To determine the effect of the mutation that changes the DNA sequence from CGACCTGAA to CGACCTCAA, we will analyze the nature of the mutation and its potential impact on the protein.
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Identify the change: The mutation involves a single base substitution where 'G' in CGACCTGAA is changed to 'C', changing the sequence to CGACCTCAA.
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Determine the implications:
- A base substitution is when one nucleotide in the DNA sequence is replaced by another. In this case, G (guanine) is replaced by C (cytosine).
- Depending on which base is replaced and what the new base is, this could either lead to a synonymous (no change in amino acid) or nonsynonymous (change in amino acid) effect on the resulting protein.
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Codon analysis:
- The original sequence CGACCTGAA, when translated, would correspond to specific codons for amino acids. If we break it down:
- CGA - Arginine (R)
- CCT - Proline (P)
- GAA - Glutamic acid (E)
- The mutated sequence CGACCTCAA:
- CGA - Arginine (R)
- CCT - Proline (P)
- CAA - Glutamine (Q)
Here, the last codon changes from GAA (Glutamic acid) to CAA (Glutamine). This means there is a change in the amino acid sequence at the end of the protein.
- The original sequence CGACCTGAA, when translated, would correspond to specific codons for amino acids. If we break it down:
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Conclusion: Since this is a substitution that results in a different amino acid being incorporated into the protein, it is a point mutation (single base alteration) that changes the protein sequence.
Thus, the correct option that describes the outcome of the mutation is: d: a point mutation substitution resulting in a different protein.