Mapping rRNA 2'-O-methylations and identification of C/D snoRNAs in Arabidopsis thaliana plants

RNA Biol. 2021 Nov;18(11):1760-1777. doi: 10.1080/15476286.2020.1869892. Epub 2021 Feb 17.

Abstract

In all eukaryotic cells, the most abundant modification of ribosomal RNA (rRNA) is methylation at the ribose moiety (2'-O-methylation). Ribose methylation at specific rRNA sites is guided by small nucleolar RNAs (snoRNAs) of C/D-box type (C/D snoRNA) and achieved by the methyltransferase Fibrillarin (FIB). Here we used the Illumina-based RiboMethSeq approach for mapping rRNA 2'-O-methylation sites in A. thaliana Col-0 (WT) plants. This analysis detected novel C/D snoRNA-guided rRNA 2'-O-methylation positions and also some orphan sites without a matching C/D snoRNA. Furthermore, immunoprecipitation of Arabidopsis FIB2 identified and demonstrated expression of C/D snoRNAs corresponding to majority of mapped rRNA sites. On the other hand, we show that disruption of Arabidopsis Nucleolin 1 gene (NUC1), encoding a major nucleolar protein, decreases 2'-O-methylation at specific rRNA sites suggesting functional/structural interconnections of 2'-O-methylation with nucleolus organization and plant development. Finally, based on our findings and existent database sets, we introduce a new nomenclature system for C/D snoRNA in Arabidopsis plants.

Keywords: 2ʹ-O-Methylation; C/D snoRNA; arabidopsis; fibrillarin; nucleolin; rRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis / genetics*
  • Methylation
  • RNA, Plant / chemistry*
  • RNA, Plant / genetics*
  • RNA, Ribosomal / chemistry*
  • RNA, Ribosomal / genetics*
  • RNA, Small Nucleolar / genetics*

Substances

  • RNA, Plant
  • RNA, Ribosomal
  • RNA, Small Nucleolar

Grants and funding

This work was supported by the CNRS, INRAE and by the ANR (Agence Nationale de la Recherche) under Grant RiboStress 17-CE12-0026-01 and MetRibo and a BQR (Bonus Qualité Recherche) from the UPVD to JSV. YM was supported by EpiARN FRCR project from Grand Est Region (France). This study is set within the framework of the “Laboratoires d’Excellence (LABEX) TULIP (ANR-10-LABX-41). Mass spectrometry experiments were supported by the French Proteomic Infrastructure (ProFI; ANR-10-INBS-08-03);ANR [17-CE12-0026-01]; ANR [MetRibo]; ANR [10-INBS-08-03]; Grand Est Region [EpiARN FRCR].