Base deletions almost always lead to loss of function of the protein as they involve a shift of the reading frame to the leftThey are therefore called frameshift mutations.Base deletions occur during DNA replication when a nucleotide fails to be incorporated into the new strand.They result in a different sequence of amino acids being added to the polypeptide chain from the point of the deletion.
Cystic fibrosis is caused by a three-nucleotide deletion causing one amino-acid to be lost.
Deletion of Bases
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Specification: AQA Biology (7401), AS-level, 3.4.3 Genetic diversity can arise as a result of mutation or during. Topic: Genetic Diversity.
Key terms in this lesson
- nucleotide
- A molecule made of a pentose sugar, a phosphate group and a nitrogen-containing base.
- mutation
- A random change in the amount, arrangement or base sequence of the DNA of an organism.
More in Genetic Diversity
- Mutations
- Chromosome Mutations
- Gene Mutations
- Substitution of Bases
- Polyploidy and Hybrids
- Meiosis
- The Process of Meiosis
- Genetic Recombination by Crossing Over
All 19 lessons in Genetic Diversity · All AQA AS-level Biology topics