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病毒RNA聚合酶对亚基因组RNA启动子的序列特异性识别。

Sequence-specific recognition of a subgenomic RNA promoter by a viral RNA polymerase.

作者信息

Siegel R W, Adkins S, Kao C C

机构信息

Department of Biology, Indiana University, Bloomington, IN 47405, USA.

出版信息

Proc Natl Acad Sci U S A. 1997 Oct 14;94(21):11238-43. doi: 10.1073/pnas.94.21.11238.

Abstract

RNA templates of 33 nucleotides containing the brome mosaic virus (BMV) core subgenomic promoter were used to determine the promoter elements recognized by the BMV RNA-dependent RNA polymerase (RdRp) to initiate RNA synthesis. Nucleotides at positions -17, -14, -13, and -11 relative to the subgenomic initiation site must be maintained for interaction with the RdRp. Changes to every other nucleotide at these four positions allow predictions for the base-specific functional groups required for RdRp recognition. RdRp contact of the nucleotide at position -17 was suggested with a template competition assay. Comparison of the BMV subgenomic promoter to those from other plant and animal alphaviruses shows a remarkable degree of conservation of the nucleotides required for BMV subgenomic RNA synthesis. We show that the RdRp of the plant-infecting BMV is capable of accurately, albeit inefficiently, initiating RNA synthesis from the subgenomic promoter of the animal-infecting Semliki Forest virus. The sequence-specific recognition of RNA by the BMV RdRp is analogous to the recognition of DNA promoters by DNA-dependent RNA polymerases.

摘要

使用含有雀麦花叶病毒(BMV)核心亚基因组启动子的33个核苷酸的RNA模板,来确定BMV RNA依赖性RNA聚合酶(RdRp)识别以启动RNA合成的启动子元件。相对于亚基因组起始位点,-17、-14、-13和-11位的核苷酸必须保持不变,以便与RdRp相互作用。这四个位置上其他每个核苷酸的变化,有助于预测RdRp识别所需的碱基特异性官能团。通过模板竞争试验表明了RdRp与-17位核苷酸的接触。将BMV亚基因组启动子与其他植物和动物甲病毒的启动子进行比较,结果显示BMV亚基因组RNA合成所需的核苷酸具有显著的保守性。我们发现,感染植物的BMV的RdRp能够准确地(尽管效率不高)从感染动物的辛德毕斯病毒的亚基因组启动子启动RNA合成。BMV RdRp对RNA的序列特异性识别类似于DNA依赖性RNA聚合酶对DNA启动子的识别。

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