Ohtsuki T, Kawai G, Watanabe Y, Kita K, Nishikawa K, Watanabe K
Department of Chemistry and Biotechnology, Graduate School of Engineering, University of Tokyo, Japan.
Nucleic Acids Res. 1996 Feb 15;24(4):662-7. doi: 10.1093/nar/24.4.662.
Ascaris suum mitochondrial tRNA Met lacking the entire T stem was prepared by enzymatic ligation of two chemically synthesized RNA fragments. The synthetic tRNA could be charged with methionine by A.suum mitochondrial extract, although the charging activity was considerably low compared with that of the native tRNA, probably due to lack of modification. Enzymatic probing of the synthetic tRNA showed a very similar digestion pattern to that of the native tRNA Met, which has already been concluded to take an L-shape-like structure [Watanabe et al. (1994) J. Biol. Chem., 269, 22902-22906]. These results suggest that the synthetic tRNA possesses almost the same conformation as the native one, irrespective of the presence or absence of modified residues. The method of preparing the bizarre tRNA used here will provide a useful tool for elucidating the tertiary structure of such tRNAs, because they can be obtained without too much difficulty in the amounts necessary for physicochemical studies such as NMR spectroscopy.
通过将两个化学合成的RNA片段进行酶促连接,制备了缺失整个T茎的猪蛔虫线粒体tRNA Met。合成的tRNA可以被猪蛔虫线粒体提取物用甲硫氨酸进行氨酰化,尽管与天然tRNA相比,氨酰化活性相当低,这可能是由于缺乏修饰所致。对合成tRNA进行酶促探测显示,其消化模式与天然tRNA Met非常相似,天然tRNA Met已被确定为具有类似L形的结构[渡边等人(1994年)《生物化学杂志》,269,22902 - 22906]。这些结果表明,无论是否存在修饰残基,合成tRNA都具有与天然tRNA几乎相同的构象。这里所使用的制备这种奇异tRNA的方法将为阐明此类tRNA的三级结构提供一个有用的工具,因为可以相对轻松地获得用于诸如核磁共振光谱等物理化学研究所需数量的tRNA。