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marker-assisted selection in wheat - ictsd

marker-assisted selection in wheat - ictsd

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132Marker-<strong>assisted</strong> <strong>selection</strong> – Current status and future perspectives <strong>in</strong> crops, livestock, forestry and fishwith up to four cycles per year, whereasphenotypic recurrent <strong>selection</strong> is limitedto one cycle per year at most. The impacton the rate of genetic ga<strong>in</strong> of such animplementation of MARS might be verypositive even if MARS did not presentany advantage over phenotypic <strong>selection</strong>on a per-cycle basis.• Cost of <strong>marker</strong> data po<strong>in</strong>ts. Large privatecompanies have made considerable effortsto reduce both the cost of <strong>marker</strong> datapo<strong>in</strong>ts and the cost of experimental fieldplots. The ratio of cost of <strong>marker</strong> datapo<strong>in</strong>t to cost of experimental field plot ismost likely lower <strong>in</strong> large private breed<strong>in</strong>gprogrammes than <strong>in</strong> most public researchlaboratories or small private programmes,potentially lead<strong>in</strong>g to different views onthe economic efficiency of MARS.Marker-based and phenotypic <strong>selection</strong>can be mobilized <strong>in</strong> many different ways,with respect to each other, <strong>in</strong> <strong>marker</strong><strong>assisted</strong>breed<strong>in</strong>g schemes. Marker andphenotypic <strong>in</strong>formation can be used eithersimultaneously or sequentially. Selectionof parents for breed<strong>in</strong>g populations canbe made us<strong>in</strong>g <strong>marker</strong> <strong>in</strong>formation alone,phenotypic <strong>in</strong>formation alone, or a comb<strong>in</strong>ationof each. Selection of <strong>in</strong>dividuals <strong>in</strong> abackcross programme can be made on thesole basis of either <strong>marker</strong> or phenotypic<strong>in</strong>formation, or us<strong>in</strong>g both. Advancementof <strong>in</strong>dividuals <strong>in</strong> a l<strong>in</strong>e development programmecan also be made at each generationon the basis of either <strong>marker</strong> <strong>in</strong>formationonly, phenotypic <strong>in</strong>formation only, or acomb<strong>in</strong>ation of each. In order to maximizethe rate of genetic ga<strong>in</strong> it is likely thatMAS breed<strong>in</strong>g schemes such as MABCand MARS will <strong>in</strong>volve generations of<strong>marker</strong>-only <strong>selection</strong> conducted at cont<strong>in</strong>uousnurseries. The advent of improvedmethods of produc<strong>in</strong>g doubled haploidswill certa<strong>in</strong>ly further <strong>in</strong>fluence the way<strong>marker</strong>-based and phenotypic <strong>selection</strong> aremobilized with respect to each other.In spite of the development of<strong>marker</strong>-only <strong>selection</strong> and regardless ofthe underly<strong>in</strong>g technology and breed<strong>in</strong>gscheme, high-quality phenotyp<strong>in</strong>g rema<strong>in</strong>svital and without substitute at severalstages; but it may become more focused.Phenotypic evaluation rema<strong>in</strong>s the ultimatescreen before any cultivar is released.MAS-derived l<strong>in</strong>es and hybrids that meetphenotypic requirements are selected forfurther evaluation and <strong>selection</strong> on the basisof their phenotypic value, while those thatdo not are discarded. Phenotypic evaluationis also critical to establish <strong>marker</strong>-traitassociations or perform the candidate genevalidations required to conduct MAS.Here, high quality phenotyp<strong>in</strong>g is necessary.Phenotyp<strong>in</strong>g protocols will thereforelikely be different from those commonlyused for phenotypic <strong>selection</strong>. Experimentsmay be conducted that <strong>in</strong>volve side-by-sidecomparisons of different treatments such aswater stress or nitrogen fertilization levelsto dissect complex traits <strong>in</strong>to their componentsand facilitate the elucidation of theirgenetic basis.Enhancements of such approachesto maize breed<strong>in</strong>g will be based on the<strong>in</strong>corporation of improved methods ofproduc<strong>in</strong>g doubled haploid <strong>in</strong>bred l<strong>in</strong>es,<strong>in</strong>formation from functional genomics andby learn<strong>in</strong>g how to <strong>in</strong>corporate favourablenative genetic variation systematically afterMAS has reduced the genetic variation<strong>in</strong> the orig<strong>in</strong>al reference populations tounacceptable levels.Advantages and limitations ofMAS <strong>in</strong> maize breed<strong>in</strong>g programmesAdvantages of MASFor private breed<strong>in</strong>g programmes, MAShas offered several attractive features, most

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