Despite several reports on directed mutagenesis using UV to induce double stranded breaks, advent of CRISPR-Cas9 system has added unambiguity to the site of excision. Employing site directed double strand breaks, Manganese sensitivity loci in Yeast was fine mapped to single polymorphism.3 While reducing the colonies to be screened, the study could also demonstrate increased confidence level of localizing the region on the genome. This principle was extrapolated to field crops by Rex Bernardo, who observed that the relative efficiency of targeted recombinations can theoretically be 212 per cent over natural recombinations, for even complex traits like grain yield in Maize. Similar results were published in Soybean, Wheat, Pea and Barley where targeted recombination in less than one third of all the chromosomes have led to same or higher predicted gains2 than natural ones.
To date, targeted recombination has only been conceptualized in theory. While, bringing into play requires fine tuning of the methodologies to fit into practical outfits. On the flip side are, population specificity of the targets. Further, desirable recombination for a given trait could turn out to be undesirable for another. Under such circumstances, selection indices are to be preferred to prioritize the target points of recombination. Potentially, the use of this concept can be felt in marker assisted backcross breeding to considerably reduce linkage drag and population size to be screened. In summary, targeted recombinations can serve as a potential tool in realizing higher crop genetic gains when put into practice.
Bibliography:
1. Allard, R. W., 1960, Principles of Plant Breeding. John Wiley and Sons, New York.
2. Ru, S. and Bernardo, R., 2019, Targeted recombination to increase genetic gain in self pollinated species. Theor. Appl. Genet., 132: 289-300.
3. Sadhu, M. J., Bloom, J. S., Day, L. and Kruglyak, L., 2016, CRISPR-directed mitotic recombination enables genetic mapping without crosses. Science, 352 (6289): 1113-1116.
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