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marker-assisted selection in wheat - ictsd

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Chapter 8 – Marker-<strong>assisted</strong> <strong>selection</strong> <strong>in</strong> maize 133of which are related to time and resourceallocations.MABC clearly provides the <strong>in</strong>formationneeded to reduce the number of generationsof backcross<strong>in</strong>g, to comb<strong>in</strong>e (i.e.“stack”) transgenes, “native” genes or QTL<strong>in</strong>to one <strong>in</strong>bred or hybrid quickly, and tomaximize the recovery of the recurrentparent’s genome <strong>in</strong> the backcross-derivedprogeny. In several private breed<strong>in</strong>g programmes,MABC has enabled the numberof backcross<strong>in</strong>g generations needed torecover 99 percent of the recurrent parentgenome to be reduced from six to three,reduc<strong>in</strong>g the time needed to develop a convertedvariety by one year (Crosbie et al.,2006; Ragot et al., 1995). As a l<strong>in</strong>e derivedby MABC can be made to be very similarto the orig<strong>in</strong>al non-converted l<strong>in</strong>e, mostof its attributes, <strong>in</strong>clud<strong>in</strong>g agronomic performance,can be assumed to be equal orsimilar to those of the orig<strong>in</strong>al l<strong>in</strong>e. Onlylimited phenotyp<strong>in</strong>g is therefore necessaryto verify these assumptions, comparedwith the extensive multiyear phenotyp<strong>in</strong>grequired when backcross<strong>in</strong>g is conductedwithout <strong>marker</strong>s. One or two years can besaved with MABC dur<strong>in</strong>g post-conversionphenotyp<strong>in</strong>g when compared with conventionalbackcross<strong>in</strong>g, result<strong>in</strong>g <strong>in</strong> an overalltime advantage of MABC over conventionalbackcross<strong>in</strong>g of up to three years.In many situations, the greatest advantagesand profits are realized by those whoare first to the market with their products.Also, for reasons related to the practicesof seed production or legal aspects of cropregistration procedures, it may be quiteimportant to be able to produce nearisogenicversions of <strong>in</strong>breds and hybrids;MABC provides such ability at a higherprobability.By contrast with MABC, SLS-MAS andMARS do not necessarily decrease the timeneeded to develop <strong>in</strong>bred l<strong>in</strong>es. The useof MARS might actually <strong>in</strong>crease it. Theadvantage of SLS-MAS and MARS resides<strong>in</strong> their ability to <strong>in</strong>crease the rate of geneticga<strong>in</strong> (Eath<strong>in</strong>gton, 2005), which potentiallyresults <strong>in</strong> higher perform<strong>in</strong>g l<strong>in</strong>es andhybrids than can be developed through phenotypic<strong>selection</strong> only. Both SLS-MAS andMARS <strong>in</strong>crease the frequency of favourablealleles <strong>in</strong> the population of selected<strong>in</strong>dividuals. The difference between thetwo approaches is that SLS-MAS operateson few loci while MARS operateson many. When SLS-MAS or MARS areused, the effective size of the populationon which <strong>selection</strong> operates is <strong>in</strong>creased,either directly for SLS-MAS or <strong>in</strong>directlythrough several consecutive generations forMARS when compared with phenotypicpedigree <strong>selection</strong>. This <strong>in</strong>crease <strong>in</strong> effectivepopulation size permits the applicationof a greater <strong>selection</strong> <strong>in</strong>tensity and henceproduces a higher genetic ga<strong>in</strong>. SLS-MASand MARS can also be seen as pre-<strong>selection</strong>steps if conducted prior to phenotypic<strong>selection</strong> and therefore improve the chancesof evaluat<strong>in</strong>g genotypes with a higher frequencyof favourable alleles phenotypicallybecause the truly undesirable portion of thepopulation may have been elim<strong>in</strong>ated priorto phenotyp<strong>in</strong>g. Phenotypic <strong>selection</strong> cantherefore be conducted with higher <strong>selection</strong><strong>in</strong>tensity than would be possible ifno pre-<strong>selection</strong> had taken place, result<strong>in</strong>gpotentially <strong>in</strong> additional genetic ga<strong>in</strong>.Alternatively, the resources used forphenotyp<strong>in</strong>g can be allocated differentlybased on whether <strong>in</strong>dividuals have beenpre-selected or not with MAS. MASschemes for forward breed<strong>in</strong>g should enablebreed<strong>in</strong>g programmes to reallocate or focusresources for phenotypic evaluation <strong>in</strong> thetarget environment. For example, if DNA<strong>marker</strong>s are l<strong>in</strong>ked to genes for resistance

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