A mutation that altered a single nucleotide within the anti-codon of a tRNA molecule could be expected to have which of the following consequences? The polypeptide amino acid sequence could be altered due to an incorrect amino acid bound to the mutant tRNA. This would be less likely to affect the amino acid sequence if the mutation occurred on nucleotide 1 or 2 of the anti-codon. The polypeptide amino acid sequence could be altered due to incorrect base-pairing between the mutant tRNA and mRNA codons. More than one option is possible.
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A mutation in DNA generates a UGA stop codon in the middle of the mRNA coding for a particular protein. A second mutation in the cell's DNA leads to a single nucleotide change in a tRNA that allows the correct translation of the protein; that is, the second mutation "suppresses" the defect caused by the first. The altered tRNA translates the UGA as tryptophan. What nucleotide change has probably occurred in the mutant tRNA molecule? What consequences would the presence of such a mutant tRNA have for the translation of the normal genes in this cell?
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A mutation in DNA generates a UGA stop codon in the middle of the mRNA coding for a particular protein. A second mutation in the cell's DNA leads to a single nucleotide change in a tRNA that allows the correct translation of this protein; that is, the second mutation 'suppresses" the defect caused by the first. The altered tRNA translates the UGA as tryptophan. What nucleotide change has probably occurred in the mutant tRNA molecule? What consequences would the presence of such a mutant tRNA have for the translation of the normal genes in this cell?
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