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In Vitro Synthesized RNA Generated from cDNA Clones of Both Genomic Components of Cucurbit yellow stunting disorder virus Replicates in Cucumber Protoplasts

机译:黄瓜黄色发育障碍病毒两个基因组成分的cDNA克隆的体外合成RNA在黄瓜原生质体中复制

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摘要

(CYSDV), a bipartite whitefly-transmitted virus, constitutes a major threat to commercial cucurbit production worldwide. Here, construction of full-length CYSDV RNA1 and RNA2 cDNA clones allowed the synthesis of RNA transcripts able to replicate in cucumber protoplasts. CYSDV RNA1 proved competent for replication; transcription of both polarities of the genomic RNA was detectable 24 h post inoculation. Hybridization of total RNA extracted from transfected protoplasts or from naturally CYSDV-infected cucurbits revealed high-level transcription of the p22 subgenomic RNA species. Replication of CYSDV RNA2 following co-transfection with RNA1 was also observed, with similar transcription kinetics. A CYSDV RNA2 cDNA clone (T3CM8Δ) comprising the 5′- and 3′-UTRs plus the 3′-terminal gene, generated a 2.8 kb RNA able to replicate to high levels in protoplasts in the presence of CYSDV RNA1. The clone T3CM8Δ will facilitate reverse genetics studies of CYSDV gene function and RNA replication determinants.
机译:(CYSDV)是由两部分粉虱传播的病毒,对全球商业葫芦的生产构成了重大威胁。在这里,全长CYSDV RNA1和RNA2 cDNA克隆的构建允许合成能够在黄瓜原生质体中复制的RNA转录本。 CYSDV RNA1被证明具有复制能力;接种后24小时可检测到基因组RNA的两个极性的转录。从转染的原生质体或从自然CYSDV感染的葫芦丝中提取的总RNA的杂交揭示了p22亚基因组RNA种类的高水平转录。在与RNA1共转染后也观察到CYSDV RNA2的复制,具有相似的转录动力学。包含5'-和3'-UTR加上3'-末端基因的CYSDV RNA2 cDNA克隆(T3CM8Δ)产生了一个2.8 kb RNA,能够在CYSDV RNA1存在下在原生质体中复制到高水平。克隆T3CM8Δ将促进CYSDV基因功能和RNA复制决定簇的反向遗传学研究。

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