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marker-assisted selection in wheat - ictsd

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Chapter 9 – Molecular <strong>marker</strong>-<strong>assisted</strong> <strong>selection</strong> for resistance to pathogens <strong>in</strong> tomato 157Figure 1Number of generations reached <strong>in</strong> backcross schemes carried out between four susceptiblerecurrent genotypes and five resistant donor genotypes5432MomorOkitzuOntarioPyrellaStevens10Sel 8 137 PI15 AD17simplified, enabl<strong>in</strong>g a faster and cheaper<strong>marker</strong> system, i.e. a sequence characterizedamplified region (SCAR; Kawchuk,Hachey and Lynch, 1998) <strong>marker</strong>, whichonly requires one PCR reaction to detectpolymorphism between the resistant andthe susceptible genotypes, to be set up.(Barone et al., 2004).The second strategy was followed todesign primers and enzymes suitable fortarget<strong>in</strong>g three resistance genes (I2, Pto andVe2). This strategy allowed gene-<strong>assisted</strong><strong>selection</strong> to be achieved through the simplePCR procedure. F<strong>in</strong>ally, the third strategywas applied <strong>in</strong> the case of one CAPS<strong>marker</strong> target<strong>in</strong>g the resistance gene Frl;it was derived from one RFLP tomato<strong>marker</strong> (TG101) l<strong>in</strong>ked to the gene (Fazio,Stevens and Scott, 1999).The <strong>marker</strong>s found were used to selectresistant genotypes <strong>in</strong> backcross breed<strong>in</strong>gschemes, while the process itself allowedthree generations to be screened annually.At present, for some cross comb<strong>in</strong>ations,the BC 5 generation has been reached, forothers the BC 2 -BC 3 (Figure 1). Where aBC 5 generation was already available, thebreed<strong>in</strong>g programme cont<strong>in</strong>ued by self<strong>in</strong>gBC 5 resistant genotypes. In all other casesthe backcross programme will cont<strong>in</strong>ue upto the fifth backcross generation. At theend of each backcross scheme, the resistantBC 5 F 3 genotypes, selected through molecular<strong>marker</strong> analysis, will also be testeddirectly for resistance by <strong>in</strong>oculat<strong>in</strong>g thepathogen and monitor<strong>in</strong>g signs of disease.This will allow verification that no l<strong>in</strong>kagebreakage and loss of resistance geneoccurred.This procedure was already adopted <strong>in</strong>the case of one backcross scheme aimedat transferr<strong>in</strong>g a resistance gene to tomatospotted wilt virus (TSWV) to the susceptiblegenotype AD17 (Langella et al., 2004).The <strong>in</strong> vivo test performed on F 1 BC 5 ,F 2 BC 5 and, F 3 BC 5 generations confirmedthe <strong>in</strong>trogression of the resistance trait andrevealed that the resistance gene Sw5 was

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