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通过大肠杆菌亮氨酰 - tRNA合成酶进行氨酰化的RNA的体外筛选。

In vitro selection of RNAs aminoacylated by Escherichia coli leucyl-tRNA synthetase.

作者信息

Asahara H, Nameki N, Hasegawa T

机构信息

Department of Biomolecular Science, Faculty of Engineering, Gifu University, Gifu, 501-1193, Japan.

出版信息

J Mol Biol. 1998 Oct 30;283(3):605-18. doi: 10.1006/jmbi.1998.2111.

DOI:10.1006/jmbi.1998.2111
PMID:9784370
Abstract

To investigate systematically the RNA sequences necessary for aminoacylation by Escherichia coli leucyl-tRNA synthetase, RNAs with leucylation activity were isolated by in vitro selection from a library of tRNALeu variants possessing randomized sequences in the D-loop, the variable arm, and the T-loop. After two rounds of selection, most of the selected variants showed the following features: (1) the tertiary interaction between nucleotides at positions 15 and 48 was A15-U48; (2) the continuous G18G19 sequence, which is invariant in canonical tRNAs, appeared at the fixed position in the D-loop; and (3) the nucleotide at position 20a in the D-loop was A. These selected nucleotides and their positions, concentrating on the hinge region of tRNA, were identical to those of native tRNALeu. In contrast, although the long variable arm is the most characteristic of the tRNALeu structure, the primary and secondary structures were not correlated with the leucylation activity. These findings indicate that A15-U48, A20a, and G18G19 located at specific positions are involved in the tertiary folding of leucine-accepting tRNA molecules. With increases in the selection cycle, the D-loop sequence and the secondary structure of the variable arm became similar to those of tRNALeu, suggesting that tRNALeu represents an optimized RNA sequence for leucylation.

摘要

为了系统地研究大肠杆菌亮氨酰 - tRNA合成酶进行氨酰化作用所需的RNA序列,通过体外筛选从D环、可变臂和T环具有随机序列的tRNALeu变体文库中分离出具有亮氨酰化活性的RNA。经过两轮筛选,大多数所选变体呈现出以下特征:(1)第15位和第48位核苷酸之间的三级相互作用为A15 - U48;(2)在典型tRNA中不变的连续G18G19序列出现在D环的固定位置;(3)D环中第20a位的核苷酸为A。这些所选核苷酸及其位置集中在tRNA的铰链区,与天然tRNALeu的相同。相比之下,尽管长可变臂是tRNALeu结构最具特征性的部分,但其一级和二级结构与亮氨酰化活性并无关联。这些发现表明,位于特定位置的A15 - U48、A20a和G18G19参与了亮氨酸接受tRNA分子的三级折叠。随着筛选周期的增加,D环序列和可变臂的二级结构变得与tRNALeu相似,这表明tRNALeu代表了一种针对亮氨酰化作用优化的RNA序列。

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