BIOLOGY 2250 Principles of Genetics Fall 2002
2. Chromosome Theory of Inheritance (Chapter 3)
- Mitosis and meiosis (prophase, metaphase, anaphase,
telophase), contrast and compare mitosis and meiosis. Chromosomes and mendelian
inheritance: correlation between the behaviour of genes and the behaviour
of chromosomes. Homologous chromososmes.
3. Gene Linkage and chromosome mapping (Chapter
5)
- Recombination: complete linkage (no recombination)
vs recommbination. Dihyrid cross (parental and recombinant gametes). Trans
vs. cis. Crossing over between non-sister chromatids. recombination fraction
(RF), map distance.
4. Extensions to Mendelian analysis (Chapter
4)
- Dominance and multiple alleles: complete dominance,
no dominance, incomplete dominance, co-dominance, > 2 alleles
- Pleiotropy (one gene affects > 1 trait) recessive
lethal , epistasis (gene interaction: > 1 gene affects a character) modified
9:3:3:1 ratio
- Penetrance and expressivity: phenotype affected
by varing degrees by variation in genetic background and the environement.
- Polygenes and heritability (Chapter 25) Phenotype
= Genotype + Environement. Many genes and the environement can result in
continuously distributed phenotypes (weight, height etc.). Additive alleles:
the more gene pairs the greater the number of phenotypic classes. Heritability
H2 = (genetic variation)/ (genetic variation +
environmental variation)
5. Linkage and gene mapping(Chapter 5)
- 3 point test cross (trihybrid = 8 gamete types):
interference, crossing over, mapping functions. Undetected multiple crossing
over results in an underestimate of map distances
- Tetrad analysis (Chapter 6): ordered tetrads,
first and second division segregation (gene to centromere distance), ordered
tetrads (gene mapping) PD, T, NPD
6. Gene and Chromosome Mutations
Chapter 15:
- Somatic vs. germinal mutation: Mutant phenotypes
- detecting mutations
Chapter 17, 18:
- changes
in chromosome structure: Karyotype, deletion (deletion mapping), duplication,
inversion (para- pericentric) inversion loop, reciprocal translocation
(reduced recombination)
- changes
in chromosome number: euploidy, polyploidy (autoployploidy, allopolyploidy,
triploid, tetraploid), aneuploidy (nondisjunction, monosomics, trisomics)
human chromosome mutations