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质粒ColIb-P9反义Inc RNA与环序列中具有5'-rUUGGCG-3'基序的靶RNA结合的结构基础。

Structural basis for binding of the plasmid ColIb-P9 antisense Inc RNA to its target RNA with the 5'-rUUGGCG-3' motif in the loop sequence.

作者信息

Asano K, Niimi T, Yokoyama S, Mizobuchi K

机构信息

Department of Biophysics and Biochemistry, Graduate School of Science, University of Tokyo, Hongo, Tokyo 113, Japan.

出版信息

J Biol Chem. 1998 May 8;273(19):11826-38. doi: 10.1074/jbc.273.19.11826.

Abstract

The sequence 5'-rUUGGCG-3' is conserved within the loop regions of antisense RNAs or their targets involved in replication of various prokaryotic plasmids. In IncIalpha plasmid ColIb-P9, the partially base paired 21-nucleotide loop of a stem-loop called structure I within RepZ mRNA contains this hexanucleotide sequence, and comprises the target site for the antisense Inc RNA. In this report, we find that the base pairing interaction at the 5'-rGGC-3' sequence in the hexanucleotide motif is important for interaction between Inc RNA and structure I. In addition, the 21-base loop domain of structure I is folded tighter than predicted, with the hexanucleotide sequence at the top. The second U residue in the sequence is favored for Inc RNA binding in a base-specific manner. On the other hand, the upper domain of the Inc RNA stem-loop is loosely structured, and maintaining the loop sequence single-stranded is important for the intermolecular interaction. Based on these results, we propose that a structural feature in the loop I domain, conferred probably by the conserved 5'-rUUGGCG-3' sequence, favors binding to a complementary, single-stranded RNA. This model also explains how the RepZ mRNA pseudoknot, described in the accompanying paper (Asano, K., and Mizobuchi, K. (1998) J. Biol. Chem. 273, 11815-11825) is formed specifically with structure I. A possible conformation adopted by the 5'-rUUGGCG-3' loop sequence is discussed.

摘要

5'-rUUGGCG-3' 序列在参与各种原核质粒复制的反义RNA或其靶标的环区域内保守。在IncIα质粒ColIb-P9中,RepZ mRNA内一个称为结构I的茎环的部分碱基配对的21核苷酸环包含此六核苷酸序列,并构成反义Inc RNA的靶位点。在本报告中,我们发现六核苷酸基序中5'-rGGC-3'序列处的碱基配对相互作用对于Inc RNA与结构I之间的相互作用很重要。此外,结构I的21碱基环结构域比预测的折叠得更紧密,六核苷酸序列在顶部。序列中的第二个U残基有利于Inc RNA以碱基特异性方式结合。另一方面,Inc RNA茎环的上部结构域结构松散,保持环序列单链对于分子间相互作用很重要。基于这些结果,我们提出环I结构域中的一种结构特征,可能由保守的5'-rUUGGCG-3'序列赋予,有利于与互补的单链RNA结合。该模型还解释了随附论文(浅野,K.,和水渊,K.(1998)J.生物化学.273,11815-11825)中描述的RepZ mRNA假结如何与结构I特异性形成。讨论了5'-rUUGGCG-3'环序列可能采用的构象。

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