Carter B J, Vold B S, Hecht S M
Department of Chemistry, University of Virginia, Charlottesville 22901.
J Biol Chem. 1990 May 5;265(13):7100-3.
Two Bacillus subtilis tRNA(His) precursors (Green, C. J., and Vold, B. S. (1988) J. Biol. Chem. 263, 652-657) were processed by Escherichia coli RNase P in the presence of varying [Mg2+]. The wild type precursor was processed under all conditions to afford a single tRNA product containing 8 base pairs in the acceptor stem. In contrast, the position of processing of a mutant tRNA(His) precursor (containing a G27----A27 alteration) was shown to be condition-dependent. Processing occurred at A27 under conditions consistent with formation of an A27-C100 base pair in the acceptor stem but at G28 under conditions that disfavored base pair formation. The ability to control the site of RNase P-mediated tRNA precursor processing is unprecedented and permits analysis of the chemical factors that promote processing.
两种枯草芽孢杆菌tRNA(His)前体(格林,C.J.,和沃尔德,B.S.(1988年)《生物化学杂志》263卷,652 - 657页)在不同的[Mg2 +]存在下由大肠杆菌核糖核酸酶P进行加工。野生型前体在所有条件下都被加工成一种在受体茎中含有8个碱基对的单一tRNA产物。相比之下,一种突变型tRNA(His)前体(含有G27→A27改变)的加工位置显示出依赖于条件。在与受体茎中形成A27 - C100碱基对一致的条件下,加工发生在A27处,但在不利于碱基对形成的条件下,加工发生在G28处。控制核糖核酸酶P介导的tRNA前体加工位点的能力是前所未有的,并且允许对促进加工的化学因素进行分析。