Name_______________________________________Date__________________Period______ Codominance Mendel’s original work seemed to show there were two types of genes: dominant and recessive. We have learned that this description is overly simple. A case of this kind is referred to as codominance. MN Blood Types An example of codominance is found in the MN blood group in humans. The two alleles for this blood group, M an N are codominant, with MM producing type M blood, NN producing type N blood, and MN producing type MN blood. Steps to Solving Genetic Problems: 1. 2. 3. 4. 5. What genetic relationship is shown? (i.e. incomplete dominance, codominance, dominant/recessive, multiple alleles, sex-linked, etc.) Write a key. (Dominant traits are underlined.) Write the cross. Show the Punnett square/ FOIL method. Answer the question(s) and circle. 1. Suppose that a person who is homozygous for the M blood type marries a person who is homozygous for the N type. Show the phenotypic and genotypic ratios of the F1 generation. 2. Now show the phenotypic and genotypic ratios of the F2 generation. Sickle Cell Anemia The genetic disease “sickle-cell anemia” in humans, is caused by two codominant alleles. Two normal genes (N) produce normal red blood cells. Two sickle cell genes (S) cause the disease to occur. Individuals afflicted with this disease have “sickled” red blood cells that are unable to carry oxygen properly. The heterozygous is not fatal and seems to offer protection against malaria infection. 1. If a man and women are tested and found to be carriers of the sickle allele, what is the probability that they will have a child who has sickle cell anemia? 2. Show a cross between a man who has sickle cell anemia and a women who is a carrier of the trait. What percentage of the offspring will have the trait? 3. Show a cross between a normal male and woman who has sickle cell anemia. What percentage of their offspring will have sickle cell anemia? Thalassemmia An anemic condition in humans called thalassemmia is controlled by codominant alleles. Homozygous for the defective allele (TT) have a severe anemia (thalassemia major), whereas heterozygotes (TN) have a mild anemia (thalassemmia minor). Normal individuals are homozygous (NN) and do not have anemia. 1. Show a cross between a man that is homozygous for thalassemmia and a woman that does not have anemia. What are the percentages of all phenotypes and genotypes? 2. What are the genotypic and phenotypic ratios for the F2 generation?