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A mutation is an alteration in a DNA sequence that can occur due to copying errors during replication or any physical or chemical damage to DNA.
The most common types of mutations are point mutations.
Here, a single nucleotide change can produce a protein that is either totally normal or completely non-functional, depending on the type of point mutation. These include silent, missense, nonsense, and frameshift mutations.
Silent mutations do not alter the amino acid sequence of a protein. For instance, if the codon CCA is changed to CCG, it will still encode for the amino acid, proline, and the protein will function normally.
Missense mutations, on the other hand, result in the substitution of one amino acid for another, such as glutamine instead of proline, which can cause the protein to malfunction.
Nonsense mutations occur when a codon for an amino acid is changed to a stop codon. This signals the cell to stop translation, resulting in a prematurely truncated protein that is often non-functional.
Finally, in the case of frameshift mutations, insertion or deletion of one or more nucleotides shifts the reading frame on the mRNA. This results in new codons that encode for a different amino acid sequence and an abnormal protein.
Mutations are changes in the sequence of DNA. These changes can occur spontaneously or they can be induced by exposure to environmental factors. Mutat…
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