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

Author:

Fan Wenwen12ORCID,Wang Ling12ORCID,Lei Zhen12ORCID,Li Hui12ORCID,Chu Jie12ORCID,Yan Mengxiao3ORCID,Wang Yuqin3,Wang Hongxia123ORCID,Yang Jun123,Cho Jungnam1245ORCID

Affiliation:

1. National Key Laboratory of Plant Molecular Genetics, CAS Center for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences, Shanghai 200032, China.

2. University of Chinese Academy of Sciences, Beijing 100049, China.

3. Shanghai Key Laboratory of Plant Functional Genomics and Resources, Shanghai Chenshan Botanical Garden, Shanghai 201602, China.

4. CAS-JIC Centre for Excellence in Plant and Microbial Science, Shanghai 200032, China.

5. Department of Biosciences, Durham University, Durham DH1 3LE, UK.

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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