Substitution mutation

Definition

noun, plural: substitution mutations

(genetics) A small-scale mutation characterized by a substitution of one or few nucleotides of a gene


Supplement

Mutation is a change in the nucleotide sequence of a gene or a chromosome. Based on the effect of mutation on the gene structure, mutations may be: (1) small-scale mutations or (2) large scale mutations. Small-scale mutations are a type of mutation where one or few nucleotides of a gene are affected. They are further classified as follows: (1) substitution mutations, (2) insertion mutations, and (3) deletion mutations.

Substitution mutations are a type of mutation in which a single nucleotide is substituted with a different nucleotide. Examples of (base-pair) substitutions: a purine is substituted with a different purine (A → G) or a [[pyrimidine],] for a different pyrimidine (C → T). This type of substitution mutation is referred to as transition. Another type of base-pair substitution is the so-called transversion. In transversion, a purine is substituted with a pyrimidine or a pyrimidine with a purine.

Substitution mutations may also be typified into: silent mutations, missense mutations, and nonsense mutations.

Substitution mutation is sometimes referred to as point mutation. However, point mutation is defined particularly as a type of mutation involving a change of only one nucleotide.


See also:

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