Chapter 6: Mutation





Chapter 6: Mutation


Chapter 6: Mutation

Concept:

  • Mutant: An organism that carries a mutated gene and expresses it as a phenotype.
  • Gene mutation: A change in the structure of a gene, involving one or a few nucleotide pairs.

Point mutation:

  • Loss or addition of nucleotides: Causes a frameshift in the reading frame of the genetic code, especially severely affecting if it occurs near the 3′ end of the template strand.
  • Nucleotide substitution:
  • May not alter the polypeptide chain due to the degeneracy of the genetic code.
  • Or change an amino acid in the polypeptide chain.
  • Cause premature termination of translation, resulting in a shorter polypeptide chain.

Mechanism of occurrence:

  • Mutagenic agents:
  • UV rays: Cause cross-linking between two thymines on the same DNA strand.
  • Chemicals:
  • 5-bromouracil: Replaces adenine with 5-bromouracil, which then pairs with guanine instead of adenine.
  • Alkylating agents: Replace guanine with 6-methylguanine, leading to pairing with thymine instead of cytosine.
  • Rare bases: Cause changes in the pairing position with the gene, leading to mispairing and nucleotide substitution.

Consequences of gene mutation:

  • Can be beneficial, harmful, or neutral.
  • The level of harm depends on environmental conditions and gene combinations.

Role:

  • Forms new alleles.
  • Is the primary fuel for evolution.

Somatic mutation:

  • Occurs in somatic cells.
  • Not inherited to offspring through sexual reproduction.



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