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FIONA1‐Mediated m(6)A Modification Regulates the Floral Transition in Arabidopsis

N (6)‐methyladenosine (m(6)A) mRNA modification represents the most widespread form of internal modifications in eukaryotic mRNAs. In the model plant Arabidopsis thaliana, those known methyltransferases mainly deposit m(6)A at their target transcripts near the stop codon or in the 3′ untranslated re...

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Detalles Bibliográficos
Autores principales: Xu, Tao, Wu, Xiaowei, Wong, Chui Eng, Fan, Sheng, Zhang, Yu, Zhang, Songyao, Liang, Zhe, Yu, Hao, Shen, Lisha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8867147/
https://www.ncbi.nlm.nih.gov/pubmed/34989479
http://dx.doi.org/10.1002/advs.202103628
Descripción
Sumario:N (6)‐methyladenosine (m(6)A) mRNA modification represents the most widespread form of internal modifications in eukaryotic mRNAs. In the model plant Arabidopsis thaliana, those known methyltransferases mainly deposit m(6)A at their target transcripts near the stop codon or in the 3′ untranslated region. Here, it is reported that FIONA1 (FIO1), a human METTL16 ortholog, acts as a hitherto unknown m(6)A methyltransferase that determines m(6)A modifications at over 2000 Arabidopsis transcripts predominantly in the coding region. Mutants of FIO1 show a decrease in global m(6)A mRNA methylation levels and an early‐flowering phenotype. Nanopore direct RNA sequencing reveals that FIO1 is required for establishing appropriate levels of m(6)A preferentially in the coding sequences of a subset of protein‐coding transcripts, which is associated with changes in transcript abundance and alternative polyadenylation. It is further demonstrated that FIO1‐mediated m(6)A methylation determines the mRNA abundance of a central flowering integrator SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1 (SOC1) and its upstream regulators, thus preventing premature flowering. The findings reveal that FIO1 acts as a unique m(6)A methyltransferase that mainly modifies the coding regions of transcripts, which underlies the key developmental transition from vegetative to reproductive growth in plants.