PART A: Work in teams of two to set up a "model" population containing male and female gametes that carry either a domin
Posted: Sat Jul 02, 2022 9:23 pm
PART B: Review that data on Chart #1 and repeat the entire experiment using adjusted numbers of beans to represent the outcomes recorded in Chart #1. Example: If Chart #1 reveals a total of 18 pairs of AA, then place 9AA (black/black) beans in the male bag for the second part of the experiment, and 9 AA (black/black) beans in the female bag. If Chart #1 shows 10 pairs of aa, then place 5aa (white/white) beans in the male bag and 5aa (white/white) beans in the female bag. After adjusting the number of black and white beans (alleles) in the "parental bags", repeat 60 trials for part two of the experiment. This provides information regarding the possible outcomes for the F₂ generation. Identify which allele (A or a) the male and female donated for the heterozygote. Record your results in Chart #2. GENOTYPE AA Aa 8 2 CHART #2 THE F₂ GENERATION TOTAL TALLY MARKS MALE ALLELES A a FEMALE ALLELES a
EXERCISE #2: Sickle-cell disease is a genetic disorder that causes erythrocytes (red blood cells; RBC's) to assume a sickled shape instead of their normal biconcave shape. It is caused by a genetic error that substitutes the amino acid valine for glutamic acid in the formation of the hemoglobin for RBC's. The sickled shape imparts partial immunity to a parasitic disease known as malaria that affects RBC's, but also prevents a healthy oxygen distribution to body cells, therefore causing symptoms of sickle-cell disease. Malaria was a deadly plague in Africa years ago, and persons who were 5s for the sickle-cell characteristic had some immunity to the malarial parasite. Persons who were born SS had no immunity to malaria and died from the malarial infection: persons who were ss for the characteristic had immunity to malaria, but also expressed all the symptoms of sickle-cell disease. Therefore, the ss individuals usually died of sickle-cell disease when they were still children, without reaching adulthood and reproducing. Hence, the genes of the ss individuals were "removed" from the population. How do your observations from Exercise #1 explain the frequency of the sickle-cell gene within populations?