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Toxoplasma gondii sequesters centromeres to a specific nuclear region throughout the cell cycle
by
Gissot, Mathieu
, Croken, Matthew M
, Brooks, Carrie F
, Francia, Maria E
, Striepen, Boris
, Kim, Kami
in
Antibodies
/ Apicomplexa
/ Biological Sciences
/ Cell cycle
/ Cell Cycle - drug effects
/ Cell division
/ Centromere - drug effects
/ Centromere - metabolism
/ Centromeres
/ chromatin
/ Chromatin Immunoprecipitation
/ Chromosome Breakage - drug effects
/ Chromosomes
/ Cryptosporidiosis
/ DNA
/ Etoposide - pharmacology
/ Eukaryotes
/ Fluorescent Antibody Technique
/ genetically modified organisms
/ genome
/ Genomes
/ Genomics
/ Histones
/ Histones - metabolism
/ human diseases
/ Humans
/ hybridization
/ Lysine - metabolism
/ Malaria
/ Methylation - drug effects
/ microarray technology
/ Mitosis
/ Mitosis - drug effects
/ mitotic spindle apparatus
/ niches
/ nuclear membrane
/ Oligonucleotide Array Sequence Analysis
/ Parasites
/ Parasitic protozoa
/ precipitin tests
/ progeny
/ Reproducibility of Results
/ Toxoplasma - cytology
/ Toxoplasma - drug effects
/ Toxoplasma - metabolism
/ Toxoplasma gondii
/ Toxoplasmosis
/ Vector-borne diseases
2011
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Toxoplasma gondii sequesters centromeres to a specific nuclear region throughout the cell cycle
by
Gissot, Mathieu
, Croken, Matthew M
, Brooks, Carrie F
, Francia, Maria E
, Striepen, Boris
, Kim, Kami
in
Antibodies
/ Apicomplexa
/ Biological Sciences
/ Cell cycle
/ Cell Cycle - drug effects
/ Cell division
/ Centromere - drug effects
/ Centromere - metabolism
/ Centromeres
/ chromatin
/ Chromatin Immunoprecipitation
/ Chromosome Breakage - drug effects
/ Chromosomes
/ Cryptosporidiosis
/ DNA
/ Etoposide - pharmacology
/ Eukaryotes
/ Fluorescent Antibody Technique
/ genetically modified organisms
/ genome
/ Genomes
/ Genomics
/ Histones
/ Histones - metabolism
/ human diseases
/ Humans
/ hybridization
/ Lysine - metabolism
/ Malaria
/ Methylation - drug effects
/ microarray technology
/ Mitosis
/ Mitosis - drug effects
/ mitotic spindle apparatus
/ niches
/ nuclear membrane
/ Oligonucleotide Array Sequence Analysis
/ Parasites
/ Parasitic protozoa
/ precipitin tests
/ progeny
/ Reproducibility of Results
/ Toxoplasma - cytology
/ Toxoplasma - drug effects
/ Toxoplasma - metabolism
/ Toxoplasma gondii
/ Toxoplasmosis
/ Vector-borne diseases
2011
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Toxoplasma gondii sequesters centromeres to a specific nuclear region throughout the cell cycle
by
Gissot, Mathieu
, Croken, Matthew M
, Brooks, Carrie F
, Francia, Maria E
, Striepen, Boris
, Kim, Kami
in
Antibodies
/ Apicomplexa
/ Biological Sciences
/ Cell cycle
/ Cell Cycle - drug effects
/ Cell division
/ Centromere - drug effects
/ Centromere - metabolism
/ Centromeres
/ chromatin
/ Chromatin Immunoprecipitation
/ Chromosome Breakage - drug effects
/ Chromosomes
/ Cryptosporidiosis
/ DNA
/ Etoposide - pharmacology
/ Eukaryotes
/ Fluorescent Antibody Technique
/ genetically modified organisms
/ genome
/ Genomes
/ Genomics
/ Histones
/ Histones - metabolism
/ human diseases
/ Humans
/ hybridization
/ Lysine - metabolism
/ Malaria
/ Methylation - drug effects
/ microarray technology
/ Mitosis
/ Mitosis - drug effects
/ mitotic spindle apparatus
/ niches
/ nuclear membrane
/ Oligonucleotide Array Sequence Analysis
/ Parasites
/ Parasitic protozoa
/ precipitin tests
/ progeny
/ Reproducibility of Results
/ Toxoplasma - cytology
/ Toxoplasma - drug effects
/ Toxoplasma - metabolism
/ Toxoplasma gondii
/ Toxoplasmosis
/ Vector-borne diseases
2011
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Toxoplasma gondii sequesters centromeres to a specific nuclear region throughout the cell cycle
Journal Article
Toxoplasma gondii sequesters centromeres to a specific nuclear region throughout the cell cycle
2011
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Overview
Members of the eukaryotic phylum Apicomplexa are the cause of important human diseases including malaria, toxoplasmosis, and cryptosporidiosis. These obligate intracellular parasites produce new invasive stages through a complex budding process. The budding cycle is remarkably flexible and can produce varied numbers of progeny to adapt to different host-cell niches. How this complex process is coordinated remains poorly understood. Using Toxoplasma gondii as a genetic model, we show that a key element to this coordination is the centrocone, a unique elaboration of the nuclear envelope that houses the mitotic spindle. Exploiting transgenic parasite lines expressing epitope-tagged centromeric H3 variant CenH3, we identify the centromeres of T. gondii chromosomes by hybridization of chromatin immunoprecipitations to genome-wide microarrays (ChIP-chip). We demonstrate that centromere attachment to the centrocone persists throughout the parasite cell cycle and that centromeres localize to a single apical region within the nucleus. Centromere sequestration provides a mechanism for the organization of the Toxoplasma nucleus and the maintenance of genome integrity.
Publisher
National Academy of Sciences,National Acad Sciences
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