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
- Crossing Over
- 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
- Linked Genes
- 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
- Phenotypic Plasticity
- Meiotic Errors
- Nondisjunction
- Failure of chromosomes to separate
- Results in aneuploidy
- Examples: Down and Turner syndromes
- Nondisjunction
- Mechanisms of Variation
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