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