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携带硫代磷酸酯(S(P))修饰的U6 RNA分子内茎环结构。

Structure of the U6 RNA intramolecular stem-loop harboring an S(P)-phosphorothioate modification.

作者信息

Reiter Nicholas J, Nikstad Laura J, Allmann Anne M, Johnson Randal J, Butcher Samuel E

机构信息

Department of Biochemistry, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

出版信息

RNA. 2003 May;9(5):533-42. doi: 10.1261/rna.2199103.

Abstract

Phosphorothioate-substitution experiments are often used to elucidate functionally important metal ion-binding sites on RNA. All previous experiments with S(P)-phosphorothioate-substituted RNAs have been done in the absence of structural information for this particular diastereomer. Yeast U6 RNA contains a metal ion-binding site that is essential for spliceosome function and includes the pro-S(P) oxygen 5' of U(80). S(P)-phosphorothioate substitution at this location creates spliceosomes dependent on thiophilic ions for the first step of splicing. We have determined the solution structure of the U(80) S(P)-phosphorothioate-substituted U6 intramolecular stem-loop (ISL), and also report the refined NMR structure of the unmodified U6 ISL. Both structures were determined with inclusion of (1)H-(13)C residual dipolar couplings. The precision of the structures with and without phosphorothioate (RMSD = 1.05 and 0.79 A, respectively) allows comparison of the local and long-range structural effect of the modification. We find that the U6-ISL structure is unperturbed by the phosphorothioate. Additionally, the thermodynamic stability of the U6 ISL is dependent on the protonation state of the A(79)-C(67) wobble pair and is not affected by the adjacent phosphorothioate. These results indicate that a single S(P)-phosphorothioate substitution can be structurally benign, and further validate the metal ion rescue experiments used to identify the essential metal-binding site(s) in the spliceosome.

摘要

硫代磷酸酯取代实验常用于阐明RNA上功能重要的金属离子结合位点。此前所有关于S(P)-硫代磷酸酯取代RNA的实验都是在缺乏这种特定非对映异构体结构信息的情况下进行的。酵母U6 RNA包含一个对剪接体功能至关重要的金属离子结合位点,其中包括U(80)的前S(P)氧5'。在此位置进行S(P)-硫代磷酸酯取代会产生依赖亲硫离子进行剪接第一步的剪接体。我们已经确定了U(80) S(P)-硫代磷酸酯取代的U6分子内茎环(ISL)的溶液结构,并且还报告了未修饰的U6 ISL的精细NMR结构。这两种结构都是在包含(1)H-(13)C剩余偶极耦合的情况下确定的。有和没有硫代磷酸酯的结构精度(均方根偏差分别为1.05和0.79 Å)允许比较修饰的局部和远程结构效应。我们发现U6-ISL结构不受硫代磷酸酯的干扰。此外,U6 ISL的热力学稳定性取决于A(79)-C(67)摆动对的质子化状态,并且不受相邻硫代磷酸酯的影响。这些结果表明单个S(P)-硫代磷酸酯取代在结构上可能是无害的,并进一步验证了用于识别剪接体中必需金属结合位点的金属离子拯救实验。

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