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FIONA1-mediated methylation of the 3’UTR of FLC affects FLC transcript levels and flowering in Arabidopsis

Adenosine bases of RNA can be transiently modified by the deposition of a methyl-group to form N(6)-methyladenosine (m(6)A). This adenosine-methylation is an ancient process and the enzymes involved are evolutionary highly conserved. A genetic screen designed to identify suppressors of late flowerin...

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Detalles Bibliográficos
Autores principales: Sun, Bin, Bhati, Kaushal Kumar, Song, Peizhe, Edwards, Ashleigh, Petri, Louise, Kruusvee, Valdeko, Blaakmeer, Anko, Dolde, Ulla, Rodrigues, Vandasue, Straub, Daniel, Yang, Junbo, Jia, Guifang, Wenkel, Stephan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543952/
https://www.ncbi.nlm.nih.gov/pubmed/36166469
http://dx.doi.org/10.1371/journal.pgen.1010386
Descripción
Sumario:Adenosine bases of RNA can be transiently modified by the deposition of a methyl-group to form N(6)-methyladenosine (m(6)A). This adenosine-methylation is an ancient process and the enzymes involved are evolutionary highly conserved. A genetic screen designed to identify suppressors of late flowering transgenic Arabidopsis plants overexpressing the miP1a microProtein yielded a new allele of the FIONA1 (FIO1) m(6)A-methyltransferase. To characterize the early flowering phenotype of fio1 mutant plants we employed an integrative approach of mRNA-seq, Nanopore direct RNA-sequencing and meRIP-seq to identify differentially expressed transcripts as well as differentially methylated RNAs. We provide evidence that FIO1 is the elusive methyltransferase responsible for the 3’-end methylation of the FLOWERING LOCUS C (FLC) transcript. Furthermore, our genetic and biochemical data suggest that 3’-methylation stabilizes FLC mRNAs and non-methylated FLC is a target for rapid degradation.