METTL15 interacts with the assembly intermediate of murine mitochondrial small ribosomal subunit to form m4C840 12S rRNA residue

• Published in: Nucleic acids research Vol. 48; no. 14; pp. 8022 - 8034
• Main Authors: Laptev, Ivan, Shvetsova, Ekaterina, Levitskii, Sergey, Serebryakova, Marina, Rubtsova, Maria, Zgoda, Victor, Bogdanov, Alexey, Kamenski, Piotr, Sergiev, Petr, Dontsova, Olga
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 20.08.2020
• Subjects: Animals; Cells, Cultured; Methylation; Methyltransferases - metabolism; Mice; Mitochondria - enzymology; Mitochondria - metabolism; Ribosome Subunits, Small, Eukaryotic - chemistry; Ribosome Subunits, Small, Eukaryotic - enzymology; Ribosome Subunits, Small, Eukaryotic - metabolism; RNA and RNA-protein complexes; RNA, Mitochondrial - chemistry; RNA, Mitochondrial - metabolism; RNA, Ribosomal - chemistry; RNA, Ribosomal - metabolism; RNA, Ribosomal, 28S - metabolism
• ISSN: 0305-1048; 1362-4962; 1362-4962
• DOI: 10.1093/nar/gkaa522

Abstract Mammalian mitochondrial ribosomes contain a set of modified nucleotides, which is distinct from that of the cytosolic ribosomes. Nucleotide m4C840 of the murine mitochondrial 12S rRNA is equivalent to the dimethylated m4Cm1402 residue of Escherichia coli 16S rRNA. Here we demonstrate that mouse METTL15 protein is responsible for the formation of m4C residue of the 12S rRNA. Inactivation of Mettl15 gene in murine cell line perturbs the composition of mitochondrial protein biosynthesis machinery. Identification of METTL15 interaction partners revealed that the likely substrate for this RNA methyltransferase is an assembly intermediate of the mitochondrial small ribosomal subunit containing an assembly factor RBFA.