BIO5: Genetic Analyses, Evolution, and Natural Selection Flashcards
Dihybrid cross
Parent x parent –> F1 generation (x F1) –> F2 generation
Autosomal recessive disorders
All affected indiviudals have 2 carrier parents
Autosomal dominant disorders
All affected individuals have 1 affected parent (appears every generation)
In order to do a pedigree
The disorder must exhibit dominance and must not be sex-linked
Testcross
Used to determine if an individual that shows the dominant phenotype is homozygous (AA) or heterozygous (Aa) by crossing the individual with a homozygous recessive individual
Backcross
Hybrid individual crossed with one of the parent to determine recombination (ie. How far a part genes are)
How do you calculate Rf from a backcross?
Rf= sum of % of recombinants in backcross progeny
Epistasis
The expression of alleles for 1 gene is dependent on the alleles for another gene (e.g. pigment gene vs color gene)
Pleiotropy
1 gene that affects multiple different traits (e.g. PKU)
Allelic series
Multiple different alleles for a gene with varying degrees of dominance (e.g. blood type IA=IB>i
Complementation test
Used to determin whether two individuals with the same phenotype carry mutations on the same gene or different genes
How is the complementation test performed?
Cross two homozygous individuals with similar mutant phenotypes (e.g. AAbb x aaBB) and see if complementation/WT phenotype (AaBb) occurs/if mutant alleles are on 2 different genes
Polygenetic
Traits that are influenced by multiple different genes (genes interact additively to produce the phenotype - e.g. skin color)
Expected phenotype ratio for two heterozygotes if completely dominant
3:01
Expected phenotype ratio for two heterozygotes if codominant/incomplete
1:02:01
Expected phenotype ratio for two double heterozygotes if complete dominance
9:3:3:1
Expected phenotype ratio for two double heterozygotes if recessive epistasis
9:3:4 (aa for gene 1 is dominant over gene 2)
Expected phenotype ratio for two double heterozygotes if dominant epistasis
12:3:1 (A for gene 1 is dominant over gene 2)