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marker-assisted selection in wheat - ictsd

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38Marker-<strong>assisted</strong> <strong>selection</strong> – Current status and future perspectives <strong>in</strong> crops, livestock, forestry and fishFigure 1Progress of microsatellite <strong>marker</strong> development <strong>in</strong> riceMcCouch et al., 2002Temnykh et al., 2001Temnykh et al., 2000Chen et al., 1997Akagi et al., 1996Panaud, Chen andMcCouch, 1996Wu and Tanksley, 1993Zhao and Kochert, 19930 500 1000 1500 2000Number of microsatellite <strong>marker</strong>sScreened libraries Genes/ESTs BAC-ends Shotgun sequences F<strong>in</strong>ished BACstracks the publication of rice microsatellite<strong>marker</strong>s derived from screen<strong>in</strong>g libraries ofclones and from the various categories ofsequences deposited <strong>in</strong> public databases. Theearliest method of develop<strong>in</strong>g microsatellite<strong>marker</strong>s <strong>in</strong> rice was by us<strong>in</strong>g microsatellitesequences as probes to isolate clones fromgenomic libraries (Zhao and Kochert, 1993;Wu and Tanksley, 1993; Panaud, Chen andMcCouch, 1996; Akagi et al., 1996; Chenet al., 1997; Temnykh et al., 2000). In 1996,Akagi et al. used microsatellite repeatsfound <strong>in</strong> rice sequences from databasesearches to develop 35 new <strong>marker</strong>s and<strong>in</strong> 2000, Temnykh et al. published 91 newmicrosatellite <strong>marker</strong>s developed fromexpressed sequence tag (EST) sequences.Temnykh et al. (2001) developed 200 new<strong>marker</strong>s, mostly from end sequences of ricebacterial artificial chromosomes (BACs).However, the most dramatic <strong>in</strong>crease <strong>in</strong>microsatellite <strong>marker</strong>s (2 240 new <strong>marker</strong>s<strong>in</strong> 2002 and 25 000 <strong>in</strong> 2004) was madepossible primarily though the use of wholegenome shotgun sequences (McCouch et al.,2002; G. Wilson, personal communication).Complete genome sequence provides anadditional advantage <strong>in</strong> electronicallydeterm<strong>in</strong><strong>in</strong>g the position of new <strong>marker</strong>son genetic and physical maps. However,full genomic sequence is not a requirementfor microsatellite <strong>marker</strong> development, andthere are a number of microsatellite <strong>marker</strong>sthat have been developed for a wide arrayof crop species (Table 3) without the benefitof full genomic sequence.Marker-<strong>assisted</strong> <strong>selection</strong>strategies and examplesMAS <strong>in</strong> a breed<strong>in</strong>g context <strong>in</strong>volves scor<strong>in</strong>g<strong>in</strong>directly for the presence or absenceof a desired phenotype or phenotypiccomponent based on the sequences orband<strong>in</strong>g patterns of molecular <strong>marker</strong>slocated <strong>in</strong> or near the genes controll<strong>in</strong>g thephenotype. The sequence polymorphismor band<strong>in</strong>g pattern of the molecular <strong>marker</strong>is <strong>in</strong>dicative of the presence or absence of aspecific gene or chromosomal segment thatis known to carry a desired allele.DNA <strong>marker</strong>s can <strong>in</strong>crease screen<strong>in</strong>gefficiency <strong>in</strong> breed<strong>in</strong>g programmes <strong>in</strong> a

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