Coefficient of coincidence
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In genetics, the coefficient of coincidence (c.o.c.) is a measure of interference in the formation of
chromosomal crossover Chromosomal crossover, or crossing over, is the exchange of genetic material during sexual reproduction between two homologous chromosomes' non-sister chromatids that results in recombinant chromosomes. It is one of the final phases of geneti ...
s during
meiosis Meiosis (; , since it is a reductional division) is a special type of cell division of germ cells in sexually-reproducing organisms that produces the gametes, such as sperm or egg cells. It involves two rounds of division that ultimately resu ...
. It is generally the case that, if there is a crossover at one spot on a chromosome, this decreases the likelihood of a crossover in a nearby spot. Griffiths AJF, Wessler SR, Lewontin RC, Carroll SB (2008) ''Introduction to Genetic Analysis''. New York: W. H. Freeman and Company. This is called interference. The coefficient of coincidence is typically calculated from recombination rates between three genes. If there are three genes in the order A B C, then we can determine how closely linked they are by frequency of recombination. Knowing the recombination rate between A and B and the recombination rate between B and C, we would naively expect the double recombination rate to be the
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of these two rates. The coefficient of coincidence is calculated by dividing the ''actual'' frequency of double recombinants by this expected frequency: :c.o.c. = actual double recombinant frequency / expected double recombinant frequency Interference is then defined as follows: :interference = 1 − c.o.c. This figure tells us how strongly a crossover in one of the DNA regions (AB or BC) interferes with the formation of a crossover in the other region.


Worked example

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females of
genotype The genotype of an organism is its complete set of genetic material. Genotype can also be used to refer to the alleles or variants an individual carries in a particular gene or genetic location. The number of alleles an individual can have in a ...
''a+a b+b c+c'' were crossed with males of genotype ''aa bb cc''. This led to 1000 progeny of the following
phenotype In genetics, the phenotype () is the set of observable characteristics or traits of an organism. The term covers the organism's morphology or physical form and structure, its developmental processes, its biochemical and physiological proper ...
s: :a+b+c+: 244 (parental genotype, shows no recombination) :a+b+c: 81 (recombinant between B and C) :a+bc+: 23 (double recombinant) :a+bc: 152 (recombinant between A and B) :ab+c+: 148 (recombinant between A and B) :ab+c: 27 (double recombinant) :abc+: 89 (recombinant between B and C) :abc: 236 (parental genotype, shows no recombination) From these numbers it is clear that the b+/b
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lies between the a+/a locus and the c+/c locus. There are 23 + 152 + 148 + 27 = 350 progeny showing recombination between genes A and B. And there are 81 + 23 + 27 + 89 = 220 progeny showing recombination between genes B and C. Thus the expected rate of double recombination is (350 / 1000) * (220 / 1000) = 0.077, or 77 per 1000. However, there are actually only 23 + 27 = 50 double recombinants. The coefficient of coincidence is therefore 50 / 77 = 0.65. Interference is 1 − 0.65 = 0.35.


High negative interference

When three genetic markers, a, b and c, are all nearby (e.g. within the same
gene In biology, the word gene (from , ; "...Wilhelm Johannsen coined the word gene to describe the Mendelian units of heredity..." meaning ''generation'' or ''birth'' or ''gender'') can have several different meanings. The Mendelian gene is a ba ...
) the coefficient of coincidence (calculated as in the above example) is generally found to be significantly greater than 1. This implies that any individual recombination event tends to be more closely associated with another nearby recombination event than would be expected by chance. This type of association is known as “negative interference”. When the coefficient of coincidence is substantially greater than 1, it is known as “high negative interference". High negative interference has been reported in
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(e.g. ) and in human imunodeficiency virus (
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) infections.Anderson JA, Teufel RJ 2nd, Yin PD, Hu WS. Correlated template-switching events during minus-strand DNA synthesis: a mechanism for high negative interference during retroviral recombination. J Virol. 1998 Feb;72(2):1186-94. PMID 9445017


References

Genetics