QTL analysis of agronomic traits in barley based on the doubled haploid progeny of two elite North American varieties representing different germplasm groups
La. Marquez-cedillo et al., QTL analysis of agronomic traits in barley based on the doubled haploid progeny of two elite North American varieties representing different germplasm groups, THEOR A GEN, 103(4), 2001, pp. 625-637
A better understanding of the genetics of complex traits, such as yield, ma
y be achieved by using molecular tools. This study was conducted to estimat
e the number, genome location, effect and allele phase of QTLs determining
agronomic traits in the two North American matting barley (Hordeum vulgare
L.) quality variety standards. Using a doubled haploid population of 140 li
nes from the cross of two-rowed Harrington x sixrowed Morex, agronomic phen
otypic data sets from nine environments, and a 107-marker linkage map, we p
erformed QTL analyses using simple interval mapping and simplified composit
e interval mapping procedures. Thirty-five QTLs were associated, either acr
oss environments or in individual environments, with five grain and agronom
ic traits (yield, kernel plumpness, test weight, heading date, and plant he
ight). Significant QTL x environment interaction was detected for all trait
s. These interactions resulted from both changes in the magnitude of respon
se and changes in the sign of the allelic effect. QTLs for multiple traits
were coincident. The vrs1 locus on chromosome 2 (2H), which determines infl
orescence row type, was coincident with the largest-effect QTL determining
four traits (yield, kernel plumpness, test weight, and plant height). QTL a
nalyses were also conducted separately for each sub-population (six-rowed a
nd two-rowed). Seven new QTLs were detected in the sub-populations. Positiv
e transgressive segregants were found for all traits, but they were more pr
evalent in the six-rowed sub-population. QTL analysis should be useful for
identifying candidate genes and introgressing favorable alleles between ger
mplasm groups.