Methyltransferase ATMETTL5 writes m6A on 18S ribosomal RNA to regulate translation in Arabidopsis

Author:

Song Peizhe1ORCID,Tian Enlin1ORCID,Cai Zhihe1ORCID,Chen Xu1ORCID,Chen Shuyan1ORCID,Yu Kemiao2ORCID,Bian Hanxiao3,He Kai4,Jia Guifang125ORCID

Affiliation:

1. Synthetic and Functional Biomolecules Center, Beijing National Laboratory for Molecular Sciences, Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry and Molecular Engineering Peking University Beijing 100871 China

2. Peking‐Tsinghua Center for Life Sciences Peking University Beijing 100871 China

3. Laboratory of Fruit Quality Biology, Zhejiang Provincial Key Laboratory of Horticultural Plant Integrative Biology Zhejiang University Zijingang Campus Hangzhou 310058 China

4. State Key Laboratory of Protein and Plant Gene Research, School of Advanced Agricultural Sciences Peking University Beijing 100871 China

5. Beijing Advanced Center of RNA Biology (BEACON) Peking University Beijing 100871 China

Abstract

Summary Aberrant RNA modifications can lead to dysregulated gene expression and impeded growth in plants. Ribosomal RNA (rRNA) constitutes a substantial portion of total RNA, while the precise functions and molecular mechanisms underlying rRNA modifications in plants remain largely elusive. Here, we elucidated the exclusive occurrence of the canonical RNA modification N6‐methyladenosine (m6A) solely 18S rRNA, but not 25S rRNA. We identified a completely uncharacterized protein, ATMETTL5, as an Arabidopsis m6A methyltransferase responsible for installing m6A methylation at the 1771 site of the 18S rRNA. ATMETTL5 is ubiquitously expressed and localized in both nucleus and cytoplasm, mediating rRNA m6A methylation. Mechanistically, the loss of ATMETTL5‐mediated methylation results in attenuated translation. Furthermore, we uncovered the role of ATMETTL5‐mediated methylation in coordinating blue light‐mediated hypocotyl growth by regulating the translation of blue light‐related messenger RNAs (mRNAs), specifically HYH and PRR9. Our findings provide mechanistic insights into how rRNA modification regulates ribosome function in mRNA translation and the response to blue light, thereby advancing our understanding of the role of epigenetic modifications in precisely regulating mRNA translation in plants.

Funder

National Key Research and Development Program of China

Beijing Municipal Natural Science Foundation

National Natural Science Foundation of China

Publisher

Wiley

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