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Osa-miR7695 enhances transcriptional priming in defense responses against the rice blast fungus

BACKGROUND: MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression at the post-transcriptional level in eukaryotes. In rice, MIR7695 expression is regulated by infection with the rice blast fungus Magnaporthe oryzae with subsequent down-regulation of an alternatively spliced tran...

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Autores principales: Sánchez-Sanuy, Ferran, Peris-Peris, Cristina, Tomiyama, Shiho, Okada, Kazunori, Hsing, Yue-Ie, San Segundo, Blanca, Campo, Sonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921540/
https://www.ncbi.nlm.nih.gov/pubmed/31852430
http://dx.doi.org/10.1186/s12870-019-2156-5
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author Sánchez-Sanuy, Ferran
Peris-Peris, Cristina
Tomiyama, Shiho
Okada, Kazunori
Hsing, Yue-Ie
San Segundo, Blanca
Campo, Sonia
author_facet Sánchez-Sanuy, Ferran
Peris-Peris, Cristina
Tomiyama, Shiho
Okada, Kazunori
Hsing, Yue-Ie
San Segundo, Blanca
Campo, Sonia
author_sort Sánchez-Sanuy, Ferran
collection PubMed
description BACKGROUND: MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression at the post-transcriptional level in eukaryotes. In rice, MIR7695 expression is regulated by infection with the rice blast fungus Magnaporthe oryzae with subsequent down-regulation of an alternatively spliced transcript of natural resistance-associated macrophage protein 6 (OsNramp6). NRAMP6 functions as an iron transporter in rice. RESULTS: Rice plants grown under high iron supply showed blast resistance, which supports that iron is a factor in controlling blast resistance. During pathogen infection, iron accumulated in the vicinity of M. oryzae appressoria, the sites of pathogen entry, and in cells surrounding infected regions of the rice leaf. Activation-tagged MIR7695 rice plants (MIR7695-Ac) exhibited enhanced iron accumulation and resistance to M. oryzae infection. RNA-seq analysis revealed that blast resistance in MIR7695-Ac plants was associated with strong induction of defense-related genes, including pathogenesis-related and diterpenoid biosynthetic genes. Levels of phytoalexins during pathogen infection were higher in MIR7695-Ac than wild-type plants. Early phytoalexin biosynthetic genes, OsCPS2 and OsCPS4, were also highly upregulated in wild-type rice plants grown under high iron supply. CONCLUSIONS: Our data support a positive role of miR7695 in regulating rice immunity that further underpin links between defense and iron signaling in rice. These findings provides a basis to better understand regulatory mechanisms involved in rice immunity in which miR7695 participates which has a great potential for the development of strategies to improve blast resistance in rice.
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spelling pubmed-69215402019-12-30 Osa-miR7695 enhances transcriptional priming in defense responses against the rice blast fungus Sánchez-Sanuy, Ferran Peris-Peris, Cristina Tomiyama, Shiho Okada, Kazunori Hsing, Yue-Ie San Segundo, Blanca Campo, Sonia BMC Plant Biol Research Article BACKGROUND: MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression at the post-transcriptional level in eukaryotes. In rice, MIR7695 expression is regulated by infection with the rice blast fungus Magnaporthe oryzae with subsequent down-regulation of an alternatively spliced transcript of natural resistance-associated macrophage protein 6 (OsNramp6). NRAMP6 functions as an iron transporter in rice. RESULTS: Rice plants grown under high iron supply showed blast resistance, which supports that iron is a factor in controlling blast resistance. During pathogen infection, iron accumulated in the vicinity of M. oryzae appressoria, the sites of pathogen entry, and in cells surrounding infected regions of the rice leaf. Activation-tagged MIR7695 rice plants (MIR7695-Ac) exhibited enhanced iron accumulation and resistance to M. oryzae infection. RNA-seq analysis revealed that blast resistance in MIR7695-Ac plants was associated with strong induction of defense-related genes, including pathogenesis-related and diterpenoid biosynthetic genes. Levels of phytoalexins during pathogen infection were higher in MIR7695-Ac than wild-type plants. Early phytoalexin biosynthetic genes, OsCPS2 and OsCPS4, were also highly upregulated in wild-type rice plants grown under high iron supply. CONCLUSIONS: Our data support a positive role of miR7695 in regulating rice immunity that further underpin links between defense and iron signaling in rice. These findings provides a basis to better understand regulatory mechanisms involved in rice immunity in which miR7695 participates which has a great potential for the development of strategies to improve blast resistance in rice. BioMed Central 2019-12-18 /pmc/articles/PMC6921540/ /pubmed/31852430 http://dx.doi.org/10.1186/s12870-019-2156-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Sánchez-Sanuy, Ferran
Peris-Peris, Cristina
Tomiyama, Shiho
Okada, Kazunori
Hsing, Yue-Ie
San Segundo, Blanca
Campo, Sonia
Osa-miR7695 enhances transcriptional priming in defense responses against the rice blast fungus
title Osa-miR7695 enhances transcriptional priming in defense responses against the rice blast fungus
title_full Osa-miR7695 enhances transcriptional priming in defense responses against the rice blast fungus
title_fullStr Osa-miR7695 enhances transcriptional priming in defense responses against the rice blast fungus
title_full_unstemmed Osa-miR7695 enhances transcriptional priming in defense responses against the rice blast fungus
title_short Osa-miR7695 enhances transcriptional priming in defense responses against the rice blast fungus
title_sort osa-mir7695 enhances transcriptional priming in defense responses against the rice blast fungus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921540/
https://www.ncbi.nlm.nih.gov/pubmed/31852430
http://dx.doi.org/10.1186/s12870-019-2156-5
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