Kim S I, Söll D
Hyonam Kidney Laboratory, Soon Chun Hyang University, Seoul, Korea.
Mol Cells. 1998 Aug 31;8(4):459-65.
Early investigations revealed that Bacillus subtilis glutamyl-tRNA synthetase [GluRS (bs)] is responsible for aminoacylating both glutamate tRNA [tRNA(Glu) (bs)] and glutamine tRNA [tRNA(Gln) (bs)] with glutamate. The same Bacillus enzyme can also efficiently attach glutamate to one isoacceptor glutamine tRNA [tRNA(Gln) (ec)] of Escherichia coli in vitro but not to tRNA2(Gln) (ec) and tRNA(Glu) (ec). To characterize identity elements of these glutamine tRNAs in the interaction with GluRS (bs), tRNA2(Gln) (ec), tRNA1(Gln) (ec), three other mutant glutamine tRNAs [tRNA2(Gln) (AU) (C34 --> U34), tRNA2(Gln) (12M) (C34 --> U34, 31A-U39 --> 31U-A39), and tRNA2(Gln) (M21) (64C --> G50 --> 64G-C50, 63U-A51 --> 63A-U51)] originated from tRNA2(Gln) (ec), tRNA(Gln) (bs), and a mutant tRNAM(Gln) (bs) whose U at the 34th position (U34), was replaced to C (C34), were produced in E. coli. All of the E. coli glutamine tRNAs containing U34 such as tRNA1(Gln), tRNA2(Gln) (AU), and tRNA2(Gln) (12M) could be charged with glutamate by GluRS (bs), whereas tRNA2(Gln) (ec) and its T-stem mutant tRNA2(Gln) (M21) containing C34 could not be charged by the same enzyme. The unique change of C34 to U34 of tRNA2(Gln) (ec) acquired glutamate acceptor activity by GluRS (bs). This result suggests that the U34 is the major identity element of tRNA1(Gln) (ec) in the recognition by GluRS (bs). The same situation was found in tRNA(Gln) (bs). The glutamate acceptor activity of tRNA(Gln) (bs) disappeared on replacement of U34 to C34. To find out whether modified bases in tRNA(Gln) (bs) are involved in the recognition by GluRS (bs), glutamylation of tRNA(Gln) (bs) produced by in vitro transcription was also examined but the in vitro transcript of tRNA(Gln) (bs) could not be charged with glutamic acid by GluRS (bs). All of these mean that the major recognition element for GluRS (bs) is U at the 34th position of both tRNA(Gln) (bs) and tRNA1(Gln) (ec) as a modified form.
早期研究表明,枯草芽孢杆菌谷氨酰胺-tRNA合成酶[GluRS(bs)]负责用谷氨酸对谷氨酸tRNA[tRNA(Glu)(bs)]和谷氨酰胺tRNA[tRNA(Gln)(bs)]进行氨酰化。同一枯草芽孢杆菌酶在体外也能有效地将谷氨酸连接到大肠杆菌的一种同功受体谷氨酰胺tRNA[tRNA(Gln)(ec)]上,但不能连接到tRNA2(Gln)(ec)和tRNA(Glu)(ec)上。为了确定这些谷氨酰胺tRNA在与GluRS(bs)相互作用中的识别元件,在大肠杆菌中产生了tRNA2(Gln)(ec)、tRNA1(Gln)(ec)、另外三种突变型谷氨酰胺tRNA[tRNA2(Gln)(AU)(C34→U34)、tRNA2(Gln)(12M)(C34→U34,31A-U39→31U-A39)和tRNA2(Gln)(M21)(64C→G50→64G-C50,63U-A51→63A-U51)],它们分别源自tRNA2(Gln)(ec)、tRNA(Gln)(bs)以及第34位的U(U34)被替换为C(C34)的突变型tRNAM(Gln)(bs)。所有含有U34的大肠杆菌谷氨酰胺tRNA,如tRNA1(Gln)、tRNA2(Gln)(AU)和tRNA2(Gln)(12M),都可以被GluRS(bs)用谷氨酸进行氨酰化,而含有C34的tRNA2(Gln)(ec)及其T-茎突变体tRNA2(Gln)(M21)则不能被同一酶氨酰化。tRNA2(Gln)(ec)的C34独特地变为U34后,获得了被GluRS(bs)用谷氨酸氨酰化的活性。这一结果表明,U34是tRNA1(Gln)(ec)在被GluRS(bs)识别时的主要识别元件。在tRNA(Gln)(bs)中也发现了同样的情况。tRNA(Gln)(bs)的U34被替换为C34后,其谷氨酸氨酰化活性消失。为了弄清楚tRNA(Gln)(bs)中的修饰碱基是否参与了被GluRS(bs)的识别,还检测了体外转录产生的tRNA(Gln)(bs)的谷氨酰化情况,但tRNA(Gln)(bs)的体外转录本不能被GluRS(bs)用谷氨酸进行氨酰化。所有这些都意味着,GluRS(bs)的主要识别元件是tRNA(Gln)(bs)和tRNA1(Gln)(ec)第34位的U,且为修饰形式。