Biedler James K, Qi Yumin, Pledger David, Macias Vanessa M, James Anthony A, Tu Zhijian
Department of Biochemistry and Fralin Life Science Institute, Virginia Tech, Blacksburg, Virginia 24061
Department of Biochemistry and Fralin Life Science Institute, Virginia Tech, Blacksburg, Virginia 24061.
G3 (Bethesda). 2014 Dec 5;5(2):157-66. doi: 10.1534/g3.114.015578.
Anopheles stephensi is a principal vector of urban malaria on the Indian subcontinent and an emerging model for molecular and genetic studies of mosquito biology. To enhance our understanding of female mosquito reproduction, and to develop new tools for basic research and for genetic strategies to control mosquito-borne infectious diseases, we identified 79 genes that displayed previtellogenic germline-specific expression based on RNA-Seq data generated from 11 life stage-specific and sex-specific samples. Analysis of this gene set provided insights into the biology and evolution of female reproduction. Promoters from two of these candidates, vitellogenin receptor and nanos, were used in independent transgenic cassettes for the expression of artificial microRNAs against suspected mosquito maternal-effect genes, discontinuous actin hexagon and myd88. We show these promoters have early germline-specific expression and demonstrate 73% and 42% knockdown of myd88 and discontinuous actin hexagon mRNA in ovaries 48 hr after blood meal, respectively. Additionally, we demonstrate maternal-specific delivery of mRNA and protein to progeny embryos. We discuss the application of this system of maternal delivery of mRNA/miRNA/protein in research on mosquito reproduction and embryonic development, and for the development of a gene drive system based on maternal-effect dominant embryonic arrest.
斯氏按蚊是印度次大陆城市疟疾的主要传播媒介,也是蚊虫生物学分子和遗传研究的新兴模式生物。为了增进我们对雌蚊繁殖的理解,并开发用于基础研究以及控制蚊媒传染病的遗传策略的新工具,我们基于从11个特定生命阶段和性别的样本中生成的RNA测序数据,鉴定出79个显示卵黄发生前生殖系特异性表达的基因。对这个基因集的分析为雌蚊繁殖的生物学和进化提供了见解。其中两个候选基因——卵黄原蛋白受体和纳米蛋白的启动子,被用于独立的转基因盒中,以表达针对疑似蚊母体效应基因——间断肌动蛋白六边形和髓样分化因子88的人工微小RNA。我们表明这些启动子具有早期生殖系特异性表达,并分别在吸血后48小时的卵巢中显示出髓样分化因子88和间断肌动蛋白六边形mRNA分别有73%和42%的敲低。此外,我们证明了mRNA和蛋白质向子代胚胎的母体特异性传递。我们讨论了这种母体传递mRNA/miRNA/蛋白质系统在蚊虫繁殖和胚胎发育研究中的应用,以及基于母体效应显性胚胎停滞的基因驱动系统的开发。