Title: The nature of mutation
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2The nature of mutation
- Change in DNA sequence
- Genetic code
- 64 codon possibilities
- 20 amino acids stop
- Redundancy, mostly at 3rd position
- Substitution
- Replace 1 nucleotide with another
- Synonymous (silent) or non-synonymous
3The nature of mutation
- Non-synonymous substitution causes change in
protein shape or function - Synonymous substitution is neutral
4The nature of mutation
- Insertions deletions
- Addition or subtraction of 1 or more nucleotides
in a sequence - Indel
- Insertions separating coding regions (exons) are
introns
5The nature of mutation
- Repetitive DNA
- Enough DNA in mammalian genomes for 300,000 genes
- Human Genome Project estimates between
25,000-30,000 genes - Most DNA is non-coding
- Most DNA is repetitive
- DNA-DNA hybridization
6The nature of mutation
- Highly repetitive DNA
- VNTR (variable number tandem repeat)
- Microsatellites
- One repeat unit (2-4 nucleotides) repeated
multiple times within a sequence - Alleles defined by length differences
- Synonyms
- Short tandem repeats (STRs)
- Simple sequence repeats (SSRs)
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8Allelic Variation at a Microsatellite Locus
GCCATGACACACACAGTAACGT
Allele A
Allele B
GCCATGACACACACACACACACACAGTAACGT
9Polymorphism at Microsatellite Loci
10Measures of Genetic Diversity
- Terms
- Locus portion of DNA (plural loci)
- Not always a gene
- Allele form that a locus can take Mendelian
- Subjective depending on resolution of measurement
- Nucleotide state difference (sequencing)
- Length difference (microsatellite)
- Functional difference (ABO blood group)
- Electrophoretic difference (allozyme)
AGGCGTTCGCTTATGATAA AGGCGTACGCTTATGATAA
AGGCGTTCACACACACACGCTTATGATAA AGGCGTTCACACACACA
CACGCTTATGATAA
11S
M
F
Direction of travel
12Measures of diversity
- Diploid genomes
- Allelic diversity (A)
- Mean number of alleles per locus
- Heterozygosity (H)
- Sum of proportions of heterozygotes at all loci
divided by number of loci - 0.1 0.2 0.25 0.05 0.1 / 5 0.14
- Percent loci polymorphic (P)
- Percent of loci with 1 allele
13Types of markers
- Co-dominant
- Allozymes
- Enzymes (proteins), not DNA
- Cheap and fast
- Requires tissue where enzyme is active
- Evolutionary relationships among alleles not
apparent - Not necessarily neutral
- American oyster
14Types of markers
- Co-dominant
- RFLP
- Restriction enzymes cut DNA at specific places
- EcoRV GATATC
- AluI AGTC
- DNA is cut into pieces by one or more enzymes
- Animation
- The number of pieces and their length can be
considered alleles - First used on circular, haploid DNA (mtDNA,
cpDNA) - Now used with PCRPCR-RFLP, allows DNA to be
characterized without large amount of tissue - Animation
15Restriction enzyme recognition sites
GAATTC CTTAAG
G AATTC CTTAA G
GATATC CTATAG
GAT ATC CTA TAG
GATC CTAG
GATC CTAG
CYCGRG GRGCYC
C YCGRG GRGCY C
Y T or C R A or G
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17PCR
- In vitro creation of DNA
- Thermochemical xerox machine
- 3 steps denature, anneal, extend
- Chain-reaction aspect invented by Kary Mullis
(Nobel Prize) - Thermus aquaticusbacteria in hot springs
- Thermostable DNA polymerase
- Animation
18Types of markers
- Co-dominant
- SNPs (pronounced snips)
- Single nucleotide polymorphisms
- A site in a DNA sequence that is variable for 2
nucleotides (alleles) - The site becomes the locus
19Types of markers
- Co-dominant
- Microsatellites
- Length mutations
- Highly variable
- Evolutionary model not known
- Infinite allele model
- Stepwise mutation model
- Two-phase model
20Mechanisms of mutation(slipped-strand mispairing)
21Types of markers
- Dominant
- RAPD (Random Amplified Polymorphic DNA)
- 1 10-bp primer used in PCR
- Multiple sites amplified
- Electrophoresis produces banding patterns
- Problems with reproducibility
- Some journals no longer accept RAPD studies
22Types of markers
- Dominant
- AFLP (Amplified Fragment Length Polymorphism)
- Cut DNA to produce fragments with sticky ends
- Attach known sequence of DNA to sticky end
- Design primer to anneal to known section
- Amplify via PCR
- Electrophorese PCR product to get banding pattern
23DNA sequences
- Co-dominant
- Ultimate level of resolution
- Neutral or functional variation
- Population-level to deep phylogeny
24Wildlife Forensics
- Molecular genetic techniques can identify
products of illegal harvest of protected species - Example Detection of Illegal hunting and sale of
meat from protected whales by Japan and Norway
(Baker and Palumbi 1996) - IWC instituted a global moratorium on commercial
whaling in 1985 - Japan and Norway continued to hunt few species
(minke) for scientific purposes - meat sold
commercially - Issue Were protected species also being
illegally harvested and meat sold as from species
that could be hunted?
25Genetic Analysis of Whale Meat
- Undercover purchase of supposedly-legally
hunted fresh whale meat (i.e. minke) in Japanese
markets - Illegal to transport tissues from protected
species - PCR-amplification of whale mtDNA control region
sequence in hotel room in Tokyo - Sequenced in US labs
26Analysis of 16 Whale Meat Samples
Samples 19b, 41, 3 11, WS4 from Protected
species 19b - Humpback 41, 3, 11, WS4 - Fin
whales 16, 13, 28 - Porpoise and dolphin
27Conclusions
- Results of analysis stricter controls over sale
of scientifically harvested whale meat - Meat harvested prior to harvest bans genotyped to
monitor distribution - Other applications species identity of caviar
and seal penises, population origin of poached
chimps
28Use of Genetic Markers to Identify Units of
Conservation in Natural Populations
- e.g. Daugherty et al.1990. Neglected taxonomy and
continuing extinctions of tuatara (Sphenodon).
Nature 347177-179. - Ancient reptilian lineage - restricted to 12
island groups off of New Zealand - For conservation purposes all populations
classified as belonging to one species (S.
punctatus) despite earlier work suggesting
multiple species - Analysis of phylogenetic relationships among
individuals using allozyme loci
293 phylogenetically distinct lineages identified
1 previously unrecognized species restricted to
single island - no special status Bad
Taxonomy Can Kill