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Fine physical and genetic mapping of powdery mildew resistance gene MlIW172 originating from wild emmer (Triticum dicoccoides)
S. Ouyang, D. Zhang, J. Han, X. Zhao, Y. Cui, W. Song, N. Huo, Y. Liang, J. Xie, Z. Wang, Q. Wu, YX. Chen, P. Lu, DY. Zhang, L. Wang, H. Sun, T. Yang, G. Keeble-Gagnere, R. Appels, J. Doležel, HQ. Ling, M. Luo, Y. Gu, Q. Sun, Z. Liu,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
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- MeSH
- Ascomycota * MeSH
- Chromosome Mapping * MeSH
- Plant Diseases genetics microbiology MeSH
- Disease Resistance genetics MeSH
- Polyploidy MeSH
- Triticum genetics microbiology MeSH
- Genes, Plant * MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Powdery mildew, caused by Blumeria graminis f. sp. tritici, is one of the most important wheat diseases in the world. In this study, a single dominant powdery mildew resistance gene MlIW172 was identified in the IW172 wild emmer accession and mapped to the distal region of chromosome arm 7AL (bin7AL-16-0.86-0.90) via molecular marker analysis. MlIW172 was closely linked with the RFLP probe Xpsr680-derived STS marker Xmag2185 and the EST markers BE405531 and BE637476. This suggested that MlIW172 might be allelic to the Pm1 locus or a new locus closely linked to Pm1. By screening genomic BAC library of durum wheat cv. Langdon and 7AL-specific BAC library of hexaploid wheat cv. Chinese Spring, and after analyzing genome scaffolds of Triticum urartu containing the marker sequences, additional markers were developed to construct a fine genetic linkage map on the MlIW172 locus region and to delineate the resistance gene within a 0.48 cM interval. Comparative genetics analyses using ESTs and RFLP probe sequences flanking the MlIW172 region against other grass species revealed a general co-linearity in this region with the orthologous genomic regions of rice chromosome 6, Brachypodium chromosome 1, and sorghum chromosome 10. However, orthologous resistance gene-like RGA sequences were only present in wheat and Brachypodium. The BAC contigs and sequence scaffolds that we have developed provide a framework for the physical mapping and map-based cloning of MlIW172.
Agriculture University of Beijing Beijing China
Maize Research Center Beijing Academy of Agricultural and Forestry Sciences Beijing China
Murdoch University Perth Western Australia Australia
USDA ARS West Regional Research Center Albany California United States of America
References provided by Crossref.org
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