Which type of mutation results in a premature stop codon?

Prepare for the HOSA Human Heredity Exam. Study with flashcards and multiple choice questions, each question has hints and explanations. Get ready for your exam!

Multiple Choice

Which type of mutation results in a premature stop codon?

Explanation:
A nonsense mutation is characterized by a change in the DNA sequence that creates a premature stop codon in the protein coding sequence. This type of mutation alters the codon that would normally code for an amino acid, resulting instead in a signal for the translation process to terminate early. The consequence of this is a truncated protein that is often nonfunctional, as the complete sequence needed for proper folding and function has not been translated. In contrast, a missense mutation results in a change of a single amino acid in the protein, which might or might not affect the protein's function. A frameshift mutation occurs when insertions or deletions of nucleotides alter the reading frame of the genetic sequence, which can lead to significant changes in the resulting protein, including potentially creating a premature stop codon, but not necessarily. Lastly, a silent mutation changes a nucleotide but does not alter the amino acid sequence due to redundancy in the genetic code, ensuring that the full-length protein is produced without premature termination.

A nonsense mutation is characterized by a change in the DNA sequence that creates a premature stop codon in the protein coding sequence. This type of mutation alters the codon that would normally code for an amino acid, resulting instead in a signal for the translation process to terminate early. The consequence of this is a truncated protein that is often nonfunctional, as the complete sequence needed for proper folding and function has not been translated.

In contrast, a missense mutation results in a change of a single amino acid in the protein, which might or might not affect the protein's function. A frameshift mutation occurs when insertions or deletions of nucleotides alter the reading frame of the genetic sequence, which can lead to significant changes in the resulting protein, including potentially creating a premature stop codon, but not necessarily. Lastly, a silent mutation changes a nucleotide but does not alter the amino acid sequence due to redundancy in the genetic code, ensuring that the full-length protein is produced without premature termination.

Subscribe

Get the latest from Examzify

You can unsubscribe at any time. Read our privacy policy