Carrara G, Calandra P, Fruscoloni P, Tocchini-Valentini G P
Istituto di Biologia Cellulare, Consiglio Nazionale delle Ricerche, Rome, Italy.
Proc Natl Acad Sci U S A. 1995 Mar 28;92(7):2627-31. doi: 10.1073/pnas.92.7.2627.
Using precursor tRNA molecules to study RNA-protein interactions, we have identified an RNA motif recognized by eukaryotic RNase P (EC 3.1.26.5). Analysis of circularly permuted precursors indicates that interruptions in the sugar-phosphate backbone are not tolerated in the acceptor stem, in the T stem-loop, or between residues A-9 and G-10. Prokaryotic RNase P will function with a minihelix consisting of the acceptor stem connected directly to the T stem-loop. Eukaryotic RNase P cannot use such a minimal substrate unless a linker sequence is added in the gap where the D stem and anticodon stem-loop were deleted.
利用前体tRNA分子研究RNA-蛋白质相互作用,我们鉴定出了一种真核核糖核酸酶P(EC 3.1.26.5)识别的RNA基序。对环形排列的前体的分析表明,在受体茎、T茎环或A-9和G-10残基之间,磷酸核糖主链的中断是不被允许的。原核核糖核酸酶P可以与一个由直接连接到T茎环的受体茎组成的小螺旋起作用。真核核糖核酸酶P不能使用这样的最小底物,除非在缺失D茎和反密码子茎环的间隙中添加一个接头序列。