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利用工程化的核糖开关控制基于甲病毒的基因表达。

Control of alphavirus-based gene expression using engineered riboswitches.

机构信息

Novartis Vaccines, Inc., Cambridge, MA, USA.

Novartis Vaccines, Inc., Cambridge, MA, USA.

出版信息

Virology. 2015 Sep;483:302-11. doi: 10.1016/j.virol.2015.04.023. Epub 2015 May 23.

Abstract

Alphavirus-based replicons are a promising nucleic acid vaccine platform characterized by robust gene expression and immune responses. To further explore their use in vaccination, replicons were engineered to allow conditional control over their gene expression. Riboswitches, comprising a ribozyme actuator and RNA aptamer sensor, were engineered into the replicon 3' UTR. Binding of ligand to aptamer modulates ribozyme activity and, therefore, gene expression. Expression from DNA-launched and VRP-packaged replicons containing riboswitches was successfully regulated, achieving a 47-fold change in expression and modulation of the resulting type I interferon response. Moreover, we developed a novel control architecture where riboswitches were integrated into the 3' and 5' UTR of the subgenomic RNA region of the TC-83 virus, leading to an 1160-fold regulation of viral replication. Our studies demonstrate that the use of riboswitches for control of RNA replicon expression and viral replication holds promise for development of novel and safer vaccination strategies.

摘要

基于甲病毒的复制子是一种有前途的核酸疫苗平台,其特点是具有强大的基因表达和免疫反应。为了进一步探索其在疫苗接种中的应用,研究人员对复制子进行了工程改造,以便对其基因表达进行条件控制。核糖开关由核酶执行器和 RNA 适体传感器组成,被工程化到复制子的 3'UTR 中。配体与适体的结合调节核酶活性,从而调节基因表达。含有核糖开关的 DNA 启动子和 VRP 包装的复制子的表达得到了成功调控,实现了表达水平 47 倍的变化,并调节了产生的 I 型干扰素反应。此外,我们开发了一种新的控制架构,其中核糖开关被整合到 TC-83 病毒的亚基因组 RNA 区域的 3'和 5'UTR 中,导致病毒复制的调节倍数达到 1160 倍。我们的研究表明,使用核糖开关来控制 RNA 复制子的表达和病毒复制具有开发新型和更安全的疫苗接种策略的潜力。

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