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Ch. 16 DNA

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Meselson-Stahl mid 1950's. DNA Replication details. Griffith: Transformation. Hershey / Chase ... How did they (Meselson-Stahl) prove this? FIG 16.10. KNOW: ... – PowerPoint PPT presentation

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Title: Ch. 16 DNA


1
Ch. 16DNA
  • DNA the Central Dogma, history, structure
  • Replication

2
History timeline, people and their
accomplishments
  • Mendel (heredity)
  • Thomas Hunt Morgan (flies, linkage)
  • Griffith (1928) transformation and mice
  • Avery and colleagues (1944)
  • proposed DNA as the transforming agent
  • Chargaff (late 40s-early 50s)
  • base pairing (AT CG)
  • Hershey-Chase (1952) DNA IS hereditary material
  • Watson and Crick (1953) (Franklin)
    chemical structure of DNA
  • Meselson-Stahl mid 1950s
  • DNA Replication details

3
Griffith
Transformation
4
Hershey / Chase (the hereditary material is not
a protein)
Radio-active P and S
5
Whose rule? A-T C-G
Purine? Pyrimidine?You have 6 billion pair in
every cell!
6
Hows it all fit?
  • DNA coiling Lets see it!

7
Chargaffs Rule
  • Purines (A, G, double rings) always pair with
    Pyrimidines (T, C, single rings)
  • A-T, C-G ( in RNA? ____)
  • Old AP test question if in a cell the DNA bases
    are 17 As then what are the s of the other
    bases?
  • CUT your PY or Pure Silver (Ag)

8
DNA Replication SEMICONSERVATIVE MODEL How did
they (Meselson-Stahl) prove this? FIG 16.10
9
KNOW Steps of ReplicationEnzymesLeading and
Lagging strands Okazaki FragmentsAnti-parallel
Video
10
Bubbles Replication forks, simultaneous
replication Eukaryotes - multiple origins of
replication Prokaryotes have one
Semi-conservative
This process is fueled bynucleoside
triphosphates
11
DNA is made from 5 to 3 and it is read from
3-5. The 3 end is the end which elongates
(grows) Why is this direction important to
consider in Replication?
12
What do the terms 5 and 3 mean?
13
Leading Lagging strands, made 5-3 Okazaki
fragments (are of the lagging strand)
ENZYMES helicase, DNA Polymerase, ligase
14
  • Enzymes
  • HelicaseSingle strand binding
    proteinsPrimase (RNA Primer)DNA
    PolymeraseLigase
  • Nuclease and DNA Polymerase (both are repair
    enzymes)

15
Lets see this in Action
  • Leading Strand (Nobelprize.org)
  • Lagging Strand (Nobelprize.org)
  • Overall (wiley)
  • Overall 3D view (wehi.edu.au or
    dnai.org) (Youtube has a music version)

16
Telomeres (Ch.16)Unfilled gap left at the ends
of the DNA strands due to the use of RNA
primersEventual shortening of DNA over
time Dolly, cancer, HeLa cells (telomerase
fig16.19)
17
Enzyme Telomerase extends the (3) long strand
so the 5 strand can finish. WOW! ? ? ? Where is
telomerase naturally found?
18
DNA from a single skin cell, if straightened out,
would be about six feet long but invisible. Half
a gram of DNA, uncoiled, would stretch to the
sun. Again, you couldn't see it.
http//www.pixar.com/featurefilms/nemo/images/inde
x_lwide.jpg
19
Story Time!! (Due Tuesday Nov. 6)
  • Select a figure, process, topic, or high level
    vocabulary word from chapter 16 or 17.
  • Your job is to make a poster of your selected
    topic.
  • The poster should be kid-friendly as to say an
    intelligent 8-10 year old would be able to
    understand it yet make sure that all information
    communicated is true to the text.
  • - Finally, you may not use English, do the best
    you can, ask friends, relatives, teachers, etc
    for help if necessary.
  • Potential topics include but are not limited to
    the following..
  • Experiments that identified DNA as the genetic
    material, DNA Structure, DNA Replication,
    Telomers and telomerase, Transcription,
    Modification of RNA, Translation, Mutations.

20
Ch.17 One gene/One polypeptide
21
Define transcription and translationCompare
Prokaryotic and Eukaryotic cellsvideo
22
  • (21 different AAs)
  • mRNA code
  • Ave. protein is 400AA long
  • Titin is 30,000AA long! (this is _____
    nucleotides?)

23
  • DNAtriplets
  • RNAcodons
  • 5 to 3
  • Pre-mRNA (primary transcript)

24
  • Promoter TATA Box
  • Transcription factors
  • RNA poly-merase
  • Transcription initiation complex
  • Movie

25
Finishing the pre-mRNA
Introns (intruding) spliced out Exons kept,
will be Expressed in the cell
26
  • snRNPs identify introns
  • Introns are cut out at a Spliceosome
  • Final mRNA has only genes that will be
    tran-scribed in cellno junk genes
  • video

27
  • Translation
  • The production of polypeptides
  • On a Ribosome
  • tRNA, transfer RNA carries in the amino acids to
    the ribosome (transfers the A.A)

Read 5 to 3
28
(No Transcript)
29
  • A P E
  • Aminoacyl-tRNA synthetase
  • Peptidyl tRNA binding site
  • Exit
  • Video
  • Movie

30
(No Transcript)
31
Termination of the translation
32
Translation of many polypeptide chains at once
33
The signal mechanism signal peptides
Free or bound ribosomes?
34
  • Coupled transcription and translation

35
One base difference out of 574 Amino acids (1722
bases)
36
The wrong protein
Nothing formed
37
(No Transcript)
38
  • Happy Homecoming (again!)
  • Have fun, be safe

39
(No Transcript)
40
Repairing mistakes
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