Identification of Aquifex aeolicus tRNA (m2(2G26) methyltransferase gene.

H. Takeda, H. Hori, Y. Endo
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引用次数: 8

Abstract

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.
风颡鱼tRNA (m2(2G26)甲基转移酶基因的鉴定。
N2,N2-二甲基鸟嘌呤(m2(2)G)的修饰存在于真核生物和古细菌的trna和rnas中。在tRNA中,G26位置的修饰是由tRNA (m2(2)G26)甲基转移酶产生的,该酶由相应的基因trm1编码。该酶通过中间修饰碱基m2G26催化s -腺苷- l-蛋氨酸的甲基转移到半保守残基G26。最近的基因组测序项目已经报道了假定的trm1编码在Aquifex aeolicus基因组中,Aquifex aeolicus是真细菌中唯一的例外。为了证实该细菌trm1基因产物是否是真正的tRNA (m2(2)G26)甲基转移酶,我们利用小麦胚芽体外无细胞翻译系统表达了该蛋白。我们的生化分析清楚地表明该基因产物具有tRNA (m2(2)G26)甲基转移酶活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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