Bucher Etienne, Lohuis Dick, van Poppel Pieter M J A, Geerts-Dimitriadou Christina, Goldbach Rob, Prins Marcel
Laboratory of Virology, Wageningen University, Binnenhaven 11, 6709 PD Wageningen, The Netherlands.
J Gen Virol. 2006 Dec;87(Pt 12):3697-3701. doi: 10.1099/vir.0.82276-0.
RNA silencing is a natural antiviral defence in plants, which can be exploited in transgenic plants for preprogramming virus recognition and ensuring enhanced resistance. By arranging viral transgenes as inverted repeats it is thus possible to obtain strong repression of incoming viruses. Due to the high sequence specificity of RNA silencing, this technology has hitherto been limited to the targeting of single viruses. Here it is shown that efficient simultaneous targeting of four different tospoviruses can be achieved by using a single small transgene based on the production of minimal sized chimaeric cassettes. Due to simultaneous RNA silencing, as demonstrated by specific siRNA accumulation, the transgenic expression of these cassettes rendered up to 82 % of the transformed plant lines heritably resistant against all four viruses. Thus RNA silencing can be further improved for high frequency multiple virus resistance by combining small RNA fragments from a series of target viruses.
RNA沉默是植物中的一种天然抗病毒防御机制,可用于转基因植物中,预先设定病毒识别程序并增强抗性。通过将病毒转基因排列成反向重复序列,从而有可能强烈抑制入侵病毒。由于RNA沉默具有高度的序列特异性,该技术迄今仅限于针对单一病毒。本文表明,通过使用基于产生最小尺寸嵌合盒的单个小转基因,可以实现对四种不同番茄斑萎病毒的有效同时靶向。如特异性siRNA积累所证明的,由于同时发生RNA沉默,这些盒的转基因表达使高达82%的转化植株系对所有四种病毒具有遗传性抗性。因此,通过组合来自一系列靶病毒的小RNA片段,RNA沉默可进一步改进以实现高频多重病毒抗性。