Tad1p, a yeast tRNA-specific adenosine deaminase, is related to the mammalian pre-mRNA editing enzymes ADAR1 and ADAR2

被引:116
作者
Gerber, A
Grosjean, H
Melcher, T
Keller, W [1 ]
机构
[1] Univ Basel, Bioctr, Dept Cell Biol, CH-4056 Basel, Switzerland
[2] CNRS, Lab Struct Enzymol & Biochem, F-91198 Gif Sur Yvette, France
[3] Max Planck Inst Med Res, Dept Mol Neurosci, D-69120 Heidelberg, Germany
关键词
adenosine deaminase; inosine; RNA editing; tRNA(Ala); yeast;
D O I
10.1093/emboj/17.16.4780
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have identified an RNA-specific adenosine deaminase (termed Tad1p/scADAT1) from Saccharomyces cerevisiae that selectively converts adenosine at position 37 of eukaryotic tRNA(Ala) to inosine. The activity of purified recombinant Tad1p depends on the conformation of its tRNA substrate and the enzyme was found to be inactive on all other types of RNA tested. Mutant strains in which the TAD1 gene is disrupted are viable but lack Tad1p enzyme activity and their tRNA(Ala) is not modified at position A(37). Transformation of the mutant cells with the TAD1 gene restored enzyme activity. Tad1p has significant sequence similarity with the mammalian editing enzymes which act on specific precursor-mRNAs and on long double-stranded RNA. These findings suggest an evolutionary link between pre-mRNA editing and tRNA modification.
引用
收藏
页码:4780 / 4789
页数:10
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