Brown Anthony E, Bugeon Laurence, Crisanti Andrea, Catteruccia Flaminia
Department of Biological Sciences, Imperial College London, Imperial College Road, London SW7 2AZ, UK.
Nucleic Acids Res. 2003 Aug 1;31(15):e85. doi: 10.1093/nar/gng085.
Heritable RNA interference (RNAi), triggered from stably expressed transgenes with an inverted repeat (IR) configuration, is an important tool for reverse genetic studies. Here we report on the development of stable RNAi in Anopheles stephensi mosquitoes, the major vector of human malaria in Asia. Trans genic mosquitoes stably expressing a RNAi transgene, designed to produce intron-spliced double-stranded RNA (dsRNA) targeting the green fluorescent protein EGFP gene, were crossed to an EGFP-expressing target line. EGFP expression was dramatically reduced at both the protein and RNA levels. The levels of gene silencing depended upon the RNAi gene copy number and its site of integration. These results demonstrate that specific RNAi-mediated knockdown of gene function can be achieved with high efficiency in Anopheles . This will be invaluable to systematically unravel the function of Anopheles genes determining the vectorial capacity of the malaria parasite.
由具有反向重复(IR)结构的稳定表达转基因引发的可遗传RNA干扰(RNAi),是反向遗传学研究的重要工具。在此,我们报告了在亚洲人类疟疾主要传播媒介斯氏按蚊中稳定RNAi的开发情况。稳定表达RNAi转基因的转基因蚊子,该转基因设计用于产生靶向绿色荧光蛋白EGFP基因的内含子剪接双链RNA(dsRNA),与表达EGFP的靶标品系进行杂交。EGFP的表达在蛋白质和RNA水平上均显著降低。基因沉默水平取决于RNAi基因的拷贝数及其整合位点。这些结果表明,在按蚊中可以高效地实现特定RNAi介导的基因功能敲低。这对于系统地阐明决定疟原虫传播能力的按蚊基因的功能将是非常宝贵的。