2002
DOI: 10.1007/s00122-002-1048-4
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"Perfect" markers for the Rht-B1b and Rht-D1b dwarfing genes in wheat

Abstract: PCR-based markers were developed to detect the point mutations responsible for the two major semi-dwarfing genes Rht-B1b ( Rht1) and Rht-D1b ( Rht2) in wheat. These markers were validated by testing 19 wheat varieties of known Rht genotype. They included Rht-B1b and Rht-D1b dwarfs, double-mutant varieties and tall wheats. These were correctly genotyped with the Rht-B1b and Rht-D1b-specific primers, as well as markers specific for the tall alleles Rht-B1a and Rht-D1a. Using a family of doubled-haploid lines seg… Show more

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Cited by 447 publications
(314 citation statements)
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“…The associations between the candidate markers and plant height detected in this study were also detected in the previous linkage mapping. Four loci (Xwmc112-2D, Xcfd23-2D, Xgwm133-2D and Xgwm192-2D) detected to associate with PH m and PH 4 , were located in a region near the centromere of chromosome 2D, where QTL for the plant height was already detected in the previous studies (Cadalen et al 1998;Ellis et al 2002;McCartney et al 2005). Loci Xgwm513-4B, Xgwm495-4B, Xgwm349-4B and Xbarc109-4B were located in a region covering 18.5 cM on chromosome 4B.…”
Section: Discussionmentioning
confidence: 93%
“…The associations between the candidate markers and plant height detected in this study were also detected in the previous linkage mapping. Four loci (Xwmc112-2D, Xcfd23-2D, Xgwm133-2D and Xgwm192-2D) detected to associate with PH m and PH 4 , were located in a region near the centromere of chromosome 2D, where QTL for the plant height was already detected in the previous studies (Cadalen et al 1998;Ellis et al 2002;McCartney et al 2005). Loci Xgwm513-4B, Xgwm495-4B, Xgwm349-4B and Xbarc109-4B were located in a region covering 18.5 cM on chromosome 4B.…”
Section: Discussionmentioning
confidence: 93%
“…The semi-dwarfing genes Rht-B1b (Rht1) and Rht-D1b (Rht2) widely present in commercial cultivars reduce plant height, increase harvest index, and improve lodging resistance, and consequently increase grain yield. Functional markers for the two genes were developed and used for discrimination of semi-dwarf (Rht-B1b and Rht-D1b) and wild-type alleles (Rht-B1a and Rht-D1a) (Ellis et al 2002;Zhang et al 2006). However, the PCR conditions are very stringent for the FMs of Rht-B1 and Rht-D1, in which Hotstar Taq DNA polymerase needs to be used for a reliable PCR amplification (Ellis et al 2002).…”
Section: Functional Markers For Agronomic Traitsmentioning
confidence: 99%
“…Functional markers for the two genes were developed and used for discrimination of semi-dwarf (Rht-B1b and Rht-D1b) and wild-type alleles (Rht-B1a and Rht-D1a) (Ellis et al 2002;Zhang et al 2006). However, the PCR conditions are very stringent for the FMs of Rht-B1 and Rht-D1, in which Hotstar Taq DNA polymerase needs to be used for a reliable PCR amplification (Ellis et al 2002). This will limit the use of these markers in breeding due to high costs (Bagge and L眉bberstedt 2008).…”
Section: Functional Markers For Agronomic Traitsmentioning
confidence: 99%
“…In wheat, some important genes, such as Rht1, Rht2 (linked to dwarfing, Peng et al 1999) and puroindoline b (linked to grain texture, Giroux and Morris 1997), have been found to contain SNPs. Some allele-specific (AS) PCR markers have been applied to detect specific alleles at these loci based on the SNPs Ellis et al 2002). The rapid development of databases of wheat gene sequences and expressed sequence tags (ESTs) provides the opportunity to identify SNPs and InDels using existing sequence information.…”
Section: Introductionmentioning
confidence: 99%