QTL Analysis of Malting Quality in Barley Based on the Doubled Haploid Progeny of Two Elite North American Varieties Representing Different Germplasm Groups

L. A. Marquez-Cedillo1, P. M. Hayes1, B. L. Jones2, A. Kleinhofs3, W. G. Legge4, B. G. Rossnagel5, K. Sato6, S. E. Ullrich3, D. M. Wesenberg7, and The North American Barley Genome Mapping Project
1Department of Crop and Soil Science
Oregon State University
Corvallis, OR 97331, USA
2Cereal Crops Research Unit
USDA-ARS
501 N. Walnut St.
Madison, WI 53705, USA
3Department of Crop and Soil Science
Washington State University
Pullman, WA 99164, USA
4Agriculture and Agri-Food Canada
Brandon MB R7A 5Y3, Canada
5Crop Development Centre
University of Saskatchewan
Saskatoon, SK S7N 5A8, Canada
6Research Institute for Bioresources
Okayama University
Kurashiki 710-0046 Japan
7National Small Grains Germplasm Research Facility
P.O. Box 307
Aberdeen, ID 83210, USA

Characterization of the determinants of economically important phenotypes showing complex inheritance should lead to more effective use of genetic resources. This study was conducted to determine the number, genome location and effects of QTLs determining malting quality in the two North American barley quality standards. Using a doubled haploid population of 140 lines from the cross of Harrington x Morex, malting quality phenotype data sets from eight environments, and a 107-marker linkage map, QTL analyses were performed using simple interval mapping and simplified composite interval mapping procedures. Seventeen QTLs were associated with seven grain and malting quality traits (percentage of plump kernels, test weight, grain protein percentage, soluble/total (S/T) protein ratio, -amylase activity, diastatic power and malt extract percentage). QTLs for multiple traits were coincident. The loci controlling inflorescence type (V on chromosome 2 and i on chromosome 4) were coincident with QTLs affecting all traits except malt extract percentage. The largest effect QTLs, for percentage of plump kernels, test weight, grain protein percentage, S/T ratio, and diastatic power, were coincident with the V locus. QTL analyses were conducted separately for each sub-population (six-rowed and two-rowed). Eleven new QTLs were detected in the subpopulations. There were significant interactions between the V and i loci for grain protein percentage and S/T protein ratio. Results suggest that this mating of two different germplasm groups caused a disruption of the balance of traits. Information on the number, position and effects of QTLs determining components of malting quality may be useful for maintaining specific allele configurations that determine target quality profiles.