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[马铃薯X病毒外壳蛋白表达水平与摆动密码子密码子使用之间的相关性]

[Relativity betweeen expression level of potato virus X coat protein and the codon usage of wobble codon].

作者信息

Feng Dejiang, Cai Huaya, Liu Xiang, Xu Junwang, Zhu Zhen

机构信息

Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.

出版信息

Wei Sheng Wu Xue Bao. 2003 Oct;43(5):569-76.

Abstract

The relationship between the quantities of rare codons and the expression levels of foreign genes is very important in gene engineering. But up to now, there is few experiment on it in multi-cellular eukaryotes, especially in plants. To study the effect of rare codons on the expression level of potato virus X (PVX) coat protein (CP) in transgenic tobacco, some preferred codons in PVX coat protein gene were substituted with synonymous rare codons without changing the encoded amino acid sequence using site-specific mutation. The modified coat protein gene (cpm) and non-modified coat protein gene (cpw) were inserted into binary vector under the control of CaMV35S promoter, and these two plant expression constructs were transferred into tobacco (Nicotiana tabacum cv. Xanthi) genomes via Agrobacterium mediated method and transgenic plants were generated. Western blot and ELISA of these transgenic tobaccos showed that the expression level of modified CP is about one third to one sixth of that of non-modified CP. Northern blot analysis of RNAs from some transformants indicated that the transcriptional levels of cpm are the same as that of cpw, which implicated that the quantity of rare codons in foreign gene was a possible limited factor in foreign gene expression process. Changing the quantity of rare codons maybe an effective method for organism to control gene expression.

摘要

在基因工程中,稀有密码子数量与外源基因表达水平之间的关系非常重要。但截至目前,在多细胞真核生物中,尤其是在植物中,针对这方面的实验较少。为了研究稀有密码子对转基因烟草中马铃薯X病毒(PVX)外壳蛋白(CP)表达水平的影响,利用定点突变技术,在不改变编码氨基酸序列的情况下,将PVX外壳蛋白基因中的一些偏爱密码子替换为同义稀有密码子。将修饰后的外壳蛋白基因(cpm)和未修饰的外壳蛋白基因(cpw)插入到CaMV35S启动子控制下的双元载体中,通过农杆菌介导法将这两种植物表达构建体转入烟草(Nicotiana tabacum cv. Xanthi)基因组中,获得了转基因植株。对这些转基因烟草进行的Western印迹和ELISA分析表明,修饰后CP的表达水平约为未修饰CP的三分之一至六分之一。对一些转化体的RNA进行Northern印迹分析表明,cpm的转录水平与cpw相同,这意味着外源基因中稀有密码子的数量可能是外源基因表达过程中的一个限制因素。改变稀有密码子的数量可能是生物体控制基因表达的一种有效方法。

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