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大肠杆菌噬菌体Qβ RNA中心发夹结构在核苷酸水平上的二维模型。

A two-dimensional model at the nucleotide level for the central hairpin of coliphage Q beta RNA.

作者信息

Skripkin E A, Jacobson A B

机构信息

Chemistry Faculty, Moscow State University, Russia.

出版信息

J Mol Biol. 1993 Sep 20;233(2):245-60. doi: 10.1006/jmbi.1993.1503.

Abstract

We describe the construction and testing of a structural model at the nucleotide level for conformation CH of the central hairpin of genomic RNA from coliphage Q beta. The model was developed with the computer program MFOLD using both optimal and suboptimal predictions. Structural information obtained by electron microscopic analysis of Kleinschmidt spreadings of Q beta RNA was used to guide the modeling. The model was tested in solution with three enzymatic probes: RNase T1, RNase T2, and RNase V1, as well as four chemical probes: dimethylsulfate, diethylpyrocarbonate, kethoxal and 1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide metho-p-toluene sulfonate (CMCT). The structural analyses in solution are consistent with the predicted structural model. The model is also supported by comparative structural analysis with the related coliphage SP. The model provides a structural basis for published biochemical and genetic studies implicating large, long-range structural features in the co-regulation of viral coat and replicase expression. In addition, we show that the read-through region of the viral protein A1 forms a separate structural domain, and we suggest that it functions as a nucleation site that participates in the folding and refolding of the molecule during replication and translation. In addition to the central hairpin, we have analyzed the structure of the viral coat initiation region. Our studies show that the entire region consists of small local hairpins and that 26 nucleotides immediately surrounding the coat initiation codon are single-stranded.

摘要

我们描述了来自大肠杆菌噬菌体Qβ基因组RNA中央发夹构象CH在核苷酸水平上的结构模型构建与测试。该模型是使用计算机程序MFOLD通过最优和次优预测开发的。通过对Qβ RNA的Kleinschmidt铺展进行电子显微镜分析获得的结构信息用于指导建模。该模型在溶液中用三种酶探针(核糖核酸酶T1、核糖核酸酶T2和核糖核酸酶V1)以及四种化学探针(硫酸二甲酯、焦碳酸二乙酯、乙二醛和1-环己基-3-(2-吗啉代乙基)碳二亚胺对甲苯磺酸盐(CMCT))进行了测试。溶液中的结构分析与预测的结构模型一致。该模型还得到了与相关噬菌体SP的比较结构分析的支持。该模型为已发表的生化和遗传学研究提供了结构基础,这些研究表明在病毒衣壳和复制酶表达的协同调节中存在大的、远距离的结构特征。此外,我们表明病毒蛋白A1的通读区域形成一个单独的结构域,并且我们认为它作为一个成核位点,在复制和翻译过程中参与分子的折叠和重新折叠。除了中央发夹,我们还分析了病毒衣壳起始区域的结构。我们的研究表明,整个区域由小的局部发夹组成,并且衣壳起始密码子周围的26个核苷酸是单链的。

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