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Phage Infections

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Title: Phage Infections


1
Phage Infections
Single Phage Infection uniform plaque morphology.
2
Phage Particles Can Recombine
r small plaque
r- large plaque
h clear plaque
h- turbid plaque
3
What is a Gene?
  • Bead Theory (1950s),
  • The gene was viewed as a fundamental unit of
    structure, indivisible by crossing over.
  • The gene was viewed as the fundamental unit of
    change.
  • The gene is the fundamental unit of function?

4
Genetic Fine Structure
  • Seymore Benzer
  • Demonstrated that a gene can be defined as a unit
    of function, a gene can be subdivided into a
    linear array of sites that are mutable and that
    can be recombined.
  • Paved the way for the understanding that the
    smallest units of mutation and recombination are
    single nucleotide pairs.

5
rII
  • A mutant T4 phage was known to produce larger,
    ragged plaques
  • this mutation was mapped to two genetic loci on
    the phage DNA molecule, rI and rII,
  • rII mutants have an altered host range than
    wild-type T4.

6
rII Host Range
7
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8
Mutation and Effect
  • Base substitutions (point mutations),
  • a change in a codon produces missense mutations,
  • different amino acids may change the function of
    the translated protein.
  • Deletions and insertions can cause frameshifts,
    usually resulting in missense and premature stop
    codons.

9
Intergenic Recombination
Frequency of recombination indicates map didtance.
10
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11
Why Stop There?
  • Deletion Mapping partial deletions in genes can
    be mapped in just the same way as other
    mutations
  • In fact, the site of the deletion can be
    determined by defining which previously mapped
    mutations fail to to recombine into a wild-type
    gene.

Please Study, and master A moment to Think, pp.
314
12
Deletion Mapping
13
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14
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15
What Did We Learn?
  • Mutations can exist within genes,
  • Genetic Exchange can take place within a gene,
  • Mutations are not produced at all locations in a
    gene,
  • and are found at higher frequencies at certain
    locations.
  • mutation hotspots correspond to key codons,
    hence key amino acids?
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