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Targets of the Entamoeba histolytica Transcription Factor URE3-BP
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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2565699/ https://www.ncbi.nlm.nih.gov/pubmed/18846235 http://dx.doi.org/10.1371/journal.pntd.0000282 |
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author | Gilchrist, Carol A. Baba, Duza J. Zhang, Yan Crasta, Oswald Evans, Clive Caler, Elisabet Sobral, Bruno W. S. Bousquet, Christina B. Leo, Megan Hochreiter, Ameilia Connell, Sarah K. Mann, Barbara J. Petri, William A. |
author_facet | Gilchrist, Carol A. Baba, Duza J. Zhang, Yan Crasta, Oswald Evans, Clive Caler, Elisabet Sobral, Bruno W. S. Bousquet, Christina B. Leo, Megan Hochreiter, Ameilia Connell, Sarah K. Mann, Barbara J. Petri, William A. |
author_sort | Gilchrist, Carol A. |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2565699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-25656992008-10-10 Targets of the Entamoeba histolytica Transcription Factor URE3-BP Gilchrist, Carol A. Baba, Duza J. Zhang, Yan Crasta, Oswald Evans, Clive Caler, Elisabet Sobral, Bruno W. S. Bousquet, Christina B. Leo, Megan Hochreiter, Ameilia Connell, Sarah K. Mann, Barbara J. Petri, William A. PLoS Negl Trop Dis Research Article 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. Public Library of Science 2008-08-27 /pmc/articles/PMC2565699/ /pubmed/18846235 http://dx.doi.org/10.1371/journal.pntd.0000282 Text en Gilchrist et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Gilchrist, Carol A. Baba, Duza J. Zhang, Yan Crasta, Oswald Evans, Clive Caler, Elisabet Sobral, Bruno W. S. Bousquet, Christina B. Leo, Megan Hochreiter, Ameilia Connell, Sarah K. Mann, Barbara J. Petri, William A. Targets of the Entamoeba histolytica Transcription Factor URE3-BP |
title | Targets of the Entamoeba histolytica Transcription Factor URE3-BP |
title_full | Targets of the Entamoeba histolytica Transcription Factor URE3-BP |
title_fullStr | Targets of the Entamoeba histolytica Transcription Factor URE3-BP |
title_full_unstemmed | Targets of the Entamoeba histolytica Transcription Factor URE3-BP |
title_short | Targets of the Entamoeba histolytica Transcription Factor URE3-BP |
title_sort | targets of the entamoeba histolytica transcription factor ure3-bp |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2565699/ https://www.ncbi.nlm.nih.gov/pubmed/18846235 http://dx.doi.org/10.1371/journal.pntd.0000282 |
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