Department of Materials Science and Biotechnology, Ehime University, Bunkyo 3, Matsuyama, Ehime 790-8577, Japan.
Nucleic Acids Res. 2010 Jan;38(3):942-57. doi: 10.1093/nar/gkp1059. Epub 2009 Nov 24.
N(7)-methylguanine at position 46 (m(7)G46) in tRNA is produced by tRNA (m(7)G46) methyltransferase (TrmB). To clarify the role of this modification, we made a trmB gene disruptant (DeltatrmB) of Thermus thermophilus, an extreme thermophilic eubacterium. The absence of TrmB activity in cell extract from the DeltatrmB strain and the lack of the m(7)G46 modification in tRNA(Phe) were confirmed by enzyme assay, nucleoside analysis and RNA sequencing. When the DeltatrmB strain was cultured at high temperatures, several modified nucleotides in tRNA were hypo-modified in addition to the lack of the m(7)G46 modification. Assays with tRNA modification enzymes revealed hypo-modifications of Gm18 and m(1)G37, suggesting that the m(7)G46 positively affects their formations. Although the lack of the m(7)G46 modification and the hypo-modifications do not affect the Phe charging activity of tRNA(Phe), they cause a decrease in melting temperature of class I tRNA and degradation of tRNA(Phe) and tRNA(Ile). (35)S-Met incorporation into proteins revealed that protein synthesis in DeltatrmB cells is depressed above 70 degrees C. At 80 degrees C, the DeltatrmB strain exhibits a severe growth defect. Thus, the m(7)G46 modification is required for cell viability at high temperatures via a tRNA modification network, in which the m(7)G46 modification supports introduction of other modifications.
N(7)-甲基鸟嘌呤位于 tRNA 的 46 位(m(7)G46),由 tRNA(m(7)G46)甲基转移酶(TrmB)产生。为了阐明这种修饰的作用,我们构建了极端嗜热真细菌 Thermus thermophilus 的 trmB 基因敲除(DeltatrmB)菌株。酶活性测定、核苷分析和 RNA 测序证实,DeltatrmB 菌株细胞提取物中缺乏 TrmB 活性,tRNA(Phe)中缺乏 m(7)G46 修饰。当 DeltatrmB 菌株在高温下培养时,除了缺乏 m(7)G46 修饰外,tRNA 中的几个修饰核苷酸也被低度修饰。用 tRNA 修饰酶进行的测定表明,Gm18 和 m(1)G37 的修饰度降低,提示 m(7)G46 对其形成有积极影响。尽管缺乏 m(7)G46 修饰和低度修饰不会影响 tRNA(Phe)的苯丙氨酸加载活性,但它们会降低 I 类 tRNA 的熔解温度并导致 tRNA(Phe)和 tRNA(Ile)的降解。(35)S-甲硫氨酸掺入蛋白质的实验表明,DeltatrmB 细胞中的蛋白质合成在 70°C 以上时受到抑制。在 80°C 时,DeltatrmB 菌株表现出严重的生长缺陷。因此,m(7)G46 修饰通过 tRNA 修饰网络对高温下的细胞活力是必需的,其中 m(7)G46 修饰支持引入其他修饰。