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Studies on the calcium-dependent regulation of URE3-BP, a transcription factor of Entamoeba histolytica: Identification and characterization of the plasma membrane-binding partner EHC2A.

机译:钙依赖调节的URE3-BP,溶血性变形杆菌的转录因子的研究:质膜结合伴侣EHC2A的鉴定和表征。

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摘要

The protozoan parasite Entamoeba histolytica is the causative agent of amebiasis, estimated to be the second leading cause of protozoan morbidity and mortality. In order to understand the molecular pathogenesis of the disease, we have studied the transcriptional regulation of important virulence genes.;Calcium (Ca2+) is a ubiquitous secondary messenger involved in many cellular signal transduction events. The E. histolytica upstream regulatory element 3-binding protein (URE3-BP) is a transcription factor that binds its cognate DNA element (URE3) in a Ca2+-inhibitable manner. The protein is located in both the nucleus and the cytoplasm, but has also been found to be enriched in the plasma membrane of amebic trophozoites. We investigated the reason for the unusual localization of URE3-BP at the amebic plasma membrane. This led to the identification and characterization of EhC2A, a 22 kDa calcium-dependent binding partner of URE3-BP and a novel member of the C2-domain superfamily.;Immunoprecipitations of URE3-BP and EhC2A demonstrated that the two proteins interact, and that the interaction was enhanced in the presence of calcium. Recombinant and native EhC2A bound phospholipid vesicles in a calcium-dependent manner, with half maximal binding occurring at 3.4 muM free Ca2+ . URE3-BP and EhC2A were observed to translocate to the amebic plasma membrane upon an increase in the intracellular Ca2+ concentration of trophozoites, as revealed by subcellular fractionation and immunofluorescent staining. In addition, shRNA mediated knockdown of EhC2A protein expression significantly modulated the mRNA levels of URE3-BP regulated transcripts. Based on these results, we propose a model for EhC2A-mediated regulation of the transcriptional activities of URE3-BP via Ca2+-dependent anchoring of the transcription factor to the amebic plasma membrane.
机译:原生动物的寄生虫组织变形虫(Entamoeba histolytica)是氨虫病的病原体,据估计是导致原生动物发病和死亡的第二大原因。为了了解该疾病的分子发病机理,我们研究了重要毒力基因的转录调控。钙(Ca2 +)是一种普遍存在的次级信使,涉及许多细胞信号转导事件。组织溶大肠杆菌上游调节元件3-结合蛋白(URE3-BP)是一种转录因子,以Ca2 +抑制的方式结合其同源DNA元件(URE3)。该蛋白质位于细胞核和细胞质中,但也发现其富含阿米巴滋养体的质膜。我们调查了URE3-BP在阿米巴质膜上异常定位的原因。这导致了EhC2A的鉴定和表征,EhC2A是URE3-BP的22 kDa钙依赖性结合伴侣,是C2结构域超家族的新成员。在钙的存在下相互作用增强。重组和天然EhC2A以钙依赖的方式结合磷脂囊泡,在3.4μM游离Ca2 +处发生最大结合的一半。亚细胞分级分离和免疫荧光染色显示,随着滋养体细胞内Ca2 +浓度的增加,URE3-BP和EhC2A易位至阿米巴质膜。此外,shRNA介导的EhC2A蛋白表达的敲低显着调节了URE3-BP调控转录本的mRNA水平。基于这些结果,我们提出了一个模型,用于EhC2A介导的通过Ca2 +依赖性锚定转录因子至阿米巴质膜的URE3-BP转录活性的调节。

著录项

  • 作者

    Moreno Aquino, Heriberto.;

  • 作者单位

    University of Virginia.;

  • 授予单位 University of Virginia.;
  • 学科 Biology Microbiology.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 139 p.
  • 总页数 139
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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