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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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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. |
format | Online Article Text |
id | pubmed-8521051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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