Level 1 Genetics Review Sheet Organize your materials in the following order: 1. Notes packet containing the following (divided by when each was done): Gregor Mendel (p. 1) Alleles/genotype/phenotypes (p. 2) Gamete formation/monohybrid cross/probability/testcross (p. 2) Dihybrid cross/testcross (p. 3) Polygenic inheritance (back p. 3) Multiple alleles/codominance (blood)/incomplete dominance (hair, sickle cell, four o’clock plants) (p.4) Viewing the chromosomes/amniocentesis/CVS (p. 5) Changes in chromosome number/nondisjunction/changes in chromosome structure/chromosome mutations (p. 6-7) Sex-linked traits (back p. 7) Linked genes (back p. 7) 2. Study guide packet (homeworks) 3. Packet of problems: Monohybrid crosses Probability practice problems Dihybrid crosses Codominance/Incomplete dominance practice problems Sex-linked trait problems 4. Laboratory: Exploring hereditary traits 5. Chapters 23 & 24 practice problems and answer key Test questions will be based on the following main ideas: Be able to explain how Mendel performed his crosses with pea plants – using an example of a trait he worked with, explain what the parents would look like, the F1 generation, and F2 generation in terms of appearance and percents for each type of appearance. Be able to explain why he got the results he got. Be able to explain each of Mendel’s laws – dominance, segregation, and independent assortment using examples of genotypes and phenotypes. Vocab: allele, phenotype, genotype, codominance, incomplete dominance, sexlinkage Be able to demonstrate (using punnett) squares the following types of problems: i. Dominance/recessiveness – monohybrid crosses, both forwards and backwards ii. Dihybrid crosses – forwards only on test iii. Codominance – blood type – forwards and backwards iv. Incomplete dominance – hair, sickle cell, four-o’clock plants – forwards and backwards v. Sex-linked traits – hemophilia, color blindness – forwards and backwards vi. Multiple probability – event happening several times in a row For each of the problems listed on the previous side of this sheet, be sure to know the genotypes to use for each type of problem, and what phenotypes each represent. Be able to explain what a testcross is, and why it would be done. Be able to explain what a polygenic trait is, and how the interaction of multiple genes affects the possible phenotypes. Be able to explain what a karyotype is and why it would be used – what can it show about the developing baby. Be able to explain the difference between amniocentesis and chorionic villus sampling (CVS) in terms of when they are done and how the cells from the fetus are acquired. Be able explain what happens to the genes on the chromosomes on each type of chromosomal mutation, and how these mutations (in general) can affect the developing baby or the genes on those affected chromosomes. Be able to explain what a linkage group is, and how Mendel’s law of independent assortment is affected by it. Be able to explain what nondisjunction is, how it can occur during meiosis I and II, and how it affects the number of chromosomes in a person. Be able to explain how sex-influenced traits occur.