Modrzynska Katarzyna, Pfander Claudia, Chappell Lia, Yu Lu, Suarez Catherine, Dundas Kirsten, Gomes Ana Rita, Goulding David, Rayner Julian C, Choudhary Jyoti, Billker Oliver
Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Cell Host Microbe. 2017 Jan 11;21(1):11-22. doi: 10.1016/j.chom.2016.12.003.
A family of apicomplexa-specific proteins containing AP2 DNA-binding domains (ApiAP2s) was identified in malaria parasites. This family includes sequence-specific transcription factors that are key regulators of development. However, functions for the majority of ApiAP2 genes remain unknown. Here, a systematic knockout screen in Plasmodium berghei identified ten ApiAP2 genes that were essential for mosquito transmission: four were critical for the formation of infectious ookinetes, and three were required for sporogony. We describe non-essential functions for AP2-O and AP2-SP proteins in blood stages, and identify AP2-G2 as a repressor active in both asexual and sexual stages. Comparative transcriptomics across mutants and developmental stages revealed clusters of co-regulated genes with shared cis promoter elements, whose expression can be controlled positively or negatively by different ApiAP2 factors. We propose that stage-specific interactions between ApiAP2 proteins on partly overlapping sets of target genes generate the complex transcriptional network that controls the Plasmodium life cycle.
在疟原虫中鉴定出了一个包含AP2 DNA结合结构域的顶复门特异性蛋白家族(ApiAP2s)。该家族包括作为发育关键调节因子的序列特异性转录因子。然而,大多数ApiAP2基因的功能仍然未知。在这里,对伯氏疟原虫进行的系统敲除筛选确定了十个对蚊子传播至关重要的ApiAP2基因:四个对感染性动合子的形成至关重要,三个是孢子生殖所必需的。我们描述了AP2-O和AP2-SP蛋白在血液阶段的非必需功能,并确定AP2-G2是在无性和有性阶段均具有活性的阻遏物。跨突变体和发育阶段的比较转录组学揭示了具有共享顺式启动子元件的共调控基因簇,其表达可由不同的ApiAP2因子正向或负向控制。我们提出,ApiAP2蛋白在部分重叠的靶基因集上的阶段特异性相互作用产生了控制疟原虫生命周期的复杂转录网络。