Question

This question is about DNA damage, repair and mutation. a) State a type of mutagen that...

This question is about DNA damage, repair and mutation.
a) State a type of mutagen that could produce a single base pair substitution mutation. Briefly describe how this mutagen can produce single base pair substitution mutations. [4 marks]
b) For your mutagen from (a), briefly describe the repair process that could repair the DNA damage. [4 marks]
c) Propose how a single base pair substitution can be a hypomorphic allele. Explain how your mutation fits the definition of a hypomorphic mutation. [3 marks]
d) State a type of mutation that is not a single base pair substitution. What type of mutagen could generate this type of mutation? Explain. [3 marks]

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

a) A type of mutagen that could cause single base pair mutation is - Base analogs. They are incorporated in the place of normal base as their structure is almost similar to natural bases with very little variation.

b) Base excision repair could be done to repair the DNA damaged by base analogs in which the faulty base is removed using enzymes like glycosylases and AP endonucleases.

c) Hypomorphic mutation is the type in which the normal function of the gene is lost . A single base pair mutation can be hypomorphic as the normal gene is altered due to base pair substitution resulting in formation of different protein.

d) A type of mutation that is not single base pair mutation is - Deletion mutation. This could be caused by both physical or chemical mutagens. Physical mutagen like UV radiation can cause dimerisation of bases which are eventually deleted from the DNA sequences causin mutation.

Add a comment
Know the answer?
Add Answer to:
This question is about DNA damage, repair and mutation. a) State a type of mutagen that...
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
  • 1. You have used a mutagen to induce mutations in a DNA sequence.  If the original DNA...

    1. You have used a mutagen to induce mutations in a DNA sequence.  If the original DNA strand is 5'-ATGGGACTAGATACC-3', then which of the following represents a nonsense mutation? (1pt) 5'-ATGGGTCTAGATACC-3' 5'-ATGCGACTAGATACC-3' 5'-ATGTGACTAGATACC-3' 5'-ATGGGACTAAGATACC-3' 2. A mutation that changes a codon sequence, and subsequently changes the amino acid that should have been placed at that point in the polypeptide chain, is called a… (1pt) silent mutation frameshift mutation missense mutation nonsense mutation 3. Excision repair corrects DNA by (1pt) correcting A=T...

  • 1. How would a mutation in the poly(A)-binding protein gene affect translation? How would an electron...

    1. How would a mutation in the poly(A)-binding protein gene affect translation? How would an electron micrograph of polyribosomes from such a mutant differ from the normal pattern? 2. Eukaryotes have repair systems that prevent mutations due to copying errors and exposure to mutagens. What are the three excision-repair systems found in eukaryotes, and which one is responsible for correcting thymine-thymine dimers that form as a result of UV light damage to DNA? 3. What is the name given to...

  • A single mutation has occurred in the following DNA sequence. 5' ATG TTG GCC CAT 3'...

    A single mutation has occurred in the following DNA sequence. 5' ATG TTG GCC CAT 3' wild-type (normal) sequence 5' ATG TTG CCC CAT 3' mutant sequence    (a) Identify and classify the mutation according to its molecular structure (i.e., insertion, deletion base substitution (transversion), or base substitution (transition)). Briefly explain why you selected this classification. (1.75 marks)    (b) Identify and classify the mutation according to its functional effects (i.e., frameshift, missense, nonsense, or silent). Briefly explain why you...

  • DNA to Protein Describe the mutation that created the HbS allele: type of mutation, location of...

    DNA to Protein Describe the mutation that created the HbS allele: type of mutation, location of mutation on HbA sequence (# of bases from beginning of sequence), nucleotide change (from which base to which base?). Describe the effect of this mutation on amino acid sequence of beta-globin polypeptide chain: effect of mutation on codon, which amino acid was changed (# amino acids from beginning of chain), what was the amino acid change (from which amino acid to which amino acid?)...

  • A single mutation has occurred in the following DNA sequence. 5' ATG TTC CAG CCA 3'...

    A single mutation has occurred in the following DNA sequence. 5' ATG TTC CAG CCA 3' wild-type (normal) sequence 5' ATG TTC TAG CCA 3' mutant sequence a) Identify and classify the mutation according to its molecular structure (i.e., insertion, deletion base substitution (transversion), or base substitution (transition)). Briefly explain why you selected this classification. b) Identify and classify the mutation according to its functional effects (i.e., frameshift, missense, nonsense, or silent). Briefly explain why you selected this classification.

  • A mutation is a permanent change in the sequence of nucleotide bases in a cell's DNA....

    A mutation is a permanent change in the sequence of nucleotide bases in a cell's DNA. Most mutations happen during DNA replication, but their effects are not seen until transcription and translation. Even a small mutation that changes a single nucleotide can have a major impact on the resulting proteins that are made in the cell. с The table following the amino acid chart lists a segment of a normal gene. Type in the corresponding mRNA strand and the amino...

  • A single mutation has occurred in the following DNA sequence. 5' ATG AAA TTA CCA 3'...

    A single mutation has occurred in the following DNA sequence. 5' ATG AAA TTA CCA 3' wild-type (normal) sequence 5' ATG AAG TTA CCA 3' mutant sequence (a) Identify and classify the mutation according to its molecular structure (i.e., insertion, deletion base substitution (transversion), or base substitution (transition)). Briefly explain why you selected this classification (1.75 marks) (b) Identify and classify the mutation according to its functional effects (i.e., frameshift, missense, nonsense, or silent). Briefly explain why you selected this...

  • Explain what classifies a mutation as “temperature‑sensitive” by comparing phenotype(s) with a wildtype allele. How is this type of phenotype explained by protein behaviour? Would the following typ...

    Explain what classifies a mutation as “temperature‑sensitive” by comparing phenotype(s) with a wildtype allele. How is this type of phenotype explained by protein behaviour? Would the following types of mutations most likely have: severe effects, mild effects, or no effect on protein function? Briefly explain your answers. Note that there may be more than one correct answer, but you need only to give one sensible answer and explain your reasoning.                                                                                                                                               [6 marks] A nonsense mutation occurring in sequences encoding amino...

  • Review Questions BIOL 260: Chapters 8-10, 13, 19 1. Consider a mutation involving the deletion of...

    Review Questions BIOL 260: Chapters 8-10, 13, 19 1. Consider a mutation involving the deletion of either 1, 2, or 3 nucleotides in the DNA of a bacterium. Which of these mutations (ie., deletion of 1, 2, or 3 nucleotides) would likely have the LEAST impact on the organism? Why? Include in your answer a comparison with the other two options to justify your reasoning. Think carefully about the impact each mutation would have on the ultimate protein coded for...

  • I-Upon heavy damage to the cell'S DNA, the normal y stall when encountering replicative DNA polymerases...

    I-Upon heavy damage to the cell'S DNA, the normal y stall when encountering replicative DNA polymerases ma damaged DNA, triggering the use of backup translesion polymerases. These backup polymerases (2 marks) A. have 5'-to-3' exonucleolytic proofreading activity B. are substituted by the replicative polymerases after adding only a few nucleotides. C. can generate mutations only on undamaged DNA D. may identify specific D NA damage and add the suitable nucleotide to restore the original sequence. E. All of the above...

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