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Function identification of miR482b, a negative regulator during tomato resistance to Phytophthora infestans

Tomato is an important horticultural and economic crop cultivated worldwide. As Phytophthora infestans becomes a huge threat to tomato production, it is necessary to study the resistance mechanisms of tomato against P. infestans. Our previous research has found that miR482 might be involved in tomat...

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Autores principales: Jiang, Ning, Meng, Jun, Cui, Jun, Sun, Guangxin, Luan, Yushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830410/
https://www.ncbi.nlm.nih.gov/pubmed/29507733
http://dx.doi.org/10.1038/s41438-018-0017-2
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author Jiang, Ning
Meng, Jun
Cui, Jun
Sun, Guangxin
Luan, Yushi
author_facet Jiang, Ning
Meng, Jun
Cui, Jun
Sun, Guangxin
Luan, Yushi
author_sort Jiang, Ning
collection PubMed
description Tomato is an important horticultural and economic crop cultivated worldwide. As Phytophthora infestans becomes a huge threat to tomato production, it is necessary to study the resistance mechanisms of tomato against P. infestans. Our previous research has found that miR482 might be involved in tomato–P. infestans interaction. In this study, miR482b precursor was cloned from Solanum pimpinellifolium “L3708” and miR482b was shown to decrease in abundance in tomato following P. infestans infection. Compared to wild-type tomato plants, tomato plants that overexpressed miR482b displayed more serious disease symptoms after P. infestans infection, with more necrotic cells, longer lesion diameters, and increased P. infestans abundance. Meanwhile, silencing of miR482b was performed by short tandem target mimic (STTM), resulting in enhancement of tomato resistance to P. infestans. Using miRNA and degradome data sets, NBS–LRR disease-resistance genes targeted by miR482b were validated. Negative correlation between the expression of miR482b and its target genes was found in all miR482b-overexpressing and -silencing tomato plants. Our results provide insight into tomato miR482b involved in the response to P. infestans infection, and demonstrate that miR482b–NBS–LRR is an important component in the network of tomato–P. infestans interaction.
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spelling pubmed-58304102018-03-05 Function identification of miR482b, a negative regulator during tomato resistance to Phytophthora infestans Jiang, Ning Meng, Jun Cui, Jun Sun, Guangxin Luan, Yushi Hortic Res Article Tomato is an important horticultural and economic crop cultivated worldwide. As Phytophthora infestans becomes a huge threat to tomato production, it is necessary to study the resistance mechanisms of tomato against P. infestans. Our previous research has found that miR482 might be involved in tomato–P. infestans interaction. In this study, miR482b precursor was cloned from Solanum pimpinellifolium “L3708” and miR482b was shown to decrease in abundance in tomato following P. infestans infection. Compared to wild-type tomato plants, tomato plants that overexpressed miR482b displayed more serious disease symptoms after P. infestans infection, with more necrotic cells, longer lesion diameters, and increased P. infestans abundance. Meanwhile, silencing of miR482b was performed by short tandem target mimic (STTM), resulting in enhancement of tomato resistance to P. infestans. Using miRNA and degradome data sets, NBS–LRR disease-resistance genes targeted by miR482b were validated. Negative correlation between the expression of miR482b and its target genes was found in all miR482b-overexpressing and -silencing tomato plants. Our results provide insight into tomato miR482b involved in the response to P. infestans infection, and demonstrate that miR482b–NBS–LRR is an important component in the network of tomato–P. infestans interaction. Nature Publishing Group UK 2018-03-01 /pmc/articles/PMC5830410/ /pubmed/29507733 http://dx.doi.org/10.1038/s41438-018-0017-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Jiang, Ning
Meng, Jun
Cui, Jun
Sun, Guangxin
Luan, Yushi
Function identification of miR482b, a negative regulator during tomato resistance to Phytophthora infestans
title Function identification of miR482b, a negative regulator during tomato resistance to Phytophthora infestans
title_full Function identification of miR482b, a negative regulator during tomato resistance to Phytophthora infestans
title_fullStr Function identification of miR482b, a negative regulator during tomato resistance to Phytophthora infestans
title_full_unstemmed Function identification of miR482b, a negative regulator during tomato resistance to Phytophthora infestans
title_short Function identification of miR482b, a negative regulator during tomato resistance to Phytophthora infestans
title_sort function identification of mir482b, a negative regulator during tomato resistance to phytophthora infestans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830410/
https://www.ncbi.nlm.nih.gov/pubmed/29507733
http://dx.doi.org/10.1038/s41438-018-0017-2
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