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成年埃及伊蚊中显微注射DNA的调控表达。

Regulated expression of microinjected DNA in adult Aedes aegypti mosquitoes.

作者信息

Isoe J, Kunz S, Manhart C, Wells M A, Miesfeld R L

机构信息

Department of Biochemistry and Molecular Biophysics, The University of Arizona, Tucson, AZ 85721, USA.

出版信息

Insect Mol Biol. 2007 Feb;16(1):83-92. doi: 10.1111/j.1365-2583.2006.00704.x.

Abstract

We have developed a novel molecular genetic approach to investigating gene regulation in adult mosquitoes called whole body transfection (WBT). This DNA microinjection method allows for both constitutive and regulated expression of plasmid vectors in the fat body and midgut of adult mosquitoes within 24 h of injection. Using a luciferase reporter gene containing the Aedes aegypti heat shock protein 70 (Hsp70) promoter, we optimized the WBT protocol at various times post-injection and used these parameters to measure the expression of a vitellogenin-luciferase reporter gene in response to blood meal feeding. These studies showed that a 843 bp fragment of the Ae. aegypti vitellogenin-C (VgC) promoter caused a greater than 200-fold induction of luciferase activity in a strict tissue-specific manner, and only in response to feeding. Functional mapping of the VgC promoter by WBT identified essential upstream regulatory elements in the region spanning -780 to -182 bp from the transcriptional start site. We also constructed a lipopolysaccharide-regulated expression vector using a 1096 bp genomic fragment of the Ae. aegypti cecropin B (CecB) promoter. Our data show that four days after WBT injection, the CecB-luciferase reporter gene could be induced more than 100-fold in the fat body following lipopolysaccharide injection. Moreover, we found that lipopolysaccharide-induction of the CecB reporter gene occurred up to 28 days post-WBT injection. These data suggest that WBT could provide a novel strategy to express recombinant proteins and RNAi constructs in adult mosquitoes using conventional microinjection methods.

摘要

我们开发了一种全新的分子遗传学方法来研究成年蚊子中的基因调控,称为全身转染(WBT)。这种DNA显微注射方法能够在注射后24小时内,使质粒载体在成年蚊子的脂肪体和中肠中进行组成型表达和调控表达。使用含有埃及伊蚊热休克蛋白70(Hsp70)启动子的荧光素酶报告基因,我们在注射后的不同时间优化了WBT方案,并利用这些参数来测量卵黄蛋白原 - 荧光素酶报告基因在血餐喂养后的表达。这些研究表明,埃及伊蚊卵黄蛋白原 - C(VgC)启动子的一个843 bp片段以严格的组织特异性方式导致荧光素酶活性诱导超过200倍,并且仅对进食有反应。通过WBT对VgC启动子进行功能定位,确定了从转录起始位点起-780至-182 bp区域内的必需上游调控元件。我们还使用埃及伊蚊天蚕素B(CecB)启动子的1096 bp基因组片段构建了一种脂多糖调控的表达载体。我们的数据表明,WBT注射四天后,脂多糖注射后脂肪体中CecB - 荧光素酶报告基因可被诱导超过100倍。此外,我们发现CecB报告基因的脂多糖诱导在WBT注射后长达28天仍会发生。这些数据表明,WBT可以提供一种新策略,使用传统显微注射方法在成年蚊子中表达重组蛋白和RNAi构建体。

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