January 10-14, 2009
Town & Country Convention Center
San Diego, CA
Scott Chapman1 , Jiankang Wang2 , Karine Chenu3 , Greg Rebetzke4 , David Bonnett5 , Claude Welcker6 , Francois Tardieu7 , Mark Dieters8 , Graeme Hammer9
Diagnostic molecular markers are available for more than 20 traits in wheat. The challenge is to combine these markers with phenotypic selection in creating new parental lines and progeny (target genotypes). Based on previous simulation work, we considered six diagnostic markers related to height, grain quality and disease. The objective was to integrate diagnostic selection (including Rht-8, a major gene to increase coleoptile length) with selection for an additional six minor QTL for this quantitative trait. The approach is to simulate (http://www.uq.edu.au/lcafs/qugene/) crosses between wheat lines with known genotypes for the markers so that the effects of linkage (among genes and between genes and markers) can be accounted for during the process of selection. We aim to identify the most efficient crossing and marker-aided process to quickly combine the desired genes together. In this case, production of doubled haploids following F2 enhancement for diagnostic markers was most efficient. In an extension of this research, we are integrating physiological models into the simulation. For each genotype to be simulated, the gene effects are linked to physiological traits (e.g. leaf growth response to temperature or water deficit) that are the inputs to a deterministic physiological model. This approach allows the scaling up of organ-level understanding of genetic response to a crop-level response. For a given QTL mapping study of leaf growth, we were able to estimate the potential outcomes of these QTL effects on the yield of maize in a range of different temperature and water deficit environments.