| First Author | Sepich-Poore C | Year | 2022 |
| Journal | J Biol Chem | Volume | 298 |
| Issue | 3 | Pages | 101590 |
| PubMed ID | 35033535 | Mgi Jnum | J:322368 |
| Mgi Id | MGI:6884948 | Doi | 10.1016/j.jbc.2022.101590 |
| Citation | Sepich-Poore C, et al. (2022) The METTL5-TRMT112 N(6)-methyladenosine methyltransferase complex regulates mRNA translation via 18S rRNA methylation. J Biol Chem 298(3):101590 |
| abstractText | Ribosomal RNAs (rRNAs) have long been known to carry chemical modifications, including 2'O-methylation, pseudouridylation, N(6)-methyladenosine (m(6)A), and N(6,6-)dimethyladenosine. While the functions of many of these modifications are unclear, some are highly conserved and occur in regions of the ribosome critical for mRNA decoding. Both 28S rRNA and 18S rRNA carry single m(6)A sites, and while the methyltransferase ZCCHC4 has been identified as the enzyme responsible for the 28S rRNA m(6)A modification, the methyltransferase responsible for the 18S rRNA m(6)A modification has remained unclear. Here, we show that the METTL5-TRMT112 methyltransferase complex installs the m(6)A modification at position 1832 of human 18S rRNA. Our work supports findings that TRMT112 is required for METTL5 stability and reveals that human METTL5 mutations associated with microcephaly and intellectual disability disrupt this interaction. We show that loss of METTL5 in human cancer cell lines and in mice regulates gene expression at the translational level; additionally, Mettl5 knockout mice display reduced body size and evidence of metabolic defects. While recent work has focused heavily on m(6)A modifications in mRNA and their roles in mRNA processing and translation, we demonstrate here that deorphanizing putative methyltransferase enzymes can reveal previously unappreciated regulatory roles for m(6)A in noncoding RNAs. |
