Cargando…

A novel Transposable element‐derived microRNA participates in plant immunity to rice blast disease

MicroRNAs (miRNAs) are small non‐coding RNAs that direct post‐transcriptional gene silencing in plant development and stress responses through cleavage or translational repression of target mRNAs. Here, we report the identification and functional characterization of a new member of the miR812 family...

Descripción completa

Detalles Bibliográficos
Autores principales: Campo, Sonia, Sánchez‐Sanuy, Ferran, Camargo‐Ramírez, Rosany, Gómez‐Ariza, Jorge, Baldrich, Patricia, Campos‐Soriano, Lidia, Soto‐Suárez, Mauricio, San Segundo, Blanca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8428829/
https://www.ncbi.nlm.nih.gov/pubmed/33780108
http://dx.doi.org/10.1111/pbi.13592
_version_ 1783750447613345792
author Campo, Sonia
Sánchez‐Sanuy, Ferran
Camargo‐Ramírez, Rosany
Gómez‐Ariza, Jorge
Baldrich, Patricia
Campos‐Soriano, Lidia
Soto‐Suárez, Mauricio
San Segundo, Blanca
author_facet Campo, Sonia
Sánchez‐Sanuy, Ferran
Camargo‐Ramírez, Rosany
Gómez‐Ariza, Jorge
Baldrich, Patricia
Campos‐Soriano, Lidia
Soto‐Suárez, Mauricio
San Segundo, Blanca
author_sort Campo, Sonia
collection PubMed
description MicroRNAs (miRNAs) are small non‐coding RNAs that direct post‐transcriptional gene silencing in plant development and stress responses through cleavage or translational repression of target mRNAs. Here, we report the identification and functional characterization of a new member of the miR812 family in rice (named as miR812w) involved in disease resistance. miR812w is present in cultivated Oryza species, both japonica and indica subspecies, and wild rice species within the Oryza genus, but not in dicotyledonous species. miR812w is a 24nt‐long that requires DCL3 for its biogenesis and is loaded into AGO4 proteins. Whereas overexpression of miR812w increased resistance to infection by the rice blast fungus Magnaporthe oryzae, CRISPR/Cas9‐mediated MIR812w editing enhances disease susceptibility, supporting that miR812w plays a role in blast resistance. We show that miR812w derives from the Stowaway type of rice MITEs (Miniature Inverted‐Repeat Transposable Elements). Moreover, miR812w directs DNA methylation in trans at target genes that have integrated a Stowaway MITE copy into their 3′ or 5′ untranslated region (ACO3, CIPK10, LRR genes), as well as in cis at the MIR812w locus. The target genes of miR812 were found to be hypo‐methylated around the miR812 recognition site, their expression being up‐regulated in transgene‐free CRISPR/Cas9‐edited miR812 plants. These findings further support that, in addition to post‐transcriptional regulation of gene expression, miRNAs can exert their regulatory function at the transcriptional level. This relationship between miR812w and Stowaway MITEs integrated into multiple coding genes might eventually create a network for miR812w‐mediated regulation of gene expression with implications in rice immunity.
format Online
Article
Text
id pubmed-8428829
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-84288292021-09-14 A novel Transposable element‐derived microRNA participates in plant immunity to rice blast disease Campo, Sonia Sánchez‐Sanuy, Ferran Camargo‐Ramírez, Rosany Gómez‐Ariza, Jorge Baldrich, Patricia Campos‐Soriano, Lidia Soto‐Suárez, Mauricio San Segundo, Blanca Plant Biotechnol J Research Articles MicroRNAs (miRNAs) are small non‐coding RNAs that direct post‐transcriptional gene silencing in plant development and stress responses through cleavage or translational repression of target mRNAs. Here, we report the identification and functional characterization of a new member of the miR812 family in rice (named as miR812w) involved in disease resistance. miR812w is present in cultivated Oryza species, both japonica and indica subspecies, and wild rice species within the Oryza genus, but not in dicotyledonous species. miR812w is a 24nt‐long that requires DCL3 for its biogenesis and is loaded into AGO4 proteins. Whereas overexpression of miR812w increased resistance to infection by the rice blast fungus Magnaporthe oryzae, CRISPR/Cas9‐mediated MIR812w editing enhances disease susceptibility, supporting that miR812w plays a role in blast resistance. We show that miR812w derives from the Stowaway type of rice MITEs (Miniature Inverted‐Repeat Transposable Elements). Moreover, miR812w directs DNA methylation in trans at target genes that have integrated a Stowaway MITE copy into their 3′ or 5′ untranslated region (ACO3, CIPK10, LRR genes), as well as in cis at the MIR812w locus. The target genes of miR812 were found to be hypo‐methylated around the miR812 recognition site, their expression being up‐regulated in transgene‐free CRISPR/Cas9‐edited miR812 plants. These findings further support that, in addition to post‐transcriptional regulation of gene expression, miRNAs can exert their regulatory function at the transcriptional level. This relationship between miR812w and Stowaway MITEs integrated into multiple coding genes might eventually create a network for miR812w‐mediated regulation of gene expression with implications in rice immunity. John Wiley and Sons Inc. 2021-04-09 2021-09 /pmc/articles/PMC8428829/ /pubmed/33780108 http://dx.doi.org/10.1111/pbi.13592 Text en © 2021 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Campo, Sonia
Sánchez‐Sanuy, Ferran
Camargo‐Ramírez, Rosany
Gómez‐Ariza, Jorge
Baldrich, Patricia
Campos‐Soriano, Lidia
Soto‐Suárez, Mauricio
San Segundo, Blanca
A novel Transposable element‐derived microRNA participates in plant immunity to rice blast disease
title A novel Transposable element‐derived microRNA participates in plant immunity to rice blast disease
title_full A novel Transposable element‐derived microRNA participates in plant immunity to rice blast disease
title_fullStr A novel Transposable element‐derived microRNA participates in plant immunity to rice blast disease
title_full_unstemmed A novel Transposable element‐derived microRNA participates in plant immunity to rice blast disease
title_short A novel Transposable element‐derived microRNA participates in plant immunity to rice blast disease
title_sort novel transposable element‐derived microrna participates in plant immunity to rice blast disease
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8428829/
https://www.ncbi.nlm.nih.gov/pubmed/33780108
http://dx.doi.org/10.1111/pbi.13592
work_keys_str_mv AT camposonia anoveltransposableelementderivedmicrornaparticipatesinplantimmunitytoriceblastdisease
AT sanchezsanuyferran anoveltransposableelementderivedmicrornaparticipatesinplantimmunitytoriceblastdisease
AT camargoramirezrosany anoveltransposableelementderivedmicrornaparticipatesinplantimmunitytoriceblastdisease
AT gomezarizajorge anoveltransposableelementderivedmicrornaparticipatesinplantimmunitytoriceblastdisease
AT baldrichpatricia anoveltransposableelementderivedmicrornaparticipatesinplantimmunitytoriceblastdisease
AT campossorianolidia anoveltransposableelementderivedmicrornaparticipatesinplantimmunitytoriceblastdisease
AT sotosuarezmauricio anoveltransposableelementderivedmicrornaparticipatesinplantimmunitytoriceblastdisease
AT sansegundoblanca anoveltransposableelementderivedmicrornaparticipatesinplantimmunitytoriceblastdisease
AT camposonia noveltransposableelementderivedmicrornaparticipatesinplantimmunitytoriceblastdisease
AT sanchezsanuyferran noveltransposableelementderivedmicrornaparticipatesinplantimmunitytoriceblastdisease
AT camargoramirezrosany noveltransposableelementderivedmicrornaparticipatesinplantimmunitytoriceblastdisease
AT gomezarizajorge noveltransposableelementderivedmicrornaparticipatesinplantimmunitytoriceblastdisease
AT baldrichpatricia noveltransposableelementderivedmicrornaparticipatesinplantimmunitytoriceblastdisease
AT campossorianolidia noveltransposableelementderivedmicrornaparticipatesinplantimmunitytoriceblastdisease
AT sotosuarezmauricio noveltransposableelementderivedmicrornaparticipatesinplantimmunitytoriceblastdisease
AT sansegundoblanca noveltransposableelementderivedmicrornaparticipatesinplantimmunitytoriceblastdisease