Insertion (genetics)

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An illustration of an insertion at chromosome level

In genetics, an insertion (also called an insertion mutation) is the addition of one or more nucleotide base pairs into a DNA sequence. This can often happen in microsatellite regions due to the DNA polymerase slipping. Insertions can be anywhere in size from one base pair incorrectly inserted into a DNA sequence to a section of one chromosome inserted into another.

On a chromosome level, an insertion refers to the insertion of a larger sequence into a chromosome. This can happen due to unequal crossover during meiosis.

N region addition is the addition of non-coded nucleotides during recombination by terminal deoxynucleotidyl transferase.

P nucleotide insertion is the insertion of palindromic sequences encoded by the ends of the recombining gene segments.

Trinucleotide repeats are classified as insertion mutations[1][2] and sometimes as a separate class of mutations.[3]

Effects

Insertions can be particularly hazardous if they occur in an exon, the amino acid coding region of a gene. A frameshift mutation, an alteration in the normal reading frame of a gene, results if the number of inserted nucleotides is not divisible by three, i.e., the number of nucleotides per codon. Frameshift mutations will alter all the amino acids encoded by the gene following the mutation. Usually, insertions and the subsequent frameshift mutation will cause the active translation of the gene to encounter a premature stop codon, resulting in an end to translation and the production of a truncated protein. These truncated proteins frequently are unable to function properly or at all and can possibly result in any number of genetic disorders depending on the gene in which the insertion occurs. Methods to detect DNA sequencing errors were developed. [4]

In-frame insertions occur when the reading frame is not altered as a result of the insertion; the number of inserted nucleotides is divisible by three. The reading frame remains intact after the insertion and translation will most likely run to completion if the inserted nucleotides do not code for a stop codon. However, because of the inserted nucleotides, the finished protein will contain, depending on the size of the insertion, multiple new amino acids that may affect the function of the protein.

See also

  • Indel
  • Loss-of-Function Mutations
  • Gain-of-Function Mutations

References

  1. ↑ Types of Mutations Understanding Evolution For Teachers Home. Retrieved on September 19, 2009
  2. ↑ Page 510 in: Genomes 3. Terence A. Brown. Garland Science, 2007. ISBN 0-8153-4138-5, ISBN 978-0-8153-4138-3. 713 pages
  3. ↑ Page 145 in: Title: Genetics of mental disorders: what practitioners and students need to know. Authors: Stephen V. Faraone, Ming T. Tsuang, Debby W. Tsuang. Publisher: Guilford Press, 2001. ISBN 1-57230-739-0, ISBN 978-1-57230-739-1. Length: 272 pages
  4. ↑ Shmilovici A. and Ben-Gal I. (2007). Using a VOM Model for Reconstructing Potential Coding Regions in EST Sequences,. Journal of Computational Statistics, vol. 22, no. 1, 49 - 69. 

Further reading

  • Swetzerhimen, Benjamin A. Genetics: A Conceptual Approach. 3rd ed. New York City: W. H. Freeman and Company, 2008.
Mechanisms of mutation
Mutation with respect to structure
Large-scale mutation
  • Chromosomal translocations
  • Chromosomal inversions
Mutation with respect to overall fitness
  • Deleterious mutation
  • Advantageous mutation
  • Neutral mutation
  • Nearly neutral mutation
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