Yamasaki Shotaro, Sanada Yuji, Imase Ryoji, Matsuura Hideyuki, Ueno Daishin, Demura Taku, Kato Ko
Graduate School of Biological Science, Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara 630-0192, Japan.
Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan.
J Biosci Bioeng. 2018 Jan;125(1):124-130. doi: 10.1016/j.jbiosc.2017.08.007. Epub 2017 Sep 11.
Transgene expression is regulated through several steps, this study focuses on the mRNA translation step. The expression level of transgenes can be increased by 5'-untranslated region (5'UTR) sequences in certain genes which act as translational enhancers. On the other hand, translation in most mRNA species is repressed by growth, development, and stress events. There is a possibility that transgene mRNA is also repressed in these conditions, despite the use of a translational enhancer. Therefore, a consistently efficient translational enhancer is needed to develop a reliable transgene expression system. Herein we searched for mRNAs translated stably under different growth, development and environmental conditions using data sets of polysome fraction assays and microarray analysis. Correct 5'UTR sequences of candidate genes were determined by cap analysis of gene expression and we tested translational ability of the candidate 5'UTRs by reporter assays. We found the 5'UTR of cold-regulated 47 gene to be an effective translational enhancer, contributing to stable high-level expression under various conditions.
转基因表达受多个步骤调控,本研究聚焦于mRNA翻译步骤。某些基因中的5'非翻译区(5'UTR)序列作为翻译增强子,可提高转基因的表达水平。另一方面,大多数mRNA种类的翻译会受到生长、发育和应激事件的抑制。尽管使用了翻译增强子,但在这些条件下转基因mRNA仍有可能受到抑制。因此,需要一种始终有效的翻译增强子来开发可靠的转基因表达系统。在此,我们利用多核糖体组分分析数据集和微阵列分析,寻找在不同生长、发育和环境条件下稳定翻译的mRNA。通过基因表达的帽分析确定候选基因的正确5'UTR序列,并通过报告基因测定法测试候选5'UTR的翻译能力。我们发现冷调节47基因的5'UTR是一种有效的翻译增强子,有助于在各种条件下实现稳定的高水平表达。