Premature polyadenylation contributes to the poor expression of the Bacillus thuringiensis cry3Ca1 gene in transgenic potato plants.

Y Z Haffani, S Overney, S Yelle, G Bellemare, F J Belzile
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引用次数: 27

Abstract

The cry genes that code for the insecticidal crystal proteins of Bacillus thuringiensis (B.t.) have been widely used to develop insect-resistant transgenic plants. The cry3Ca1 gene has been reported to code for a crystal protein which is particularly potent against the Colorado potato beetle (CPB). To explore the biotechnological potential of cry3Ca1, we introduced this gene into transgenic potato plants under the control of the CaMV 35S promoter. In the resulting transformants, the cry3-Ca1 gene was very poorly expressed. In fact, no full-length transcript (2300 nt) could be detected. Instead, only short transcripts of approximately 1100 nt were observed. Analysis of these short transcripts by Northern hybridization, RT-PCR as well as by cloning and sequencing showed that they resulted from premature polyadenylation. These processing events occurred at four sites within the cry3Ca1 coding region (at positions 652, 669, 914 and 981 relative to the translation start site). The sites at which premature polyadenylation took place were not those that showed the highest degree of identity to the canonical AAUAAA motif. Together with other recent data, our findings suggest that premature polyadenylation is an important mechanism which can contribute to the poor expression of transgenes in a foreign host.

过早聚腺苷化导致苏云金芽孢杆菌cry3Ca1基因在转基因马铃薯植株中的表达较差。
苏云金芽孢杆菌(Bacillus thuringiensis, B.t.)杀虫晶体蛋白的编码基因已被广泛用于开发抗虫转基因植物。据报道,cry3Ca1基因编码了一种晶体蛋白,该蛋白对科罗拉多马铃薯甲虫(CPB)特别有效。为了探索cry3Ca1的生物技术潜力,我们在CaMV 35S启动子的控制下,将该基因导入转基因马铃薯植株。在由此产生的转化子中,cry3-Ca1基因表达非常低。事实上,没有检测到全长转录本(2300 nt)。相反,只观察到大约1100 nt的短转录本。对这些短转录本进行Northern杂交、RT-PCR以及克隆和测序分析表明,它们是由过早聚腺苷酸化引起的。这些处理事件发生在cry3Ca1编码区的四个位点上(相对于翻译起始位点,在位置652、669、914和981)。早聚腺苷化发生的位点并不是那些与标准AAUAAA基序具有最高一致性的位点。结合其他最近的数据,我们的研究结果表明,过早的聚腺苷酸化是导致转基因在外源宿主中表达不良的一个重要机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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