Transcriptome-Wide Mapping of 5-methylcytidine RNA Modifications in Bacteria, Archaea, and Yeast Reveals m5C within Archaeal mRNAs

• Published in: PLoS genetics Vol. 9; no. 6; p. e1003602
• Main Authors: Edelheit, Sarit, Schwartz, Schraga, Mumbach, Maxwell R., Wurtzel, Omri, Sorek, Rotem
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 01.06.2013; Public Library of Science (PLoS)
• Subjects: Archaea - genetics; Bacillus subtilis - genetics; Bacteria; Biology; Cytidine - analogs & derivatives; Cytidine - genetics; DNA methylation; E coli; Escherichia coli - genetics; Eukaryotes; Gene Expression Profiling; Genes; Genetics; Genome; Genomes; High-Throughput Nucleotide Sequencing; Methylation; Organisms; Proteins; RNA, Messenger - genetics; RNA, Ribosomal - genetics; RNA, Transfer - genetics; Saccharomyces cerevisiae - genetics; Studies; Transfer RNA; Yeast
• ISSN: 1553-7404; 1553-7390; 1553-7404
• DOI: 10.1371/journal.pgen.1003602

The presence of 5-methylcytidine (m(5)C) in tRNA and rRNA molecules of a wide variety of organisms was first observed more than 40 years ago. However, detection of this modification was limited to specific, abundant, RNA species, due to the usage of low-throughput methods. To obtain a high resolution, systematic, and comprehensive transcriptome-wide overview of m(5)C across the three domains of life, we used bisulfite treatment on total RNA from both gram positive (B. subtilis) and gram negative (E. coli) bacteria, an archaeon (S. solfataricus) and a eukaryote (S. cerevisiae), followed by massively parallel sequencing. We were able to recover most previously documented m(5)C sites on rRNA in the four organisms, and identified several novel sites in yeast and archaeal rRNAs. Our analyses also allowed quantification of methylated m(5)C positions in 64 tRNAs in yeast and archaea, revealing stoichiometric differences between the methylation patterns of these organisms. Molecules of tRNAs in which m(5)C was absent were also discovered. Intriguingly, we detected m(5)C sites within archaeal mRNAs, and identified a consensus motif of AUCGANGU that directs methylation in S. solfataricus. Our results, which were validated using m(5)C-specific RNA immunoprecipitation, provide the first evidence for mRNA modifications in archaea, suggesting that this mode of post-transcriptional regulation extends beyond the eukaryotic domain.