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提高 Anastrepha suspensa 胚胎条件致死性转基因品系开发的策略。

Strategy for enhanced transgenic strain development for embryonic conditional lethality in Anastrepha suspensa.

机构信息

United States Department of Agriculture, Agriculture Research Service, Center for Medical, Agricultural and Veterinary Entomology, 1700 SW 23rd Drive, Gainesville, FL 32608, USA.

出版信息

Proc Natl Acad Sci U S A. 2012 Jun 12;109(24):9348-53. doi: 10.1073/pnas.1203352109. Epub 2012 May 30.

Abstract

Here the first reproductive sterility system for the tephritid fruit fly pest, Anastrepha suspensa, is presented, based on lethality primarily limited to embryos heterozygous for a conditional lethal transgene combination. This tetracycline (Tet)-suppressible system uses a driver construct having the promoter from the newly isolated embryo-specific A. suspensa serendipity α gene linked to the Tet-transactivator. This was used to drive expression of a phosphomutated variant of the pro-apoptotic cell death gene, hid, from A. ludens, that was isolated, based on its identity to A. suspensa hid. The Alhid(Ala2) variant was shown to have the highest cell death activity in an in vitro A. suspensa cell death assay compared to the orthologous genes Ashid, Dmhid, and the variant Dmhid(Ala5). These cell death assays also allowed a determination of the most-efficient driver-effector cassette combinations for use in A. suspensa transformants, resulting in two hybrid strains exhibiting 100% lethality. One strain was 96% lethal in embryos in the absence of tetracycline, with none surviving past the first larval instar, which is critical for pests that are most damaging in late-larval stages. We demonstrate that the isolation and in vitro validation of species-specific promoters and lethal effector genes can greatly improve the efficiency of creating high-performance conditional lethality strains that may be extended to other insect pest species.

摘要

这里提出了第一个用于桔小实蝇害虫的生殖不育系统,该系统主要基于对杂合子条件致死转基因组合的胚胎致死率。该四环素(Tet)抑制系统使用了一个驱动构建体,该构建体具有从新分离的胚胎特异性 A. suspensa 天意α基因连接到 Tet 转录激活子的启动子。这用于驱动来自 A. ludens 的磷酸化突变体凋亡细胞死亡基因 hid 的表达,该基因基于其与 A. suspensa hid 的同一性被分离。与同源基因 Ashid、Dmhid 和变体 Dmhid(Ala5)相比,在体外 A. suspensa 细胞死亡测定中,Alhid(Ala2)变体显示出最高的细胞死亡活性。这些细胞死亡测定还允许确定用于 A. suspensa 转化体的最有效的驱动子-效应子盒组合,导致两种杂种品系表现出 100%的致死率。一种品系在没有四环素的情况下,胚胎的致死率为 96%,没有一个能存活到第一龄幼虫期,这对于在幼虫后期危害最大的害虫来说是至关重要的。我们证明,分离和体外验证物种特异性启动子和致死效应基因可以大大提高创建高性能条件致死性菌株的效率,这些菌株可能扩展到其他昆虫害虫物种。

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