De Niz Mariana, Helm Susanne, Horstmann Sebastian, Annoura Takeshi, Del Portillo Hernando A, Khan Shahid M, Heussler Volker T
Institute of Cell Biology, University of Bern, Bern, Switzerland.
Molecular Parasitology, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
PLoS One. 2015 Apr 15;10(4):e0123473. doi: 10.1371/journal.pone.0123473. eCollection 2015.
Little is known about stage-specific gene regulation in Plasmodium parasites, in particular the liver stage of development. We have previously described in the Plasmodium berghei rodent model, a liver stage-specific (lisp2) gene promoter region, in vitro. Using a dual luminescence system, we now confirm the stage specificity of this promoter region also in vivo. Furthermore, by substitution and deletion analyses we have extended our in vitro characterization of important elements within the promoter region. Importantly, the dual luminescence system allows analyzing promoter constructs avoiding mouse-consuming cloning procedures of transgenic parasites. This makes extensive mutation and deletion studies a reasonable approach also in the malaria mouse model. Stage-specific expression constructs and parasite lines are extremely valuable tools for research on Plasmodium liver stage biology. Such reporter lines offer a promising opportunity for assessment of liver stage drugs, characterization of genetically attenuated parasites and liver stage-specific vaccines both in vivo and in vitro, and may be key for the generation of inducible systems.
关于疟原虫寄生虫中阶段特异性基因调控,尤其是发育的肝脏阶段,我们所知甚少。我们之前在伯氏疟原虫啮齿动物模型中,在体外描述了一个肝脏阶段特异性(lisp2)基因启动子区域。现在我们使用双荧光系统,在体内也证实了该启动子区域的阶段特异性。此外,通过替换和缺失分析,我们扩展了对启动子区域内重要元件的体外表征。重要的是,双荧光系统允许分析启动子构建体,避免了转基因寄生虫消耗小鼠的克隆程序。这使得广泛的突变和缺失研究在疟疾小鼠模型中也是一种合理的方法。阶段特异性表达构建体和寄生虫系是疟原虫肝脏阶段生物学研究的极其有价值的工具。此类报告系为体内和体外评估肝脏阶段药物、表征基因减毒寄生虫以及肝脏阶段特异性疫苗提供了一个有前景的机会,并且可能是诱导系统生成的关键。