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新城疫病毒意大利株小基因救系统的构建。

Construction of a minigenome rescue system for Newcastle disease virus strain Italien.

机构信息

Cell Engineering Research Centre and Department of Cell Biology, State Key Laboratory of Cancer Biology, Fourth Military Medical University, No.17 Changle West Road, Xi'an, China.

出版信息

Arch Virol. 2011 Apr;156(4):611-6. doi: 10.1007/s00705-010-0898-3. Epub 2011 Jan 5.

Abstract

Newcastle disease virus (NDV) Italien, a velogenic strain, is an oncolytic virus that is considered to be a potential agent for antitumor viral therapy. We constructed three helper plasmids expressing the NP, P and L genes of NDV Italien based on the eukaryotic expression plasmid pcDNA3.1(+). The minigenome consisting of the 3' leader and 5' trailer regions of NDV Italien flanking a reporter gene encoding firefly luciferase was constructed to examine the efficacy of the three helper plasmids in viral genome replication and transcription. After co-transfection of BSR-T7/5 cells with the three helper plasmids and the minigenome plasmid, replication of minigenome RNA was evaluated by determining luciferase activity. In the minigenome rescue system, expression of the reporter gene was detected. Our results indicate that the three proteins NP, P, and L are correctly expressed and can assemble into a functional ribonucleoprotein complex that effectively directs the transcription of minigenome RNA.

摘要

新城疫病毒(NDV)意大利毒株,是一种强毒力毒株,被认为是抗肿瘤病毒治疗的潜在药物。我们基于真核表达质粒 pcDNA3.1(+)构建了三个表达 NDV 意大利 NP、P 和 L 基因的辅助质粒。该小基因组由 NDV 意大利的 3' 启动子和 5' 尾部区域侧翼的报告基因编码萤火虫荧光素酶组成,用于检测三个辅助质粒在病毒基因组复制和转录中的功效。在 BSR-T7/5 细胞中转染三个辅助质粒和小基因组质粒后,通过测定荧光素酶活性来评估小基因组 RNA 的复制。在小基因组拯救系统中,检测到报告基因的表达。我们的结果表明,NP、P 和 L 三种蛋白正确表达,并能组装成功能性核糖核蛋白复合物,有效地指导小基因组 RNA 的转录。

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