Johnson B W, Olson K E, Allen-Miura T, Rayms-Keller A, Carlson J O, Coates C J, Jasinskiene N, James A A, Beaty B J, Higgs S
Arthropod-Borne and Infectious Diseases Laboratory (AIDL), Department of Microbiology, Colorado State University, Fort Collins, CO 80523, USA.
Proc Natl Acad Sci U S A. 1999 Nov 9;96(23):13399-403. doi: 10.1073/pnas.96.23.13399.
A rapid and reproducible method of inhibiting the expression of specific genes in mosquitoes should further our understanding of gene function and may lead to the identification of mosquito genes that determine vector competence or are involved in pathogen transmission. We hypothesized that the virus expression system based on the mosquito-borne Alphavirus, Sindbis (Togaviridae), may efficiently transcribe effector RNAs that inhibit expression of a targeted mosquito gene. To test this hypothesis, germ-line-transformed Aedes aegypti that express luciferase (LUC) from the mosquito Apyrase promoter were intrathoracically inoculated with a double subgenomic Sindbis (dsSIN) virus TE/3'2J/anti-luc (Anti-luc) that transcribes RNA complementary to the 5' end of the LUC mRNA. LUC activity was monitored in mosquitoes infected with either Anti-luc or control dsSIN viruses expressing unrelated antisense RNAs. Mosquitoes infected with Anti-luc virus exhibited 90% reduction in LUC compared with uninfected and control dsSIN-infected mosquitoes at 5 and 9 days postinoculation. We demonstrate that a gene expressed from the mosquito genome can be inhibited by using an antisense strategy. The dsSIN antisense RNA expression system is an important tool for studying gene function in vivo.
一种快速且可重复的抑制蚊子体内特定基因表达的方法,应能增进我们对基因功能的理解,并可能有助于鉴定决定蚊子传播能力或参与病原体传播的蚊子基因。我们推测,基于蚊媒α病毒辛德毕斯病毒(披膜病毒科)的病毒表达系统,可能会高效转录抑制目标蚊子基因表达的效应RNA。为了验证这一假设,将从蚊子ATP双磷酸酶启动子表达荧光素酶(LUC)的种系转化埃及伊蚊经胸腔接种双亚基因组辛德毕斯病毒(dsSIN)TE/3'2J/抗luc(Anti-luc),该病毒转录与LUC mRNA 5'端互补的RNA。在感染了Anti-luc或表达无关反义RNA的对照dsSIN病毒的蚊子中监测LUC活性。与未感染和感染对照dsSIN病毒的蚊子相比,感染Anti-luc病毒的蚊子在接种后5天和9天时LUC活性降低了90%。我们证明,使用反义策略可以抑制从蚊子基因组表达的基因。dsSIN反义RNA表达系统是研究体内基因功能的重要工具。