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脊髓灰质炎病毒不同型间重组体交叉区域的一级结构:RNA基因组间重组的模型

The primary structure of crossover regions of intertypic poliovirus recombinants: a model of recombination between RNA genomes.

作者信息

Romanova L I, Blinov V M, Tolskaya E A, Viktorova E G, Kolesnikova M S, Guseva E A, Agol V I

出版信息

Virology. 1986 Nov;155(1):202-13. doi: 10.1016/0042-6822(86)90180-7.

Abstract

The nucleotide sequence of crossover sites in the genome of four intertypic (type 3/type 1) poliovirus recombinants has been determined. The approximate boundaries of the crossover regions were first estimated by RNase T1 oligonucleotide mapping of the recombinant genomes; then appropriate regions were sequenced by the chain termination method using oligonucleotide-primed reverse transcription of the recombinant RNAs. The crossover sites (defined as the contiguous sequences shared by the recombinant and both parental genomes flanked, in the recombinant genome, by heterotypic RNA segments) are 5, 5, 7, and 11 nucleotides long, respectively. The recombination was precise and was not accompanied by any other genetic alterations. The recombination sites were found to be located within genome segments having a potential to form secondary structure elements. Based on this observation, a model of recombination between picornaviral RNA genomes has been proposed. The essence of this model consists in bringing together homologous regions of two recombining RNA genomes via formation of intermolecular duplexes, detachment of the nascent 3' end of the newly synthesized complementary RNA from a "parting" site on the first template and its subsequent "jumping" to the identical (or closely related) "anchoring" site on the other template. Features of this model are discussed in some detail.

摘要

已确定了四种脊髓灰质炎病毒重组体(3型/1型)基因组中交叉位点的核苷酸序列。交叉区域的大致边界首先通过重组基因组的核糖核酸酶T1寡核苷酸图谱进行估计;然后使用重组RNA的寡核苷酸引发的逆转录,通过链终止法对适当区域进行测序。交叉位点(定义为重组体与两个亲本基因组共有的连续序列,在重组基因组中两侧为异型RNA片段)分别长5、5、7和11个核苷酸。重组是精确的,且未伴随任何其他基因改变。发现重组位点位于具有形成二级结构元件潜力的基因组片段内。基于这一观察结果,提出了小核糖核酸病毒RNA基因组之间的重组模型。该模型的本质在于通过形成分子间双链体,将两个重组RNA基因组的同源区域聚集在一起,使新合成的互补RNA的新生3'末端从第一个模板上的“分离”位点脱离,并随后“跳跃”到另一个模板上相同(或密切相关)的“锚定”位点。对该模型的特点进行了较为详细的讨论。

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