TytoAlba95
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I got this question in an exam. Why do silent mutations always affect the third position of a codon? I have no clue about it.
Silent mutations predominantly affect the third position of a codon due to the redundancy in the genetic code, where the first two bases determine the specific amino acid. Changes in these first two bases typically result in a different amino acid, leading to potential deleterious effects. The phenomenon is explained by the concept of "wobble base," which allows for variability in the third position without altering the encoded amino acid. Understanding tRNA recognition of codons during translation is crucial for grasping this topic.
PREREQUISITESStudents studying genetics, molecular biologists, and anyone interested in the mechanisms of mutation and protein synthesis.
SanjuktaGhosh said:I got this question in an exam. Why do silent mutations always affect the third position of a codon? I have no clue about it.
Because the first two bases are necessary to specify the type of amino acid to be encoded. And they are both the same base. It wouldn't be silent if it was one of the first two bases because then it would be deleterious. Only the third base can change and you can still encode the same amino acid.SanjuktaGhosh said:I got this question in an exam. Why do silent mutations always affect the third position of a codon? I have no clue about it.