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

H. Takeda, H. Hori, Y. Endo
{"title":"Identification of Aquifex aeolicus tRNA (m2(2G26) methyltransferase gene.","authors":"H. Takeda, H. Hori, Y. Endo","doi":"10.1093/NASS/2.1.229","DOIUrl":null,"url":null,"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.","PeriodicalId":19724,"journal":{"name":"Nucleic acids research. Supplement","volume":"37 1","pages":"229-30"},"PeriodicalIF":0.0000,"publicationDate":"2002-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"8","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nucleic acids research. Supplement","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/NASS/2.1.229","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Stereocontrolled synthesis of phosphorothioate DNA by an oxazaphospholidine approach. Identification of Aquifex aeolicus tRNA (m2(2G26) methyltransferase gene. Crystal structure of d(GCGAAAGCT) containing parallel-stranded duplex with homo base pairs and anti-parallel duplex with Watson-Crick base pairs. X-ray structure of d(GCGAAGC); switching of partner for G:A pair in duplex form. Synthesis and characterization of oligonucleotides containing formamidopyrimidine lesions (Fapy.dA, Fapy.dG) at defined sites.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1