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DNA structure and replication

Ifeoma Ezepue Fundamentals of Medicine University Inglés 3,5Valoración media 3,5 de 5 (2 valoraciones) 24 fichas

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  1. 1Why is DNA important?molecular basis for inheritance
    contains the code for all other cellular molecules
    its complementary structure allows it to be replicated and the code to be read
    variations in DNA sequence lead to phenotypic differences and susceptibility to disease
    defects in DNA replication and repair lead to many diseases
  2. 2What is a DNA nucleotide made out of?phosphate
    deoxyribose sugar
    organic nitrogenous base (GCAT)
  3. 3What can be said about the strands of DNA?double stranded DNA
    strands in antiparallel directions linked through hydrogen bonding
    A and T = 2 H bonds
    C and G = 3 H bonds
    A and G = 2 rings, purines
    T and C = 3 rings, pyrimidines
  4. 4What is the 5' end?free phosphate group at the 5' position on the sugar backbone
  5. 5What is the 3' end?unlinked OH group at 3' position on sugar
  6. 6Explain the compaction of DNADNA exists as double helix
    wraps around histones
    to form nucleosomes
    undergoes further folding to form 30nm chromatin fibre
    compacted further to form chromosome
  7. 7Describe the differences in compaction at interphase and metaphaseeach cell has 2m of DNA
    1,000x compaction at interphase
    10,000x compaction at metaphase
  8. 8What is the role of linker histones?histone H1
    keeps DNA wrapped around the histones in place by binding nucleosome at exit and entry sites
    binds to linker DNA region between nucleosomes, helping stabilize the zig-zagged 30nm chromatin fibre
  9. 9Why are histones abundant in the nucleus?form the framework around which DNA is wrapped
  10. 10What are core histones?four different types
    H2A H2B H3 H4
    these all exist as dimers
    form octameric nucleosome core
    which DNA strands wrap around twice
  11. 11With chromosomes in interphase nucleus what do you see?you don't see separate chromosomes but rather chromosome families
  12. 12What is the difference between the sense and anti-sense strand?sense - runs from 5' to 3'
    antisense - runs from 3' to 5'
  13. 13What is the difference between the lagging and leading strand?lagging - synthesized discontinuously
    leading - synthesized continually
  14. 14Explain the process of DNA replication in terms of leading and lagging strandsreplication starts at the point of origin
    here DNA polymerase moves in opposite directions
    continuous synthesis if DNA polymerase is moving in 5' to 3' direction (in terms of new strand) - leading strand
    if polymerase is moving in the 3' to 5' direction simple replication not possible as no free OH 3' end for polymerase to bind
    replication needs to happen in chunks thus forming okazaki fragments that are then fused together by DNA ligase - lagging strand
  15. 15Explain the role of DNA topoisomerasesany protein that propels itself alone along a DNA strand of a double helix e.g. helicase tends to generate superhelical tension
    DNA topoisomerase enzymes rapidly remove this tension
    prevents DNA supercoiling
  16. 16What targets topoisomerases? What is the result of this?quinolones
    this leads to supercoiling of DNA
    so double strand breaks
  17. 17Some antibiotics interfere with DNA replication in bacteria. Give some examplesfluoroquinolones e.g. gemifloxacin target topoisomerases
    in aerobic gram negative and positive species
    trimethoprim targets nucleotide synthesis in aerobic gram negative and positive species
  18. 18There are three ways to repair single strand defects. Explain base excision repaireach DNA glycosylases can recognise a specific type of altered base in DNA and catalyse its hydrolytic removal
    flipping out of altered nucleotide base from helix
    DNA glycosylase probes all faces of base for damage
    once an enzyme finds damaged base it recognises it and removes base from sugar
    sugar phosphate with missing base cut out by the sequential action of AP endonucleases and phosphodiesterase
    DNA polymerase adds new nucleotide
    DNA ligase seals nick
  19. 19There are three ways to repair single strand defects. Explain nucleotide excision repairmultienzyme complex recognises pyrimidine dimer
    one cut is made on each side of lesion
    DNA helicase removes entire portion of damaged strand
    leaves a gap of 12 nucleotides
    gap in DNA helix repaired by DNA polymerase and DNA ligase
  20. 20What is a pyrimidine dimer and what is it caused by?pyrimidines become chemically bonded together
    e.g. T-T, C-T, C-C
    caused by sunlight
  21. 21What is the major concern with double strand breaks?means no intact template strand to enable accurate repair
    if not repaired leads to breakdown of chromosomes into smaller fragments and loss of genes when the cell divides
  22. 22Double strand breaks can be joined by end-joining. Explain how non-homologous end-joining worksbroken ends brought together and joined by DNA ligation
    with a loss of nucleotides at sight of joining due to degradation from ends
    common in mammalian somatic cells
    although there's a change in DNA sequence alright for chromosomes as little of genome is essential for life
  23. 23Double strand breaks can be joined by end-joining. Explain how homologous end-joining worksoccurs in newly replicated DNA
    uses sister chromatid as template
    only happens in S and G2 phases
    (when SC available to serve as templates)
    the copying process involves homologous recombination
    a complete sequence restored by copying second chromosome
  24. 24Draw a table depicting some examples of inherited DNA repair defects. Include name, phenotype and affected processesBRCA2
    breast and ovarian cancer
    repair by homologous recombination
    MutS, MutL
    colon cancer
    mismatch repair
    Xeroderma pigmentosum (XP)
    skin cancer, cellular UV sensitivity, neurological abnormalities
    nucleotide excision repair

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Descripción
University (Molecular Biology and Genetics) Fundamentals of Medicine Fichas sobre DNA structure and replication, creado por Ifeoma Ezepue el 05/11/2015.
Creado por
Ifeoma Ezepue
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Valoración media 3,5 de 5 (2 valoraciones)

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