Department of Biochemistry and Biophysics and Center for RNA Biology, University of Rochester School of Medicine, Rochester, New York 14642, USA.
RNA. 2013 Feb;19(2):243-56. doi: 10.1261/rna.035808.112. Epub 2012 Dec 18.
tRNAs are highly modified, each with a unique set of modifications. Several reports suggest that tRNAs are hypomodified or, in some cases, hypermodified under different growth conditions and in certain cancers. We previously demonstrated that yeast strains depleted of tRNA(His) guanylyltransferase accumulate uncharged tRNA(His) lacking the G(-1) residue and subsequently accumulate additional 5-methylcytidine (m(5)C) at residues C(48) and C(50) of tRNA(His), due to the activity of the m(5)C-methyltransferase Trm4. We show here that the increase in tRNA(His) m(5)C levels does not require loss of Thg1, loss of G(-1) of tRNA(His), or cell death but is associated with growth arrest following different stress conditions. We find substantially increased tRNA(His) m(5)C levels after temperature-sensitive strains are grown at nonpermissive temperature, and after wild-type strains are grown to stationary phase, starved for required amino acids, or treated with rapamycin. We observe more modest accumulations of m(5)C in tRNA(His) after starvation for glucose and after starvation for uracil. In virtually all cases examined, the additional m(5)C on tRNA(His) occurs while cells are fully viable, and the increase is neither due to the GCN4 pathway, nor to increased Trm4 levels. Moreover, the increased m(5)C appears specific to tRNA(His), as tRNA(Val(AAC)) and tRNA(Gly(GCC)) have much reduced additional m(5)C during these growth arrest conditions, although they also have C(48) and C(50) and are capable of having increased m(5)C levels. Thus, tRNA(His) m(5)C levels are unusually responsive to yeast growth conditions, although the significance of this additional m(5)C remains unclear.
tRNA 高度修饰,每种都具有独特的修饰集。有几项报告表明,在不同的生长条件下和某些癌症中,tRNA 的修饰程度较低,或者在某些情况下修饰程度较高。我们之前证明,耗尽 tRNA(His)鸟苷酰转移酶的酵母菌株会积累无 G(-1)残基的未负载 tRNA(His),随后在 tRNA(His)的 C(48)和 C(50)残基处积累额外的 5-甲基胞嘧啶 (m(5)C),这是由于 m(5)C-甲基转移酶 Trm4 的活性所致。我们在这里表明,tRNA(His) m(5)C 水平的增加不需要 Thg1 的缺失、tRNA(His)的 G(-1)缺失或细胞死亡,但与不同应激条件下的生长停滞有关。我们发现,在温度敏感菌株在非允许温度下生长后,以及在野生型菌株生长到静止期、缺乏必需氨基酸饥饿或用雷帕霉素处理后,tRNA(His)的 m(5)C 水平会显著增加。在饥饿葡萄糖和饥饿尿嘧啶后,tRNA(His)中的 m(5)C 积累量更大。在几乎所有检查的情况下,tRNA(His)上额外的 m(5)C 是在细胞完全存活的情况下发生的,并且这种增加既不是由于 GCN4 途径,也不是由于 Trm4 水平增加所致。此外,增加的 m(5)C 似乎是 tRNA(His)特有的,因为在这些生长停滞条件下,tRNA(Val(AAC))和 tRNA(Gly(GCC))的额外 m(5)C 减少很多,尽管它们也具有 C(48)和 C(50),并且能够具有增加的 m(5)C 水平。因此,尽管这种额外的 m(5)C 的意义尚不清楚,但 tRNA(His)的 m(5)C 水平对酵母生长条件的反应异常敏感。