首页> 美国卫生研究院文献>The EMBO Journal >Ribosomal frameshifting in plants: a novel signal directs the -1 frameshift in the synthesis of the putative viral replicase of potato leafroll luteovirus.
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Ribosomal frameshifting in plants: a novel signal directs the -1 frameshift in the synthesis of the putative viral replicase of potato leafroll luteovirus.

机译:植物中的核糖体移码:一种新型信号指导马铃薯卷叶黄体病毒的假定病毒复制酶合成中的-1移码。

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摘要

The 5.8 kb RNA genome of potato leafroll luteovirus (PLRV) contains two overlapping open reading frames, ORF2a and ORF2b, which are characterized by helicase and RNA polymerase motifs, respectively, and possibly represent the viral replicase. Within the overlap, ORF2b lacks an AUG translational start codon and is therefore presumably translated by -1 ribosomal frameshifting as a transframe protein with ORF2a. This hypothesis was studied by introducing the putative frameshift region into an internal position of the beta-glucuronidase (GUS) gene and testing for the occurrence of frameshifting in vivo by transient expression of GUS activity in potato protoplasts as well as in vitro by translation in the reticulocyte system. Both experimental approaches demonstrate that a -1 frameshift occurs at a frequency of approximately 1%. Site-directed mutagenesis identified the frameshift region and the involvement of the novel heptanucleotide motif UUUAAAU in conjunction with an adjacent stem-loop structure. Part of this stem-loop encodes a basic region in the ORF2b moiety of the transframe protein which was shown by binding experiments with PLRV RNA to represent a nucleic acid-binding domain. These data support a possible biological significance of the frameshift to occur at this position of the large overlap by including the putative RNA template-binding site of the PLRV replicase in the ORF2a/ORF2b transframe protein.
机译:马铃薯卷叶黄体病毒(PLRV)的5.8 kb RNA基因组包含两个重叠的开放阅读框ORF2a和ORF2b,分别以解旋酶和RNA聚合酶为特征,并可能代表病毒复制酶。在重叠内,ORF2b缺少AUG翻译起始密码子,因此可能被-1核糖体移码翻译为ORF2a的超帧蛋白。通过将假定的移码区引入β-葡萄糖醛酸苷酶(GUS)基因的内部位置并通过马铃薯原生质体中GUS活性的瞬时表达以及通过体外翻译在马铃薯中体外测试GUS活性来测试体内移码的发生,从而研究了这一假设。网织红细胞系统。两种实验方法都表明-1移码的发生频率约为1%。定点诱变确定了移码区域和新型七核苷酸基序UUUAAAU与相邻茎环结构的结合。该茎环的一部分编码跨框架蛋白的ORF2b部分中的基本区域,通过与PLRV RNA的结合实验显示了该区域,以代表核酸结合结构域。这些数据通过在ORF2a / ORF2b跨框架蛋白中包含PLRV复制酶的推定RNA模板结合位点,支持在大重叠的此位置发生移码的可能的生物学意义。

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