Sickle-cell anemia is caused by a point mutation which alters the shape of erythrocytes. Individuals with two normal alleles have normal erythrocytes, individuals with two mutated alleles have C-shaped erythrocytes and experience anemia. Heterozygous individuals produce both types of erythrocytes and experience protection from the parasite that causes malaria. If a anemic man and a normal woman have children, what percentage of the offspring are expected to be protected from malaria? 50% 0% 75% O 100% 25%
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- Sickle cell anemia is an autosomal recessive genetic disorder. Because individuals affected bysickle cell anemia have defective hemoglobin proteins, their blood cannot transport oxygenproperly. There appears to be a relationship between the incidence of malaria and sickle cellanemia. Individuals with sickle cell anemia and carriers of the sickle cell allele have someresistance to malaria. Malaria is caused by the parasite Plasmodium and is transmitted among humans by mosquitoes. If scientists are successful in reducing significantly or eliminating malaria, the best predictionfor what will happen to the allele for sickle cell anemia in the population is that it willa. not be affected by the elimination of malariab. increase as its selective advantage is increasedc. be reduced as its selective advantage is decreasedd. disappear quickly as its selective advantage is increasedSickle cell anemia is an autosomal recessive genetic disorder. Because individuals affected bysickle cell anemia have defective hemoglobin proteins, their blood cannot transport oxygenproperly. There appears to be a relationship between the incidence of malaria and sickle cellanemia. Individuals with sickle cell anemia and carriers of the sickle cell allele have someresistance to malaria. Malaria is caused by the parasite Plasmodium and is transmitted amonghumans by mosquitoes.4. If scientists are successful in reducing significantly or eliminating malaria, the best predictionfor what will happen to the allele for sickle cell anemia in the population is that it willa. not be affected by the elimination of malariab. increase as its selective advantage is increasedc. be reduced as its selective advantage is decreasedd. disappear quickly as its selective advantage is increasedSickle cell anemia is an inheritable red blood cell disorder that results in sickle-shaped red blood cells. The sickle-shaped red blood cells can stick to blood vessel walls and cause a blockage or slow the movement of blood throughout the body. Individuals who are heterozygous produce both normal and sickle-shaped red blood cells which gives them resistance to malaria but they do not develop sickle cell anemia (so heterozygotes are unaffected on the pedigree).Let HbS be the allele for sickle cell anemia and let HbA be the allele for normal red blood cells. Which of the following rows provides the correct genotypes for individuals I-2, I-4, II-1, and III-1? Select one: a. I-2 I-4 II-1 III-1 HbA_ HbAHbS HbAHbS HbA_ b. I-2 I-4 II-1 III-1 HbA_ HbAHbS HbAHbS HbAHbS c. I-2 I-4 II-1 III-1 HbAHbS HbAHbS HbAHbS HbAHbS d. I-2 I-4 II-1 III-1 HbAHbA HbAHbA HbAHbA HbAHbA
- In a region of Africa, where malaria is prevalent, 40% of the population are found to have sickle-cell anemia. The disease is caused by an abnormal hemoglobin that is found in both homozygotes (S2S2) and heterozygotes (S1S2). Many homozygotes (S2S2) suffer from anemia and often die. Heterozygotes (S1S2) incur a much less debilitating malady called "sickling trait". Approximately 3% of the people with abnormal hemoglobin are homozygotes (1.2\% of the entire population). The fitness of the S2S2 homozygotes is only 1/4 that of the heterozygotes. Where malaria is prevalent, heterozygotes exhibit overdominance with respect to fitness. How would you calculate relative fitness of the S1S1 homozygotes if you're assuming the population is at an equilibrium frequency for S2?Astigmatism and polydactyly are dominant over normal vision and finger traits. Sickle-cell anemia onthe other hand, is an overdominant lethal trait due to its recessive genes (ss). Individuals with this traitdie prematurely. Heterozygotes (Ss), however, have some RBCs that sickle while others remainnormal, thus, not lethal. They are referred to as sickle-trait carriers. A polydactylous, normal-visioned, brown-eyed man with wavy hair has a nonpolydactylous, blue-eyed mother. He proposed marriage to a nonpolydactylous, astigmatic, blue-eyed, and curly-hairedlady whose mother has normal vision. However, the lady is worried about the proposal since sickle-cell anemia has been known to run in both their families. a. Is there a genetic basis for her worry? Explain. b. If it turned out that the lady is a carrier and the man has normal RBC, what would be their COMPLETE genotypes? Male genotype:_________________________________Female genotype: ______________________________ c. Based on their…Astigmatism and polydactyly are dominant over normal vision and finger traits. Sickle-cell anemia onthe other hand, is an overdominant lethal trait due to its recessive genes (ss). Individuals with this traitdie prematurely. Heterozygotes (Ss), however, have some RBCs that sickle while others remainnormal, thus, not lethal. They are referred to as sickle-trait carriers. A polydactylous, normal-visioned, brown-eyed man with wavy hair has a nonpolydactylous, blue-eyed mother. He proposed marriage to a nonpolydactylous, astigmatic, blue-eyed, and curly-hairedlady whose mother has normal vision. However, the lady is worried about the proposal since sickle-cell anemia has been known to run in both their families. a. Is there a genetic basis for her worry? Explain. b. If it turned out that the lady is a carrier and the man has normal RBC, what would be their COMPLETE genotypes? Male genotype:_________________________________Female genotype: ______________________________ c. Based on their…
- In humans, hemophilia is a sex-linked condition and normal blood clotting (H) is dominant to the condition of hemophilia (h). A woman with hemophilia marries a normal man. The hat are the probabilities of them having children with hemophilia and their sexes?In a pop, 1/10 men has Hemophilia B. HWE conditions are met, what is the incidence of Hemophilia B between women?Hereditary hemochromatosis is an autosomal recessive genetic disorder that causes the body to absorb too much iron from the diet. This excess iron is stored in the body's tissues and organs, particularly the skin, heart, liver, pancreas, and joints. Because humans cannot increase the excretion of iron, excess iron can overload and eventually damage tissues and organs. Anthony and Melinda met at a support group for individuals who have hereditary hemochromatosis. They were advised by their genetic counselor that it would be risky to have children, since both of them are homozygous for the same recessive allele that causes this condition. Nevertheless, they decided to have a child together. During Melinda’s pregnancy, amniocentesis and genetic testing were performed, and it was confirmed the fetus was homozygous for the hereditary hemochromatosis allele. At birth, the baby appeared completely normal, and as the child continued to grow and mature, the couple were surprised that he seemed…
- Astigmatism and polydactyly are dominant over normal vision and finger traits. Sickle-cell anemia on the other hand, is an overdominant lethal trait due to its recessive genes (ss). Individuals with this trait die prematurely. Heterozygotes (Ss), however, have some RBCs that sickle while others remain normal, thus, not lethal. They are referred to as sickle-trait carriers. A polydactylous, normal-visioned, brown-eyed man with wavy hair has a nonpolydactylous, blue-eyed mother. He proposed marriage to a nonpolydactylous, astigmatic, blue-eyed, and curly-haired lady whose mother has normal vision. However, the lady is worried about the proposal since sickle-cell anemia has been known to run in both their families. Is there a genetic basis for her worry? Explain.Describe how the Bombay phenotype is epistatic to the ABO blood phenotype in humans, and discuss some implications of this phenotype in blood typing and blood donation.Introduction: A person’s blood type is an inherited trait governing special marker proteins appear-ing on the surface of their red blood cells. Blood typing is important, because it governs who anindividual can give or receive blood donations from; blood with proteins markers not present in theirown blood will be rejected by an individual’s immune system.There are two separate genes that govern blood type; the ABO gene has two dominant options, Aand B, and a recessive option called O. For example, an individual with AO or AA would presentthe A protein, and an individual with AB will present both the A and B proteins on their blood;an individual with OO has no proteins from this gene. The Rh gene has two options; the dominantoption is called positive (or + for short), while the recessive option is called negative or null (or –for short). For example, an individual with ++ or +– would present the Rh protein on their blood,while an individual with – – would not present the Rh…