Green C J, Vold B S, Morch M D, Joshi R L, Haenni A L
SRI International, Menlo Park, California 94025.
J Biol Chem. 1988 Aug 25;263(24):11617-20.
The 3'-end of the RNA genome of turnip yellow mosaic virus can form a pseudoknotted tRNA-like structure that can be recognized by several tRNA-specific enzymes. We have found that the catalytic RNA component of Bacillus subtilis RNase P can cleave this structure in unusually low ionic strength buffers at a site analogous to the 5'-end of an aminoacyl stem of a tRNA. Most other precursors can only be processed under low ionic strength conditions if the RNase P holoenzyme is used; processing by the catalytic RNA component alone requires a higher ionic strength buffer. The cleavage of the turnip yellow mosaic virus tRNA-like structure demonstrates the importance of the substrate in determining the optimal buffer conditions for this reaction and also shows that high ionic strength buffers are not always necessary for cleavage by the catalytic RNA.
芜菁黄花叶病毒RNA基因组的3'末端可形成一种假结状的tRNA样结构,该结构能被多种tRNA特异性酶识别。我们发现,枯草芽孢杆菌核糖核酸酶P的催化RNA组分可在异常低离子强度的缓冲液中,于一个类似于tRNA氨酰茎5'末端的位点切割该结构。大多数其他前体只有在使用核糖核酸酶P全酶时才能在低离子强度条件下进行加工;仅由催化RNA组分进行加工则需要更高离子强度的缓冲液。芜菁黄花叶病毒tRNA样结构的切割证明了底物在确定该反应最佳缓冲条件方面的重要性,同时也表明高离子强度缓冲液并非催化RNA切割所必需。