Genomic targeting and high-resolution mapping of the domestication gene Q in wheat

被引:36
作者
Faris, JD
Gill, BS
机构
[1] ARS, USDA, Cereal Crops Res Unit, No Crop Sci Lab, Fargo, ND 58105 USA
[2] Kansas State Univ, Dept Plant Pathol, Throckmorton Plant Sci Ctr 4024, Manhattan, KS 66506 USA
关键词
Triticum aestivum; positional cloning; physical mapping;
D O I
10.1139/G02-036
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The Q locus is largely responsible for the domestication of bread wheat. Q confers the free-threshing character of the spike and influences other important agronomic traits. Using chromosome deletion lines, Q was placed on the physical map within a submicroscopic segment of the long arm of chromosome 5A. We targeted markers to the segment by comparative mapping of anonymous RFLP clones, AFLP, and mRNA differential display analysis of deletion lines 5AL-7 and -23, which have deletion breakpoints that flank the Q locus. Differentially expressed sequences detected fragments at various loci on group 5 chromosomes suggesting that Q may be a regulatory gene. We identified 18 markers within the Q gene deletion interval and used them to construct a genetic linkage map of the region in F-2 populations derived from chromosome 5A disomic substitution lines. The genetic map corresponding to the deletion segment was 20-cM long, and we identified markers as close as 0.7 cM to the Q gene. An estimate of base pairs per centimorgan within the region is 250 kb/cM, an 18-fold increase in recombination compared with the genomic average. Genomic targeting and high-density mapping provide a basis for the map-based cloning of the Q gene.
引用
收藏
页码:706 / 718
页数:13
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