AP BIOLOGY

THE MOLECULAR BASIS OF INHERITANCE

GENE MUTATION

Question [CLICK ON ANY CHOICE TO KNOW THE RIGHT ANSWER]
Which mutation causes an amino acid change, in every codon following the mutation? (check all that apply)
A
Deletion
B
Insertion
C
Substitution
Explanation: 

Detailed explanation-1: -A frameshift variant occurs when there is an addition or loss of nucleotides that shifts the grouping and changes the code for all downstream amino acids. The resulting protein is usually nonfunctional. Insertions, deletions, and duplications can all be frameshift variants.

Detailed explanation-2: -Definition. A missense mutation is a DNA change that results in different amino acids being encoded at a particular position in the resulting protein.

Detailed explanation-3: -A point mutation is a change in a single nucleotide in DNA. This type of mutation is usually less serious than a chromosomal alteration. An example of a point mutation is a mutation that changes the codon UUU to the codon UCU. Point mutations can be silent, missense, or nonsense mutations, as shown in Table below.

Detailed explanation-4: -A mutation in the amino acid sequence may alter the structure of a protein but it does not necessarily alter its function, although, the mutation at specific sites such as conserved residues can bring about a change in the structure and function of the protein.

Detailed explanation-5: -Mutations can be of many types, such as substitution, deletion, insertion, and translocation.

There is 1 question to complete.