rRNA adenine methylation requires T07A9.8 gene as rram-1 in Caenorhabditis elegans
Author(s) -
Wataru Yokoyama,
Keiko Hirota,
Huahua Wan,
Naoaki Sumi,
Mai Miyata,
Sho Araoi,
Naoto Nomura,
Koichiro Kako,
Akiyoshi Fukamizu
Publication year - 2018
Publication title -
the journal of biochemistry
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 115
eISSN - 1756-2651
pISSN - 0021-924X
DOI - 10.1093/jb/mvy018
Subject(s) - ribosomal rna , caenorhabditis elegans , biology , n6 methyladenosine , rna , 18s ribosomal rna , genetics , 23s ribosomal rna , internal transcribed spacer , gene , methylation , microbiology and biotechnology , methyltransferase , ribosome
RNAs are post-transcriptionally modified in all kingdoms of life. Of these modifications, base methylations are highly conserved in eukaryote ribosomal RNA (rRNA). Recently, rRNA processing protein 8 (Rrp8) and nucleomethylin (NML) were identified as factors of N1-methyladenosine (m1A) modification in yeast 25 S and mammalian 28 S rRNA, respectively. However, m1A modification of rRNA is still poorly understood in Caenorhabditis elegans (C. elegans). Here, using the liquid chromatography/tandem mass spectrometry analysis and RNA immunoprecipitation assay, we have identified that the m1A modification is located around position 674 (A674) of 26 S rRNA in C. elegans. Furthermore, quantitative PCR-based analysis revealed that T07A9.8, a C. elegans homolog of yeast Rrp8 and human NML, is responsible for m1A modification at A674 of 26 S rRNA. This m1A modification site in C. elegans corresponds to those in yeast 25 S rRNA and human 28 S rRNA. Intriguingly, T07A9.8 is not associated with pre-rRNA transcription under normal nutrient conditions. Since the m1A modification of 26 S rRNA requires T07A9.8 in C. elegans, we designated the gene as rRNA adenine methyltransferase-1 (rram-1).
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