Skavdis G, Sidén-Kiamos I, Müller H M, Crisanti A, Louis C
Institute of Molecular Biology and Biotechnology, Heraklion, Crete, Greece.
EMBO J. 1996 Jan 15;15(2):344-50.
Control of malaria by a methodology that would permit the effective blockage of the Anopheles gambiae midgut wall penetration by Plasmodium parasites requires a detailed understanding of both the physiology of the mosquito's digestion, and of the interactions between the parasite and its host. We have transformed Drosophila melanogaster with several constructs that allow the study of the promoter region of two of the major late trypsin genes of A. gambiae. Using several deletions, we have identified, for both genes, small genomic segments that are sufficient to confer tissue specificity to the promoter in a species that is far away in evolution from the mosquito. This will allow further studies that will enable both the understanding of the blood meal digestion, and may potentially be useful for the design of anti-plasmodial constructs at a later stage.
通过一种能够有效阻断疟原虫对冈比亚按蚊中肠壁穿透的方法来控制疟疾,需要详细了解蚊子的消化生理以及寄生虫与其宿主之间的相互作用。我们用几种构建体转化了黑腹果蝇,这些构建体可用于研究冈比亚按蚊两个主要晚期胰蛋白酶基因的启动子区域。通过几个缺失片段,我们已针对这两个基因鉴定出小的基因组片段,这些片段足以在与蚊子进化关系甚远的物种中赋予启动子组织特异性。这将有助于进一步开展研究,既能增进对血餐消化的理解,也可能在后期抗疟原虫构建体的设计中发挥作用。