino acids features in the AP2 domain that binds to the DNA. Interestingly, all P. patens members of the PpERF24 subclade are induced by fungal pathogens. The function of PpERF24 during plant immunity was assessed by an overexpression approach and transcriptomic analysis. Overexpressing lines showed increased defenses to infection by the fungal pathogens Botrytis cinerea and Colletotrichum gloeosporioides evidenced by reduced cellular damage and fungal biomass compared to wild-type plants. Transcriptomic and RT-qPCR analysis revealed that PpERF24 positively regulates the expression levels of defense genes involved in transcriptional regulation, phenylpropanoid and jasmonate pathways, oxidative burst and pathogenesis-related (PR) genes. These findings give novel insights into potential mechanism by which PpERF24 increases plant defenses against several pathogens by regulating important players in plant immunity. Frontiers Media S.A. 2022-09-15 /pmc/articles/PMC9520294/ /pubmed/36186018 http://dx.doi.org/10.3389/fpls.2022.908682 Text en Copyright © 2022 Reboledo, Agorio, Vignale, Alvarez and Ponce De León. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Reboledo, Guillermo
Agorio, Astrid
Vignale, Lucía
Alvarez, Alfonso
Ponce De León, Inés
The moss-specific transcription factor PpERF24 positively modulates immunity against fungal pathogens in Physcomitrium patens
title The moss-specific transcription factor PpERF24 positively modulates immunity against fungal pathogens in Physcomitrium patens
title_full The moss-specific transcription factor PpERF24 positively modulates immunity against fungal pathogens in Physcomitrium patens
title_fullStr The moss-specific transcription factor PpERF24 positively modulates immunity against fungal pathogens in Physcomitrium patens
title_full_unstemmed The moss-specific transcription factor PpERF24 positively modulates immunity against fungal pathogens in Physcomitrium patens
title_short The moss-specific transcription factor PpERF24 positively modulates immunity against fungal pathogens in Physcomitrium patens
title_sort moss-specific transcription factor pperf24 positively modulates immunity against fungal pathogens in physcomitrium patens
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520294/
https://www.ncbi.nlm.nih.gov/pubmed/36186018
http://dx.doi.org/10.3389/fpls.2022.908682
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