Inversion

Last updated on: 04.07.2024

Dieser Artikel auf Deutsch

Requires free registration (medical professionals only)

Please login to access all articles, images, and functions.

Our content is available exclusively to medical professionals. If you have already registered, please login. If you haven't, you can register for free (medical professionals only).


Requires free registration (medical professionals only)

Please complete your registration to access all articles and images.

To gain access, you must complete your registration. You either haven't confirmed your e-mail address or we still need proof that you are a member of the medical profession.

Finish your registration now

HistoryThis section has been translated automatically.

The first evidence of chromosomal inversion was provided by Alfred Sturtevant in Drosophila melanogaster in 1921. Since then, inversions have been found in all eukaryotes.

DefinitionThis section has been translated automatically.

Inversion is a genetic term used to describe a chromosome rearrangement. If two breaks occur in a chromosome, a segment of the chromosome can be inverted in its original position and reinserted at this position. The break sites of inversions are often located in regions with repeating nucleotides, and these regions can be reused in other inversions. Chromosome segments in inversions can be very small, e.g. one kilobase, or very large, e.g. 100 megabases. The number of genes affected by an inversion can range from a few to hundreds of genes.

PathophysiologyThis section has been translated automatically.

Basically, two types of inversions can be distinguished:

  • paracentric inversions
  • and
  • pericentric inversions.

Paracentric inv ersions do not include the centromere, and both breakpoints occur in one arm of the chromosome.

Pericentric inv ersions include the centromere; there is a breakpoint in each arm of the chromosome.

Inversions do not usually cause abnormalities in carriers as long as the rearrangement is balanced. However, in individuals who are heterozygous for an inversion, there is an increased production of abnormal chromatids (this occurs through crossing-over within the inversion span). This leads to reduced fertility, as unbalanced germ cells are produced.

In inversions, there is neither a loss nor a gain of genetic information; only the linear DNA sequence is rearranged.

Note(s)This section has been translated automatically.

Inversions were of crucial importance for the evolution of sex chromosomes. In mammals, the Y chromosome is unable to recombine with the X chromosome along almost its entire length. This non-recombining part results from a series of inversions that overlap.

LiteratureThis section has been translated automatically.

  1. Dagilis AJ (2022) What inversion lengths can tell us about their evolution. Mol Ecol 31:3513-3515.
  2. Miller K et al. (1990) Paracentric inversion 14. Ann Genet 33:225-227.
  3. Madan K (1995) Paracentric inversions: a review. Hum Genet 96:503-515.
  4. Villoutreix R et al. (2021) Inversion breakpoints and the evolution of supergenes. Mol Ecol 30:2738-2755.

Last updated on: 04.07.2024