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芜菁黄花叶病毒RNA依赖的RNA聚合酶:体外负链合成的起始

Turnip yellow mosaic virus RNA-dependent RNA polymerase: initiation of minus strand synthesis in vitro.

作者信息

Singh R N, Dreher T W

机构信息

Department of Agricultural Chemistry, Oregon State University, Corvallis 97331-7301, USA.

出版信息

Virology. 1997 Jul 7;233(2):430-9. doi: 10.1006/viro.1997.8621.

Abstract

An RNA-dependent RNA polymerase (RdRp) activity was detergent-solubilized from the chloroplast membranes of Chinese cabbage leaves infected with turnip yellow mosaic virus (TYMV). The template-dependent, micrococcal nuclease-treated activity synthesized full-length minus strands from TYMV RNA and 3'-fragments as short as a 28-nucleotide-long RNA comprising the amino acid acceptor stem of the 3'-tRNA-like structure (TLS). Minus strands were shown to arise by de novo initiation with the insertion of GTP opposite the penultimate (C) residue of the 3'-terminal -CCA. The TYMV RdRp activity was template specific in that poly(A) RNA was not copied, and alfalfa mosaic virus (AIMV) RNA, which does not contain a 3'-TLS, was a very poor template. However, other viral RNAs with a 3'-TLS and in vitro transcripts of tRNAs were copied to varying degrees. Fully modified tRNAs were either inactive or poorly active templates, and AIMV 3'-RNA, even when provided with a 3'-terminal -ACCA, was not copied detectably. A potential role of the acceptor stem pseudoknot as a promoter element was assessed with mutations that drastically altered the structure and sequence of the pseudoknot, revealing only a twofold effect in decreasing template activity. The data show that RNAs with both a tRNA-like conformation and a -CCA 3'-terminus are potential templates for TYMV RdRp and suggest that promoter elements are not limited to the acceptor stem pseudoknot.

摘要

从感染芜菁黄花叶病毒(TYMV)的大白菜叶片叶绿体膜中,通过去污剂增溶获得了一种依赖RNA的RNA聚合酶(RdRp)活性。经微球菌核酸酶处理后的模板依赖性活性,能从TYMV RNA合成全长负链以及短至28个核苷酸长的3'-片段,该3'-片段包含3'-类tRNA结构(TLS)的氨基酸接受茎。负链是通过从头起始产生的,在3'-末端-CCA的倒数第二个(C)残基相对位置插入GTP。TYMV RdRp活性具有模板特异性,即不复制聚(A)RNA,且不含3'-TLS的苜蓿花叶病毒(AIMV)RNA是非常差的模板。然而,其他具有3'-TLS的病毒RNA和tRNA的体外转录本在不同程度上被复制。完全修饰的tRNA要么是无活性的模板,要么是活性很差的模板,并且即使为AIMV 3'-RNA提供3'-末端-ACCA,也未检测到其被复制。通过对显著改变假结结构和序列的突变进行评估,探讨了接受茎假结作为启动子元件的潜在作用,结果显示其对降低模板活性仅有两倍的影响。数据表明,具有类tRNA构象和-CCA 3'-末端的RNA是TYMV RdRp的潜在模板,并表明启动子元件不限于接受茎假结。

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