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Amplified fragment length polymorphism‐ and simple sequence repeat‐based molecular tagging and mapping of greenbug resistance gene Gb3 in wheat
Author(s) -
Weng Y.,
Lazar M. D.
Publication year - 2002
Publication title -
plant breeding
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.583
H-Index - 71
eISSN - 1439-0523
pISSN - 0179-9541
DOI - 10.1046/j.1439-0523.2002.00693.x
Subject(s) - amplified fragment length polymorphism , biology , locus (genetics) , genetics , genetic linkage , population , genetic marker , gene mapping , microsatellite , sequence tagged site , marker assisted selection , gene , molecular marker , chromosome , cleaved amplified polymorphic sequence , restriction fragment length polymorphism , genotype , allele , genetic diversity , demography , sociology
The greenbug, Schizaphis graminum (Rondani), is the most economically damaging aphid pest of wheat in the southern Great Plains of the USA. In this study, the single, dominant greenbug resistance gene, Gb3 , was molecularly tagged and genetically mapped using amplified fragment length polymorphism (AFLP) and simple sequence repeat(SSR) markers. Three AFLP loci were associated with the Gb3 locus in linkage analysis with 75 F 2:3 families from the cross between two near‐isogenic lines (NILs) for Gb3 ,‘TXGBE273’ and ‘TXGBE281′. Two of these loci, XMgcc Pagg and Xmagg Patg cosegregate with Gb3 in the population analysed. Further analysis indicated that XMgcc Pagg and Xmagg Patg are specific for the Gb3 locus in diverse genetic backgrounds. Two SSR markers, Xgwm111 and Xgwm428 previously mapped in wheat chromosome 7D, were shown to be linked with Gb3 , 22.5 cM and 33.1 cM from Gb3 , respectively, in an F 2 population of ‘Largo’בTAM 107’, suggesting that Gb3 is located in the long arm of chromosome 7D. The two AFLP markers cosegregating with Gb3 are valuable tools in developing molecular markers for marker‐assisted selection of greenbug resistance in wheat breeding.