首页> 外文期刊>Molecular biology of the cell >A Cluster of Ring Stage–specific Genes Linked to a Locus Implicated in Cytoadherence in Plasmodium falciparum Codes for PEXEL-negative and PEXEL-positive Proteins Exported into the Host Cell
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A Cluster of Ring Stage–specific Genes Linked to a Locus Implicated in Cytoadherence in Plasmodium falciparum Codes for PEXEL-negative and PEXEL-positive Proteins Exported into the Host Cell

机译:环阶段特异性基因的簇与恶性疟原虫代码中细胞粘附相关的基因座相关,PEXEL阴性和PEXEL阳性蛋白输出到宿主细胞。

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Blood stages of Plasmodium falciparum export proteins into their erythrocyte host, thereby inducing extensive host cell modifications that become apparent after the first half of the asexual development cycle (ring stage). This is responsible for a major part of parasite virulence. Export of many parasite proteins depends on a sequence motif termed Plasmodium export element (PEXEL) or vacuolar transport signal (VTS). This motif has allowed the prediction of the Plasmodium exportome. Using published genome sequence, we redetermined the boundaries of a previously studied region linked to P . falciparum virulence, reducing the number of candidate genes in this region to 13. Among these, we identified a cluster of four ring stage-specific genes, one of which is known to encode an exported protein. We demonstrate that all four genes code for proteins exported into the host cell, although only two genes contain an obvious PEXEL/VTS motif. We propose that the systematic analysis of ring stage-specific genes will reveal a cohort of exported proteins not present in the currently predicted exportome. Moreover, this provides further evidence that host cell remodeling is a major task of this developmental stage. Biochemical and photobleaching studies using these proteins reveal new properties of the parasite-induced membrane compartments in the host cell. This has important implications for the biogenesis and connectivity of these structures.
机译:恶性疟原虫的血液阶段将蛋白质输出到其红细胞宿主中,从而诱导了广泛的宿主细胞修饰,这些修饰在无性发育周期的前半部分(环期)后变得很明显。这是造成寄生虫毒力的主要部分。许多寄生虫蛋白的输出取决于序列基序,称为疟原虫输出元件(PEXEL)或液泡转运信号(VTS)。这种主题可以预测疟原虫的出口。使用公开的基因组序列,我们重新确定了先前研究的与P关联的区域的边界。恶性疟原虫的毒力,使该区域的候选基因数量减少至13个。在这些基因中,我们鉴定了一组由四个环阶段特异性基因组成的簇,其中一个已知编码输出蛋白。我们证明所有四个基因编码输出到宿主细胞中的蛋白质,尽管只有两个基因包含一个明显的PEXEL / VTS基序。我们建议对环阶段特异性基因的系统分析将揭示当前预测的输出基因组中不存在的一组输出蛋白。此外,这提供了进一步的证据表明宿主细胞重塑是该发育阶段的主要任务。使用这些蛋白质的生化和光漂白研究揭示了宿主细胞中寄生虫诱导的膜区室的新特性。这对这些结构的生物发生和连通性具有重要意义。

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