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首页> 外文期刊>Parasitology >Molecular characterization and analysis of a novel calcium-dependent protein kinase from Eimeria tenella
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Molecular characterization and analysis of a novel calcium-dependent protein kinase from Eimeria tenella

机译:一种新型的艾美耳球虫钙依赖性蛋白激酶的分子表征和分析

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SUMMARY The calcium-dependent protein kinases (CDPKs) are unique enzymes found only in plants, green algae, ciliates and apicomplexan parasites. In this study, a novel CDPK gene of Eimeria tenella, designed EtCDPK3, was cloned using rapid amplification of cDNA ends (RACE) based on the expressed sequence tag (EST). The entire cDNA of EtCDPK3 contained 1637 nucleotides encoding 433 amino acids and the deduced EtCDPK3 protein had canonical characteristic domains identified in other CDPKs, including a well-conserved amino-terminal kinase domain and a carboxy-terminal calmodulin-like structure with 4 EF-hand motifs for calcium binding. The expression profiles of the EtCDPK3 gene in different development stages were investigated by real-time quantitative PCR. Messenger RNA levels from the EtCDPK3 gene were higher in sporozoites than in other stages (unsporulated oocysts, sporulated oocysts and merozoites). Western blot analysis showed that rabbit antiserum against recombinant EtCDPK3 could recognize a native 49? kDa protein band of parasite. Indirect immunofluorescent antibody labelling revealed dispersed localization of EtCDPK3 during the first schizogony and intense specific staining. EtCDPK3 was located at the apical end of the sporozoites after early infection of DF-1 cells and the protein was highly expressed. Inhibition of EtCDPK3 function using specific antibodies reduced the ability of E. tenella to invade host cells. These results suggested that EtCDPK3 may be involved in invasion and survival of the parasite intracellular stages of E. tenella. Because this kinase family is absent from hosts, it represents a valid target that could be exploited for chemotherapy against Eimeria spp. ? Cambridge University Press 2013.
机译:发明内容钙依赖性蛋白激酶(CDPK)是仅在植物,绿藻,纤毛虫和apicomplexan寄生虫中发现的独特酶。在这项研究中,基于表达的序列标签(EST),使用cDNA末端(RACE)的快速扩增,克隆了设计为EtCDPK3的艾美尔球虫的新型CDPK基因。 EtCDPK3的整个cDNA包含1637个核苷酸,编码433个氨基酸,推导的EtCDPK3蛋白具有在其他CDPK中鉴定出的规范特征域,包括一个保守的氨基末端激酶结构域和一个羧基末端钙调蛋白样结构,带有4个EF-手钙结合的基序。通过实时定量PCR研究了EtCDPK3基因在不同发育阶段的表达情况。子孢子中EtCDPK3基因的信使RNA水平高于其他阶段(未孢子卵囊,孢子卵囊和裂殖子)。蛋白质印迹分析表明,兔抗重组EtCDPK3的抗血清可以识别天然的49?寄生虫的kDa蛋白带。间接免疫荧光抗体标记显示在第一次精神分裂期间EtCDPK3的分散定位和强烈的特异性染色。早期感染DF-1细胞后,EtCDPK3位于子孢子的顶端,并且该蛋白高度表达。使用特异性抗体抑制EtCDPK3功能会降低大肠杆菌的入侵宿主细胞的能力。这些结果表明,EtCDPK3可能参与大肠杆菌的寄生虫细胞内阶段的入侵和生存。由于宿主中不存在该激酶家族,因此它代表了可用于针对艾美尔球菌属的化学疗法开发的有效靶标。 ?剑桥大学出版社,2013年。

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