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体外参与苜蓿花叶病毒RNA复制的顺式作用元件。

cis-acting elements involved in replication of alfalfa mosaic virus RNAs in vitro.

作者信息

van der Kuyl A C, Langereis K, Houwing C J, Jaspars E M, Bol J F

机构信息

Department of Biochemistry, Leiden University, The Netherlands.

出版信息

Virology. 1990 Jun;176(2):346-54. doi: 10.1016/0042-6822(90)90004-b.

Abstract

A DNA copy of alfalfa mosaic virus (AIMV) RNA3 was transcribed in vitro in two different orientations with T7 RNA polymerase and the transcripts were used as templates for a virus-specific RNA-dependent RNA polymerase (RdRp) purified from AIMV-infected bean plants. Minus-stranded templates were transcribed by the RdRp into subgenomic plus-stranded RNA4. A deletion analysis showed that a sequence in minus-strand RNA3, located between nucleotides -8 and -55 upstream of the initiation site for RNA4 synthesis, was sufficient for subgenomic promoter activity in vitro. Plus-stranded templates were transcribed by the RdRp into full-length minus-stranded copies. A deletion analysis indicated that a sequence located between nucleotides 133 and 163 from the 3'-end of AIMV RNA3 was sufficient to direct the synthesis of minus-stranded products by the RdRp. Thus, the 3'-terminal region of the AIMV RNAs, which contains the binding sites with a high affinity for coat protein, appears not to be involved in recognition of the RNAs by the RdRp in vitro.

摘要

用T7 RNA聚合酶以两种不同方向在体外转录苜蓿花叶病毒(AIMV)RNA3的DNA拷贝,转录本用作从感染AIMV的菜豆植株中纯化的病毒特异性RNA依赖性RNA聚合酶(RdRp)的模板。负链模板被RdRp转录成亚基因组正链RNA4。缺失分析表明,负链RNA3中位于RNA4合成起始位点上游核苷酸-8至-55之间的序列,足以在体外发挥亚基因组启动子活性。正链模板被RdRp转录成全长负链拷贝。缺失分析表明,位于AIMV RNA3 3'-末端核苷酸133至163之间的序列足以指导RdRp合成负链产物。因此,AIMV RNA的3'-末端区域含有与衣壳蛋白具有高亲和力的结合位点,在体外似乎不参与RdRp对RNA的识别。

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