Meyhack B, Pace B, Uhlenbeck O C, Pace N R
Proc Natl Acad Sci U S A. 1978 Jul;75(7):3045-9. doi: 10.1073/pnas.75.7.3045.
RNase M5 of Bacillus subtilis specifically cleaves a 179-nucleotide precursor 5S rRNA to yield mature 5S rRNA (116 nucleotides) and two fragments derived from the termini. Possible recognition elements for RNase M5 within the precursor structure include nucleotide sequences arranged with 2-fold rotational and translational symmetry about the substrate bonds. We have used bacteriophage T4 RNA ligase to construct, from synthetic oligonucleotides and mature or precursor 5S rRNA fragments, test substrates lacking these symmetry elements. The susceptibilities of the artificial substrates to RNase M5 demonstrate that the symmetrically arranged sequences are not used in the RNase M5 interaction with the precursor. Additionally, the synthetic protocols permitted the invention of an acid-soluble assay for RNase M5 and, potentially, other specific endoribonucleases.
枯草芽孢杆菌的核糖核酸酶M5能特异性切割一段179个核苷酸的前体5S核糖体RNA,产生成熟的5S核糖体RNA(116个核苷酸)以及两个源自末端的片段。前体结构中核糖核酸酶M5可能的识别元件包括围绕底物键以2倍旋转和平移对称排列的核苷酸序列。我们利用噬菌体T4 RNA连接酶,从合成寡核苷酸以及成熟或前体5S核糖体RNA片段构建了缺乏这些对称元件的测试底物。这些人工底物对核糖核酸酶M5的敏感性表明,对称排列的序列在核糖核酸酶M5与前体的相互作用中未被利用。此外,这些合成方案使得能够发明一种针对核糖核酸酶M5以及可能的其他特异性核糖核酸内切酶的酸溶性检测方法。