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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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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
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author Xu, Tao
Wu, Xiaowei
Wong, Chui Eng
Fan, Sheng
Zhang, Yu
Zhang, Songyao
Liang, Zhe
Yu, Hao
Shen, Lisha
author_facet Xu, Tao
Wu, Xiaowei
Wong, Chui Eng
Fan, Sheng
Zhang, Yu
Zhang, Songyao
Liang, Zhe
Yu, Hao
Shen, Lisha
author_sort Xu, Tao
collection PubMed
description 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.
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spelling pubmed-88671472022-02-27 FIONA1‐Mediated m(6)A Modification Regulates the Floral Transition in Arabidopsis Xu, Tao Wu, Xiaowei Wong, Chui Eng Fan, Sheng Zhang, Yu Zhang, Songyao Liang, Zhe Yu, Hao Shen, Lisha Adv Sci (Weinh) Research Articles 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. John Wiley and Sons Inc. 2022-01-05 /pmc/articles/PMC8867147/ /pubmed/34989479 http://dx.doi.org/10.1002/advs.202103628 Text en © 2022 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Xu, Tao
Wu, Xiaowei
Wong, Chui Eng
Fan, Sheng
Zhang, Yu
Zhang, Songyao
Liang, Zhe
Yu, Hao
Shen, Lisha
FIONA1‐Mediated m(6)A Modification Regulates the Floral Transition in Arabidopsis
title FIONA1‐Mediated m(6)A Modification Regulates the Floral Transition in Arabidopsis
title_full FIONA1‐Mediated m(6)A Modification Regulates the Floral Transition in Arabidopsis
title_fullStr FIONA1‐Mediated m(6)A Modification Regulates the Floral Transition in Arabidopsis
title_full_unstemmed FIONA1‐Mediated m(6)A Modification Regulates the Floral Transition in Arabidopsis
title_short FIONA1‐Mediated m(6)A Modification Regulates the Floral Transition in Arabidopsis
title_sort fiona1‐mediated m(6)a modification regulates the floral transition in arabidopsis
topic Research Articles
url 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
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