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纳米基因控制DNA介导黄热病蚊子埃及伊蚊中发育调控的转座。

nanos gene control DNA mediates developmentally regulated transposition in the yellow fever mosquito Aedes aegypti.

作者信息

Adelman Zach N, Jasinskiene Nijole, Onal Sedef, Juhn Jennifer, Ashikyan Aurora, Salampessy Michael, MacCauley Todd, James Anthony A

机构信息

Department of Molecular Biology and Biochemistry, University of California, Irvine, CA 92697, USA.

出版信息

Proc Natl Acad Sci U S A. 2007 Jun 12;104(24):9970-5. doi: 10.1073/pnas.0701515104. Epub 2007 Jun 4.

Abstract

Transposable elements (TEs) are proposed as a basis for developing drive systems to spread pathogen resistance genes through vector mosquito populations. The use of transcriptional and translational control DNA elements from genes expressed specifically in the insect germ line to mediate transposition offers possibilities for mitigating some of the concerns about transgene behavior in the target vector species and eliminating effects on nontarget organisms. Here, we describe the successful use of the promoter and untranslated regions from the nanos (nos) orthologous gene of the yellow fever mosquito, Aedes aegypti, to control sex- and tissue-specific expression of exogenously derived mariner MosI transposase-encoding DNA. Transgenic mosquitoes expressed transposase mRNA in abundance near or equal to the endogenous nos transcript and exclusively in the female germ cells. In addition, MosI mRNA was deposited in developing oocytes and localized and maintained at the posterior pole during early embryonic development. Importantly, four of five transgenic lines examined were capable of mobilizing a second MosI transgene into the mosquito genome, indicating that functional transposase was being produced. Thus, the nos control sequences show promise as part of a TE-based gene drive system.

摘要

转座元件(TEs)被提议作为开发驱动系统的基础,以便将病原体抗性基因传播到媒介蚊虫种群中。利用在昆虫生殖系中特异性表达的基因的转录和翻译控制DNA元件来介导转座,为减轻对目标媒介物种中转基因行为的一些担忧以及消除对非目标生物的影响提供了可能性。在此,我们描述了成功利用黄热病蚊埃及伊蚊的nanos(nos)直系同源基因的启动子和非翻译区,来控制性特异性和组织特异性表达外源来源的编码水手MosI转座酶的DNA。转基因蚊子在接近或等于内源性nos转录本的水平大量表达转座酶mRNA,并且仅在雌性生殖细胞中表达。此外,MosI mRNA沉积在发育中的卵母细胞中,并在胚胎发育早期定位于并维持在后极。重要的是,所检测的五个转基因品系中有四个能够将第二个MosI转基因转移到蚊子基因组中,这表明正在产生功能性转座酶。因此,nos控制序列有望作为基于转座元件的基因驱动系统的一部分。

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