AP Biology Unit 5: Heredity — Mind Map
Reviews Mendelian genetics (monohybrid and dihybrid crosses, test crosses), pedigrees, sex-linked vs. autosomal inheritance, linkage and crossing over, chromosomal disorders, non-Mendelian patterns (codominance, incomplete dominance, pleiotropy), and meiosis as a source of genetic variation.
Heredity
Mechanisms of Variation
Crossing Over
Occurs in Prophase I
Exchange between non-sister chromatids
Creates recombinant chromosomes
Independent Assortment
Random orientation in Metaphase I
Formula: 2^n combinations
8.4 million possibilities in humans
Random Fertilization
Random union of unique gametes
Multiplies meiotic variation
Genetic Linkage and Mapping
Linked Genes
Located close on same chromosome
Inherited together as a unit
Recombination frequency < 50%
Linkage Maps
Based on recombination frequencies
1% RF = 1 centimorgan (map unit)
Distance reflects crossover probability
Non-Nuclear Inheritance
Maternal inheritance
Mitochondrial DNA
Chloroplast DNA in plants
Environmental Effects
Phenotypic Plasticity
One genotype, multiple phenotypes
Influence of temperature and pH
Nutrition and UV exposure
Meiotic Errors
Nondisjunction
Failure of chromosomes to separate
Results in aneuploidy
Examples: Down and Turner syndromes
AcornPrep