Mapping pre-harvest sprouting resistance loci in AAC Innova x AAC Tenacious spring wheat population

被引:9
|
作者
Dhariwal, Raman [1 ]
Hiebert, Colin W. [2 ]
Sorrells, Mark E. [3 ]
Spaner, Dean [4 ]
Graf, Robert J. [1 ]
Singh, Jaswinder [5 ]
Randhawa, Harpinder S. [1 ]
机构
[1] Agr & Agri Food Canada, Lethbridge Res & Dev Ctr, 5403 1st Ave South, Lethbridge, AB T1J 4B1, Canada
[2] Agr & Agri Food Canada, Morden Res & Dev Ctr, 101 Route 100, Morden, MB R6M 1Y5, Canada
[3] Cornell Univ, Sch Integrat Plant Sci, Plant Breeding & Genet Sect, 240 Emerson Hall, Ithaca, NY 14853 USA
[4] Univ Alberta, Dept Agr Food & Nutr Sci, Edmonton, AB T6G 2P5, Canada
[5] McGill Univ, Dept Plant Sci, Ste Anne De Bellevue, PQ H9X 3V9, Canada
关键词
Seed dormancy; Seed coat color; Phytohormones; Genetic and epigenetic factors; Epistasis interactions; QUANTITATIVE TRAIT LOCI; SEED COAT COLOR; TRITICUM-AESTIVUM; GRAIN DORMANCY; BREAD-WHEAT; SOFT WHITE; GENEALOGICAL ANALYSIS; HISTONE DEACETYLASES; HEXAPLOID WHEAT; JAPANESE WHEAT;
D O I
10.1186/s12864-021-08209-6
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
Background Pre-harvest sprouting (PHS) is a major problem for wheat production due to its direct detrimental effects on wheat yield, end-use quality and seed viability. Annually, PHS is estimated to cause > 1.0 billion USD in losses worldwide. Therefore, identifying PHS resistance quantitative trait loci (QTLs) is crucial to aid molecular breeding efforts to minimize losses. Thus, a doubled haploid mapping population derived from a cross between white-grained PHS susceptible cv AAC Innova and red-grained resistant cv AAC Tenacious was screened for PHS resistance in four environments and utilized for QTL mapping. Results Twenty-one PHS resistance QTLs, including seven major loci (on chromosomes 1A, 2B, 3A, 3B, 3D, and 7D), each explaining >= 10% phenotypic variation for PHS resistance, were identified. In every environment, at least one major QTL was identified. PHS resistance at most of these loci was contributed by AAC Tenacious except at two loci on chromosomes 3D and 7D where it was contributed by AAC Innova. Thirteen of the total twenty-one identified loci were located to chromosome positions where at least one QTL have been previously identified in other wheat genotype(s). The remaining eight QTLs are new which have been identified for the first time in this study. Pedigree analysis traced several known donors of PHS resistance in AAC Tenacious genealogy. Comparative analyses of the genetic intervals of identified QTLs with that of already identified and cloned PHS resistance gene intervals using IWGSC RefSeq v2.0 identified MFT-A1b (in QTL interval QPhs.lrdc-3A.1) and AGO802A (in QTL interval QPhs.lrdc-3A.2) on chromosome 3A, MFT-3B-1 (in QTL interval QPhs.lrdc-3B.1) on chromosome 3B, and AGO802D, HUB1, TaVp1-D1 (in QTL interval QPhs.lrdc-3D.1) and TaMyb10-D1 (in QTL interval QPhs.lrdc-3D.2) on chromosome 3D. These candidate genes are involved in embryo- and seed coat-imposed dormancy as well as in epigenetic control of dormancy. Conclusions Our results revealed the complex PHS resistance genetics of AAC Tenacious and AAC Innova. AAC Tenacious possesses a great reservoir of important PHS resistance QTLs/genes supposed to be derived from different resources. The tracing of pedigrees of AAC Tenacious and other sources complements the validation of QTL analysis results. Finally, comparing our results with previous PHS studies in wheat, we have confirmed the position of several major PHS resistance QTLs and candidate genes.
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页数:20
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