School of Life Sciences, University of Nottingham, Nottingham, UK.
Pathogen Genomics Group, BESE Division, King Abdullah University of Science and Technology (KAUST), Thuwal, Kingdom of Saudi Arabia.
Commun Biol. 2021 Jun 18;4(1):760. doi: 10.1038/s42003-021-02273-0.
PP1 is a conserved eukaryotic serine/threonine phosphatase that regulates many aspects of mitosis and meiosis, often working in concert with other phosphatases, such as CDC14 and CDC25. The proliferative stages of the malaria parasite life cycle include sexual development within the mosquito vector, with male gamete formation characterized by an atypical rapid mitosis, consisting of three rounds of DNA synthesis, successive spindle formation with clustered kinetochores, and a meiotic stage during zygote to ookinete development following fertilization. It is unclear how PP1 is involved in these unusual processes. Using real-time live-cell and ultrastructural imaging, conditional gene knockdown, RNA-seq and proteomic approaches, we show that Plasmodium PP1 is implicated in both mitotic exit and, potentially, establishing cell polarity during zygote development in the mosquito midgut, suggesting that small molecule inhibitors of PP1 should be explored for blocking parasite transmission.
PP1 是一种保守的真核丝氨酸/苏氨酸磷酸酶,它调节有丝分裂和减数分裂的许多方面,通常与其他磷酸酶(如 CDC14 和 CDC25)协同作用。疟原虫生命周期的增殖阶段包括在蚊子媒介中的有性发育,雄性配子的形成以非典型的快速有丝分裂为特征,包括三轮 DNA 合成、具有聚集动粒的连续纺锤体形成,以及受精后合子到卵囊母细胞发育的减数分裂阶段。目前尚不清楚 PP1 如何参与这些不寻常的过程。通过实时活细胞和超微结构成像、条件性基因敲低、RNA-seq 和蛋白质组学方法,我们表明 Plasmodium PP1 参与有丝分裂退出,并且可能在蚊子中肠合子发育过程中建立细胞极性,这表明 PP1 的小分子抑制剂应该被探索用于阻断寄生虫传播。