Genome structures. Table 7.2 Genomes 3 (© Garland Science 2007)

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  • Genome structures
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  • Table 7.2 Genomes 3 ( Garland Science 2007)
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  • Fritillaria assyriaca
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  • Figure 7.20 Genomes 3 ( Garland Science 2007) A processed pseudogene
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  • Figure 7.21 Genomes 3 ( Garland Science 2007)
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  • Repetitive DNA in genomes Mostly DNA and RNA transposons Satellite DNA (micro-, mini-, satellites)
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  • Figure 7.24 Genomes 3 ( Garland Science 2007) Microsatellite analysis (24 samples)
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  • Figure 7.18 Genomes 3 ( Garland Science 2007) Relationship between the human gene catalog and the catalogs of other organisms
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  • Chromatin organization
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  • General features of eukaryotic chromosomes Origin of replication
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  • Centromeres are necessary for correct segregation of chromosomes to daughter cells in cell division Centromeres associate with proteins to form kinetochores, i.e. attachment sites for microtubules
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  • Centromeres vary in size. Most consist of tandem repeats.
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  • General features of eukaryotic chromosomes Origin of replication
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  • Telomeres consist of tandemly repeated DNA (minisatellites) at the ends of chromosomes. They maintain the ends of linear chromosomes. 5-TTAGGG-3 is the repeat unit in humans.
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  • Chromatin organization is not fixed Cell cycle
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  • Chromatin organization is not fixed
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  • Cohesin- and condensin protein complexes induce formation of M phase chromosomes.
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  • Chromatin organization is not fixed
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  • Proteolysis of cohesins allows segregation of sister chromatids. Proteolysis of condensins leads to interphase chromosomes.
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  • Mitosis Meiosis
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  • Chromatin organization is not fixed Interphase M-phase
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  • General organization of interphase chromatin in the nucleus
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  • Nucleosomes
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  • Histones are the core proteins of nucleosomes
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  • Histones are the core proteins of nucleosomes
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  • Histones are the core proteins of nucleosomes
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  • Histones are the core proteins of nucleosomes
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  • Assembly of nucleosomes is promoted by histone chaperones
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  • Assembly of nucleosomes is promoted by histone chaperones
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  • Histone H1 is a linker histone
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  • Structural changes in nucleosome positioning in the presence of linker histone H1 no H1 + H1
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  • General organization of interphase chromatin in the nucleus
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  • Possible organization of the 30 nm fiber
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  • Histone core modifications: CENP-A can replace histone H3 in centromeres. H2A and H2B variants are found in histone cores.
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  • General organization of interphase chromatin in the nucleus
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  • Nucleosome remodeling complexes alter the position of nucleosomes
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  • Nucleosome remodeling complexes alter the position of nucleosomes
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  • Histone tail modifications influence chromatin structure
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  • Histone tail modifications alter chromatin structure
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  • Histone modifying protein complexes
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  • Histone tail modifications cause changes in chromatin structure loosetight
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  • Histone tail modifications create binding sites for protein complexes that alter the structure of chromatin
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  • DNA methylation alters chromatin structure
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  • Genomic imprinting