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J Biochem ; 163(6): 465-474, 2018 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-29385568

RESUMO

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).


Assuntos
Adenina/metabolismo , Caenorhabditis elegans/genética , RNA Ribossômico/metabolismo , DNA Metiltransferases Sítio Específica (Adenina-Específica)/metabolismo , Animais , Caenorhabditis elegans/enzimologia , Caenorhabditis elegans/metabolismo , Metilação , RNA Ribossômico/química , Reação em Cadeia da Polimerase Via Transcriptase Reversa , DNA Metiltransferases Sítio Específica (Adenina-Específica)/genética
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