32
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Identification of Four Entamoeba histolytica Organellar DNA Polymerases of the Family B and Cellular Localization of the Ehodp1 Gene and EhODP1 Protein

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          We report the identification of a family of four active genes ( Ehodp1, Ehodp2, Ehodp3, and Ehodp4) encoding putative DNA polymerases in Entamoeba histolytica, the protozoan parasite responsible of human amoebiasis. The four Ehodp genes show similarity to DNA polymerases encoded in fungi and plant mitochondrial plasmids. EhODP polypeptides conserve the 3′-5′ exonuclease II and 5′-3′ polymerization domains, and they have the I, II, and III conserved boxes that characterize them as DNA polymerases of family B. Furthermore, we found in EhODP polymerases two novel A and B boxes, present also in DNA polymerases encoded in fungi mitochondrial plasmids. By in situ PCR, Ehodp1 gene was located in nuclei and in DNA-containing cytoplasmic structures. Additionally, using polyclonal antibodies against a recombinant rEhODP1-168 polypeptide, and confocal microscopy, EhODP1 was located in cytoplasmic DNA-containing structures.

          Related collections

          Most cited references49

          • Record: found
          • Abstract: found
          • Article: not found

          The genome of the protist parasite Entamoeba histolytica.

          Entamoeba histolytica is an intestinal parasite and the causative agent of amoebiasis, which is a significant source of morbidity and mortality in developing countries. Here we present the genome of E. histolytica, which reveals a variety of metabolic adaptations shared with two other amitochondrial protist pathogens: Giardia lamblia and Trichomonas vaginalis. These adaptations include reduction or elimination of most mitochondrial metabolic pathways and the use of oxidative stress enzymes generally associated with anaerobic prokaryotes. Phylogenomic analysis identifies evidence for lateral gene transfer of bacterial genes into the E. histolytica genome, the effects of which centre on expanding aspects of E. histolytica's metabolic repertoire. The presence of these genes and the potential for novel metabolic pathways in E. histolytica may allow for the development of new chemotherapeutic agents. The genome encodes a large number of novel receptor kinases and contains expansions of a variety of gene families, including those associated with virulence. Additional genome features include an abundance of tandemly repeated transfer-RNA-containing arrays, which may have a structural function in the genome. Analysis of the genome provides new insights into the workings and genome evolution of a major human pathogen.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            A new medium for the axenic cultivation of Entamoeba histolytica and other Entamoeba.

              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              A new medium for the axenic cultivation of Entamoeba histolytica and other Entamoeba

                Bookmark

                Author and article information

                Journal
                J Biomed Biotechnol
                JBB
                Journal of Biomedicine and Biotechnology
                Hindawi Publishing Corporation
                1110-7243
                1110-7251
                2010
                15 March 2010
                : 2010
                : 734898
                Affiliations
                1Posgrado en Ciencias Genómicas, Universidad Autónoma de la Ciudad de México, San Lorenzo 290, Col. Del Valle, CP 03100 México, DF, Mexico
                2Departmento de Biología Celular, Cinvestav-IPN, Av. IPN 2508, Col. Zacatenco, CP 07360 México, DF, Mexico
                3Departmento de Infectómica y Patogénesis Molecular, Cinvestav-IPN, Av. IPN 2508, Col. Zacatenco, CP 07360 México, DF, Mexico
                Author notes

                Academic Editor: Isaac K. O. Cann

                Article
                10.1155/2010/734898
                2840583
                20300437
                939304bb-2fa0-427d-8244-a0d7daf05465
                Copyright © 2010 María Esther Herrera-Aguirre et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 18 August 2009
                : 15 December 2009
                Categories
                Research Article

                Molecular medicine
                Molecular medicine

                Comments

                Comment on this article