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

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 repea...

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Autores principales: de Vries, Sophie, Kukuk, Andreas, von Dahlen, Janina K., Schnake, Anika, Kloesges, Thorsten, Rose, Laura E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832704/
https://www.ncbi.nlm.nih.gov/pubmed/29491170
http://dx.doi.org/10.1098/rspb.2017.2560
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author de Vries, Sophie
Kukuk, Andreas
von Dahlen, Janina K.
Schnake, Anika
Kloesges, Thorsten
Rose, Laura E.
author_facet de Vries, Sophie
Kukuk, Andreas
von Dahlen, Janina K.
Schnake, Anika
Kloesges, Thorsten
Rose, Laura E.
author_sort de Vries, Sophie
collection PubMed
description 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.
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spelling pubmed-58327042018-03-14 Expression profiling across wild and cultivated tomatoes supports the relevance of early miR482/2118 suppression for Phytophthora resistance de Vries, Sophie Kukuk, Andreas von Dahlen, Janina K. Schnake, Anika Kloesges, Thorsten Rose, Laura E. Proc Biol Sci Evolution 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. The Royal Society 2018-02-28 2018-02-28 /pmc/articles/PMC5832704/ /pubmed/29491170 http://dx.doi.org/10.1098/rspb.2017.2560 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolution
de Vries, Sophie
Kukuk, Andreas
von Dahlen, Janina K.
Schnake, Anika
Kloesges, Thorsten
Rose, Laura E.
Expression profiling across wild and cultivated tomatoes supports the relevance of early miR482/2118 suppression for Phytophthora resistance
title Expression profiling across wild and cultivated tomatoes supports the relevance of early miR482/2118 suppression for Phytophthora resistance
title_full Expression profiling across wild and cultivated tomatoes supports the relevance of early miR482/2118 suppression for Phytophthora resistance
title_fullStr Expression profiling across wild and cultivated tomatoes supports the relevance of early miR482/2118 suppression for Phytophthora resistance
title_full_unstemmed Expression profiling across wild and cultivated tomatoes supports the relevance of early miR482/2118 suppression for Phytophthora resistance
title_short Expression profiling across wild and cultivated tomatoes supports the relevance of early miR482/2118 suppression for Phytophthora resistance
title_sort expression profiling across wild and cultivated tomatoes supports the relevance of early mir482/2118 suppression for phytophthora resistance
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832704/
https://www.ncbi.nlm.nih.gov/pubmed/29491170
http://dx.doi.org/10.1098/rspb.2017.2560
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