Genetics! Gene mapping in 4 steps!

Gene mapping, describes the methods used to identify the locus of a gene and the distances between genes.[1]

Genetic linkage was first discovered by the British geneticists William Bateson, Edith Rebecca Saunders and Reginald Punnett shortly after Mendel's laws were rediscovered.[1][2] The understanding of genetic linkage was expanded by the work of Thomas Hunt Morgan. Morgan's observation that the amount of crossing over between linked genes differs led to the idea that crossover frequency might indicate the distance separating genes on the chromosome.

Alfred Sturtevant, a student of Morgan's, first developed genetic maps, also known as linkage maps. Sturtevant proposed that the greater the distance between linked genes, the greater the chance that non-sister chromatids would cross over in the region between the genes. By working out the number of recombinants it is possible to obtain a measure for the distance between the genes. This distance is expressed in terms of a genetic map unit (m.u.), or a centimorgan and is defined as the distance between genes for which one product of meiosis in 100 is recombinant. A recombinant frequency (RF) of 1% is equivalent to 1 m.u. But this equivalence is only a good approximation for small percentages; the largest percentage of recombinants cannot exceed 50%, which would be the situation where the two genes are at the extreme opposite ends of the same chromosomes. In this situation, any crossover events would result in an exchange of genes, but only an odd number of crossover events (a 50-50 chance between even and odd number of crossover events) would result in a recombinant product of meiotic crossover. A statistical interpretation of this is through the Haldane mapping function or the Kosambi mapping function, among others. A linkage map is created by finding the map distances between a number of traits that are present on the same chromosome, ideally avoiding having significant gaps between traits to avoid the inaccuracies that will occur due to the possibility of multiple recombination events.



The essence of all genome mapping is to place a collection of molecular markers onto their respective positions on the genome. Molecular markers come in all forms. Genes can be viewed as one special type of genetic markers in the construction of genome maps, and mapped the same way as any other markers.




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