Respuesta :
The nonsense mutation is a point mutation that originates a new stop codon within the sequence. The result of this single base-pair substitution is A nonsense mutation resulting in early termination of translation. OPTION E
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When a change occurs in a single base pair, it is known as a point mutation.
Points mutations might be either silent, missense, or nonsense.
- In silent mutations, the resulting mRNA codon codes for the same amino acid as the unmutated sequence.
- If the mutation causes the mRNA codon to code for a different amino acid, this mutation is a missense mutation.
- Finally, if the mutation causes the mRNA codon to be a stop codon, we are referring to a nonsense mutation.
In the exposed example,
30 31 32 33 34 35 36 37 38 39
Original sequence G C U A U U A A C A
Mutated sequence G C U A U A A A C A
The mutation occurs in base number 35. An adenine replaces the original uracil.
Since only a single base changes, this is a point mutation.
This point mutation originates a new stop codon, which places before the stop codon of the original sequence (UAG) .
We are referring, then, to a NONSENSE MUTATION.
The options are:
A. a silent mutation (no change in the amino acid sequence of the protein)
INCORRECT. It is not a silent mutation
B. a frameshift mutation causing extensive change in the amino acid sequence of the protein
INCORRECT. It does not extensive change in the amino acid sequence
C. a missense mutation causing a single amino acid change in the protein
INCORRECT. It is not a missense mutation.
D. a frameshift mutation causing a single amino acid change in the protein
INCORRECT. It is not a frameshift mutation.
E. a nonsense mutation resulting in early termination of translation
CORRECT. The change of a single base produces a new stop codon placed before the original one.
The result of this single base-pair substitution is A nonsense mutation resulting in early termination of translation. OPTION E
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