Department of Biochemistry and Biophysics, Center for RNA Biology, University of Rochester School of Medicine, Rochester, New York, United States of America.
PLoS Genet. 2022 Jul 28;18(7):e1010215. doi: 10.1371/journal.pgen.1010215. eCollection 2022 Jul.
All tRNAs have numerous modifications, lack of which often results in growth defects in the budding yeast Saccharomyces cerevisiae and neurological or other disorders in humans. In S. cerevisiae, lack of tRNA body modifications can lead to impaired tRNA stability and decay of a subset of the hypomodified tRNAs. Mutants lacking 7-methylguanosine at G46 (m7G46), N2,N2-dimethylguanosine (m2,2G26), or 4-acetylcytidine (ac4C12), in combination with other body modification mutants, target certain mature hypomodified tRNAs to the rapid tRNA decay (RTD) pathway, catalyzed by 5'-3' exonucleases Xrn1 and Rat1, and regulated by Met22. The RTD pathway is conserved in the phylogenetically distant fission yeast Schizosaccharomyces pombe for mutants lacking m7G46. In contrast, S. cerevisiae trm6/gcd10 mutants with reduced 1-methyladenosine (m1A58) specifically target pre-tRNAiMet(CAU) to the nuclear surveillance pathway for 3'-5' exonucleolytic decay by the TRAMP complex and nuclear exosome. We show here that the RTD pathway has an unexpected major role in the biology of m1A58 and tRNAiMet(CAU) in both S. pombe and S. cerevisiae. We find that S. pombe trm6Δ mutants lacking m1A58 are temperature sensitive due to decay of tRNAiMet(CAU) by the RTD pathway. Thus, trm6Δ mutants had reduced levels of tRNAiMet(CAU) and not of eight other tested tRNAs, overexpression of tRNAiMet(CAU) restored growth, and spontaneous suppressors that restored tRNAiMet(CAU) levels had mutations in dhp1/RAT1 or tol1/MET22. In addition, deletion of cid14/TRF4 in the nuclear surveillance pathway did not restore growth. Furthermore, re-examination of S. cerevisiae trm6 mutants revealed a major role of the RTD pathway in maintaining tRNAiMet(CAU) levels, in addition to the known role of the nuclear surveillance pathway. These findings provide evidence for the importance of m1A58 in the biology of tRNAiMet(CAU) throughout eukaryotes, and fuel speculation that the RTD pathway has a major role in quality control of body modification mutants throughout fungi and other eukaryotes.
所有 tRNA 都有许多修饰,缺乏这些修饰通常会导致芽殖酵母酿酒酵母生长缺陷和人类神经或其他疾病。在酿酒酵母中,缺乏 tRNA 体修饰会导致 tRNA 稳定性受损,并导致一部分低修饰 tRNA 降解。缺乏 G46 上的 7-甲基鸟嘌呤(m7G46)、N2,N2-二甲基鸟嘌呤(m2,2G26)或 4-乙酰胞苷(ac4C12)的突变体与其他体修饰突变体结合,将某些成熟的低修饰 tRNA 靶向快速 tRNA 降解(RTD)途径,该途径由 5'-3'外切核酸酶 Xrn1 和 Rat1 催化,并受 Met22 调节。RTD 途径在系统发育上遥远的裂殖酵母 Schizosaccharomyces pombe 中是保守的,对于缺乏 m7G46 的突变体也是如此。相比之下,酿酒酵母 trm6/gcd10 突变体中 1-甲基腺苷(m1A58)减少,特异性地将 pre-tRNAiMet(CAU)靶向核监视途径,通过 TRAMP 复合物和核核酶进行 3'-5'外切核酸酶降解。我们在这里表明,RTD 途径在 m1A58 和 tRNAiMet(CAU)在 S. pombe 和 S. cerevisiae 中的生物学中具有意想不到的重要作用。我们发现,由于 RTD 途径的作用,缺乏 m1A58 的 S. pombe trm6Δ 突变体对 tRNAiMet(CAU)的降解表现出温度敏感性。因此,trm6Δ 突变体的 tRNAiMet(CAU)水平降低,而其他八种测试的 tRNA 水平不变,过表达 tRNAiMet(CAU)可恢复生长,自发抑制子恢复 tRNAiMet(CAU)水平的突变位于 dhp1/RAT1 或 tol1/MET22。此外,核监视途径中 cid14/TRF4 的缺失并不能恢复生长。此外,对酿酒酵母 trm6 突变体的重新检查表明,RTD 途径除了已知的核监视途径的作用外,在维持 tRNAiMet(CAU)水平方面也起着重要作用。这些发现为 m1A58 在真核生物中 tRNAiMet(CAU)生物学中的重要性提供了证据,并引发了这样一种猜测,即 RTD 途径在真菌和其他真核生物中体修饰突变体的质量控制中起着重要作用。