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marker-assisted selection in wheat - ictsd

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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 75Table 3Identification of the 19 targeted regions mapped on 15 different chromosomes and compris<strong>in</strong>g oneor several co–localized fibre quality QTL from G. barbadense for <strong>in</strong>trogression <strong>in</strong>to a G. hirsutumgenetic backgroundCarrier chromosomeChromosomelength(cM)Target <strong>in</strong>terval(cM)Target size(cM)Traitc14 197 28–57 29 Lengthc3 153 32–67 35 Length, f<strong>in</strong>eness90–138 48 Length, strength, f<strong>in</strong>enessc4 190 102–118 16 F<strong>in</strong>enessc22 139 112–139 27 F<strong>in</strong>enessc5 360 78–101 23 Strengthc6 296 137–144 7 Length, f<strong>in</strong>enessc25 183 44–73 29 Length, strengthc16 168 65–117 52 Strength, f<strong>in</strong>eness, colourc23 173 45–66 21 Strength (elongation –, colour –)113–135 22 Length, strengthc10 192 0–21 21 F<strong>in</strong>eness78–120 42 Length, f<strong>in</strong>eness, colourc20 268 88–161 73 Elongation, f<strong>in</strong>enessc26 195 67–143 76 Length (colour –)A01 233 16–54 38 Length171–209 38 Strengthc18 158 32–46 14 F<strong>in</strong>enessA03 271 209–234 25 Strength, uniformityTotal 3176 Total 636Note: All targeted QTL show a positive contribution from the G. barbadense allele, except for a few negative cases <strong>in</strong>dicated<strong>in</strong> brackets. The target region is def<strong>in</strong>ed as situated between the two loci flank<strong>in</strong>g the QTL peak LOD value at a one LODconfidence <strong>in</strong>terval.along chromosome 3 for QTL for fibrestrength and f<strong>in</strong>eness, and chromosome 23for QTL for fibre strength and length.The chromosome regions carry<strong>in</strong>gco-localized QTL (correspond<strong>in</strong>g to as<strong>in</strong>gle or to several traits measured on as<strong>in</strong>gle or on several populations) whosepositive alleles derived from the G. barbadensedonor genome, were reduced to19 QTL-rich regions that were carriedby 15 different “carrier” chromosomes(Table 3). Altogether, the confidence <strong>in</strong>tervals(one LOD) of the <strong>in</strong>volved QTL-richregions delimited a total length of 636 cM(20 percent of the carrier genome), or11.5 percent of the total genome (Table 3).Eleven non-carrier chromosomes weredevoid of positive QTL, or harboured negative(positive alleles derived from the G.hirsutum alleles) QTL.MAS <strong>in</strong> the BC 3 and BC 4 generationsand allelic transmission throughoutgenerationsThe early <strong>selection</strong> of BC 3 and BC 4 plantsus<strong>in</strong>g SSR <strong>marker</strong>s that framed the 19 targetedregions of <strong>in</strong>terest made it possibleto choose those plants that showed anallelic constitution with as many <strong>in</strong>trogressedloci with<strong>in</strong> the targeted regions aspossible. In total, 43 BC 3 plants out of 411(11.4 percent) and 37 BC 4 plants out of 450(8.2 percent) were reta<strong>in</strong>ed based upon the<strong>in</strong>formation provided by the <strong>marker</strong>s, i.e.without any phenotypic <strong>selection</strong> at thisstage. These plants were backcrossed to therecurrent parent (and self-poll<strong>in</strong>ated <strong>in</strong> thecase of the BC 4 plants).The allelic transmission observed <strong>in</strong> thefour groups of BC 4 derived from fourdifferent BC 1 plants is given <strong>in</strong> Table 4.

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