Santerre A, Britt A B
Section of Plant Biology, University of California, Davis 95616.
Proc Natl Acad Sci U S A. 1994 Mar 15;91(6):2240-4. doi: 10.1073/pnas.91.6.2240.
We have isolated an Arabidopsis thaliana cDNA that complements the methyl methanesulfonate-sensitive phenotype of an Escherichia coli double mutant deficient in 3-methyladenine glycosylases (DNA-3-methyladenine glycosidases I and II, EC 3.2.2.20 and 3.2.2.21, respectively, encoded by tag and alkA). Expression of the Arabidopsis cDNA enhances the methyl methanesulfonate resistance of the E. coli double mutant by nearly four orders of magnitude. The cDNA corresponds to a single-copy, nuclearly encoded sequence which specifies a predicted 28.1-kDa protein with a charge of +8 at pH 7.0. Enzymatic analysis of extracts prepared from the transformed mutants indicates that the cDNA encodes a 3-methyladenine glycosylase. The predicted amino acid sequence of the Arabidopsis glycosylase has significant homology to other eukaryotic 3-methyladenine glycosylases.
我们分离出了一个拟南芥cDNA,它能互补大肠杆菌双突变体对甲磺酸甲酯敏感的表型,该双突变体缺乏3-甲基腺嘌呤糖基化酶(DNA-3-甲基腺嘌呤糖基化酶I和II,分别由tag和alkA编码,EC 3.2.2.20和3.2.2.21)。拟南芥cDNA的表达使大肠杆菌双突变体对甲磺酸甲酯的抗性提高了近四个数量级。该cDNA对应一个单拷贝、核编码序列,它指定了一个预测的28.1 kDa蛋白,在pH 7.0时带 +8电荷。对从转化突变体中制备的提取物进行酶分析表明,该cDNA编码一种3-甲基腺嘌呤糖基化酶。拟南芥糖基化酶的预测氨基酸序列与其他真核生物3-甲基腺嘌呤糖基化酶具有显著同源性。