Le Chat Ludovic, Sinden Robert E, Dessens Johannes T
Department of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, Keppel Street, London WC1E 7HT, United Kingdom.
Mol Biochem Parasitol. 2007 May;153(1):41-7. doi: 10.1016/j.molbiopara.2007.01.016. Epub 2007 Feb 2.
The malaria parasite encodes a wide range of proteases necessary to facilitate its many developmental transitions in vertebrate and insect hosts. Amongst these is a predicted cysteine protease structurally related to caspases, named Plasmodium metacaspase 1 (PxMC1). We have generated Plasmodium berghei parasites in which the PbMC1coding sequence is removed and replaced with a green fluorescent reporter gene to investigate the expression of PbMC1, its contribution to parasite development, and its involvement in previously reported apoptosis-like cell death of P. berghei ookinetes. Our results show that the pbmc1 gene is expressed in female gametocytes and all downstream mosquito stages including sporozoites, but not in asexual blood stages. We failed to detect an apparent loss-of-function phenotype, suggesting that PbMC1 constitutes a functionally redundant gene. We discuss these findings in the context of two other putative Plasmodium metacaspases that we describe here.
疟原虫编码了多种蛋白酶,这些蛋白酶对于疟原虫在脊椎动物和昆虫宿主体内的多种发育转变至关重要。其中有一种预测的半胱氨酸蛋白酶,其结构与胱天蛋白酶相关,名为疟原虫间型半胱天冬酶1(PxMC1)。我们构建了伯氏疟原虫寄生虫,其中PbMC1编码序列被去除,并用绿色荧光报告基因取代,以研究PbMC1的表达、其对寄生虫发育的贡献以及其参与先前报道的伯氏疟原虫动合子凋亡样细胞死亡的情况。我们的结果表明,pbmc1基因在雌配子体以及包括子孢子在内的所有下游蚊子阶段表达,但在无性血液阶段不表达。我们未能检测到明显的功能丧失表型,这表明PbMC1构成了一个功能冗余的基因。我们在此背景下讨论这些发现,同时还描述了另外两种假定的疟原虫间型半胱天冬酶。