Conservation Genetics Flashcards
Problems in conservation
genetics 1. Survival of small populations
E.g. Javan black rhinoceros (Rhinoceros sondaicus)
* 40-60 individuals of subspecies in Java
* Another population of <8 in Cat Loc reserve, Vietnam
* No individuals in captivity
* Brink of extinction
GENETIC INSTABILITY
* Not just animals
* Remote tribes of humans “uncontacted tribes”
* Often small populations, inbreeding can be a problem
- Survival of managed populations
E.g. Zoos
* Typically contain very small numbers of individuals of the
same species, subject to inbreeding
* Siberian tigers: ~300 left in the wild in Russia and China,
~200 in Zoos
* The issue is many of the “Zoo’s 200” have come from a
small number of individual founders
- Conservation of breeds
E.g. Domestic animals – dogs, cats, horses, cattle etc.
* Highly inbred
* Bred for particular traits e.g. high milk yield in dairy cows,
desirable characteristics in pet dogs
* Because of this inbreeding, they behave like small
populations and are subjected to inbreeding depression
Reduction in reproductive fitness
Reduction in survivability
Inbreeding Depression
What happens in the next generation?
Reduced heterozygosity and reduced hybrid vigour
Siberian Tigers
Inbreeding vs. Hybrid Vigour
- Siberian tigers: the Hengadoahezi tiger breeding centre
(China) they bred >200 tigers in captivity since the 1980s - They are derived from just eight founding individuals
- The observed inbreeding led to physical deformities in
the offspring e.g. blurred striped pattern, general genetic
degradation
inbreeding vs. Hybrid Vigour in HUMANS
Founder effects example: Retinitis pigmentosa on
Tristan de Cuhna (night blindness)
* Island was first colonised in 1810 by 15 people
– Just one person had night blindness
– Current population today has a high frequency of the condition
Inbreeding does two things:
- Reduces the number of heterozygotes in the population
(and therefore reduces hybrid vigour) - It encourages the accumulation of individuals with the
double-recessive phenotype
– If this phenotype is for a harmful trait, it increases the probability
the harmful trait spreads through the population
Measuring inbreeding
- Inbreeding coefficient (F) = probability of two alleles of a
gene being identical, because they descended from the
same copy of the alleles in an ancestor - Between 0 to 1 (or 0-100%)
F is the degree to which two alleles are more likely to be
homozygous (AA/aa) than heterozygous (Aa) in an
individual, because their parents are related
- Population size
- Effective population size Ne
- The key measure of population size is the number of
individuals that are able to breed Ne - If all the rhino’s were male, there would be no potential
for breeding - If all the rhino’s were too young/old to mate, there would
be no breeding - Ne accounts for sex ratio and population age structure
- Inbreeding
– Inbreeding coefficient F
Measuring inbreeding
Conservation of populations
3 Situations
- Unmanaged population – random breeding
- Managed population – zoos, wildlife parks etc.
- Wild animals – mate choice
* E.g. Sorraia, a horse breed native to Portugal
– During 1900s the breed was approaching extinction
– In 1937 it was conserved: only 5 males, 7 females left
– Horses were allowed to randomly interbreed
– By 2001, 160 animals living derived from 7 females
Ex situ conservation
– When you look at the family pedigrees, you see that
only families derived from two particular females had
survived to the current generation
– The remaining five died out, so the remaining
population is highly inbred
– Genetic bottleneck
- Managed population – zoos, wildlife parks etc.
- Pedigree
- Choose mates that maximise outbreeding
- Studbook (or electronic equivalent)
- Wild animals
Mate Choice
How to measure genetic variation in populations?
- Pedigree – not always available or known, more useful for
captive populations - Genetic testing – techniques similar to DNA fingerprinting
in humans using microsatellites or minisatellites
Measuring genetic variation
* Microsatellite DNA – repeat unit length of 1-7 bases
– 5-100 repeats at each microsatellites
– 1000s of different microsatellites, randomly scattered throughout
genome
Measuring genetic variation
* Microsatellite DNA – repeat unit length of 1-7 bases
– 5-100 repeats at each microsatellites
– 1000s of different microsatellites, randomly scattered throughout
genome
* Minisatellite DNA – repeat unit length of 6-100 bases
– 2-1000s repeats at each minisatellite
– 1000s of different minisatellites, scattered throughout genome,
but often clustered near the ends of chromosomes (telomeres)
Measuring genetic variation
* Microsatellite DNA – repeat unit length of 1-7 bases
– 5-100 repeats at each microsatellites
– 1000s of different microsatellites, randomly scattered throughout
genome
* Minisatellite DNA – repeat unit length of 6-100 bases
– 2-1000s repeats at each minisatellite
– 1000s of different minisatellites, scattered throughout genome,
but often clustered near the ends of chromosomes (telomeres)