Cargando…

The Vacuolar ATPase from Entamoeba histolytica: Molecular cloning of the gene encoding for the B subunit and subcellular localization of the protein

BACKGROUND: Entamoeba histolytica is a professional phagocytic cell where the vacuolar ATPase plays a key role. This enzyme is a multisubunit complex that regulates pH in many subcellular compartments, even in those that are not measurably acidic. It participates in a wide variety of cellular proces...

Descripción completa

Detalles Bibliográficos
Autores principales: Meléndez-Hernández, Mayra Gisela, Barrios, María Luisa Labra, Orozco, Esther, Luna-Arias, Juan Pedro
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2629482/
https://www.ncbi.nlm.nih.gov/pubmed/19108705
http://dx.doi.org/10.1186/1471-2180-8-235
_version_ 1782163785224552448
author Meléndez-Hernández, Mayra Gisela
Barrios, María Luisa Labra
Orozco, Esther
Luna-Arias, Juan Pedro
author_facet Meléndez-Hernández, Mayra Gisela
Barrios, María Luisa Labra
Orozco, Esther
Luna-Arias, Juan Pedro
author_sort Meléndez-Hernández, Mayra Gisela
collection PubMed
description BACKGROUND: Entamoeba histolytica is a professional phagocytic cell where the vacuolar ATPase plays a key role. This enzyme is a multisubunit complex that regulates pH in many subcellular compartments, even in those that are not measurably acidic. It participates in a wide variety of cellular processes such as endocytosis, intracellular transport and membrane fusion. The presence of a vacuolar type H(+)-ATPase in E. histolytica trophozoites has been inferred previously from inhibition assays of its activity, the isolation of the Ehvma1 and Ehvma3 genes, and by proteomic analysis of purified phagosomes. RESULTS: We report the isolation and characterization of the Ehvma2 gene, which encodes for the subunit B of the vacuolar ATPase. This polypeptide is a 55.3 kDa highly conserved protein with 34 to 80% identity to orthologous proteins from other species. Particularly, in silico studies showed that EhV-ATPase subunit B displays 78% identity and 90% similarity to its Dictyostelium ortholog. A 462 bp DNA fragment of the Ehvma2 gene was expressed in bacteria and recombinant polypeptide was used to raise mouse polyclonal antibodies. EhV-ATPase subunit B antibodies detected a 55 kDa band in whole cell extracts and in an enriched fraction of DNA-containing organelles named EhkOs. The V-ATPase subunit B was located by immunofluorescence and confocal microscopy in many vesicles, in phagosomes, plasma membrane and in EhkOs. We also identified the genes encoding for the majority of the V-ATPase subunits in the E. histolytica genome, and proposed a putative model for this proton pump. CONCLUSION: We have isolated the Ehvma2 gene which encodes for the V-ATPase subunit B from the E. histolytica clone A. This gene has a 154 bp intron and encodes for a highly conserved polypeptide. Specific antibodies localized EhV-ATPase subunit B in many vesicles, phagosomes, plasma membrane and in EhkOs. Most of the orthologous genes encoding for the EhV-ATPase subunits were found in the E. histolytica genome, indicating the conserved nature of V-ATPase in this parasite.
format Text
id pubmed-2629482
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-26294822009-01-22 The Vacuolar ATPase from Entamoeba histolytica: Molecular cloning of the gene encoding for the B subunit and subcellular localization of the protein Meléndez-Hernández, Mayra Gisela Barrios, María Luisa Labra Orozco, Esther Luna-Arias, Juan Pedro BMC Microbiol Research Article BACKGROUND: Entamoeba histolytica is a professional phagocytic cell where the vacuolar ATPase plays a key role. This enzyme is a multisubunit complex that regulates pH in many subcellular compartments, even in those that are not measurably acidic. It participates in a wide variety of cellular processes such as endocytosis, intracellular transport and membrane fusion. The presence of a vacuolar type H(+)-ATPase in E. histolytica trophozoites has been inferred previously from inhibition assays of its activity, the isolation of the Ehvma1 and Ehvma3 genes, and by proteomic analysis of purified phagosomes. RESULTS: We report the isolation and characterization of the Ehvma2 gene, which encodes for the subunit B of the vacuolar ATPase. This polypeptide is a 55.3 kDa highly conserved protein with 34 to 80% identity to orthologous proteins from other species. Particularly, in silico studies showed that EhV-ATPase subunit B displays 78% identity and 90% similarity to its Dictyostelium ortholog. A 462 bp DNA fragment of the Ehvma2 gene was expressed in bacteria and recombinant polypeptide was used to raise mouse polyclonal antibodies. EhV-ATPase subunit B antibodies detected a 55 kDa band in whole cell extracts and in an enriched fraction of DNA-containing organelles named EhkOs. The V-ATPase subunit B was located by immunofluorescence and confocal microscopy in many vesicles, in phagosomes, plasma membrane and in EhkOs. We also identified the genes encoding for the majority of the V-ATPase subunits in the E. histolytica genome, and proposed a putative model for this proton pump. CONCLUSION: We have isolated the Ehvma2 gene which encodes for the V-ATPase subunit B from the E. histolytica clone A. This gene has a 154 bp intron and encodes for a highly conserved polypeptide. Specific antibodies localized EhV-ATPase subunit B in many vesicles, phagosomes, plasma membrane and in EhkOs. Most of the orthologous genes encoding for the EhV-ATPase subunits were found in the E. histolytica genome, indicating the conserved nature of V-ATPase in this parasite. BioMed Central 2008-12-23 /pmc/articles/PMC2629482/ /pubmed/19108705 http://dx.doi.org/10.1186/1471-2180-8-235 Text en Copyright © 2008 Meléndez-Hernández et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Meléndez-Hernández, Mayra Gisela
Barrios, María Luisa Labra
Orozco, Esther
Luna-Arias, Juan Pedro
The Vacuolar ATPase from Entamoeba histolytica: Molecular cloning of the gene encoding for the B subunit and subcellular localization of the protein
title The Vacuolar ATPase from Entamoeba histolytica: Molecular cloning of the gene encoding for the B subunit and subcellular localization of the protein
title_full The Vacuolar ATPase from Entamoeba histolytica: Molecular cloning of the gene encoding for the B subunit and subcellular localization of the protein
title_fullStr The Vacuolar ATPase from Entamoeba histolytica: Molecular cloning of the gene encoding for the B subunit and subcellular localization of the protein
title_full_unstemmed The Vacuolar ATPase from Entamoeba histolytica: Molecular cloning of the gene encoding for the B subunit and subcellular localization of the protein
title_short The Vacuolar ATPase from Entamoeba histolytica: Molecular cloning of the gene encoding for the B subunit and subcellular localization of the protein
title_sort vacuolar atpase from entamoeba histolytica: molecular cloning of the gene encoding for the b subunit and subcellular localization of the protein
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2629482/
https://www.ncbi.nlm.nih.gov/pubmed/19108705
http://dx.doi.org/10.1186/1471-2180-8-235
work_keys_str_mv AT melendezhernandezmayragisela thevacuolaratpasefromentamoebahistolyticamolecularcloningofthegeneencodingforthebsubunitandsubcellularlocalizationoftheprotein
AT barriosmarialuisalabra thevacuolaratpasefromentamoebahistolyticamolecularcloningofthegeneencodingforthebsubunitandsubcellularlocalizationoftheprotein
AT orozcoesther thevacuolaratpasefromentamoebahistolyticamolecularcloningofthegeneencodingforthebsubunitandsubcellularlocalizationoftheprotein
AT lunaariasjuanpedro thevacuolaratpasefromentamoebahistolyticamolecularcloningofthegeneencodingforthebsubunitandsubcellularlocalizationoftheprotein
AT melendezhernandezmayragisela vacuolaratpasefromentamoebahistolyticamolecularcloningofthegeneencodingforthebsubunitandsubcellularlocalizationoftheprotein
AT barriosmarialuisalabra vacuolaratpasefromentamoebahistolyticamolecularcloningofthegeneencodingforthebsubunitandsubcellularlocalizationoftheprotein
AT orozcoesther vacuolaratpasefromentamoebahistolyticamolecularcloningofthegeneencodingforthebsubunitandsubcellularlocalizationoftheprotein
AT lunaariasjuanpedro vacuolaratpasefromentamoebahistolyticamolecularcloningofthegeneencodingforthebsubunitandsubcellularlocalizationoftheprotein