Takeda Hiroshi, Hori Hiroyuki, Endo Yaeta
Department of Applied Chemistry, Faculty of Engineering, Ehime University, Matsuyama 790-8577, Japan.
Nucleic Acids Res Suppl. 2002(2):229-30.
The modifications of N2,N2-dimethylguanine (m2(2)G) are found in tRNAs and rRNAs from eukarya and archaea. In tRNAs, modification at position G26 is generated by tRNA (m2(2)G26) methyltransferase, which is encoded by the corresponding gene, trm1. This enzyme catalyzes the methyl-transfer from S-adenosyl-L-methionine to the semi-conserved residue, G26, via the intermediate modified base, m2G26. Recent genome sequencing project has been reported that the putative trm1 is encoded in the genome of Aquifex aeolicus, a hyper-thermophilic eubacterium as only one exception among eubacteria. In order to confirm whether this bacterial trm1 gene product is a real tRNA (m2(2)G26) methyltransferase or not, we expressed this protein by wheat germ in vitro cell-free translation system. Our biochemical analysis clearly showed that this gene product possessed tRNA (m2(2)G26) methyltransferase activity.
N2,N2-二甲基鸟嘌呤(m2(2)G)修饰存在于真核生物和古细菌的转运RNA(tRNA)和核糖体RNA(rRNA)中。在tRNA中,G26位置的修饰由tRNA(m2(2)G26)甲基转移酶产生,该酶由相应的基因trm1编码。这种酶通过中间修饰碱基m2G26催化从S-腺苷-L-甲硫氨酸到半保守残基G26的甲基转移。最近的基因组测序项目报道,嗜热栖热菌(一种嗜热真细菌)的基因组中编码了假定的trm1,这是真细菌中唯一的例外。为了确定这种细菌trm1基因产物是否是真正的tRNA(m2(2)G26)甲基转移酶,我们在小麦胚体外无细胞翻译系统中表达了这种蛋白质。我们的生化分析清楚地表明,这种基因产物具有tRNA(m2(2)G26)甲基转移酶活性。