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Originally published In Press as doi:10.1074/jbc.M006866200 on October 18, 2000

J. Biol. Chem., Vol. 276, Issue 2, 1602-1609, January 12, 2001
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Identification of Two Entamoeba histolytica Sequence-specific URE4 Enhancer-binding Proteins with Homology to the RNA-binding Motif RRM*

Joanna M. SchaenmanDagger , Carol A. Gilchrist§, Barbara J. MannDagger §, and William A. Petri Jr.Dagger §||

From the Departments of Dagger  Microbiology, § Internal Medicine, and  Pathology, University of Virginia, Charlottesville, Virginia 22908

To study transcriptional regulation in the lower branching eukaryote Entamoeba histolytica, we have identified two sequence-specific DNA-binding proteins that recognize the upstream regulatory element URE4, an enhancer that regulates expression of the Gal/GalNAc lectin heavy subunit gene hgl5. A chromatographic purification of E. histolytica nuclear extracts by gel filtration, cation exchange, and sequence-specific DNA affinity chromatography led to a 700-fold increase in URE4 binding activity and the appearance of two dominant protein species with molecular masses of 28 and 18 kDa. These proteins, termed E. histolytica enhancer-binding proteins 1 and 2 (EhEBP1 and EhEBP2), were sequenced by tandem mass spectroscopy and their corresponding cDNA clones identified. Recombinant EhEBP1 and EhEBP2 were able to bind double-stranded oligonucleotides bearing the URE4 motif in a sequence-specific manner, and antibodies raised against EhEBP1 were able to interfere with the formation of URE4-protein complexes in crude nuclear extracts. Overexpression of EhEBP1 in E. histolytica trophozoites resulted in a 7-fold drop in promoter activity in transiently transfected reporter gene constructs when the URE4 motif was present, confirming its ability to specifically recognize the URE4 motif and suggesting that additional cofactors may be required for transcriptional activation by URE4. Further characterization and identification of binding partners for EhEBP1 and EhEBP2, the first proteins with demonstrated sequence-specific DNA binding activity to be identified in E. histolytica, should provide new insights into transcriptional regulation in this protozoan parasite.


* This work was supported in part by National Institutes of Health Grant AI 37941.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EMBL Data Bank with accession number(s) AF224345 and AF224346 (for EhEBP1 and EhEBP2, respectively).

|| A Burroughs Wellcome Fund Scholar in Molecular Parasitology. To whom correspondence should be addressed: University of Virginia HSC, MR4 Bldg., Rm. 2115, 300 Park Pl., Charlottesville, VA 22908. Tel.: 804-924-0075; Fax: 804-924-0075; E-mail address: wap3g@virginia.edu.


Copyright © 2001 by The American Society for Biochemistry and Molecular Biology, Inc.


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