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There are two popular and overlapping theories that explain the origins of crossing-over, coming from the different theories on the origin of meiosis.The first theory rests upon the idea that meiosis evolved as another method of DNA repair, and thus crossing-over is a novel way to replace possibly damaged sections of DNA. [9]
Gene conversion is the process by which one DNA sequence replaces a homologous sequence such that the sequences become identical after the conversion. [1] Gene conversion can be either allelic, meaning that one allele of the same gene replaces another allele, or ectopic, meaning that one paralogous DNA sequence converts another.
In genetics, the crossover value is the linked frequency of chromosomal crossover between two gene loci ().For a fixed set of genetic and environmental conditions, recombination in a particular region of a linkage structure tends to be constant and the same is then true for the crossover value which is used in the production of genetic maps.
Unequal crossing over is the process most responsible for creating regional gene duplications in the genome. [1] Repeated rounds of unequal crossing over cause the homogenization of the two sequences. With the increase in the duplicates, unequal crossing over can lead to dosage imbalance in the genome and can be highly deleterious. [1] [2]
Meiotic recombination through crossing over is thought to be a mechanism by which a cell promotes correct segregation of homologous chromosomes and the repair of DNA damages. Crossing over requires a DNA double-stranded break followed by strand invasion of the homolog and subsequent repair. [ 3 ]
This is an accepted version of this page This is the latest accepted revision, reviewed on 26 January 2025. Cell division producing haploid gametes For the figure of speech, see Meiosis (figure of speech). For the process whereby cell nuclei divide to produce two copies of themselves, see Mitosis. For excessive constriction of the pupils, see Miosis. For the parasitic infestation, see Myiasis ...
Points of crossing over become visible as chiasma after the synaptonemal complex dissembles and the homologous chromosomes slightly apart from each other. The phenomenon of genetic chiasmata ( chiasmatypie ) was discovered and described in 1909 by Frans Alfons Janssens , a Professor at the University of Leuven in Belgium .
Resolution of the DNA recombination intermediate into a crossover exchanges DNA segments between the two homologous chromosomes at a site called a chiasma (plural: chiasmata). This physical strand exchange and the cohesion between the sister chromatids along each chromosome ensure robust pairing of the homologs in diplotene phase.