Question

The allele that causes sickle-cell anemia is the result of __________. a. two chromosomal translocations followed...

The allele that causes sickle-cell anemia is the result of __________.

a. two chromosomal translocations followed by fusions

b. an insertion leading to a frameshift mutation that changed all downstream codons

c. a single base substitution causing a transversion mutation

d. a silent mutation, which is why it goes unnoticed until adulthood

0 0
Add a comment Improve this question Transcribed image text
Answer #1

The allele that causes sickle-cell anemia is the result of --

c. a single base substitution causing a transversion mutation.

Explanation - sickle-cell anemia is caused due changes a single base substitution of the beta-globin gene known as sickle hemoglobin (Hb S). Here mistakenly Valine is coded instead of glutamic acid, so here U-uracil(pyrimidine) is coded instead of A- adenine (purine) thus causing a transversion mutation.

Add a comment
Know the answer?
Add Answer to:
The allele that causes sickle-cell anemia is the result of __________. a. two chromosomal translocations followed...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • Sickle Cell Anemia Sickle cell anemia is the result of a type of mutation in the...

    Sickle Cell Anemia Sickle cell anemia is the result of a type of mutation in the gene that codes for part of the hemoglobin molecule. Recall that hemoglobin carries oxygen in your red blood cells. The mutation causes these red blood cells to become stiff & sickle-shaped when they release their oxygen. The sickled cells tend to get stuck in blood vessels, causing pain and increased risk of stroke, blindness, damage to the heart & lungs, and other conditions. Analyze...

  • A mutation in one of the hemoglobin genes causes sickle cell anemia. The sickle cell allele,...

    A mutation in one of the hemoglobin genes causes sickle cell anemia. The sickle cell allele, S, severely reduces fitness in people who are homozygotes, SS. In contrast, people with at least one normal hemoglobin allele, A, do not suffer the effects of sickle cell anemia, even if the individual is a heterozygote, AS. Interestingly, though, in areas with a high rate of malaria, heterozygotes that carry the sickle cell allele have a higher fitness than do individuals that are...

  • Explain how the allele that causes the fatal condition of sickle-cell anemia has been preserved in...

    Explain how the allele that causes the fatal condition of sickle-cell anemia has been preserved in certain populations that are exposed to malaria. Why is sickle-cell anemia relatively frequent today even among populations who live in geographic regions where malaria is under control?

  • - What is the likelihood that two individual who are both heterozygous for the sickle-cell allele...

    - What is the likelihood that two individual who are both heterozygous for the sickle-cell allele will have offspring with Sickle-Cell Anemia? 0% 25% 50% 75% - An individual who is heterozygous for the sickle-cell allele is said to have: Sickle-Cell Anemia Sickle-Cell Disease Sickle-Cell Trait Malaria - The sickle-cell allele is an example of: a chromosomal mutation a point mutation recombination genetic drift - Which of the following piece of evidence supports Anthony Allison’s hypothesis that there is a...

  • A mutation in one of the hemoglobin genes causes sickle cell anemia. The sickle cell allele,...

    A mutation in one of the hemoglobin genes causes sickle cell anemia. The sickle cell allele, S, severely reduces fitness in people who are homozygotes, SS. In contrast, people with at least one normal hemoglobin allele, A, do not suffer the effects of sickle cell anemia, even if the individual is a heterozygote, AS. Interestingly, in areas with high rates of malaria, a single Sallele confers some resistance to malarial infection. Suppose there is a population with the observed and...

  • Sickle cell anemia is a genetic disease resulting from a single amino acid substitution (glutamate to...

    Sickle cell anemia is a genetic disease resulting from a single amino acid substitution (glutamate to valine in the sixth position, or E6V) in the hemoglobin β chain. This mutation causes hemoglobin to polymerize into strands in the deoxygenated state, leading to the erythrocytes forming a sickled shape. Speculate as to why the mutation leads to the polymerization of hemoglobin and why this only happens in the deoxygenated state.

  • Use the following information to answer the next two questions. Sickle cell anemia is a disease...

    Use the following information to answer the next two questions. Sickle cell anemia is a disease that is caused by a mutation in the gene that produces haemoglobin. Hemoglobin carries oxygen in red blood cells. The HbA allele produces normal hemoglobin and the HbS allele produces haemoglobin that sticks together and causes red blood cells to sickle. Heterozygous individuals (HbAHbS) produce both normal and "sickle" hemoglobin so the HbA and HbS alleles are codominant. Heterozygotes do not develop sickle cell...

  • Sickle-cell Anemia Study Sickle-cell anemia or Sickle-cell disease, is a hereditary disorder. characterized by aryabnormality in...

    Sickle-cell Anemia Study Sickle-cell anemia or Sickle-cell disease, is a hereditary disorder. characterized by aryabnormality in the oxygen-carrying hemoglobin molecule in erythrocytes. Sickle-cell conditions have an autosomal recessive pattern of inheritance from parents. The sickle cell defect is a mutation of a single nucleotide of the hemoglobin B gene, which results in glutamic acid being substituted by a different amino acid at position 6. Hemoglobin with this mutation is referred to as Hbs, as opposed to the normal hemoglobin HbA....

  • D) Consider that during replication of the cell. the following mutations were generated within the gene...

    D) Consider that during replication of the cell. the following mutations were generated within the gene sequence. Find the mutation (in bold Italics-underlined Specify the protein sequences for each mutant sequence. mutation type 1: This is a non-sense mutation because the codon does not code for an amino acid any more 5' -..AACTAATGCCGTAAGACGTATTTTGACTAAT..-3' (substitution of a C 7 A in codon 3) 3'- TTGATTACGGCAT ICTGCATAAAACTGATTA..-5 S mutation type 2: This is a missense mutation because the codon now codes for...

  • please andwer all the questions 7) Describe at least two major intramolecular forces that help stabilize...

    please andwer all the questions 7) Describe at least two major intramolecular forces that help stabilize the DNA double-helix? 8) In mammalian female cells, the DNA of the Barr Body is characteristic of: a) Heterochromatin b) Euchromatin c) Dispersed chromatin d) Patemal DNA ONLY e) Maternal DNA ONLY 9) When used to describe the RNA polymerases' activity, the term “processivity” refers to: a) The ability to recognize and bind to a promoter region b) The ability to remain attached to...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT