Cargando…

Amoebozoa Possess Lineage-Specific Globin Gene Repertoires Gained by Individual Horizontal Gene Transfers

The Amoebozoa represent a clade of unicellular amoeboid organisms that display a wide variety of lifestyles, including free-living and parasitic species. For example, the social amoeba Dictyostelium discoideum has the ability to aggregate into a multicellular fruiting body upon starvation, while the...

Descripción completa

Detalles Bibliográficos
Autores principales: Dröge, Jasmin, Buczek, Dorota, Suzuki, Yutaka, Makałowski, Wojciech
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4081604/
https://www.ncbi.nlm.nih.gov/pubmed/25013378
http://dx.doi.org/10.7150/ijbs.8327
_version_ 1782324130478030848
author Dröge, Jasmin
Buczek, Dorota
Suzuki, Yutaka
Makałowski, Wojciech
author_facet Dröge, Jasmin
Buczek, Dorota
Suzuki, Yutaka
Makałowski, Wojciech
author_sort Dröge, Jasmin
collection PubMed
description The Amoebozoa represent a clade of unicellular amoeboid organisms that display a wide variety of lifestyles, including free-living and parasitic species. For example, the social amoeba Dictyostelium discoideum has the ability to aggregate into a multicellular fruiting body upon starvation, while the pathogenic amoeba Entamoeba histolytica is a parasite of humans. Globins are small heme proteins that are present in almost all extant organisms. Although several genomes of amoebozoan species have been sequenced, little is known about the phyletic distribution of globin genes within this phylum. Only two flavohemoglobins (FHbs) of D. discoideum have been reported and characterized previously while the genomes of Entamoeba species are apparently devoid of globin genes. We investigated eleven amoebozoan species for the presence of globin genes by genomic and phylogenetic in silico analyses. Additional FHb genes were identified in the genomes of four social amoebas and the true slime mold Physarum polycephalum. Moreover, a single-domain globin (SDFgb) of Hartmannella vermiformis, as well as two truncated hemoglobins (trHbs) of Acanthamoeba castellanii were identified. Phylogenetic evidence suggests that these globin genes were independently acquired via horizontal gene transfer from some ancestral bacteria. Furthermore, the phylogenetic tree of amoebozoan FHbs indicates that they do not share a common ancestry and that a transfer of FHbs from bacteria to amoeba occurred multiple times.
format Online
Article
Text
id pubmed-4081604
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Ivyspring International Publisher
record_format MEDLINE/PubMed
spelling pubmed-40816042014-07-10 Amoebozoa Possess Lineage-Specific Globin Gene Repertoires Gained by Individual Horizontal Gene Transfers Dröge, Jasmin Buczek, Dorota Suzuki, Yutaka Makałowski, Wojciech Int J Biol Sci Research Paper The Amoebozoa represent a clade of unicellular amoeboid organisms that display a wide variety of lifestyles, including free-living and parasitic species. For example, the social amoeba Dictyostelium discoideum has the ability to aggregate into a multicellular fruiting body upon starvation, while the pathogenic amoeba Entamoeba histolytica is a parasite of humans. Globins are small heme proteins that are present in almost all extant organisms. Although several genomes of amoebozoan species have been sequenced, little is known about the phyletic distribution of globin genes within this phylum. Only two flavohemoglobins (FHbs) of D. discoideum have been reported and characterized previously while the genomes of Entamoeba species are apparently devoid of globin genes. We investigated eleven amoebozoan species for the presence of globin genes by genomic and phylogenetic in silico analyses. Additional FHb genes were identified in the genomes of four social amoebas and the true slime mold Physarum polycephalum. Moreover, a single-domain globin (SDFgb) of Hartmannella vermiformis, as well as two truncated hemoglobins (trHbs) of Acanthamoeba castellanii were identified. Phylogenetic evidence suggests that these globin genes were independently acquired via horizontal gene transfer from some ancestral bacteria. Furthermore, the phylogenetic tree of amoebozoan FHbs indicates that they do not share a common ancestry and that a transfer of FHbs from bacteria to amoeba occurred multiple times. Ivyspring International Publisher 2014-06-19 /pmc/articles/PMC4081604/ /pubmed/25013378 http://dx.doi.org/10.7150/ijbs.8327 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Research Paper
Dröge, Jasmin
Buczek, Dorota
Suzuki, Yutaka
Makałowski, Wojciech
Amoebozoa Possess Lineage-Specific Globin Gene Repertoires Gained by Individual Horizontal Gene Transfers
title Amoebozoa Possess Lineage-Specific Globin Gene Repertoires Gained by Individual Horizontal Gene Transfers
title_full Amoebozoa Possess Lineage-Specific Globin Gene Repertoires Gained by Individual Horizontal Gene Transfers
title_fullStr Amoebozoa Possess Lineage-Specific Globin Gene Repertoires Gained by Individual Horizontal Gene Transfers
title_full_unstemmed Amoebozoa Possess Lineage-Specific Globin Gene Repertoires Gained by Individual Horizontal Gene Transfers
title_short Amoebozoa Possess Lineage-Specific Globin Gene Repertoires Gained by Individual Horizontal Gene Transfers
title_sort amoebozoa possess lineage-specific globin gene repertoires gained by individual horizontal gene transfers
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4081604/
https://www.ncbi.nlm.nih.gov/pubmed/25013378
http://dx.doi.org/10.7150/ijbs.8327
work_keys_str_mv AT drogejasmin amoebozoapossesslineagespecificglobingenerepertoiresgainedbyindividualhorizontalgenetransfers
AT buczekdorota amoebozoapossesslineagespecificglobingenerepertoiresgainedbyindividualhorizontalgenetransfers
AT suzukiyutaka amoebozoapossesslineagespecificglobingenerepertoiresgainedbyindividualhorizontalgenetransfers
AT makałowskiwojciech amoebozoapossesslineagespecificglobingenerepertoiresgainedbyindividualhorizontalgenetransfers