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苜蓿花叶病毒RNA3的3'非翻译区包含一个负链RNA合成的核心启动子和一个增强子元件。

The 3' untranslated region of alfalfa mosaic virus RNA3 contains a core promoter for minus-strand RNA synthesis and an enhancer element.

作者信息

van Rossum C M, Reusken C B, Brederode F T, Bol J F

机构信息

Institute of Molecular Plant Sciences, Gorlaeus Laboratories, Leiden University, The Netherlands.

出版信息

J Gen Virol. 1997 Nov;78 ( Pt 11):3045-9. doi: 10.1099/0022-1317-78-11-3045.

Abstract

The 3' untranslated regions (UTRs) of the three genomic RNAs of alfalfa mosaic virus consist of a 3' homologous sequence of 145 nt and upstream unique sequences 18-34 nt in length. Mutations were made in the 3' UTR of a cDNA clone of RNA3. Point mutations in five AUGC motifs which interfere with specific binding of coat protein to the 3' UTR had no effect on template activity of RNA3 for minus-strand RNA synthesis in vitro by purified viral RNA-dependent RNA polymerase (RdRp). Deletion analysis showed that the 3' homologous sequence of 145 nt was sufficient for a low level of template activity in the in vitro RdRp assay and a similarly low level of RNA3 accumulation in plants. The presence of an additional sequence of nucleotides 145-165 from the 3' end of RNA3 enhanced template recognition by RdRp in vitro and accumulation of RNA3 in vivo to wild-type levels.

摘要

苜蓿花叶病毒三种基因组RNA的3'非翻译区(UTR)由一个145个核苷酸的3'同源序列和长度为18 - 34个核苷酸的上游独特序列组成。对RNA3的cDNA克隆的3'UTR进行了突变。五个AUGC基序中的点突变干扰了外壳蛋白与3'UTR的特异性结合,但对纯化的病毒RNA依赖性RNA聚合酶(RdRp)体外合成负链RNA时RNA3的模板活性没有影响。缺失分析表明,145个核苷酸的3'同源序列足以在体外RdRp测定中产生低水平的模板活性,并且在植物中RNA3积累水平同样较低。来自RNA3 3'端额外的145 - 165个核苷酸序列的存在增强了RdRp在体外对模板的识别以及RNA3在体内积累至野生型水平。

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