Question

In: Biology

Beta-thalessemia is caused by mutations in the hemoglobin B gene we discussed along with sickle cell...

Beta-thalessemia is caused by mutations in the hemoglobin B gene we discussed along with sickle cell anemia. There are some anemia-causing mutations that are dominant while other mutations act in a recessive manner. The anemia caused by either type can be debilitating in affected genotypes and would be selected against in areas which do not have malaria.

a) Assuming both forms of beta-thalessemia in the affected genotypes show similar fitness relative to unaffected genotypes, which type of allele (recessive or dominant) will disappear more quickly from a population with a similar negative selection coefficient (s)?  Explain why there is a difference.

b) Why would these mutations fail to disappear from a population in an area that has malaria-infected mosquitoes? Why do allele frequencies stabilize?

Solutions

Expert Solution


Related Solutions

Sickle cell anemia is a recessive disorder caused by a mutation in the hemoglobin A gene....
Sickle cell anemia is a recessive disorder caused by a mutation in the hemoglobin A gene. Persons with the disease have a variety of serious health issues related to fragile and sickling red blood cells including premature death, and infants sometimes die from complications. In regions of central Africa where malaria is endemic, the relative fitnesses for individuals that are homozygous for the wild type hemoglobin allele (HbA), heterozygous (HbAHbS), and homozygous for the sickle cell allele (HbS) are 0.8,...
abnormal hemoglobin that causes sickle cell is an example of a mutation that is: a)both adaptive...
abnormal hemoglobin that causes sickle cell is an example of a mutation that is: a)both adaptive in areas without malaria and maladaptive in areas with malaria b)adaptive in areas with malaria c)maladaptive in areas with malaria d)adaptive in areas without malaria
Sketch photograph and submit the scheme of transcription and translation for normal hemoglobin and sickle cell...
Sketch photograph and submit the scheme of transcription and translation for normal hemoglobin and sickle cell anemia. Use your knowledge of codons, mutations, DNA, RNA and amino acids
4. (10 pts) Hemoglobin S or sickle cell hemoglobin forms fibers in red blood cells because...
4. (10 pts) Hemoglobin S or sickle cell hemoglobin forms fibers in red blood cells because of a Glu→Val mutation on the surface of the protein. The mutated residue interacts with Leu and Phe residues located on the surface of a different protein molecule. This interaction drives the formation of the fibers. Explain why higher concentrations are needed to form fibers at lower temperatures.
Cystic fibrosis is genetic disease caused by mutations in the CFTR gene. The consequence of this...
Cystic fibrosis is genetic disease caused by mutations in the CFTR gene. The consequence of this is production of an abnormal transmembrane protein that is responsible for producing sweat, mucus, and digestive fluids. Explain in depth the correlation between the defective gene and the abnormal protein that is produced. Be sure to mention the process involved in protein production, whether or not those process(s) have occurred, and their end products. Provide details in your explanation and support your answer with...
Sickle cell anemia is a recessive disorder in which hemoglobin loses the ability to effectively deliver...
Sickle cell anemia is a recessive disorder in which hemoglobin loses the ability to effectively deliver oxygen to the tissues. Gene therapy in which hemoglobin gamma-chain is introduced to sickle cell anemia patients seems to be a promising new therapy to correct the disease. Why do you think this is possible, based on your knowledge of the sickle cell mutation and the different hemoglobin polypeptide chains?
Neither myoglobin or sickle-cell hemoglobin will work for oxygen transport in the body. Using your extensive...
Neither myoglobin or sickle-cell hemoglobin will work for oxygen transport in the body. Using your extensive knowledge of these proteins, explain why this is true. Additionally, explain the effect of decreasing pH and 2,3-BPG on the action of a normal molecule of hemoglobin.
QUESTION 15: Sickle cell anemia is usually detected at birth because fetal hemoglobin is affected by...
QUESTION 15: Sickle cell anemia is usually detected at birth because fetal hemoglobin is affected by the genetic mutation. True False QUESTION 16: Pruritic linear lesions that itch more at night that may have more vesicles and papules describes which of the following conditions? Atopic dermatitis Tinea corporis Impetigo Staphylococcal scalded-skin syndrome QUESTION 17: The most common cause of chronic hepatitis in children is: A and B A and C B and C B and D QUESTION 18: Before the...
HbS, the variant of hemoglobin responsible for sickle-cell anemia, aggregates into long chains in aqueous, biological...
HbS, the variant of hemoglobin responsible for sickle-cell anemia, aggregates into long chains in aqueous, biological conditions (pH 7.4, 37oC, some salt and buffer present). Explain this phenomenon from a molecular point of view. Why does it form chains, not globular aggregates? Why is this phenomenon unsurprising to biochemists familiar with the details of protein folding?
Please answer the following question: Sickle-cell anemia is a disease in which one subunit of hemoglobin...
Please answer the following question: Sickle-cell anemia is a disease in which one subunit of hemoglobin protein contains a single amino acid substitution: a Glu (glutamic acid residue is replaced with Val (valine) Examine the structures of Glu and Val and your answers to the previous two questions. How do you expect each of the following to be affected in the hemoglobin protein of a sickle-cell anemia patient compared to the hemoglobin protein of a normal individual? 1. Primary protein...
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT