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Single Amino Acid Substitution in the DNA Repairing Gene Radiation-Sensitive 4 Contributes to Ultraviolet Tolerance of a Plant Pathogen

To successfully survive and reproduce, all species constantly modify the structure and expression of their genomes to cope with changing environmental conditions including ultraviolet (UV) radiation. Thus, knowledge of species adaptation to environmental changes is a central theme of evolutionary st...

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Autores principales: Wang, Yan-Ping, Yang, Li-Na, Feng, Yuan-Yuan, Liu, Songqing, Zhan, Jiasui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330021/
https://www.ncbi.nlm.nih.gov/pubmed/35910660
http://dx.doi.org/10.3389/fmicb.2022.927139
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author Wang, Yan-Ping
Yang, Li-Na
Feng, Yuan-Yuan
Liu, Songqing
Zhan, Jiasui
author_facet Wang, Yan-Ping
Yang, Li-Na
Feng, Yuan-Yuan
Liu, Songqing
Zhan, Jiasui
author_sort Wang, Yan-Ping
collection PubMed
description To successfully survive and reproduce, all species constantly modify the structure and expression of their genomes to cope with changing environmental conditions including ultraviolet (UV) radiation. Thus, knowledge of species adaptation to environmental changes is a central theme of evolutionary studies which could have important implication for disease management and social-ecological sustainability in the future but is generally insufficient. Here, we investigated the evolution of UV adaptation in organisms by population genetic analysis of sequence structure, physiochemistry, transcription, and fitness variation in the radiation-sensitive 4 (RAD4) gene of the Irish potato famine pathogen Phytophthora infestans sampled from various altitudes. We found that RAD4 is a key gene determining the resistance of the pathogen to UV stress as indicated by strong phenotype-genotype-geography associations and upregulated transcription after UV exposure. We also found conserved evolution in the RAD4 gene. Only five nucleotide haplotypes corresponding to three protein isoforms generated by point mutations were detected in the 140 sequences analyzed and the mutations were constrained to the N-terminal domain of the protein. Physiochemical changes associated with non-synonymous mutations generate severe fitness penalty to mutants, which are purged out by natural selection, leading to the conserved evolution observed in the gene.
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spelling pubmed-93300212022-07-29 Single Amino Acid Substitution in the DNA Repairing Gene Radiation-Sensitive 4 Contributes to Ultraviolet Tolerance of a Plant Pathogen Wang, Yan-Ping Yang, Li-Na Feng, Yuan-Yuan Liu, Songqing Zhan, Jiasui Front Microbiol Microbiology To successfully survive and reproduce, all species constantly modify the structure and expression of their genomes to cope with changing environmental conditions including ultraviolet (UV) radiation. Thus, knowledge of species adaptation to environmental changes is a central theme of evolutionary studies which could have important implication for disease management and social-ecological sustainability in the future but is generally insufficient. Here, we investigated the evolution of UV adaptation in organisms by population genetic analysis of sequence structure, physiochemistry, transcription, and fitness variation in the radiation-sensitive 4 (RAD4) gene of the Irish potato famine pathogen Phytophthora infestans sampled from various altitudes. We found that RAD4 is a key gene determining the resistance of the pathogen to UV stress as indicated by strong phenotype-genotype-geography associations and upregulated transcription after UV exposure. We also found conserved evolution in the RAD4 gene. Only five nucleotide haplotypes corresponding to three protein isoforms generated by point mutations were detected in the 140 sequences analyzed and the mutations were constrained to the N-terminal domain of the protein. Physiochemical changes associated with non-synonymous mutations generate severe fitness penalty to mutants, which are purged out by natural selection, leading to the conserved evolution observed in the gene. Frontiers Media S.A. 2022-07-14 /pmc/articles/PMC9330021/ /pubmed/35910660 http://dx.doi.org/10.3389/fmicb.2022.927139 Text en Copyright © 2022 Wang, Yang, Feng, Liu and Zhan. 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 Microbiology
Wang, Yan-Ping
Yang, Li-Na
Feng, Yuan-Yuan
Liu, Songqing
Zhan, Jiasui
Single Amino Acid Substitution in the DNA Repairing Gene Radiation-Sensitive 4 Contributes to Ultraviolet Tolerance of a Plant Pathogen
title Single Amino Acid Substitution in the DNA Repairing Gene Radiation-Sensitive 4 Contributes to Ultraviolet Tolerance of a Plant Pathogen
title_full Single Amino Acid Substitution in the DNA Repairing Gene Radiation-Sensitive 4 Contributes to Ultraviolet Tolerance of a Plant Pathogen
title_fullStr Single Amino Acid Substitution in the DNA Repairing Gene Radiation-Sensitive 4 Contributes to Ultraviolet Tolerance of a Plant Pathogen
title_full_unstemmed Single Amino Acid Substitution in the DNA Repairing Gene Radiation-Sensitive 4 Contributes to Ultraviolet Tolerance of a Plant Pathogen
title_short Single Amino Acid Substitution in the DNA Repairing Gene Radiation-Sensitive 4 Contributes to Ultraviolet Tolerance of a Plant Pathogen
title_sort single amino acid substitution in the dna repairing gene radiation-sensitive 4 contributes to ultraviolet tolerance of a plant pathogen
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330021/
https://www.ncbi.nlm.nih.gov/pubmed/35910660
http://dx.doi.org/10.3389/fmicb.2022.927139
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