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由虾白斑综合征病毒(WSSV)的内部核糖体进入位点(IRES)介导的昆虫细胞中mRNA翻译的内部起始。

Internal initiation of mRNA translation in insect cell mediated by an internal ribosome entry site (IRES) from shrimp white spot syndrome virus (WSSV).

作者信息

Han Fang, Zhang Xiaobo

机构信息

Key Laboratory of Marine Biogenetic Resources, Third Institute of Oceanography, State Oceanic Administration Xiamen 361005, PR China.

出版信息

Biochem Biophys Res Commun. 2006 Jun 9;344(3):893-9. doi: 10.1016/j.bbrc.2006.03.229. Epub 2006 Apr 19.

Abstract

Internal initiation of mRNA translation can be mediated by internal ribosome entry site (IRES) elements which are located mainly in RNA viruses as well as certain mammalian and insect mRNA molecules. Thus far, only one DNA virus has been discovered to contain IRES element. In this investigation, an IRES element from white spot syndrome virus (WSSV), a DNA virus of marine shrimp, was demonstrated to direct the efficient translation of dicistronic mRNA in Trichoplusia ni insect cells. The IRES was inserted between glutathione S-transferase (GST) and green fluorescent protein (GFP) genes to construct a dicistronic cassette (GST-IRES-GFP). After transfection of this dicistronic cassette in insect cell, the Northern blot indicated that only one transcript corresponding to the mRNA of GST-IRES-GFP could be detected. However, the GST and GFP genes were simultaneously translated as revealed by Western blot and fluorescent microscopy, respectively. Based on sequence orientation and deletion analyses, the IRES element was 180 nucleotides (nt) in length and orientation-dependent. By comparison with that of cap-dependent initiation, the translation efficiency mediated by IRES was 98.77%. This finding promises that the WSSV IRES could be very useful to co-express two or more proteins due to its shorter length and higher translation efficiency.

摘要

mRNA翻译的内部起始可由内部核糖体进入位点(IRES)元件介导,这些元件主要存在于RNA病毒以及某些哺乳动物和昆虫的mRNA分子中。到目前为止,仅发现一种DNA病毒含有IRES元件。在本研究中,来自海洋虾的DNA病毒白斑综合征病毒(WSSV)的IRES元件被证明可在粉纹夜蛾昆虫细胞中指导双顺反子mRNA的有效翻译。将该IRES插入谷胱甘肽S-转移酶(GST)和绿色荧光蛋白(GFP)基因之间,构建双顺反子盒(GST-IRES-GFP)。将此双顺反子盒转染到昆虫细胞后,Northern印迹表明只能检测到一个与GST-IRES-GFP的mRNA相对应的转录本。然而,分别通过Western印迹和荧光显微镜观察发现,GST和GFP基因同时被翻译。基于序列方向和缺失分析,IRES元件长度为180个核苷酸(nt),且具有方向依赖性。与帽依赖性起始相比,IRES介导的翻译效率为98.77%。这一发现表明,由于WSSV IRES长度较短且翻译效率较高,它可能对共表达两种或更多种蛋白质非常有用。

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