Table of Contents
- 1 Which of the following mutations would change the amino acid sequence of a protein?
- 2 Which of the following mutation or change in amino acid would most likely affect the protein function the most?
- 3 Which of the following mutations will not result in a change to the amino acid sequence of a protein?
- 4 Which of the following mutation will not result in a change to amino acid sequence of protein?
- 5 What gene mutations have the greatest effect?
- 6 What are the 3 types of mutations?
- 7 What is it called when only one amino acid changes?
- 8 Which Mutation ultimately ends up affecting the position of the reading?
Which of the following mutations would change the amino acid sequence of a protein?
A missense mutation is a mistake in the DNA which results in the wrong amino acid being incorporated into a protein because of change, that single DNA sequence change, results in a different amino acid codon which the ribosome recognizes. Changes in amino acid can be very important in the function of a protein.
Which of the following mutation or change in amino acid would most likely affect the protein function the most?
Although there are other possibilities, the most likely mutation would be a silent point mutation where a single base is changed, but the changed codon still codes for the same amino acid.
Which type of mutation creates the greatest change in the protein sequence?
The type of mutation that is likely to have the greatest effect on a protein is B. Nonsense mutation. This is because a nonsense mutation creates a premature stop codon, leading to an incomplete formation of a protein, severely affecting protein structure and function.
Which of the following types of mutations Cannot change the amino acid sequence of a protein?
If a mutation does not alter the amino acid sequence of a protein, it is considered a silent mutation. A neutral mutation changes the amino acid, but not the function of the protein. Both frameshift and nonsense mutations can severely affect the function and structure of a protein.
Which of the following mutations will not result in a change to the amino acid sequence of a protein?
A silent mutation is a mutation that occurs within the DNA sequence, but does not alter the amino acid sequence. Silent mutations can occur in introns, which are spliced out before translation.
Which of the following mutation will not result in a change to amino acid sequence of protein?
What are the 4 types of gene mutations?
Summary
- Germline mutations occur in gametes. Somatic mutations occur in other body cells.
- Chromosomal alterations are mutations that change chromosome structure.
- Point mutations change a single nucleotide.
- Frameshift mutations are additions or deletions of nucleotides that cause a shift in the reading frame.
Which of the following types of mutations can result in a frameshift?
A frameshift mutation is a genetic mutation caused by a deletion or insertion in a DNA sequence that shifts the way the sequence is read.
What gene mutations have the greatest effect?
Indels can have a wide variety of lengths. At the short end of the spectrum, indels of one or two base pairs within coding sequences have the greatest effect, because they will inevitably cause a frameshift (only the addition of one or more three-base-pair codons will keep a protein approximately intact).
What are the 3 types of mutations?
There are three types of DNA Mutations: base substitutions, deletions and insertions.
- Base Substitutions. Single base substitutions are called point mutations, recall the point mutation Glu —–> Val which causes sickle-cell disease.
- Deletions.
- Insertions.
Which mutation would cause the most change to the final amino acid sequence?
Frameshift mutations The outcome of a frameshift mutation is complete alteration of the amino acid sequence of a protein. This alteration occurs during translation because ribosomes read the mRNA strand in terms of codons, or groups of three nucleotides.
What is the difference between substitution and deletion mutation?
Results in an amino acid substitution nonsense mutation Substitutes a stop codon(which is a three nucleotide) for an amino acid. Deletion mutation (chromosomal) is a mutation (a genetic aberration) in which a part of a chromosome or a sequence of DNA is lost during DNA replication.
What is it called when only one amino acid changes?
A type of substitution in which one amino acid changes is called Missense A type of substitution in which no amino acids change is called silent If you are missing or have an extra base at the end of your mutated DNA. What type of mutation occurred?
Which Mutation ultimately ends up affecting the position of the reading?
A frameshift mutation ultimately ends up affecting the position of the Reading frame WHAT TYPE OF GENE MUTATION RESULTS FROM THE INSERTION OR DELETION OF NUCLEOTIDES AND ALTERS THE ENTIRE AMINO ACID SEGUENCE FROM THAT POINT FORWARD? FRAMESHIFT