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A novel miRNA negatively regulates resistance to Glomerella leaf spot by suppressing expression of an NBS gene in apple

Glomerella leaf spot (GLS) of apple (Malus×domestica Borkh.), caused by Glomerella cingulata, is an emerging fungal epidemic threatening the apple industry. Little is known about the molecular mechanism underlying resistance to this devastating fungus. In this study, high-throughput sequencing techn...

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Autores principales: Zhang, Yi, Zhang, Qiulei, Hao, Li, Wang, Shengnan, Wang, Shengyuan, Zhang, Wenna, Xu, Chaoran, Yu, Yunfei, Li, Tianzhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804642/
https://www.ncbi.nlm.nih.gov/pubmed/31645951
http://dx.doi.org/10.1038/s41438-019-0175-x
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author Zhang, Yi
Zhang, Qiulei
Hao, Li
Wang, Shengnan
Wang, Shengyuan
Zhang, Wenna
Xu, Chaoran
Yu, Yunfei
Li, Tianzhong
author_facet Zhang, Yi
Zhang, Qiulei
Hao, Li
Wang, Shengnan
Wang, Shengyuan
Zhang, Wenna
Xu, Chaoran
Yu, Yunfei
Li, Tianzhong
author_sort Zhang, Yi
collection PubMed
description Glomerella leaf spot (GLS) of apple (Malus×domestica Borkh.), caused by Glomerella cingulata, is an emerging fungal epidemic threatening the apple industry. Little is known about the molecular mechanism underlying resistance to this devastating fungus. In this study, high-throughput sequencing technology was used to identify microRNAs (miRNAs) involved in GLS resistance in apple. We focused on miRNAs that target genes related to disease and found that expression of a novel miRNA, Md-miRln20, was higher in susceptible apple varieties than in resistant ones. Furthermore, its target gene Md-TN1-GLS exhibited the opposite expression pattern, which suggested that the expression levels of Md-miRln20 and its target gene are closely related to apple resistance to GLS. Furthermore, downregulation of Md-miRln20 in susceptible apple leaves resulted in upregulation of Md-TN1-GLS and reduced the disease incidence. Conversely, overexpression of Md-miRln20 in resistant apple leaves suppressed Md-TN1-GLS expression, with increased disease incidence. We demonstrated that Md-miRln20 negatively regulates resistance to GLS by suppressing Md-TN1-GLS expression and showed, for the first time, a crucial role for miRNA in response to GLS in apple.
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spelling pubmed-68046422019-10-23 A novel miRNA negatively regulates resistance to Glomerella leaf spot by suppressing expression of an NBS gene in apple Zhang, Yi Zhang, Qiulei Hao, Li Wang, Shengnan Wang, Shengyuan Zhang, Wenna Xu, Chaoran Yu, Yunfei Li, Tianzhong Hortic Res Article Glomerella leaf spot (GLS) of apple (Malus×domestica Borkh.), caused by Glomerella cingulata, is an emerging fungal epidemic threatening the apple industry. Little is known about the molecular mechanism underlying resistance to this devastating fungus. In this study, high-throughput sequencing technology was used to identify microRNAs (miRNAs) involved in GLS resistance in apple. We focused on miRNAs that target genes related to disease and found that expression of a novel miRNA, Md-miRln20, was higher in susceptible apple varieties than in resistant ones. Furthermore, its target gene Md-TN1-GLS exhibited the opposite expression pattern, which suggested that the expression levels of Md-miRln20 and its target gene are closely related to apple resistance to GLS. Furthermore, downregulation of Md-miRln20 in susceptible apple leaves resulted in upregulation of Md-TN1-GLS and reduced the disease incidence. Conversely, overexpression of Md-miRln20 in resistant apple leaves suppressed Md-TN1-GLS expression, with increased disease incidence. We demonstrated that Md-miRln20 negatively regulates resistance to GLS by suppressing Md-TN1-GLS expression and showed, for the first time, a crucial role for miRNA in response to GLS in apple. Nature Publishing Group UK 2019-08-01 /pmc/articles/PMC6804642/ /pubmed/31645951 http://dx.doi.org/10.1038/s41438-019-0175-x Text en © The Author(s) 2019 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
Zhang, Yi
Zhang, Qiulei
Hao, Li
Wang, Shengnan
Wang, Shengyuan
Zhang, Wenna
Xu, Chaoran
Yu, Yunfei
Li, Tianzhong
A novel miRNA negatively regulates resistance to Glomerella leaf spot by suppressing expression of an NBS gene in apple
title A novel miRNA negatively regulates resistance to Glomerella leaf spot by suppressing expression of an NBS gene in apple
title_full A novel miRNA negatively regulates resistance to Glomerella leaf spot by suppressing expression of an NBS gene in apple
title_fullStr A novel miRNA negatively regulates resistance to Glomerella leaf spot by suppressing expression of an NBS gene in apple
title_full_unstemmed A novel miRNA negatively regulates resistance to Glomerella leaf spot by suppressing expression of an NBS gene in apple
title_short A novel miRNA negatively regulates resistance to Glomerella leaf spot by suppressing expression of an NBS gene in apple
title_sort novel mirna negatively regulates resistance to glomerella leaf spot by suppressing expression of an nbs gene in apple
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804642/
https://www.ncbi.nlm.nih.gov/pubmed/31645951
http://dx.doi.org/10.1038/s41438-019-0175-x
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