Home > Term: frameshift mutation
frameshift mutation
1) An insertion or deletion involving a number of base pairs that is not a multiple of three and consequently disrupts the triplet reading frame, usually leading to the creation of a premature termination (stop) codon and resulting in a truncated protein product
2) A frameshift mutation is a type of mutation involving the insertion or deletion of a nucleotide in which the number of deleted base pairs is not divisible by three. "Divisible by three" is important because the cell reads a gene in groups of three bases. Each group of three bases corresponds to one of 20 different amino acids used to build a protein. If a mutation disrupts this reading frame, then the entire DNA sequence following the mutation will be read incorrectly.
- Μέρος του λόγου: noun
- Κλάδος/Τομέας: Medical
- Category: Human genome
- Company: National Library of Medicine
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Δημιουργός
- Max Bryant
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