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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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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. |
format | Online Article Text |
id | pubmed-10686560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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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