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具有非对称串联GxU摆动碱基对的14碱基RNA双链体的晶体结构

Crystal structure of a 14 bp RNA duplex with non-symmetrical tandem GxU wobble base pairs.

作者信息

Trikha J, Filman D J, Hogle J M

机构信息

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Nucleic Acids Res. 1999 Apr 1;27(7):1728-39. doi: 10.1093/nar/27.7.1728.

Abstract

Adjacent GxU wobble base pairs are frequently found in rRNA. Atomic structures of small RNA motifs help to provide a better understanding of the effects of various tandem mismatches on duplex structure and stability, thereby providing better rules for RNA structure prediction and validation. The crystal structure of an RNA duplex containing the sequence r(GGUAUUGC-GGUACC)2 has been solved at 2.1 A resolution using experimental phases. Novel refinement strategies were needed for building the correct solvent model. At present, this is the only short RNA duplex structure containing 5'-U-U-3'/3'-G-G-5' non-symmetric tandem GxU wobble base pairs. In the 14mer duplex, the six central base pairs are all displaced away from the helix axis, yielding significant changes in local backbone conformation, helix parameters and charge distribution that may provide specific recognition sites for biologically relevant ligand binding. The greatest deviations from A-form helix occur where the guanine of a wobble base pair stacks over a purine from the opposite strand. In this vicinity, the intra-strand phosphate distances increase significantly, and the major groove width increases up to 3 A. Structural comparisons with other short duplexes containing symmetrical tandem GxU or GxT wobble base pairs show that nearest-neighbor sequence dependencies govern helical twist and the occurrence of cross-strand purine stacks.

摘要

相邻的GxU摆动碱基对在rRNA中经常出现。小RNA基序的原子结构有助于更好地理解各种串联错配对双链体结构和稳定性的影响,从而为RNA结构预测和验证提供更好的规则。使用实验相位已在2.1埃分辨率下解析了包含序列r(GGUAUUGC-GGUACC)2的RNA双链体的晶体结构。构建正确的溶剂模型需要新的优化策略。目前,这是唯一包含5'-U-U-3'/3'-G-G-5'非对称串联GxU摆动碱基对的短RNA双链体结构。在14聚体双链体中,六个中心碱基对均偏离螺旋轴,导致局部主链构象、螺旋参数和电荷分布发生显著变化,这可能为生物相关配体结合提供特定的识别位点。与A-型螺旋的最大偏差发生在摆动碱基对的鸟嘌呤堆积在相反链的嘌呤上方的位置。在这个附近,链内磷酸距离显著增加,大沟宽度增加至3埃。与其他包含对称串联GxU或GxT摆动碱基对的短双链体的结构比较表明,近邻序列依赖性决定螺旋扭曲和跨链嘌呤堆积的出现。

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