European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, Cambridgeshire CB10 1SD, UK; Malaria Programme, Wellcome Trust Sanger Institute, Hinxton, Cambridgeshire CB10 1SA, UK.
Malaria Programme, Wellcome Trust Sanger Institute, Hinxton, Cambridgeshire CB10 1SA, UK; Department of Microbiology & Molecular Medicine, CMU, University of Geneva, 1211 Geneva 4, Geneva, Switzerland.
Cell Rep. 2017 Nov 14;21(7):2017-2029. doi: 10.1016/j.celrep.2017.10.071.
The transmission of malaria parasites to mosquitoes relies on the rapid induction of sexual reproduction upon their ingestion into a blood meal. Haploid female and male gametocytes become activated and emerge from their host cells, and the males enter the cell cycle to produce eight microgametes. The synchronized nature of gametogenesis allowed us to investigate phosphorylation signaling during its first minute in Plasmodium berghei via a high-resolution time course of the phosphoproteome. This revealed an unexpectedly broad response, with proteins related to distinct cell cycle events undergoing simultaneous phosphoregulation. We implicate several protein kinases in the process, and we validate our analyses on the plant-like calcium-dependent protein kinase 4 (CDPK4) and a homolog of serine/arginine-rich protein kinases (SRPK1). Mutants in these kinases displayed distinct phosphoproteomic disruptions, consistent with differences in their phenotypes. The results reveal the central role of protein phosphorylation in the atypical cell cycle regulation of a divergent eukaryote.
疟原虫向蚊子的传播依赖于它们在摄入血餐时迅速诱导有性繁殖。单倍体雌性和雄性配子体被激活并从宿主细胞中逸出,雄性进入细胞周期产生 8 个小配子。配子发生的同步性使我们能够通过对疟原虫伯氏疟原虫的磷酸化蛋白质组进行高分辨率的时间过程研究,在其最初的一分钟内研究磷酸化信号转导。这揭示了一个出乎意料的广泛反应,与不同细胞周期事件相关的蛋白质同时经历磷酸化调节。我们在该过程中涉及几个蛋白激酶,并在植物样钙依赖性蛋白激酶 4(CDPK4)和丝氨酸/精氨酸丰富蛋白激酶(SRPK1)的同源物上验证了我们的分析。这些激酶的突变体显示出不同的磷酸蛋白质组破坏,与其表型差异一致。研究结果揭示了蛋白磷酸化在一个不同的真核生物的典型细胞周期调控中的核心作用。