Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/13332
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Type: Journal article
Title: Construction of three linkage maps in bread wheat, Triticum aestivum
Author: Chalmers, K.
Campbell, A.
Kretschmer, J.
Karakousis, A.
Henschke, P.
Pierens, S.
Harker, N.
Pallotta, M.
Cornish, G.
Shariflou, M.
Rampling, L.
McLauchlan, A.
Daggard, G.
Sharp, P.
Holton, T.
Sutherland, M.
Appels, R.
Langridge, P.
Citation: Australian Journal of Agricultural Research, 2001; 52(11-Dec):1089-1119
Publisher: C S I R O Publishing
Issue Date: 2001
ISSN: 0004-9409
Statement of
Responsibility: 
K. J. Chalmers, A. W. Campbell, J. Kretschmer, A. Karakousis, P. H. Henschke, S. Pierens, N. Harker, M. Pallotta, G. B. Cornish, M. R. Shariflou, L. R. Rampling, A. McLauchlan, G. Daggard, P. J. Sharp, T. A. Holton, M. W. Sutherland, R. Appels and P. Langridge
Abstract: Genetic maps were compiled from the analysis of 160–180 doubled haploid lines derived from 3 crosses: Cranbrook × Halberd, CD87 × Katepwa, and Sunco × Tasman. The parental wheat lines covered a wide range of the germplasm used in Australian wheat breeding. The linkage maps were constructed with RFLP, AFLP, microsatellite markers, known genes, and proteins. The numbers of markers placed on each map were 902 for Cranbrook × Halberd, 505 for CD87 × Katepwa, and 355 for Sunco × Tasman. Most of the expected linkage groups could be determined, but 10–20% of markers could not be assigned to a specific linkage group. Homologous chromosomes could be aligned between the populations described here and linkage groups reported in the literature, based around the RFLP, protein, and microsatellite markers. For most chromosomes, colinearity of markers was found for the maps reported here and those recorded on published physical maps of wheat. AFLP markers proved to be effective in filling gaps in the maps. In addition, it was found that many AFLP markers defined specific genetic loci in wheat across all 3 populations. The quality of the maps and the density of markers differs for each population. Some chromosomes, particularly D genome chromosomes, are poorly covered. There was also evidence of segregation distortion in some regions, and the distribution of recombination events was uneven, with substantial numbers of doubled haploid lines in each population displaying one or more parental chromosomes. These features will affect the reliability of the maps in localising loci controlling some traits, particularly complex quantitative traits and traits of low heritability. The parents used to develop the mapping populations were selected based on their quality characteristics and the maps provide a basis for the analysis of the genetic control of components of processing quality. However, the parents also differ in resistance to several important diseases, in a range of physiological traits, and in tolerance to some abiotic stresses.
Keywords: Genetic map; RFLP; AFLP; microsatellites; map alignment; non-recombinant chromosomes
RMID: 0020010103
DOI: 10.1071/AR01081
Published version: http://www.publish.csiro.au/nid/40/paper/AR01081.htm
Appears in Collections:Agriculture, Food and Wine publications

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