LmxMPK4, a mitogen-activated protein (MAP) kinase homologue essential for promastigotes and amastigotes of Leishmania mexicana.

Qiong Wang, Inga M Melzer, Martin Kruse, Claudia Sander-Juelch, Martin Wiese
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引用次数: 48

Abstract

Background: Leishmania parasites undergo profound morphological and biochemical changes while passing through their life cycle. Protein kinases have been shown to be involved in the differentiation from the extracellular flagellated promastigotes to the intracellular "non-flagellated" amastigotes and vice versa. Moreover, these enzymes are likely involved in the regulation of the proliferation of the different life stages.

Results: Here, we characterize LmxMPK4, a mitogen-activated protein (MAP) kinase homologue from Leishmania mexicana. The kinase reveals all sequence motifs for classification as a MAP kinase. LmxMPK4 proved to be active as a recombinant protein. The kinase is expressed in promastigotes and amastigotes. It was impossible to generate homozygous gene deletion mutants for LmxMPK4 in promastigotes. Moreover, amastigotes bearing only an episomal copy of the gene stably retained LmxMPK4 over a prolonged period without antibiotic pressure in infected mice.

Conclusion: LmxMPK4 is essential for promastigotes and amastigotes of Leishmania. It shows significant amino acid sequence divergence to mammalian MAP kinases. Thus, LmxMPK4 is a promising new drug target.

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LmxMPK4,一种分裂原活化蛋白(MAP)激酶同源物,对墨西哥利什曼原虫的promastigotes和amastigotes至关重要。
背景:利什曼原虫在整个生命周期中经历了深刻的形态和生化变化。蛋白质激酶已被证明参与了从细胞外有鞭毛的前体向细胞内“无鞭毛”的无尾体的分化,反之亦然。此外,这些酶可能参与调节不同生命阶段的增殖。结果:在这里,我们对来自墨西哥利什曼原虫的丝裂原活化蛋白(MAP)激酶同源物LmxMPK4进行了表征。该激酶显示所有序列基序,可归类为MAP激酶。结果表明,LmxMPK4作为重组蛋白具有活性。该激酶在promastigotes和amastigotes中表达。在原孢子中不可能产生LmxMPK4纯合基因缺失突变体。此外,在没有抗生素压力的感染小鼠中,仅携带该基因的一个片段拷贝的无尾线虫在很长一段时间内稳定地保留了LmxMPK4。结论:LmxMPK4对利什曼原虫的原毛体和无尾毛体是必需的。与哺乳动物MAP激酶存在显著的氨基酸序列差异。因此,LmxMPK4是一个很有前景的新药物靶点。
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Consultation meeting on the development of therapeutic vaccines for post kala azar dermal leishmaniasis. In silico, biologically-inspired modelling of genomic variation generation in surface proteins of Trypanosoma cruzi. Genetic diversity of Leishmania amazonensis strains isolated in northeastern Brazil as revealed by DNA sequencing, PCR-based analyses and molecular karyotyping. Dynamics of infection and competition between two strains of Trypanosoma brucei brucei in the tsetse fly observed using fluorescent markers. Consultative meeting to develop a strategy for treatment of cutaneous leishmaniasis. Institute Pasteur, Paris. 13-15 June, 2006.
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