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What mutation?

Published in Genetics and Heredity 2 mins read

A mutation is a change in the DNA sequence of an organism.

Understanding Mutations

According to the provided reference, a mutation is defined as:

  • A change in the DNA sequence of an organism. This change can alter the genetic instructions that cells follow.

Causes of Mutations

Mutations can arise from several sources:

  • Errors in DNA replication during cell division: When cells divide, they must copy their DNA. Mistakes can happen during this copying process.
  • Exposure to mutagens: Mutagens are agents that can damage DNA. Examples include:
    • Certain chemicals
    • Radiation (e.g., UV radiation, X-rays)
  • Viral infection: Some viruses can insert their DNA into the host cell's DNA, causing mutations.

Example of Mutation

Mutation Type Description Example
Point Mutation Change in a single nucleotide base. Sickle cell anemia caused by a single base change in the beta-globin gene.
Insertion Addition of one or more nucleotide base pairs. Some cases of Huntington's disease due to increased repeats of a specific DNA sequence.
Deletion Loss of one or more nucleotide base pairs. Cystic fibrosis caused by deletion of a specific amino acid in the CFTR protein.

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