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Transcript
BCH 4054 Spring 2001 Chapter 29 Lecture Notes
Slide 1
Chapter 29
DNA: Genetic Information,
Recombination, and Mutation
Slide 2
DNA as the Genetic Material
• Griffith Experiment on pneumococcal
transformation (Fig 29.1)
• Avery, MacLeod and McCarty showed the
principle was DNA
• Hershey-Chase experiment on
bacteriophage infection (Fig 29.3)
• DNA and coat protein labeled differently.
Slide 3
Recombination of DNA
• Mendel recognized how genes could
rearrange in different combinations, with
some genes being linked and sorting
together
• Explained by random sorting of chromosomes
• Some linkages weren’t complete, with some
rearrangement of pieces of chromosomes
Chapter 29, Page 1
Slide 4
Recombination in Meiosis
• Sister chromatids pair duing meiosis
• Chromosome ends can exchange in a
process called “crossing over”
• Occurs with equal probability along entire
chromosome
• Frequency of recombination measures
distance between genes, and is used for
mapping
Slide 5
Importance of Recombination
• Phenomenon seen in many different
situations
• Provides a means for nature to
“experiment”
• Probably important in evolution of new
combinations of genes and pieces of genes
• Also important in salvaging damaged genes
• Lets look at some specific examples
Slide 6
Recombination in Bacteria
• Lederberg-Tatum experiments on
rearrangement of genes between strains of
bacteria (Fig 29.4)
• Explanation comes from sexual
conjugation followed by genetic
recombination
• F factor is plasmid carrying genes for
conjugation (Fig 29.6)
Chapter 29, Page 2
Slide 7
Hfr stands for “high frequency of
recombination”
Recombination in Bacteria, con’t.
• F factor integration into bacterial chromosome
creases Hfr cells
• Integrated F factor plus part of chromosome is
transferred.
• Creates diploid condition for some genes.
• Recombinationexchanges portions of the diploid
genes.
• Can be used for mapping position of genes on
chromosome. (Fig 29.7)
Slide 8
Recombination in
Bacteriophage
• Two strains of bacterial viruses infecting a
bacterial cell can produce a diploid condition for
the viral genes.
• Recombination between viral genes can occur to
produce a heteroduplex DNA
• See Fig 29.10
• Messelson and Weigle showed by 13 C and 15N
labeling that recombinant phage contained DNA
from both “parents”
Slide 9
Classification of Recombination
Events
• General recombination
• Occurs between homologous DNA regions
• Site-specific recombination
• Insertion of bacterial virus genomes into
bacterial chromosomes at specific sites
• Transposition
• Insertion and removal of DNA
Chapter 29, Page 3
Slide
10
Mechanism of Homologous
Recombination
• Model proposed by Robin Holliday in 1964
• Duplex unwinding, strand invasion and
ligation to create a Holliday junction
• See Fig 29.11
• Resolution can produce either a “patch
recombinant” heteroduplex, or a “splice
recombinant heteroduplex”.
Slide
11
Enzymes in Recombination
• Bacterial recombination requires a number
of proteins
• First analyzed as mutations lacking in ability to
recombine, hence the proteins are referred to by
the genetic identification: recA, recB, etc.
• RecBCD initiates the process (Fig 29.12)
• RecA forms filament that binds to single
stranded DNA (Fig 29.13)
Slide
12
Enzymes in Recombination,
con’t.
• RecA-SSDNA complex binds to duplex DNA and
searches for homologous sequences
• RecA catalyzes “strand invasion” at homologous
sequence
• See Fig’s 29.14 and 29.15
• RuvA, RuvB, and RuvC bind to “Holliday
junction”, drive branch migration, and resolve the
junction into recombination products.
Chapter 29, Page 4
Slide
13
Other Recombination Phenomena
• Transposons—”jumping genes”
• First recognized in corn genetics by Barbara
McClintock
• Many variation now known. For example, bacterial
plasmids integrating at various places in bacterial
chromosome
• DNA rearrangement in Immunoglobulin genes
• Produces great diversity in IgG sequences.
• Skip the details
Slide
14
Molecular Nature of Mutations
• Point mutations
• Tautomer mistake
• Base analogue induced
• Chemical mutagens
• Insertions and Deletions
• Intercalating agents
• Transposon insertion
Slide
15
Point Mutations
• Transitions or Transversions
• Wrong tautomer at replication
• About one in 10 -10 per base pair
Transition: Purine replaced by
purine (A by G or G by A);
pyrimidine replaced by pyrimidine
(C by T or T by C)
Transversion: Purine replaced by
pyrimidine or pyrimidine replaced
by purine
• Conformation shift syn to anti
• Water mediated H bonding between
pyrimidines
• See Fig 29.24
Chapter 29, Page 5
Slide
16
Point Mutations, con’t.
• Base analog induced
• 5-bromouracil and 2 amino purine
• Fig 29.25 and 29.26
• Chemical mutagens
• Nitrous acid (oxidative deamination)
• Fig 29.28a
• Alkylating agents alter H-bonding
• Fig 29.28d
Slide
17
Insertions and Deletions
• Acridine orange and other aromatic
molecules
• Intercalation between bases causes added
or skipped bases during replication
• Transposons
• Insertion of a transposon can shift reading
frame
Slide
18
UV, X-ray, and Radiation
We’ll have more to say about these
in discussing DNA repair
mechanisms
• Not discussed in book at this point
• Causes DNA damage
• Example, UV can cause thymine dimers
• Can lead to mispairing
• Also induces an enzyme system for
repair of damage that is called “error
prone repair”
Chapter 29, Page 6
Slide
19
RNA as Genetic Material
• Most plant viruses, some animal and
bacterial viruses, use RNA as genetic
material
• Retroviruses make DNA from the
RNA, and the DNA can be
“recombined” into the genome of the
host
Slide
20
Transgenic animals
• Recombinant DNA technology now
allows for genetic manipulation
• Insertion of genes
• Ex. Is growth hormone gene in mice
• Destruction (“knock-out”) of genes
• Useful in determining the function of a gene
Slide
21
Prions
1997 Nobel Prize awarded to
Stanley Prusiner for discovery of
prions
• Protein infectious particle
• A seeming case of a protein causing a “genetic”
change
• Protein can exist in two conformational forms,
normal and “diseased” form
• Infection by “diseased” conformation can induce
conformational change in normal form
• See Fig and discussion, page 979
Chapter 29, Page 7