| First Author | Thalalla Gamage S | Year | 2025 |
| Journal | Sci Adv | Volume | 11 |
| Issue | 12 | Pages | eads2923 |
| PubMed ID | 40106564 | Mgi Jnum | J:363949 |
| Mgi Id | MGI:8164814 | Doi | 10.1126/sciadv.ads2923 |
| Citation | Thalalla Gamage S, et al. (2025) Transfer RNA acetylation regulates in vivo mammalian stress signaling. Sci Adv 11(12):eads2923 |
| abstractText | Transfer RNA (tRNA) modifications are crucial for protein synthesis, but their position-specific physiological roles remain poorly understood. Here, we investigate the impact of N(4)-acetylcytidine (ac(4)C), a highly conserved tRNA modification catalyzed by the essential acetyltransferase Nat10. By targeting Thumpd1, a nonessential adapter protein required for Nat10-catalyzed tRNA acetylation, we determine that loss of tRNA acetylation leads to reduced levels of tRNA(Leu), increased ribosome stalling, and activation of eIF2alpha phosphorylation. Thumpd1 knockout mice exhibit growth defects and sterility. Concurrent knockout of Thumpd1 and the stress-sensing kinase Gcn2 causes penetrant postnatal lethality in mice, indicating a critical genetic interaction. Our findings demonstrate that a modification restricted to a single position within type II cytosolic tRNAs can regulate ribosome-mediated stress signaling in mammalian organisms, with implications for our understanding of translational control and therapeutic interventions. |
