Wellcome Trust Centre for Molecular Parasitology, University of Glasgow.
Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Nature. 2014 Mar 13;507(7491):253-257. doi: 10.1038/nature12970. Epub 2014 Feb 23.
Commitment to and completion of sexual development are essential for malaria parasites (protists of the genus Plasmodium) to be transmitted through mosquitoes. The molecular mechanism(s) responsible for commitment have been hitherto unknown. Here we show that PbAP2-G, a conserved member of the apicomplexan AP2 (ApiAP2) family of DNA-binding proteins, is essential for the commitment of asexually replicating forms to sexual development in Plasmodium berghei, a malaria parasite of rodents. PbAP2-G was identified from mutations in its encoding gene, PBANKA_143750, which account for the loss of sexual development frequently observed in parasites transmitted artificially by blood passage. Systematic gene deletion of conserved ApiAP2 genes in Plasmodium confirmed the role of PbAP2-G and revealed a second ApiAP2 member (PBANKA_103430, here termed PbAP2-G2) that significantly modulates but does not abolish gametocytogenesis, indicating that a cascade of ApiAP2 proteins are involved in commitment to the production and maturation of gametocytes. The data suggest a mechanism of commitment to gametocytogenesis in Plasmodium consistent with a positive feedback loop involving PbAP2-G that could be exploited to prevent the transmission of this pernicious parasite.
性发育的启动和完成对于疟原虫(疟原虫属)通过蚊子传播至关重要。负责启动的分子机制迄今尚不清楚。在这里,我们表明,PbAP2-G 是一种保守的顶复体 AP2(ApiAP2)家族的 DNA 结合蛋白,对于啮齿动物疟原虫(Plasmodium berghei)无性繁殖形式向性发育的启动是必需的。PbAP2-G 是从其编码基因 PBANKA_143750 的突变中鉴定出来的,该基因的突变导致寄生虫在通过血液传播时经常失去性发育。对顶复体中保守的 ApiAP2 基因进行系统的基因缺失,证实了 PbAP2-G 的作用,并揭示了第二个 ApiAP2 成员(PBANKA_103430,这里称为 PbAP2-G2)显著调节但不能消除配子体形成,表明一连串的 ApiAP2 蛋白参与了启动配子体的产生和成熟。这些数据表明了疟原虫向配子体发生启动的一种机制,与涉及 PbAP2-G 的正反馈环一致,该机制可以被利用来防止这种有害寄生虫的传播。