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流感病毒3'和5'非翻译区特征分析的快速方法

Rapid method for the characterization of 3' and 5' UTRs of influenza viruses.

作者信息

Szymkowiak Christopher, Kwan Wan-Sang, Su Qin, Toner Timothy J, Shaw Alan R, Youil Rima

机构信息

Department of Virus and Cell Biology, Merck and Co Inc, 44L-206B West Point, PA 19486, USA.

出版信息

J Virol Methods. 2003 Jan;107(1):15-20. doi: 10.1016/s0166-0934(02)00184-2.

Abstract

A T4 RNA ligase based strategy is demonstrated that allows for the full characterization of 3' and 5' UTR regions of negative strand RNA viruses. Negative strand RNA viruses such as influenza have 3'OH and 5'P terminal ends that are capable of being ligated using T4 RNA ligase. Each segment can form a mixture of linear concatamers between like and different viral segments or can itself form a circular structure upon ligation. RT-PCR can then be performed on these circular RNA segments using gene specific primers subsequently allowing for the characterization of the true terminal sequence for each viral segment. The UTR regions of a number of influenza virus strains were defined accurately using this approach.

摘要

本文展示了一种基于T4 RNA连接酶的策略,该策略可对负链RNA病毒的3'和5'非翻译区(UTR)进行全面表征。诸如流感病毒之类的负链RNA病毒具有3'OH和5'P末端,能够使用T4 RNA连接酶进行连接。每个片段可在相同和不同的病毒片段之间形成线性串联体混合物,或者在连接后自身形成环状结构。然后可以使用基因特异性引物对这些环状RNA片段进行逆转录聚合酶链反应(RT-PCR),随后可对每个病毒片段的真实末端序列进行表征。使用这种方法准确地定义了多种流感病毒株的UTR区域。

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