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marker-assisted selection in wheat

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Chapter 6 – Targeted <strong>in</strong>trogression of cotton fibre quality quantitative trait loci us<strong>in</strong>g molecular <strong>marker</strong>s 77Figure 3Graphical genotypes (26 chromosomes) of a BC 1 plant (No. BC1/16) (upper panel) and of twoselected BC 4 plant (Nos. BC 4 /104 and BC 4 /419) (lower panel) derived from itBC 1/16c25 c16 c23topc26A01topA01botc3topc4c3botc6c23botc20A03BC 4 /104 BC 4/419c25 c16 c23topc25c26A01botc6c23botA03The two possible allelic forms, homozygous Gh/Gh and heterozygous Gh/Gb, are denoted <strong>in</strong> dark grey and black respectively.Regions <strong>in</strong> black are <strong>in</strong>trogressed with G. barbadense alleles. Light grey areas <strong>in</strong>dicate portions of unknown alleliccomposition. Boxed areas represent the localization of QTL-rich regions localized on 15 carrier chromosomes shown to theleft (11 non-carrier chromosomes are shown to the right). Arrows <strong>in</strong>dicate the regions totally or partially <strong>in</strong>trogressed.Fibre characteristics of BC 3 and BC 4generation plantsOw<strong>in</strong>g to the limited number of <strong>in</strong>dividualsand the unbalanced frequenciesof genotypic classes <strong>in</strong> the BC 3 and BC 4material, significant <strong>marker</strong>-trait associationswere less frequent than observedfrom the BC 1 and BC 2 data. For example,<strong>marker</strong>s mapped along five, n<strong>in</strong>e and sixchromosome regions contributed (P=0.01),respectively, to length, strength or f<strong>in</strong>enessvariation us<strong>in</strong>g BC 4 <strong>marker</strong>-trait data,as compared with 15, 12 and 21 from theBC 1 and BC 2 data (Table 2). However,the majority of significant associations,particularly those determ<strong>in</strong>ed <strong>in</strong> the BC 4generation, were observed with<strong>in</strong> previouslydetected regions (not shown). Us<strong>in</strong>gfibre strength as an example, out of the eightstrength QTL-harbour<strong>in</strong>g regions on chromosomesc3bot, c5, c16, c23sup, c23bot,c25, A01 and A03 identified from the comb<strong>in</strong>edBC 1 and BC 2 data (Table 3), theBC 4 data confirmed significant <strong>marker</strong>-traitassociations <strong>in</strong> five of these regions, i.e. for<strong>marker</strong>s mapped on chromosomes c3bot,

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