2 research outputs found

    New eSSR and gSSR markers added to Australian barley maps

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    To enhance genetic maps of barley previously developed in Australia for identifying markers useable in molecular breeding, a new set of simple sequence repeat (SSR) and indel markers was added to the maps. These markers were developed through (i) database mining of barley expressed sequence tag (EST) sequences, (ii) comparative barley-rice genome analysis, and (iii) screening of a genomic library with SSR probes. The primer set selected for this study comprised 216 EST-SSR (eSSR) and 25 genomic SSR (gSSR) markers, which were screened for polymorphism on 4 doubled haploid (DH) or recombinant inbred line (RIL) populations. In total, 81 new markers were added to the maps, with good coverage on all 7 chromosomes, except 6H, which only had 2 new markers added. The marker order of previously published maps was re-evaluated by comparing recombination fractions calculated by 2 methods to discover the best position for each marker. The new SSR markers were then added to the updated maps. Several of these new markers are linked to important barley disease resistance genes such as those for cereal cyst nematode, spot form of net blotch, and leaf scald resistance, and are readily useable for marker-assisted barley breeding. The new maps are available on-line at www.genica.net.au

    Genetic mapping in the Triticeae

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    Genetic maps are the fundamental tools to identify features of phenotypes that are linked to specific genetic loci and eventually DNA sequences or genes. The major use of genetic linkage maps has, therefore, been to identify quantitative trait loci (QTL). Genetic maps are also essential for marker assisted selection, comparative mapping, high-resolution mapping and map based cloning. To date, over 40 maps with at least 300 markers have been published for different Triticeae populations. The quality of genetic maps can be affected by a number of factors and map curation ensures that map quality issues are identified and, where possible, resolved. We report on the issues involved in the production of quality genetic linkage maps by inspection of marker genotype data after map construction
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