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m(6)A RNA demethylase AtALKBH9B promotes mobilization of a heat-activated long terminal repeat retrotransposon in Arabidopsis

Transposons are mobile and ubiquitous DNA molecules that can cause vast genomic alterations. In plants, it is well documented that transposon mobilization is strongly repressed by DNA methylation; however, its regulation at the posttranscriptional level remains relatively uninvestigated. Here, we su...

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Autores principales: Fan, Wenwen, Wang, Ling, Lei, Zhen, Li, Hui, Chu, Jie, Yan, Mengxiao, Wang, Yuqin, Wang, Hongxia, Yang, Jun, Cho, Jungnam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686560/
https://www.ncbi.nlm.nih.gov/pubmed/38019921
http://dx.doi.org/10.1126/sciadv.adf3292
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author Fan, Wenwen
Wang, Ling
Lei, Zhen
Li, Hui
Chu, Jie
Yan, Mengxiao
Wang, Yuqin
Wang, Hongxia
Yang, Jun
Cho, Jungnam
author_facet Fan, Wenwen
Wang, Ling
Lei, Zhen
Li, Hui
Chu, Jie
Yan, Mengxiao
Wang, Yuqin
Wang, Hongxia
Yang, Jun
Cho, Jungnam
author_sort Fan, Wenwen
collection PubMed
description Transposons are mobile and ubiquitous DNA molecules that can cause vast genomic alterations. In plants, it is well documented that transposon mobilization is strongly repressed by DNA methylation; however, its regulation at the posttranscriptional level remains relatively uninvestigated. Here, we suggest that transposon RNA is marked by m(6)A RNA methylation and can be localized in stress granules (SGs). Intriguingly, SG-localized AtALKBH9B selectively demethylates a heat-activated retroelement, Onsen, and thereby releases it from spatial confinement, allowing for its mobilization. In addition, we show evidence that m(6)A RNA methylation contributes to transpositional suppression by inhibiting virus-like particle assembly and extrachromosomal DNA production. In summary, this study unveils a previously unknown role for m(6)A in the suppression of transposon mobility and provides insight into how transposons counteract the m(6)A-mediated repression mechanism by hitchhiking the RNA demethylase of the host.
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spelling pubmed-106865602023-11-30 m(6)A RNA demethylase AtALKBH9B promotes mobilization of a heat-activated long terminal repeat retrotransposon in Arabidopsis Fan, Wenwen Wang, Ling Lei, Zhen Li, Hui Chu, Jie Yan, Mengxiao Wang, Yuqin Wang, Hongxia Yang, Jun Cho, Jungnam Sci Adv Biomedicine and Life Sciences Transposons are mobile and ubiquitous DNA molecules that can cause vast genomic alterations. In plants, it is well documented that transposon mobilization is strongly repressed by DNA methylation; however, its regulation at the posttranscriptional level remains relatively uninvestigated. Here, we suggest that transposon RNA is marked by m(6)A RNA methylation and can be localized in stress granules (SGs). Intriguingly, SG-localized AtALKBH9B selectively demethylates a heat-activated retroelement, Onsen, and thereby releases it from spatial confinement, allowing for its mobilization. In addition, we show evidence that m(6)A RNA methylation contributes to transpositional suppression by inhibiting virus-like particle assembly and extrachromosomal DNA production. In summary, this study unveils a previously unknown role for m(6)A in the suppression of transposon mobility and provides insight into how transposons counteract the m(6)A-mediated repression mechanism by hitchhiking the RNA demethylase of the host. American Association for the Advancement of Science 2023-11-29 /pmc/articles/PMC10686560/ /pubmed/38019921 http://dx.doi.org/10.1126/sciadv.adf3292 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Fan, Wenwen
Wang, Ling
Lei, Zhen
Li, Hui
Chu, Jie
Yan, Mengxiao
Wang, Yuqin
Wang, Hongxia
Yang, Jun
Cho, Jungnam
m(6)A RNA demethylase AtALKBH9B promotes mobilization of a heat-activated long terminal repeat retrotransposon in Arabidopsis
title m(6)A RNA demethylase AtALKBH9B promotes mobilization of a heat-activated long terminal repeat retrotransposon in Arabidopsis
title_full m(6)A RNA demethylase AtALKBH9B promotes mobilization of a heat-activated long terminal repeat retrotransposon in Arabidopsis
title_fullStr m(6)A RNA demethylase AtALKBH9B promotes mobilization of a heat-activated long terminal repeat retrotransposon in Arabidopsis
title_full_unstemmed m(6)A RNA demethylase AtALKBH9B promotes mobilization of a heat-activated long terminal repeat retrotransposon in Arabidopsis
title_short m(6)A RNA demethylase AtALKBH9B promotes mobilization of a heat-activated long terminal repeat retrotransposon in Arabidopsis
title_sort m(6)a rna demethylase atalkbh9b promotes mobilization of a heat-activated long terminal repeat retrotransposon in arabidopsis
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686560/
https://www.ncbi.nlm.nih.gov/pubmed/38019921
http://dx.doi.org/10.1126/sciadv.adf3292
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