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Expression profiling across wild and cultivated tomatoes supports the relevance of early miR482/2118 suppression for Phytophthora resistance.

Identifieur interne : 000779 ( Main/Exploration ); précédent : 000778; suivant : 000780

Expression profiling across wild and cultivated tomatoes supports the relevance of early miR482/2118 suppression for Phytophthora resistance.

Auteurs : Sophie De Vries [Canada, Allemagne] ; Andreas Kukuk [Allemagne] ; Janina K. Von Dahlen [Allemagne] ; Anika Schnake [Allemagne] ; Thorsten Kloesges [Allemagne] ; Laura E. Rose [Allemagne]

Source :

RBID : pubmed:29491170

Descripteurs français

English descriptors

Abstract

Plants possess a battery of specific pathogen resistance (R-)genes. Precise R-gene regulation is important in the presence and absence of a pathogen. Recently, a microRNA family, miR482/2118, was shown to regulate the expression of a major class of R-genes, nucleotide-binding site leucine-rich repeats (NBS-LRRs). Furthermore, RNA silencing suppressor proteins, secreted by pathogens, prevent the accumulation of miR482/2118, leading to an upregulation of R-genes. Despite this transcriptional release of R-genes, RNA silencing suppressors positively contribute to the virulence of some pathogens. To investigate this paradox, we analysed how the regulation of NBS-LRRs by miR482/2118 has been shaped by the coevolution between Phytophthora infestans and cultivated and wild tomatoes. We used degradome analyses and qRT-PCR to evaluate and quantify the co-expression of miR482/2118 and their NBS-LRR targets. Our data show that miR482/2118-mediated targeting contributes to the regulation of NBS-LRRs in Solanum lycopersicum. Based on miR482/2118 expression profiling in two additional tomato species-with different coevolutionary histories with P. infestans-we hypothesize that pathogen-mediated RNA silencing suppression is most effective in the interaction between S. lycopersicum and P. infestans Furthermore, an upregulation of miR482/2118 early in the infection may increase susceptibility to P. infestans.

DOI: 10.1098/rspb.2017.2560
PubMed: 29491170
PubMed Central: PMC5832704


Affiliations:


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<term>Biological Coevolution (MeSH)</term>
<term>Disease Resistance (genetics)</term>
<term>Lycopersicon esculentum (genetics)</term>
<term>Lycopersicon esculentum (microbiology)</term>
<term>MicroRNAs (genetics)</term>
<term>Phytophthora (physiology)</term>
<term>Plant Diseases (genetics)</term>
<term>Plant Diseases (microbiology)</term>
<term>RNA, Plant (genetics)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>ARN des plantes (génétique)</term>
<term>Coévolution biologique (MeSH)</term>
<term>Lycopersicon esculentum (génétique)</term>
<term>Lycopersicon esculentum (microbiologie)</term>
<term>Maladies des plantes (génétique)</term>
<term>Maladies des plantes (microbiologie)</term>
<term>Phytophthora (physiologie)</term>
<term>Résistance à la maladie (génétique)</term>
<term>microARN (génétique)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>MicroRNAs</term>
<term>RNA, Plant</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Disease Resistance</term>
<term>Lycopersicon esculentum</term>
<term>Plant Diseases</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>ARN des plantes</term>
<term>Lycopersicon esculentum</term>
<term>Maladies des plantes</term>
<term>Résistance à la maladie</term>
<term>microARN</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr">
<term>Lycopersicon esculentum</term>
<term>Maladies des plantes</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiology" xml:lang="en">
<term>Lycopersicon esculentum</term>
<term>Plant Diseases</term>
</keywords>
<keywords scheme="MESH" qualifier="physiologie" xml:lang="fr">
<term>Phytophthora</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en">
<term>Phytophthora</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Biological Coevolution</term>
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<div type="abstract" xml:lang="en">Plants possess a battery of specific pathogen resistance (
<i>R-</i>
)genes. Precise
<i>R-</i>
gene regulation is important in the presence and absence of a pathogen. Recently, a microRNA family, miR482/2118, was shown to regulate the expression of a major class of
<i>R-</i>
genes
<i>,</i>
nucleotide-binding site leucine-rich repeats (
<i>NBS-LRRs</i>
). Furthermore, RNA silencing suppressor proteins, secreted by pathogens, prevent the accumulation of miR482/2118, leading to an upregulation of
<i>R-</i>
genes. Despite this transcriptional release of
<i>R</i>
-genes, RNA silencing suppressors positively contribute to the virulence of some pathogens
<i>.</i>
To investigate this paradox, we analysed how the regulation of
<i>NBS-LRRs</i>
by miR482/2118 has been shaped by the coevolution between
<i>Phytophthora infestans</i>
and cultivated and wild tomatoes. We used degradome analyses and qRT-PCR to evaluate and quantify the co-expression of miR482/2118 and their
<i>NBS-LRR</i>
targets. Our data show that miR482/2118-mediated targeting contributes to the regulation of
<i>NBS-LRRs</i>
in
<i>Solanum lycopersicum.</i>
Based on miR482/2118 expression profiling in two additional tomato species-with different coevolutionary histories with
<i>P. infestans</i>
-we hypothesize that pathogen-mediated RNA silencing suppression is most effective in the interaction between
<i>S. lycopersicum</i>
and
<i>P. infestans</i>
Furthermore, an upregulation of miR482/2118 early in the infection may increase susceptibility to
<i>P. infestans</i>
.</div>
</front>
</TEI>
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<DateCompleted>
<Year>2019</Year>
<Month>01</Month>
<Day>04</Day>
</DateCompleted>
<DateRevised>
<Year>2019</Year>
<Month>01</Month>
<Day>30</Day>
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<JournalIssue CitedMedium="Internet">
<Volume>285</Volume>
<Issue>1873</Issue>
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<ArticleTitle>Expression profiling across wild and cultivated tomatoes supports the relevance of early miR482/2118 suppression for
<i>Phytophthora</i>
resistance.</ArticleTitle>
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<ELocationID EIdType="doi" ValidYN="Y">10.1098/rspb.2017.2560</ELocationID>
<Abstract>
<AbstractText>Plants possess a battery of specific pathogen resistance (
<i>R-</i>
)genes. Precise
<i>R-</i>
gene regulation is important in the presence and absence of a pathogen. Recently, a microRNA family, miR482/2118, was shown to regulate the expression of a major class of
<i>R-</i>
genes
<i>,</i>
nucleotide-binding site leucine-rich repeats (
<i>NBS-LRRs</i>
). Furthermore, RNA silencing suppressor proteins, secreted by pathogens, prevent the accumulation of miR482/2118, leading to an upregulation of
<i>R-</i>
genes. Despite this transcriptional release of
<i>R</i>
-genes, RNA silencing suppressors positively contribute to the virulence of some pathogens
<i>.</i>
To investigate this paradox, we analysed how the regulation of
<i>NBS-LRRs</i>
by miR482/2118 has been shaped by the coevolution between
<i>Phytophthora infestans</i>
and cultivated and wild tomatoes. We used degradome analyses and qRT-PCR to evaluate and quantify the co-expression of miR482/2118 and their
<i>NBS-LRR</i>
targets. Our data show that miR482/2118-mediated targeting contributes to the regulation of
<i>NBS-LRRs</i>
in
<i>Solanum lycopersicum.</i>
Based on miR482/2118 expression profiling in two additional tomato species-with different coevolutionary histories with
<i>P. infestans</i>
-we hypothesize that pathogen-mediated RNA silencing suppression is most effective in the interaction between
<i>S. lycopersicum</i>
and
<i>P. infestans</i>
Furthermore, an upregulation of miR482/2118 early in the infection may increase susceptibility to
<i>P. infestans</i>
.</AbstractText>
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