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Composite genome map and recombination parameters derived from three archetypal lineages of Toxoplasma gondii

Toxoplasma gondii is a highly successful protozoan parasite in the phylum Apicomplexa, which contains numerous animal and human pathogens. T.gondii is amenable to cellular, biochemical, molecular and genetic studies, making it a model for the biology of this important group of parasites. To facilita...

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Autores principales: Khan, Asis, Taylor, Sonya, Su, Chunlei, Mackey, Aaron J., Boyle, Jon, Cole, Robert, Glover, Darius, Tang, Keliang, Paulsen, Ian T., Berriman, Matt, Boothroyd, John C., Pfefferkorn, Elmer R., Dubey, J. P., Ajioka, James W., Roos, David S., Wootton, John C., Sibley, L. David
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1137028/
https://www.ncbi.nlm.nih.gov/pubmed/15911631
http://dx.doi.org/10.1093/nar/gki604
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author Khan, Asis
Taylor, Sonya
Su, Chunlei
Mackey, Aaron J.
Boyle, Jon
Cole, Robert
Glover, Darius
Tang, Keliang
Paulsen, Ian T.
Berriman, Matt
Boothroyd, John C.
Pfefferkorn, Elmer R.
Dubey, J. P.
Ajioka, James W.
Roos, David S.
Wootton, John C.
Sibley, L. David
author_facet Khan, Asis
Taylor, Sonya
Su, Chunlei
Mackey, Aaron J.
Boyle, Jon
Cole, Robert
Glover, Darius
Tang, Keliang
Paulsen, Ian T.
Berriman, Matt
Boothroyd, John C.
Pfefferkorn, Elmer R.
Dubey, J. P.
Ajioka, James W.
Roos, David S.
Wootton, John C.
Sibley, L. David
author_sort Khan, Asis
collection PubMed
description Toxoplasma gondii is a highly successful protozoan parasite in the phylum Apicomplexa, which contains numerous animal and human pathogens. T.gondii is amenable to cellular, biochemical, molecular and genetic studies, making it a model for the biology of this important group of parasites. To facilitate forward genetic analysis, we have developed a high-resolution genetic linkage map for T.gondii. The genetic map was used to assemble the scaffolds from a 10X shotgun whole genome sequence, thus defining 14 chromosomes with markers spaced at ∼300 kb intervals across the genome. Fourteen chromosomes were identified comprising a total genetic size of ∼592 cM and an average map unit of ∼104 kb/cM. Analysis of the genetic parameters in T.gondii revealed a high frequency of closely adjacent, apparent double crossover events that may represent gene conversions. In addition, we detected large regions of genetic homogeneity among the archetypal clonal lineages, reflecting the relatively few genetic outbreeding events that have occurred since their recent origin. Despite these unusual features, linkage analysis proved to be effective in mapping the loci determining several drug resistances. The resulting genome map provides a framework for analysis of complex traits such as virulence and transmission, and for comparative population genetic studies.
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spelling pubmed-11370282005-05-23 Composite genome map and recombination parameters derived from three archetypal lineages of Toxoplasma gondii Khan, Asis Taylor, Sonya Su, Chunlei Mackey, Aaron J. Boyle, Jon Cole, Robert Glover, Darius Tang, Keliang Paulsen, Ian T. Berriman, Matt Boothroyd, John C. Pfefferkorn, Elmer R. Dubey, J. P. Ajioka, James W. Roos, David S. Wootton, John C. Sibley, L. David Nucleic Acids Res Article Toxoplasma gondii is a highly successful protozoan parasite in the phylum Apicomplexa, which contains numerous animal and human pathogens. T.gondii is amenable to cellular, biochemical, molecular and genetic studies, making it a model for the biology of this important group of parasites. To facilitate forward genetic analysis, we have developed a high-resolution genetic linkage map for T.gondii. The genetic map was used to assemble the scaffolds from a 10X shotgun whole genome sequence, thus defining 14 chromosomes with markers spaced at ∼300 kb intervals across the genome. Fourteen chromosomes were identified comprising a total genetic size of ∼592 cM and an average map unit of ∼104 kb/cM. Analysis of the genetic parameters in T.gondii revealed a high frequency of closely adjacent, apparent double crossover events that may represent gene conversions. In addition, we detected large regions of genetic homogeneity among the archetypal clonal lineages, reflecting the relatively few genetic outbreeding events that have occurred since their recent origin. Despite these unusual features, linkage analysis proved to be effective in mapping the loci determining several drug resistances. The resulting genome map provides a framework for analysis of complex traits such as virulence and transmission, and for comparative population genetic studies. Oxford University Press 2005 2005-05-23 /pmc/articles/PMC1137028/ /pubmed/15911631 http://dx.doi.org/10.1093/nar/gki604 Text en © The Author 2005. Published by Oxford University Press. All rights reserved
spellingShingle Article
Khan, Asis
Taylor, Sonya
Su, Chunlei
Mackey, Aaron J.
Boyle, Jon
Cole, Robert
Glover, Darius
Tang, Keliang
Paulsen, Ian T.
Berriman, Matt
Boothroyd, John C.
Pfefferkorn, Elmer R.
Dubey, J. P.
Ajioka, James W.
Roos, David S.
Wootton, John C.
Sibley, L. David
Composite genome map and recombination parameters derived from three archetypal lineages of Toxoplasma gondii
title Composite genome map and recombination parameters derived from three archetypal lineages of Toxoplasma gondii
title_full Composite genome map and recombination parameters derived from three archetypal lineages of Toxoplasma gondii
title_fullStr Composite genome map and recombination parameters derived from three archetypal lineages of Toxoplasma gondii
title_full_unstemmed Composite genome map and recombination parameters derived from three archetypal lineages of Toxoplasma gondii
title_short Composite genome map and recombination parameters derived from three archetypal lineages of Toxoplasma gondii
title_sort composite genome map and recombination parameters derived from three archetypal lineages of toxoplasma gondii
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1137028/
https://www.ncbi.nlm.nih.gov/pubmed/15911631
http://dx.doi.org/10.1093/nar/gki604
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