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Genetic dissection of starch paste viscosity characteristics in waxy maize revealed by high-density SNPs in a recombinant inbred line population
Authors:Derong Hao  Lin Xue  Jianhua Yuan  Zhenliang Zhang  Huhua Lu  Yuxiang Mao  Mingliang Shi  Xiaolan Huang  Guangfei Zhou  Guoqing Chen
Affiliation:1.Nantong Key Laboratory for Exploitation of Crop Genetic Resources and Molecular Breeding,Jiangsu Yanjiang Institute of Agricultural Sciences,Nantong,China;2.Jiangsu Collaborative Innovation Center for Modern Crop Production,Nanjing,China;3.Institute of Food Crops,Jiangsu Academy of Agricultural Sciences,Nanjing,China
Abstract:Starch paste viscosity properties are widely used as important indicators for quality estimation in waxy maize. To elucidate the genetic basis of paste viscosity characteristics of waxy maize, seven parameters from the rapid visco analyzer (RVA) profile were analyzed for quantitative trait loci (QTLs) in this study, using a recombinant inbred line population derived from a cross between the inbred lines Tongxi5 and Hengbai522. A high-density linkage map was constructed using 2703 bin markers, covering 1876.20 cM of the whole genome with an average genetic distance of 0.73 cM between adjacent bin markers. Seventy-two QTLs were detected for RVA parameters across 3 years, of which 17 could be identified in 2 years, and 6 identified in all 3 years. Eight QTL clusters were observed to be co-associated with two or more RVA parameters. Three major QTLs, qPV4-1, qTV4-1, and qFV5-2, which explained over 10% of the phenotypic variation, were stably mapped to the chromosomes 4 or 5 in all years. Based on functional annotations, two genes were considered as potential candidate genes for the identified major QTLs. The QTLs and candidate genes identified in this study will be useful for further understanding of the genetic architecture of starch paste viscosity characteristics in waxy maize, and may facilitate molecular breeding for grain quality improvement in breeding programs, and simultaneously provide a basis for cloning of the genes underlying these QTLs.
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