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雀麦花叶病毒中同源RNA重组的高效系统:序列、结构要求及交叉准确性

Efficient system of homologous RNA recombination in brome mosaic virus: sequence and structure requirements and accuracy of crossovers.

作者信息

Nagy P D, Bujarski J J

机构信息

Plant Molecular Biology Center, Northern Illinois University, De Kalb 60115.

出版信息

J Virol. 1995 Jan;69(1):131-40. doi: 10.1128/JVI.69.1.131-140.1995.

Abstract

Brome mosaic virus (BMV), a tripartite positive-stranded RNA virus of plants engineered to support intersegment RNA recombination, was used for the determination of sequence and structural requirements of homologous crossovers. A 60-nucleotide (nt) sequence, common between wild-type RNA2 and mutant RNA3, supported efficient repair (90%) of a modified 3' noncoding region in the RNA3 segment by homologous recombination with wild-type RNA2 3' noncoding sequences. Deletions within this sequence in RNA3 demonstrated that a nucleotide identity as short as 15 nt can support efficient homologous recombination events, while shorter (5-nt) sequence identity resulted in reduced recombination frequency (5%) within this region. Three or more mismatches within a downstream portion of the common 60-nt RNA3 sequence affected both the incidence of recombination and the distribution of crossover sites, suggesting that besides the length, the extent of sequence identity between two recombining BMV RNAs is an important factor in homologous recombination. Site-directed mutagenesis of the common sequence in RNA3 did not reveal a clear correlation between the stability of predicted secondary structures and recombination activity. This indicates that homologous recombination does not require similar secondary structures between two recombining RNAs at the sites of crossovers. Nearly 20% of homologous recombinants were imprecise (aberrant), containing either nucleotide mismatches, small deletions, or small insertions within the region of crossovers. This implies that homologous RNA recombination is not as accurate as proposed previously. Our results provide experimental evidence that the requirements and thus the mechanism of homologous recombination in BMV differ from those of previously described heteroduplex-mediated nonhomologous recombination (P. D. Nagy and J. J. Bujarski, Proc. Natl. Acad. Sci. USA 90:6390-6394, 1993).

摘要

雀麦花叶病毒(BMV)是一种经过改造以支持片段间RNA重组的植物三分体正链RNA病毒,用于确定同源交叉的序列和结构要求。野生型RNA2和突变型RNA3之间共有的一段60个核苷酸(nt)的序列,通过与野生型RNA2 3'非编码序列的同源重组,支持了RNA3片段中一个修饰的3'非编码区的高效修复(90%)。RNA3中该序列内的缺失表明,短至15 nt的核苷酸同一性就能支持高效的同源重组事件,而较短(5 nt)的序列同一性会导致该区域内重组频率降低(5%)。共同的60 nt RNA3序列下游部分的三个或更多错配会影响重组发生率和交叉位点分布,这表明除了长度之外,两个重组BMV RNA之间的序列同一性程度也是同源重组的一个重要因素。对RNA3中共同序列进行定点诱变并未揭示预测二级结构稳定性与重组活性之间的明显相关性。这表明同源重组在交叉位点处不需要两个重组RNA之间具有相似的二级结构。近20%的同源重组体是不精确的(异常的),在交叉区域内包含核苷酸错配、小缺失或小插入。这意味着同源RNA重组并不像之前所提出的那样精确。我们的结果提供了实验证据,表明BMV中同源重组的要求及机制与先前描述的异源双链介导的非同源重组(P. D. Nagy和J. J. Bujarski,《美国国家科学院院刊》90:6390 - 6394,1993)不同。

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