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Biology 2120 recitation

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[C] The outer membrane of the nuclear envelope is continuous with the endoplasmic ... [C] DNA replication requires an RNA primer Fig. 19-11 ... – PowerPoint PPT presentation

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Title: Biology 2120 recitation


1
Biology 2120 recitation
  • (Date)

2
Todays schedule
  • Lecture review
  • Quiz
  • Review Quiz

3
  • Lecture 9- Nuclear structure and DNA replication
  • A The Big Picture 
  • A The nucleus contains and protects most of a
    eukaryotic cell's DNA
  • B The nuclear envelope is a double membrane
    structure
  • C The outer membrane of the nuclear envelope is
    continuous with the endoplasmic reticulum Fig.
    18-26
  • C Nuclear pore complexes regulate molecular
    traffic into and out of the nucleus Figs. 18-27,
    18-28, 18-29
  • B The interior of the nucleus is highly
    organized and contains many subcompartments Fig.
    18-32
  • C The nucleolus contains DNA that encodes
    ribosomal RNAs Fig. 18-33
  • C The nuclear matrix helps to organize
    chromosomes Fig. 18-31
  • C DNA replication occurs at sites called
    replication factories
  • C RNA polymerase complexes, and spliceosomes
    are distinct structures within the nucleus

4
A DNA replication is a complex, tightly
regulated process Fig. 19-13 B DNA polymerases
are enzymes that replicate DNA C DNA
polymerases add new deoxyribonucleotides to the
3 end of a DNA strand Fig. 19-7 C DNA
polymerases proofread their work Fig. 19-10A
DNA replication is a complex, tightly regulated
process Fig. 19-13 B DNA replication is
semi-discontinuous Fig. 19-9 C DNA replication
begins at sites on chromosomes called origins of
replication Fig. 19-5 C Specialized proteins
unwind and separate the two strands during
replication to form a replication fork Origin
Replication Complex, MiniChromosome Maintenance
proteins Fig. 19-6, 19-12, 19-14 C DNA
replication requires an RNA primer Fig. 19-11 C
DNA ligases join fragments of single-stranded
DNA C Replication of DNA at the end of
chromosomes requires additional steps Fig. 19-15,
19-16 B Cells have two main DNA repair
mechanisms Fig. 19-17 C Excision systems remove
one strand of damaged DNA and replace it Fig.
19-18 C Recombination systems repair
large-scale DNA damage
5
A Mitosis Separates Replicated Chromosomes B
Mitosis is divided into stages Fig. 19-20 B
Prophase prepares the cell for division Fig.
19-20. 19-25 B Chromosomes attach to the
mitotic spindle during prometaphase C
Kinetochores attach chromosomes to the mitotic
spindle Fig. 19-22 B Arrival of the chromosomes
at the spindle equator signals the beginning of
metaphase Fig. 19-26 B Separation of chromatids
at the metaphase plate occurs during anaphase C
The onset of anaphase requires dissolving the
connections between sister chromatids condensins
and cohesins C Anaphase is subdivided into two
phases, anaphase A and anaphase B Fig. 19-24,
19-27 B Telophase begins to reverse the
structural rearrangements that occurred in
prophase B Cytokinesis completes mitosis by
partitioning the cytoplasm to form two new
daughter cells Fig. 19-28 C Fragmentation of
nonnuclear organelles ensures their equal
distribution in the daughter cells
6
Macromolecular Transport into and out of the
Nucleus
Figure 18-29
7
PYROPHOSPHATE
Figure 19-7
8
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9
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10
Arrangement of Proteins at the Replication Fork
Figure 19-14
11
The Extension of Telomeres by Telomerase
Figure 19-16c
12
Figure 19-25
13
Figure 19-24
14
Figure 19-25 Microtubule Polarity in the Mitotic
Spindle
Figure 19-27a Mitotic Motors
15
Quiz Time!
16
Research article
  • Rationale
  • Cancer cells have extra copies of some
    advantageous genes, and these are in
    extrachromosomal structures called double minutes
    (pronounced my-noots)
  • Getting rid of double minutes will make cancer
    cells more sensitive to chemotherapy drugs by
    reducing the number of advantageous
    genes/proteins
  • http//en.wikipedia.org/wiki/Double_minute

17
Research strategy
  • Create a human colon cancer cell line that has
    easy-to-identify genes that are present in double
    minutes
  • Introduce three pieces of foreign DNA
  • a piece of bacterial DNA encoding multiple copies
    of a gene operator (lacO, a regulatory sequence)
    this sequence will end up in the double minutes
  • a bacterial gene encoding a protein that binds to
    lacO (lacR), fused to Green Fluorescent Protein
    (easy to see with fluorescence microscope)
  • a piece of DNA containing sequences necessary to
    create double minutes
  • The cells form lacO-containing double minutes
    that are bound by GFP-tagged lacR protein

18
Research strategy
  • Add hydroxurea to cells HU removes double
    minutes by introducing double-stranded breaks in
    DNA
  • Look for evidence of double stranded breaks by
    immunofluorescence microscopy use a primary
    antibody that binds to the phosphorylated form of
    a histone (histone H2AX)
  • DATA Green fluorescence shows presence of double
    minutes, phospho-H2AX (red), and position of all
    DNA (blue)

19
Exercise form groups
  • Translate the title
  • Write out the hypothesis
  • Identify three premises look in Figures 1, 2,
    and 3
  • Write out one logical argument containing at
    least two of your premises
  • Does this argument support or disprove their
    hypothesis?
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