Reininger Luc, Tewari Rita, Fennell Clare, Holland Zoe, Goldring Dean, Ranford-Cartwright Lisa, Billker Oliver, Doerig Christian
INSERM U609-Wellcome Centre for Molecular Parasitology, Biomedical Research Centre, Faculty of Biomedical and Life Sciences, University of Glasgow, 120 University Place, Glasgow G12 8TA, Scotland.
J Biol Chem. 2009 Jul 31;284(31):20858-68. doi: 10.1074/jbc.M109.017988. Epub 2009 Jun 2.
The molecular control of cell division and development in malaria parasites is far from understood. We previously showed that a Plasmodium gametocyte-specific NIMA-related protein kinase, nek-4, is required for completion of meiosis in the ookinete, the motile form that develops from the zygote in the mosquito vector. Here, we show that another NIMA-related kinase, Pfnek-2, is also predominantly expressed in gametocytes, and that Pfnek-2 is an active enzyme displaying an in vitro substrate preference distinct from that of Pfnek-4. A functional nek-2 gene is required for transmission of both Plasmodium falciparum and the rodent malaria parasite Plasmodium berghei to the mosquito vector, which is explained by the observation that disruption of the nek-2 gene in P. berghei causes dysregulation of DNA replication during meiosis and blocks ookinete development. This has implications (i) in our understanding of sexual development of malaria parasites and (ii) in the context of control strategies aimed at interfering with malaria transmission.
疟原虫细胞分裂和发育的分子调控机制仍远未明确。我们之前的研究表明,疟原虫配子体特异性的NIMA相关蛋白激酶nek - 4是动合子减数分裂完成所必需的,动合子是在蚊媒中由合子发育而来的运动形式。在此,我们发现另一种NIMA相关激酶Pfnek - 2也主要在配子体中表达,并且Pfnek - 2是一种活性酶,其体外底物偏好与Pfnek - 4不同。功能性的nek - 2基因对于恶性疟原虫和啮齿类疟原虫伯氏疟原虫传播至蚊媒是必需的,这可以通过以下观察结果来解释:伯氏疟原虫中nek - 2基因的破坏会导致减数分裂期间DNA复制失调,并阻断动合子发育。这在以下两方面具有重要意义:(i)有助于我们理解疟原虫的有性发育;(ii)对于旨在干扰疟疾传播的控制策略而言。