Abstract

BackgroundN6-methyladenosine (m6A) mRNA modification is essential for mammalian and plant viability. The U6 m6A methyltransferases in other species regulate S-adenosylmethionine (SAM) homeostasis through installing m6A in pre-mRNAs of SAM synthetases. However, U6 m6A methyltransferase has not been characterized in Arabidopsis and little is known about its role in regulating photomorphogenesis and flowering.ResultsHere we characterize that FIONA1 is an Arabidopsis U6 m6A methyltransferase that installs m6A in U6 snRNA and a small subset of poly(A)+ RNA. Disruption of FIONA1 leads to phytochrome signaling-dependent hypocotyl elongation and photoperiod-independent early flowering. Distinct from mammalian METTL16 and worm METT-10, FIONA1 neither installs m6A in the mRNAs of Arabidopsis SAM synthetases nor affects their transcript expression levels under normal or high SAM conditions. We confirm that FIONA1 can methylate plant mRNA m6A motifs in vitro and in vivo. We further show that FIONA1 installs m6A in several phenotypic related transcripts, thereby affecting downstream mRNA stability and regulating phytochrome signaling and floral transition.ConclusionFIONA1 is functional as a U6 m6A methyltransferase in Arabidopsis, distinct from mammalian METTL16 and worm METT-10. Our results demonstrate that FIONA1-mediated m6A post-transcriptional regulation is an autonomous regulator for flowering and phytochrome signaling-dependent photomorphogenesis.

Highlights

  • N6-methyladenosine (m6A) mRNA modification is essential for mammalian and plant viability

  • FIONA1 installs m6A modification in U6 snRNA and a small subset of poly(A)+ RNA in Arabidopsis To characterize Arabidopsis U6 m6A methyltransferase, we processed phylogenetic analysis and sequence alignments and found a single, putative homolog of human methyltransferase like 16 (METTL16) in Arabidopsis, FIONA1 (AT2G21070) (Additional file 1: Fig. S1), which prompted us to test whether FIONA1 deposits m6A modification in plants

  • We identified 1137 confident hypomethylated m6A peaks corresponding 1128 transcripts/genes in fiona1-1(Fig. 5a, b; Additional file 6: Table S4), which predominantly belong to mRNA (Fig. 5c)

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Summary

Introduction

N6-methyladenosine (m6A) mRNA modification is essential for mammalian and plant viability. The most abundant internal mRNA modification N6-methyladenosine (m6A) is reversible and vital in many biological processes through post-transcriptional regulation of mRNA processing and metabolism [6,7,8,9,10,11,12,13,14,15,16,17]. In both mammals and plants, the m6A modification is written by methyltransferase, erased by demethylase, and read by m6Abinding proteins [18,19,20,21]. Plant WTAP homolog (Arabidopsis FIP37 and rice OsFIP) affects Arabidopsis shoot stem cell fate and early degeneration of rice microspores [38, 41]

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