Page Banner

United States Department of Agriculture

Agricultural Research Service

Title: Identifying and Utilizing High-Temperature Adult-Plant Resistance to Combat Stripe Rust in Wheat

Authors
item Kidwell, K - WASHINGTON STATE UNIV
item Santra, D - WASHINGTON STATE UNIV
item Uauy, C - UNIV OF CA, DAVIS, CA
item Chen, Xianming
item Garland-Campbell, Kimberly
item Dubcovsky, J - UNIV OF CA, DAVIS, CA

Submitted to: Agronomy Society of America, Crop Science Society of America, Soil Science Society of America Meeting
Publication Type: Abstract Only
Publication Acceptance Date: September 1, 2005
Publication Date: November 1, 2005
Citation: Kidwell, K.K., Santra, D.K., Uauy, C., Chen, X., Garland Campbell, K.A., Dubcovsky, J. 2005. Identifying and utilizing high-temperature adult-plant resistance to combat stripe rust in wheat. ASA/CSSA/SSSA Annual meeting, Nov. 7-10, Salt Lake City, UT, S1277.

Technical Abstract: Stripe rust (caused by Puccinia striiformis Westend. f. sp. tritici) is one of the most destructive diseases of wheat (Triticum aestivum L.) grown worldwide. Two major types of genetic resistance have been identified; seedling resistance that is race-specific and is not durable, and high-temperature adult-plant (HTAP) resistance that is race nonspecific and durable. High levels of HTAP resistance have been identified in T. dicoccoides, which is a tetraploid, as well as in several hexaploid wheat cultivars. HTAP resistance from the winter wheat cultivars ‘Stephens' and ‘Druchamp' have provided significant levels of protection from stripe rust in winter wheat for over 25 years. Full utilization of these sources requires efficient strategies for incorporating HTAP resistance into susceptible germplasm, as well as an enhanced understanding of the underlying mechanisms governing this type of resistance. The objectives of this research are to: 1) clone the HTAP resistance gene Yr36 on chromosome 6BS from T. dicoccoides using a map-based cloning approach; and 2) identify major QTL for HTAP resistance in Stephens and Druchamp through genetic linkage analysis. We recently identified a major QTL associated with HTAP resistance on chromosome 6BS in Stephens, and flanking markers associated with this region have been identified. Comparative mapping results indicate that this QTL region from Stephens partially overlaps with the chromosomal location of Yr36 in T. dicoccoides. We intend to develop breeder friendly molecular markers for use in marker-assisted selection strategies to efficiently incorporate HTAP resistance into regionally adapted cultivars.

Last Modified: 10/22/2014
Footer Content Back to Top of Page