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Part VI. Assessment 1. People with Sickle Cell Anemia have distorted red blood cells. They make hemoglobin S instead of the normal hemoglobin A. Hemoglobin S moves slower during electrophoresis. Carriers of the disease make hemoglobin A and S. Look at the gel below and answer the next three questions.
Which lane was loaded with a sample from a normal person?
Which lane contains a sample from a carrier for sickle cell anemia?
2. Another Hemoglobin Genetic Variant: Hemoglobin Saverne: The normal DNA for the end of the beta chain of hemoglobin reads: 143 Fill in the second strand of DNA on the line above. Make a messenger RNA from this second DNA strand:
Translate the mRNA into a protein until you reach the STOP signal; do not translate further – why? In the disease Hemoglobin Saverne, the A in triplet CAC #143 is deleted, causing a frameshift mutation. Delete that A in triplet #143, and reorder the remaining bases downstream as triplets, three at a time, without that A. The new DNA would then read: 143 Fill in the second strand of DNA above. Now use the second strand of DNA to make the mRNA:
Translate the mRNA into protein; what is the result?
What effect do you think this would have on the functioning of the hemoglobin molecule? _____________________________________
3. If you look up the HBB gene on the OMIM database, # 141900, you will see that other kinds of mutations in this gene result in different kinds of beta-thalassemias – what is the difference between sickle cell anemia and beta-thalassemias?
4. Use the following terms to fill in the blanks below: chromosome, DNA, gene, genome, protein. The challenge is to use each term only once! The _______________ hemoglobin is coded by the _______ made of the molecule ___________ . The genes are organized in the nucleus within _________________ , and all together they make up the entire human ________________.
Credits: Gel image and question compliments of Dennis Anderson, OCCC.
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