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RNA干扰触发物导入冈比亚按蚊蛹体

RNAi Trigger Delivery into Anopheles gambiae Pupae.

作者信息

Regna Kimberly, Harrison Rachel M, Heyse Shannon A, Chiles Thomas C, Michel Kristin, Muskavitch Marc A T

机构信息

Biology Department, Boston College.

Division of Biology, Kansas State University.

出版信息

J Vis Exp. 2016 Mar 8(109):53738. doi: 10.3791/53738.

Abstract

RNA interference (RNAi), a naturally occurring phenomenon in eukaryotic organisms, is an extremely valuable tool that can be utilized in the laboratory for functional genomic studies. The ability to knockdown individual genes selectively via this reverse genetic technique has allowed many researchers to rapidly uncover the biological roles of numerous genes within many organisms, by evaluation of loss-of-function phenotypes. In the major human malaria vector Anopheles gambiae, the predominant method used to reduce the function of targeted genes involves injection of double-stranded (dsRNA) into the hemocoel of the adult mosquito. While this method has been successful, gene knockdown in adults excludes the functional assessment of genes that are expressed and potentially play roles during pre-adult stages, as well as genes that are expressed in limited numbers of cells in adult mosquitoes. We describe a method for the injection of Serine Protease Inhibitor 2 (SRPN2) dsRNA during the early pupal stage and validate SRPN2 protein knockdown by observing decreased target protein levels and the formation of melanotic pseudo-tumors in SRPN2 knockdown adult mosquitoes. This evident phenotype has been described previously for adult stage knockdown of SRPN2 function, and we have recapitulated this adult phenotype by SRPN2 knockdown initiated during pupal development. When used in conjunction with a dye-labeled dsRNA solution, this technique enables easy visualization by simple light microscopy of injection quality and distribution of dsRNA in the hemocoel.

摘要

RNA干扰(RNAi)是真核生物中自然发生的一种现象,是一种极其有价值的工具,可在实验室中用于功能基因组学研究。通过这种反向遗传学技术选择性敲低单个基因的能力,使许多研究人员能够通过评估功能缺失表型,快速揭示许多生物体中众多基因的生物学作用。在主要的人类疟疾传播媒介冈比亚按蚊中,用于降低目标基因功能的主要方法是将双链(dsRNA)注射到成年蚊子的血腔中。虽然这种方法已经取得成功,但在成年蚊子中进行基因敲除排除了对在成虫前期表达并可能发挥作用的基因,以及在成年蚊子中有限数量细胞中表达的基因的功能评估。我们描述了一种在蛹早期注射丝氨酸蛋白酶抑制剂2(SRPN2)dsRNA的方法,并通过观察SRPN2敲除的成年蚊子中目标蛋白水平的降低和黑色素瘤样假肿瘤的形成来验证SRPN2蛋白的敲低。这种明显的表型先前已在成年期敲低SRPN2功能时被描述过,并且我们通过在蛹发育期间启动的SRPN2敲除重现了这种成年表型。当与染料标记的dsRNA溶液一起使用时,该技术能够通过简单的光学显微镜轻松观察dsRNA在血腔中的注射质量和分布情况。

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