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DNA Structure and Function

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Experiment with viruses showed that the genetic information was in DNA, not protein. ... dividing, the DNA strands are apart. A change in the DNA has no ... – PowerPoint PPT presentation

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Title: DNA Structure and Function


1
DNA Structure and Function
2
Griffith
  • Griffith showed some heredity material could move
    into live harmless bacteria and make a lethal
    strain

3
Griffiths Experiment
Mice injected with live cells of harmless strain
R.
Mice live. No live R cells in their blood.
Heat killed S strain, but releases the killer
genes that the R strain incorporated.
4
Virus
  • Basically only two parts
  • DNA inside
  • Protein Coat outside
  • Carries genetic material in which part?

5
genetic material
bacterial cell wall
plasma membrane
viral coat
sheath
base plate
tail fiber
cytoplasm
6
Hershey-Chase
  • Experiment with viruses showed that the genetic
    information was in DNA, not protein.

7
virus particle labeled with 35S
virus particle labeled with 32P
bacterial cell
Hershey and Chase showed DNA carries genetic
information
label inside cell
label outside cell
8
The Hershey-Chase experiment phages
9
Fig. 9.5a
10
Fig. 9.5bc
11
Fig. 9.6a
12
Fig. 9.6b
13
Watson and Crick
14
Rosalind Franklins X-ray Crystallography
15
DNA
  • Deoxyribonucleic Acid DNA
  • Made up of nucleotides
  • Nucleotides have three parts
  • Sugar
  • Phosphate group
  • Nitrogenous base
  • Sugar-phosphates make the DNA back bone that is
    covalently bonded

16
adenine (A) base with a double-ring structure
guanine (G) base with a double-ring structure
phosphate group
sugar (ribose)
thymine (T) base with a single-ring structure
cytosine (C) base with a single-ring structure
17
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18
Nitrogenous bases
  • Four different nitrogenous bases
  • Have one or two rings
  • Form 2 or 3 hydrogen bonds
  • Bases can only pair one way
  • A-T
  • C-G
  • The sequence of nitrogenous bases carries the
    genetic information

19
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20
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21
or
or
one base pair
22
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23
DNA Structure
  • Forms a double helix
  • Two complementary strands held together by
    hydrogen bonds

24
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25
Fig. 9.5a
26
Fig. 9.5bc
27
Meselson- Stahl
  • Heavier isotope falls to bottom of flask
  • Timed to capture each new generation of bacteria
  • Shows radiation diluted by half each generation,
    didnt stay together.
  • Showed semi-conservative replication

28
Fig. 9.6a
29
Fig. 9.6b
30
DNA replication
  • Semiconservative one old and one new strand in
    each daughter molecule
  • Each original strand acts as a template to form a
    new complementary strand

31
DNA Replication
32
Three enzymes
  • Helicase unwinds DNA
  • DNA Polymerase adds new nucleotides off the
    template
  • Works in one direction only
  • One side makes separate fragments
  • Ligase seals up the fragments
  • Proofreads DNA, fixes mistakes

33
Three Enzymes
34
Helicase Unwinds helix
Polymerase adds nucleotides Ligase Seals
fragments
35
continuous assembly on one strand
discontinuous assembly on other strand
newly forming DNA strand
one parent DNA strand
36
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37
DNA Replication
  • Starts in several spots
  • Pretty rapid process.
  • Very accurate, few errors

38
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39
Chromosomes
  • DNA Replication forms the sister chromatids just
    before Mitosis or meiosis

40
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41
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42
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43
Fig. 9.10
44
Mutations
  • When cells are dividing, the DNA strands are
    apart.
  • A change in the DNA has no complementary strand
    to fix it.
  • These changes get incorporated into new strand
  • They are passed on in all the new divisions.
  • Dividing cells collect mutations, can become
    cancerous
  • Skin, lungs, liver

45
Transcription
Translation
protein
DNA
RNA
nucleus
cytoplasm
  • DNA to RNA
  • Copies only select genes, not all at once
  • Each gene is on only one strand of DNA, not the
    complimentary strand
  • RNA to Protein
  • In cytoplasm
  • Uses ribosome
  • Can make multiple copies
  • Relatively short lived

46
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47
RNA
  • Always a single strand
  • Use Ribose as a sugar
  • Uses Uracil
  • and Adenine, Cytosine, Guanine
  • mRNA carries genetic info. From nucleus to
    cytoplasm
  • tRNA carries amino acids to ribosome, links the
    genetic code
  • rRNA makes up most of ribosome

48
URACIL (U) base with a single-ring structure
phosphate group
sugar (ribose)
49
DNA ? RNA ? protein
50
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51
Chromosome during transcription
52
Transcription
  • At Initiation RNA polymerase binds start of gene
    and uncoils DNA.
  • At Elongation RNA polymerase moves along the gene
    briefly binding nucleotides to DNA (only about 10
    nucleotides at a time), as the RNA nucleotides
    join together in a making a single complimentary
    strand
  • At Termination the mRNA moves out of nucleus,
    detaches and DNA recoils

53
RNA polymerase
DNA
54
transcribed DNA winds up again
DNA to be transcribed unwinds
newly forming RNA transcript
DNA template at the assembly site
55
Fig. 9.11
56
growing RNA transcript
3
5
3
5
direction of transcription
5
3
57
m RNA modification
  • new pre-mRNA includes extra nucleotides called
    introns must be cut out.
  • The exons remain to go on to the cytoplasm
    carrying the information for the protein
    synthesis.

58
Fig. 9.17
59
Translation
  • mRNA code directs sequence of amino acids in
    protein.
  • Uses ribosomes to assemble proteins
  • At Initiation a tRNA attaches to the mRNA and the
    ribosome subunits combine.
  • Start codon is AUG
  • At Elongation the ribosome moves down the mRNA
    assembling the amino acids
  • Only 6 nucleotides at at time
  • Each triplet codes for one amino acid
  • At Termination a stop codon causes the protein
    chain and the ribosome and mRNA to separate from
    each other.

60
base sequence of gene region
mRNA
amino acids
arginine
glycine
tyrosine
tyrosine
tryptophan
61
Genetic Code uses triplets of Nucleotides to
place amino acids in sequence
62
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63
Fig. 9.13
64
Fig. 9.14
65
Fig. 9.15
66
Fig. 9.16
67
Mutations
  • a Point Mutation is a single base pair nucleotide
    substitution
  • May cause a single amino acid change, or none
  • Insertions and Deletions (adding or removing
    nucleotides) reset the reading frame and change
    subsequent amino acids.
  • Missense makes a new amino acid chains
  • Nonsense adds stop codons and synthesis cuts off.

68
Fig. 9.23
69
original base triplet in a DNA strand
a base substitution within the triplet (red)
During replication, proofreading enzymes make a
substitution
possible outcomes
or
original, unmutated sequence
a gene mutation
70
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71
Mutations
72
mRNA
parental DNA
amino acids
arginine
glycine
tyrosine
tryptophan
asparagine
altered mRNA
DNA with base insertion
altered amino- acid sequence
arginine
glycine
leucine
glutamate
leucine
73
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74
Polyribosomes make multiple copies of the
protein at the same time on the same mRNA
75
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76
Fig. 9.18
77
Transcription
mRNA
rRNA
tRNA
protein subunits
mRNA transcripts
ribosomal subunits
tRNA
Translation
amino acids, tRNAs, ribosomal subunits
Protein
78
From DNA to protein
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