Chromosomal rearrangement

Some chromosomal regions are more prone to rearrangement than others and thus are the source of genetic diseases and cancer. This instability is usually due to the propensity of these regions to misalign during DNA repair, exacerbated by defects of the appearance of replication proteins (like FEN1 or Pol δ) that ubiquitously affect the integrity of the genome. Complex chromosomal rearrangements (CCR) are rarely seen in the general population and are defined as structural chromosomal rearrangements with at least three breakpoints with exchange of genetic material between two or more chromosomes. Some forms of campomelic dysplasia, for example, result from CCRs.

Heng and Gorelick and Heng reviewed evidence that sexual reproduction helps preserve species identity by acting as a coarse filter, weeding out chromosomal rearrangements, but permitting minor variation, such as changes at the nucleotide or gene level (that are often neutral) to pass through the sexual sieve.

In the liver of mice, genome rearrangements do not increase with age until after 27 months when they increase rapidly. In mouse brain the frequency of genome rearrangements is lower than in liver and this frequency does not increase with age.

It is possible that speciation frequently occurs when a population becomes fixed for one or more chromosomal rearrangements that reduce fitness when they are heterozygous. This theory is lacking in theoretical support because mutations that cause a large reduction in fitness can only be fixed through genetic drift in small, inbred populations, and the effects of chromosomal rearrangements on fitness are unpredictable and vary greatly in plant and animal species. However, a potential mechanism that could promote speciation is that rearrangements reduce gene flow more by suppressing recombination (and extending the effects of linked isolation genes) than by reducing fitness.

Exemplifying (extensive) chromosome rearrangements can be found in the complete and haplotype-resolved African cassava (TME204) genome that was reconstructed and made available using the Hi-C technology.