The posttranscriptional modification of messenger RNA (mRNA) and transfer RNA (tRNA) provides an additional layer of regulatory complexity during gene expression. Here, we show that a tRNA methyltransferase, TRMT10A, interacts with an mRNA demethylase FTO (ALKBH9), both in vitro and inside cells. TRMT10A installs -methylguanosine (mG) in tRNA, and FTO performs demethylation on -methyladenosine (mA) and ,2'--dimethyladenosine (mA) in mRNA. We show that TRMT10A ablation not only leads to decreased mG in tRNA but also significantly increases mA levels in mRNA. Cross-linking and immunoprecipitation, followed by high-throughput sequencing results show that TRMT10A shares a significant overlap of associated mRNAs with FTO, and these mRNAs have accelerated decay rates potentially through the regulation by a specific mA reader, YTHDF2. Furthermore, transcripts with increased mA upon TRMT10A ablation contain an overrepresentation of mG9-containing tRNAs codons read by tRNA, tRNA, and tRNA These findings collectively reveal the presence of coordinated mRNA and tRNA methylations and demonstrate a mechanism for regulating gene expression through the interactions between mRNA and tRNA modifying enzymes.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7149399 | PMC |
http://dx.doi.org/10.1073/pnas.1913448117 | DOI Listing |
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