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来自小鼠乳腺肿瘤病毒的非移码RNA假结的构象。

Conformation of a non-frameshifting RNA pseudoknot from mouse mammary tumor virus.

作者信息

Kang H, Hines J V, Tinoco I

机构信息

Department of Chemistry, University of California, Berkeley, USA.

出版信息

J Mol Biol. 1996 May 31;259(1):135-47. doi: 10.1006/jmbi.1996.0308.

Abstract

The solution conformation of an RNA pseudoknot, which is a mutant of the pseudoknot required for ribosomal frameshifting in mouse mammary tumor virus, has been determined by NMR. The 32-nucleotide RNA pseudoknot does not promote efficient frameshifting, although its sequence is very similar to the efficient frameshifting pseudoknot whose structure was recently determined by our group. 13C-labeling of the RNA and 13C-edited NMR techniques were used to facilitate spectral assignment. The three-dimensional structure of the RNA pseudoknot was determined by restrained molecular dynamics based on NMR-derived interproton distances and torsion angle constraints. The conformation is very different from that previously determined for the efficient-frameshifting pseudoknot. Two unpaired nucleotides are stacked between stem 1 and stem 2, in contrast to the one unpaired nucleotide at the same junction region as found previously. The two stems of the pseudoknot are not coaxial, they are twisted and bent relative to each other. Loop 2 does not cross the shallow minor groove of stem 1, in contrast to the pseudoknots with one or no intervening nucleotides between the stems. The fact that a specific conformation is required for efficient frameshifting implies a specific interaction of the pseudoknot with the ribosome.

摘要

一种RNA假结的溶液构象已通过核磁共振(NMR)确定,该假结是小鼠乳腺肿瘤病毒核糖体移码所需假结的突变体。这个32个核苷酸的RNA假结虽然其序列与我们小组最近确定结构的高效移码假结非常相似,但它并不能促进有效的移码。对RNA进行13C标记并使用13C编辑的NMR技术来促进光谱归属。基于NMR得出的质子间距离和扭转角约束,通过受限分子动力学确定了RNA假结的三维结构。该构象与先前确定的高效移码假结的构象非常不同。与之前在相同连接区域发现的一个未配对核苷酸不同,有两个未配对核苷酸堆积在茎1和茎2之间。假结的两个茎不同轴,它们彼此扭曲和弯曲。与茎之间有一个或没有间隔核苷酸的假结不同,环2不穿过茎1的浅小沟。高效移码需要特定构象这一事实意味着假结与核糖体之间存在特定相互作用。

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