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Targets of the Entamoeba histolytica Transcription Factor URE3-BP
Author(s) -
Carol A. Gilchrist,
Duza Baba,
Yan Zhang,
Oswald Crasta,
Clive Evans,
Elisabet Caler,
Bruno Sobral,
Christina B. Bousquet,
Megan Leo,
Ameilia Hochreiter,
Sarah K. Connell,
Barbara J. Mann,
William A. Petri
Publication year - 2008
Publication title -
plos neglected tropical diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.99
H-Index - 135
eISSN - 1935-2735
pISSN - 1935-2727
DOI - 10.1371/journal.pntd.0000282
Subject(s) - transcription factor , promoter , entamoeba histolytica , biology , electrophoretic mobility shift assay , gene , response element , dna binding protein , microbiology and biotechnology , genetics , gene expression
The Entamoeba histolytica transcription factor Upstream Regulatory Element 3-Binding Protein (URE3-BP) is a calcium-responsive regulator of two E. histolytica virulence genes, hgl 5 and fdx 1. 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 hgl 5 and fdx 1. 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.

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