tRNA nucleotidyltransferases: ancient catalysts with an unusual mechanism of polymerization

被引:52
作者
Betat, Heike [1 ]
Rammelt, Christiane [2 ]
Moerl, Mario [1 ]
机构
[1] Univ Leipzig, Inst Biochem, D-04103 Leipzig, Germany
[2] Univ Halle Wittenberg, Inst Biochem, D-06120 Halle, Germany
关键词
CCA-adding enzyme; tRNA nucleotidyltransferase; tRNA; Template-independent polymerization; CCA-ADDING ENZYME; BACTERIAL POLY(A) POLYMERASE; ESCHERICHIA-COLI; MESSENGER-RNA; ACTIVE-SITE; 3' TERMINUS; ENCODED NUCLEOTIDES; HD DOMAIN; DNA; SUPERFAMILY;
D O I
10.1007/s00018-010-0271-4
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
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.
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页码:1447 / 1463
页数:17
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