Institute for Biochemistry, University of Leipzig, Brüderstr. 34, 04103 Leipzig, Germany.
Cell Mol Life Sci. 2010 May;67(9):1447-63. doi: 10.1007/s00018-010-0271-4. Epub 2010 Feb 14.
RNA polymerases are important enzymes involved in the realization of the genetic information encoded in the genome. Thereby, DNA sequences are used as templates to synthesize all types of RNA. Besides these classical polymerases, there exists another group of RNA polymerizing enzymes that do not depend on nucleic acid templates. Among those, tRNA nucleotidyltransferases show remarkable and unique features. These enzymes add the nucleotide triplet C-C-A to the 3'-end of tRNAs at an astonishing fidelity and are described as "CCA-adding enzymes". During this incorporation of exactly three nucleotides, the enzymes have to switch from CTP to ATP specificity. How these tasks are fulfilled by rather simple and small enzymes without the help of a nucleic acid template is a fascinating research area. Surprising results of biochemical and structural studies allow scientists to understand at least some of the mechanistic principles of the unique polymerization mode of these highly unusual enzymes.
RNA 聚合酶是参与实现基因组中编码的遗传信息的重要酶。因此,DNA 序列被用作合成所有类型 RNA 的模板。除了这些经典的聚合酶之外,还有另一组不依赖核酸模板的 RNA 聚合酶。其中,tRNA 核苷酸转移酶表现出显著而独特的特征。这些酶以惊人的保真度将三核苷酸 C-C-A 添加到 tRNA 的 3' 端,被描述为“CCA 添加酶”。在这个精确添加三个核苷酸的过程中,酶必须从 CTP 切换到 ATP 特异性。这些相当简单和小的酶在没有核酸模板帮助的情况下如何完成这些任务,是一个引人入胜的研究领域。生化和结构研究的惊人结果使科学家们至少能够理解这些高度异常的酶独特聚合模式的一些机制原则。