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The m(6)A RNA Demethylase ALKBH9B Plays a Critical Role for Vascular Movement of Alfalfa Mosaic Virus in Arabidopsis

The N(6)-methyladenosine (m(6)A) pathway has been widely described as a viral regulatory mechanism in animals. We previously reported that the capsid protein (CP) of alfalfa mosaic virus (AMV) interacts with the Arabidopsis m(6)A demethylase ALKBH9B regulating m(6)A abundance on viral RNAs (vRNAs) a...

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Autores principales: Martínez-Pérez, Mireya, Gómez-Mena, Concepción, Alvarado-Marchena, Luis, Nadi, Riad, Micol, José Luis, Pallas, Vicente, Aparicio, Frederic
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8521051/
https://www.ncbi.nlm.nih.gov/pubmed/34671333
http://dx.doi.org/10.3389/fmicb.2021.745576
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author Martínez-Pérez, Mireya
Gómez-Mena, Concepción
Alvarado-Marchena, Luis
Nadi, Riad
Micol, José Luis
Pallas, Vicente
Aparicio, Frederic
author_facet Martínez-Pérez, Mireya
Gómez-Mena, Concepción
Alvarado-Marchena, Luis
Nadi, Riad
Micol, José Luis
Pallas, Vicente
Aparicio, Frederic
author_sort Martínez-Pérez, Mireya
collection PubMed
description The N(6)-methyladenosine (m(6)A) pathway has been widely described as a viral regulatory mechanism in animals. We previously reported that the capsid protein (CP) of alfalfa mosaic virus (AMV) interacts with the Arabidopsis m(6)A demethylase ALKBH9B regulating m(6)A abundance on viral RNAs (vRNAs) and systemic invasion of floral stems. Here, we analyze the involvement of other ALKBH9 proteins in AMV infection and we carry out a detailed evaluation of the infection restraint observed in alkbh9b mutant plants. Thus, via viral titer quantification experiments and in situ hybridization assays, we define the viral cycle steps that are altered by the absence of the m(6)A demethylase ALKBH9B in Arabidopsis. We found that ALKBH9A and ALKBH9C do not regulate the AMV cycle, so ALKBH9B activity seems to be highly specific. We also define that not only systemic movement is affected by the absence of the demethylase, but also early stages of viral infection. Moreover, our findings suggest that viral upload into the phloem could be blocked in alkbh9b plants. Overall, our results point to ALKBH9B as a possible new component of phloem transport, at least for AMV, and as a potential target to obtain virus resistance crops.
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spelling pubmed-85210512021-10-19 The m(6)A RNA Demethylase ALKBH9B Plays a Critical Role for Vascular Movement of Alfalfa Mosaic Virus in Arabidopsis Martínez-Pérez, Mireya Gómez-Mena, Concepción Alvarado-Marchena, Luis Nadi, Riad Micol, José Luis Pallas, Vicente Aparicio, Frederic Front Microbiol Microbiology The N(6)-methyladenosine (m(6)A) pathway has been widely described as a viral regulatory mechanism in animals. We previously reported that the capsid protein (CP) of alfalfa mosaic virus (AMV) interacts with the Arabidopsis m(6)A demethylase ALKBH9B regulating m(6)A abundance on viral RNAs (vRNAs) and systemic invasion of floral stems. Here, we analyze the involvement of other ALKBH9 proteins in AMV infection and we carry out a detailed evaluation of the infection restraint observed in alkbh9b mutant plants. Thus, via viral titer quantification experiments and in situ hybridization assays, we define the viral cycle steps that are altered by the absence of the m(6)A demethylase ALKBH9B in Arabidopsis. We found that ALKBH9A and ALKBH9C do not regulate the AMV cycle, so ALKBH9B activity seems to be highly specific. We also define that not only systemic movement is affected by the absence of the demethylase, but also early stages of viral infection. Moreover, our findings suggest that viral upload into the phloem could be blocked in alkbh9b plants. Overall, our results point to ALKBH9B as a possible new component of phloem transport, at least for AMV, and as a potential target to obtain virus resistance crops. Frontiers Media S.A. 2021-10-04 /pmc/articles/PMC8521051/ /pubmed/34671333 http://dx.doi.org/10.3389/fmicb.2021.745576 Text en Copyright © 2021 Martínez-Pérez, Gómez-Mena, Alvarado-Marchena, Nadi, Micol, Pallas and Aparicio. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Martínez-Pérez, Mireya
Gómez-Mena, Concepción
Alvarado-Marchena, Luis
Nadi, Riad
Micol, José Luis
Pallas, Vicente
Aparicio, Frederic
The m(6)A RNA Demethylase ALKBH9B Plays a Critical Role for Vascular Movement of Alfalfa Mosaic Virus in Arabidopsis
title The m(6)A RNA Demethylase ALKBH9B Plays a Critical Role for Vascular Movement of Alfalfa Mosaic Virus in Arabidopsis
title_full The m(6)A RNA Demethylase ALKBH9B Plays a Critical Role for Vascular Movement of Alfalfa Mosaic Virus in Arabidopsis
title_fullStr The m(6)A RNA Demethylase ALKBH9B Plays a Critical Role for Vascular Movement of Alfalfa Mosaic Virus in Arabidopsis
title_full_unstemmed The m(6)A RNA Demethylase ALKBH9B Plays a Critical Role for Vascular Movement of Alfalfa Mosaic Virus in Arabidopsis
title_short The m(6)A RNA Demethylase ALKBH9B Plays a Critical Role for Vascular Movement of Alfalfa Mosaic Virus in Arabidopsis
title_sort m(6)a rna demethylase alkbh9b plays a critical role for vascular movement of alfalfa mosaic virus in arabidopsis
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8521051/
https://www.ncbi.nlm.nih.gov/pubmed/34671333
http://dx.doi.org/10.3389/fmicb.2021.745576
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