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RNA重排和点突变都有助于修复有缺陷的嵌合病毒基因组,从而在植物中形成功能性杂种病毒。

Both RNA rearrangement and point mutation contribute to repair of defective chimeric viral genomes to form functional hybrid viruses in plants.

作者信息

Reade R, Wu Z, Rochon D

机构信息

Pacific Agri-Food Research Centre, Agriculture and Agri-Food Canada, Summerland, British Columbia, Canada.

出版信息

Virology. 1999 Jun 5;258(2):217-31. doi: 10.1006/viro.1999.9726.

Abstract

The putative movement protein gene (p27) plus 5' and 3' flanking sequences of cucumber leaf spot aureusvirus (CLSV) was inserted into an infectious cucumber necrosis tombusvirus (CNV) cDNA clone containing a deletion in the cell-to-cell movement protein gene. Approximately 5% of plants inoculated with synthetic transcripts of two such defective chimeric CNV/CLSV cDNA clones developed systemic symptoms 7-19 days postinoculation. Reverse transcription-polymerase chain reaction and sequence analysis of virus obtained from systemically infected leaves indicated that both point mutation and RNA rearrangement (deletion) contributed to the formation of movement competent CNV/CLSV hybrid viruses. The hybrid viruses were found to accumulate to high levels in infected plants, to form stable virions, and to be mechanically transmissible. In addition, a hybrid virus that lacked 50 amino acids at the carboxyl-terminal region of CLSV p27 was still capable of facilitating CNV movement. These data provide experimental evidence for the role of CLSV p27 in viral cell-to-cell movement and demonstrate that p27 can enable efficient movement of the CNV genome. Moreover, the data show that RNA rearrangements known to occur during CNV RNA replication can contribute to rapid evolution of the CNV genome.

摘要

将黄瓜叶斑金黄病毒(CLSV)的推定运动蛋白基因(p27)及其5'和3'侧翼序列插入到一个感染性黄瓜坏死番茄病毒(CNV)的cDNA克隆中,该克隆在细胞间运动蛋白基因处有一个缺失。用两个这种有缺陷的嵌合CNV/CLSV cDNA克隆的合成转录本接种的植物中,约5%在接种后7 - 19天出现系统症状。对从系统感染叶片中获得的病毒进行逆转录 - 聚合酶链反应和序列分析表明,点突变和RNA重排(缺失)都促成了具有运动能力的CNV/CLSV杂交病毒的形成。发现杂交病毒在受感染植物中积累到高水平,形成稳定的病毒粒子,并且可以机械传播。此外,一种在CLSV p27羧基末端区域缺少50个氨基酸的杂交病毒仍然能够促进CNV的运动。这些数据为CLSV p27在病毒细胞间运动中的作用提供了实验证据,并证明p27能够使CNV基因组有效运动。此外,数据表明已知在CNV RNA复制过程中发生的RNA重排可促成CNV基因组的快速进化。

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