Student A believes that a missense mutation would lead to a nonfunctioning protein. Student B believes that the insertion of 3 nucleotides would be more likely to lead to a nonfunctioning protein. Student C disagrees with both student A and B claiming that such mutations would not alter the function of the protein. WHos perspective is the most correct and why?
A nonsense mutation may be a mutation during a DNA sequence that leads to a shorter, unfinished protein product. DNA may be a chain of the many smaller molecules called nucleotides. During protein formation, DNA (or RNA) nucleotide sequences are read three nucleotides at a time in units called codons, and every codon corresponds to a selected aminoalkanoic acid or stop signal (stop codon). Stop codons also are called nonsense codons because they are doing not code for an aminoalkanoic acid and instead signal the top of protein synthesis. Thus, nonsense mutations occur when a premature nonsense or stop codon is introduced within the DNA sequence. When the mutated sequence is translated into a protein, the resulting protein is incomplete and shorter than normal. Consequently, most nonsense mutations end in nonfunctional proteins.
Missense mutation means change in one amino acid in a protein, arising from a point mutation in a single nucleotide AND it is a type of nonsynonymous substitution in a DNA sequence. Another type of nonsynonymous substitution is a nonsense mutation in which a codon is changed to a premature stop codon that results in truncation of the resulting protein. Missense mutations can resulting protein nonfunctional.
An insertion changes the number of DNA bases in a gene by adding a piece of DNA. As a result, the protein made by the gene may not function properly.
so student A is more correct
Student A believes that a missense mutation would lead to a nonfunctioning protein. Student B believes...
11. Match each type of mutation with the corresponding description. (4 points) Missense An insertion or deletion of nucleotides that are not in multiples of 3. Nonsense A mutation that does not alter the protein sequence. Silent A mutation that confers an amino acid substitution. Frameshift A mutation that confers a premature stop codon.
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...
Why is an insertion or deletion more likely to result in a damaging mutation than a point mutation? 1.Point mutations only change two or three nucleotides 2.Point mutations never change the amino acid that is called for in the protein 3.Insertions/deletions change all codons that follow them, unless they are indels of 3, 6, 9, etc 4.Point mutations cannot result in a stop codon, whereas insertions and deletions can.
Genetics Worksheet Week 3: Gene Regulation and Epigenetics 1. Duchenne muscular dystrophy is caused by a mutation in a gene that is 2.5 million nucleotides in length and encodes a protein called dystrophin. The dystrophin protein itself is 3684 amino acids in length. Calculate below the approximate size of the mRNA that encodes dystrophin. Approximately what percentage of the gene that encodes dystrophin is intron sequence? The human genome encodes a much greater variety and number of proteins than the...
A mutation occurs that causes the promoter of a gene to over-express a protein. Would this most likely be a gain of function or loss of function mutation? Why?
How could an early stop mutation lead to an N-terminal truncated protein? What experiments would you conduct to confirm this hypothesis? (This is in regard to an article on BRCA 1 mutations, but this question is in general)
1. Tryptophan (Trp) is encoded by the codon UGG. Suppose that a cell was treated with high levels of 5-Bromouracil such that mutations were induced at Trp codons. Would you expect that these mutations would results in a non-sense mutation, a silent mutation, a missense mutation. Explain your answer.What is a tautomeric shift and explain how it contributes to transition mutations? 2.Draw the structure of the rare tautomeric enol form of guanine. Draw the structure of the monophosphate deoxynucleotide which...
Which of the following mutations would be most likely to have a harmful effect on an organism? (A) a deletion of three nucleotides near the middle of a gene (B) a single nucleotide deletion in the middle of an intron (C) a single nucleotide deletion near the end of the coding sequence (D) a single nucleotide insertion downstream of, and close to, the start of the coding sequence In this problem, why (c) cannot be the answer?? Single nucleotide deletion...
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...
Please answer 2-5
2. Consider a gene with a particular function. Mutation X and mutation Y cach cause defects in the function of the encoded protein, yet a gene containing both mutations X and Y encodes a protein that works even better than the original protein. The odds are exceedingly small that a single mutational event will generate both mutations X and Y. Explain a simple way that an organism with a mutant gene containing both mutations X and Y...