Waugh D S, Green C J, Pace N R
Department of Biology, Indiana University, Bloomington 47405.
Science. 1989 Jun 30;244(4912):1569-71. doi: 10.1126/science.2472671.
Ribonuclease P (RNase P) RNA is the catalytic moiety of the ribonucleoprotein enzyme that removes precursor sequences from the 5' ends of pre-transfer RNAs in eubacteria. Phylogenetic variation according to recently proposed secondary structure models was used to identify structural elements of the RNase P RNA that are dispensable for catalysis. A simplified RNase P RNA that consists only of evolutionarily conserved features was designed, synthesized, and characterized. Although the simplified RNA (Min 1 RNA) is only 263 nucleotides in length, in contrast to the 354 to 417 nucleotides of naturally occurring RNase P RNAs, its specificity of pre-tRNA cleavage is identical to that of the native enzymes. Moreover, the catalytic efficiencies of the Min 1 RNA and the native RNA enzymes are similar. These results focus the search for the catalytic elements of RNase P RNAs to their conserved structure.
核糖核酸酶P(RNase P)RNA是核糖核蛋白酶的催化部分,该酶可从真细菌中前体转运RNA的5'末端去除前体序列。根据最近提出的二级结构模型的系统发育变异用于识别RNase P RNA中对催化作用可有可无的结构元件。设计、合成并表征了一种仅由进化保守特征组成的简化RNase P RNA。尽管简化RNA(Min 1 RNA)长度仅为263个核苷酸,而天然存在的RNase P RNA长度为354至417个核苷酸,但其对前体tRNA切割的特异性与天然酶相同。此外,Min 1 RNA和天然RNA酶的催化效率相似。这些结果将对RNase P RNA催化元件的搜索集中到其保守结构上。