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Genome-wide Functional Analysis of Plasmodium Protein Phosphatases Reveals Key Regulators of Parasite Development and Differentiation

机译:疟原虫蛋白磷酸酶的全基因组功能分析揭示了寄生虫发育和分化的关键调控因素。

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Reversible protein phosphorylation regulated by kinases and phosphatases controls many cellular processes. Although essential functions for the malaria parasite kinome have been reported, the roles of most protein phosphatases (PPs) during Plasmodium development are unknown. We report a functional analysis of the Plasmodium berghei protein phosphatome, which exhibits high conservation with the P. falciparum phosphatome and comprises 30 predicted PPs with differential and distinct expression patterns during various stages of the life cycle. Gene disruption analysis of P. berghei PPs reveals that half of the genes are likely essential for asexual blood stage development, whereas six are required for sexual development/sporogony in mosquitoes. Phenotypic screening coupled with transcriptome sequencing unveiled morphological changes and altered gene expression in deletion mutants of two N-myristoylated PPs. These findings provide systematic functional analyses of PPs in Plasmodium, identify how phosphatases regulate parasite development and differentiation, and can inform the identification of drug targets for malaria
机译:由激酶和磷酸酶调节的可逆蛋白质磷酸化控制许多细胞过程。尽管已报道了疟疾寄生虫激酶组的基本功能,但尚不清楚大多数蛋白磷酸酶(PPs)在疟原虫发育过程中的作用。我们报告了疟原虫疟原虫蛋白质磷原子的功能分析,它与恶性疟原虫磷原子具有很高的保守性,并包括30个预测的PP,它们在生命周期的各个阶段具有不同的表达模式。对伯氏疟原虫PPs的基因破坏分析表明,一半的基因可能是无性血液阶段发育必不可少的,而蚊子的性发育/口语化则需要六个。表型筛选与转录组测序揭示了两种N-豆蔻酰化PP缺失突变体的形态学变化和基因表达的改变。这些发现提供了疟原虫中PP的系统功能分析,确定了磷酸酶如何调节寄生虫的发育和分化,并可以为疟疾药物靶标的鉴定提供信息

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