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51 Cards in this Set

  • Front
  • Back
gene pool
all the alleles of every gene in a population
population
group of individuals of the same species that occupy the same region and can interbreed with one another
polymorphism
the prevalence of two or more phenotypic forms in a population
the phenomenon in which a gene exists in two or more alleles within a population
allele frequencies
number of copies of an allele in a pop/ total # of alleles for that gene in a pop
genotype frequency
# of indiv with a particular genotype in a pop/ tot # of indiv in a pop
conditions of Hardy- Weinberg
no new mutations, no genetic drift, no migration, no natural selection, random mating
random genetic drift
changes in allele frequencies in a population due to chance fluctuations. favors the loss of an allele of its fixation at 100%
depends on pop size
small pop- likelihood of fixation high
probability of fixation
1/2N
expected number of new mutations
2Nmu
probability of elimination
1- (1/2N)
# of generations until fixation
t=4N
bottle neck effect
type of genetic drift that occurs when most of the population is eliminated without regards to genetic composition
founder effect
changes in allele frequencies that occur when a small population separates from a larger population and establishes a colony in a new location
gene flow
individuals migrate between populations that have different allele frequencies, and the migrants breed successfully with the recipient population
darwinian fitness
the relative likelihood that a genotype will contribute to the gene pool of the next generation
directional selection
favors individuals at one extreme of a phenotypic distribution that are more likely to survive and reproduce in a particular environment
stabilizing selection
the extreme phenotypes for a trait are selected against, and those with the intermediate phenotypes have the highest fitness values
-decreases genetic diversity
Disruptive selection
favors the survival of two or more different genotypes that produce different phenotypes
-diverse environments
balancing selection
genetic polymorphisms
- a pattern of natural selection that favors the maintenance of two or more alleles
ex: heterozygote advantage and negative frequency dependent selection
microevolution
changes in a
population gene pool
from one generation to
the next
haplotype
a set of alleles that are closely linked and inherited as a group
heteroplasmy
variation in the genomic DNA of organelles (chloroplasts or mitochondria) within a cell
cytogenetic mapping
localizes genes to microscopically visible positions on a chromosome
linkage mapping
places genes on chromosomes according to the frequency of recombination btw different loci
physical mapping
identifies the position of genes within the sequenced DNA
Fluorescent in situ hybridization (FISH)
localization of genes to general region of particular chromosome
simple translocation
when a single piece of chromosome is attached to another chromosome
reciprocal translocation
when two different types of chromosomes exchange pieces - producing two abnormal chromosomes carrying translocations
homologues
genes derived from a single ancestral gene
paralogues
homolgous genes within a single species
orthologues
homologous genes found in different species
pericentric inversion
centromere lies within the inverted region of the chromosome
(duplicated/deleted)
paracentric inversion
centromere is found outside the inverted region
(acentric fragment & dicentric chromosome)
inversion heterozygote
carries one copy of a normal chr4omosome and one copy of an inverted chromosome
dicentric chromosome
two centromeres
acentric fragment
chromosome without any centromere
robertsonian translocation
two non-homologous acrocentric chromosomes are joined at breaks that occur near the centromere
alternate segregation haploid cells
two normal chromosomes, two reciprocal balanced translocations
adjacent-1 segregation haploid cells
4 unbalanced cells (one of each type of centromere)
adjacent-2 segregation haploid cells
4 cells unbalanced (both copies of the centromere on same chromosome into daughter cell)
requires incorrect segregation of the centromeres during meiosis I)
euploid
chromosome number is an exact multiple of a chromosome set
polyploid
chromosome number is a multiple greater than 3 of a chromosome set
aneuploid
not euploid; chromosome number is NOT an exact multiple chromosome set
trisomy
having 3 copies of a particular chromosome
monosomy
having 1 copy of a particular chromosome
endopolyploidy
occurrence of polyploid tissues in otherwise diploid organism
polytene chromosomes
repeated rounds of replication without cellular division
mechanisms of aneuploidy
meiotic nondisjunction, mitotic nondisjunction, alloploidy
meiotic nondisjunction
failure of correct chromosomal segregation in meiosis
mitotic nondisjunction
failure of correct chromosomal segregation in mitosis
alloploidy
having two or more sets of chromosomes from different species