Marker-based selection of QTL affecting grain and malt quality in two-row barley

Citation
E. Igartua et al., Marker-based selection of QTL affecting grain and malt quality in two-row barley, CROP SCI, 40(5), 2000, pp. 1426-1433
Citations number
26
Categorie Soggetti
Agriculture/Agronomy
Journal title
CROP SCIENCE
ISSN journal
0011183X → ACNP
Volume
40
Issue
5
Year of publication
2000
Pages
1426 - 1433
Database
ISI
SICI code
0011-183X(200009/10)40:5<1426:MSOQAG>2.0.ZU;2-4
Abstract
Malt quality traits of barley (Hordeum vulgare L.) may be suitable candidat es for marker-assisted selection, as their evaluation involves laborious an d costly procedures. Four regions of the genome were previously reported to affect several grain and malt quality traits in the two-row barley cross ' Harrington'/'TR306'. This study used an independent set of lines derived fr om the same cross to verify the existence of quantitative trait loci (QTL) in these regions. Molecular marker genotypes were used to select 47 lines f rom among 410 Harrington/TR306 lines that had not been used in the original mapping experiment. Four groups of lines were selected on the basis of the ir genotype at marker Loci in two regions on chromosome 7 (5H) with QTL, af fecting kernel weight and plumpness, grain protein, extract beta-glucan con tent, the difference between fine-grind and coarse-grind extract, soluble p rotein, diastatic power, alpha-amylase activity and fine-grind extract, and in regions on chromosomes 3 (3H) and 6 (6H) with QTL affecting extract bet a-glucan content and fine-coarse difference. Grain and malt quality traits of these lines were determined from grain grown in five held environments i n western Canada. The results confirmed the presence of QTL on chromosome 7 affecting all traits previously reported. Marker-based selection for two r egions on chromosome 7 was effective in identifying phenotypically superior lines, and the magnitudes of the combined effects for these regions were c lose to the estimates calculated in the mapping experiment. The presence of QTL on chromosomes 3 and 6 could not be confirmed as categorically, but co mbined selection for extract beta-glucan content and fine-coarse difference at all four QTL regions was more effective than selection for only the two regions on chromosome 7.