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Targets of the Entamoeba histolytica Transcription Factor URE3-BP

机译:溶组织性变形杆菌的靶标因子URE3-BP

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摘要

The Entamoeba histolytica transcription factor Upstream Regulatory Element 3-Binding Protein (URE3-BP) is a calcium-responsive regulator of two E. histolytica virulence genes, hgl5 and fdx1. URE3-BP was previously identified by a yeast one-hybrid screen of E. histolytica proteins capable of binding to the sequence TATTCTATT (Upstream Regulatory Element 3 (URE3)) in the promoter regions of hgl5 and fdx1. In this work, precise definition of the consensus URE3 element was performed by electrophoretic mobility shift assays (EMSA) using base-substituted oligonucleotides, and the consensus motif validated using episomal reporter constructs. Transcriptome profiling of a strain induced to produce a dominant-positive URE3-BP was then used to identify additional genes regulated by URE3-BP. Fifty modulated transcripts were identified, and of these the EMSA defined motif T[atg]T[tc][cg]T[at][tgc][tg] was found in over half of the promoters (54% p<0.0001). Fifteen of the URE3-BP regulated genes were potential membrane proteins, suggesting that one function of URE3-BP is to remodel the surface of E. histolytica in response to a calcium signal. Induction of URE3-BP leads to an increase in tranwell migration, suggesting a possible role in the regulation of cellular motility.
机译:变形杆菌肠溶菌转录因子上游调节元件3-结合蛋白(URE3-BP)是两个溶酶链球菌毒力基因hgl5和fdx1的钙响应调节剂。 URE3-BP以前是通过酵母组织蛋白酶的一杂交筛选来鉴定的,该蛋白能够与hgl5和fdx1的启动子区域中的序列TATTCTATT(上游调节元件3(URE3))结合。在这项工作中,使用碱基取代的寡核苷酸通过电泳迁移率变动分析(EMSA)对共有URE3元件进行了精确定义,并使用游离型报告基因构建体验证了共有基序。然后使用诱导产生显性阳性URE3-BP的菌株的转录组谱分析来鉴定由URE3-BP调控的其他基因。鉴定出五十个调制的转录本,其中有EMSA定义的基序T [atg] T [tc] [cg] T [at] [tgc] [tg]在一半以上的启动子中发现(54%p <0.0001) 。 URE3-BP调控的基因中有15个是潜在的膜蛋白,这表明URE3-BP的功能之一是响应钙信号重塑溶组织性大肠杆菌的表面。 URE3-BP的诱导导致tranwell迁移的增加,表明在调节细胞运动性中可能发挥作用。

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