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ARS Home » Pacific West Area » Pullman, Washington » WHGQ » Research » Publications at this Location » Publication #288960
Title: The dissection and SSR mapping of a high-temperature adult-plant stripe rust resistance gene in American spring wheat cultivar Alturas

Author
item ZHAO, LEI - Shenyang Agricultural University
item FENG, JING - Plant Protection Institute Hebei China
item ZHANG, CHUN-YU - Shenyang Agricultural University
item XU, XIAO-DAN - Shenyang Agricultural University
item Chen, Xianming
item SUN, QUAN - Shenyang Agricultural University
item MIAO, QING - Shenyang Agricultural University
item XU, SHI-CHANG - Plant Protection Institute Hebei China
item LIN, FENG - Shenyang Agricultural University

Submitted to: European Journal of Plant Pathology
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: 4/2/2012
Publication Date: 10/1/2012
Citation: Zhao, L., Feng, J., Zhang, C., Xu, X., Chen, X., Sun, Q., Miao, Q., Xu, S., Lin, F. 2012. The dissection and SSR mapping of a high-temperature adult-plant stripe rust resistance gene in American spring wheat cultivar Alturas. European Journal of Plant Pathology. 134:281-288. Available: http://www.springerlink.com/content/t27110v866wg1141/fulltext.pdf.

Interpretive Summary: Stripe rust is one of major diseases in wheat production worldwide. The best economic and efficient method is to utilize resistant varieties. Alturas has high-temperature adult-plant (HTAP) resistance. In order to determine stripe rust resistance characteristics, resistance gene combination and molecular map of the resistance gene(s), Alturas was crossed with Chinese susceptible cultivar Taichung 29 and the F1 and F2 progenies were tested together with the parents with Chinese predominant mixed races CYR31, CYR32 and CYR33 in one field location in 2010 and F3 progenies were tested at two locations in 2011. Infection type (IT) and disease severity (DS) were recorded three times for each plant for F1 and F2, and each line for F3 during each growing season. The DS data were used to calculate relative area under the disease progress curve (AUDPC) values. Both IT and AUDPC data showed continuous distributions, indicating that the Alturas HTAP resistance was controlled by quantitative trait loci (QTL). A major HTAP QTL, designated as QYrAlt.syau-3BS, was consistently detected across environments and was located on chromosome 3BS. The gene contributed to 34.28% of the phenotypic variation for average AUDPC and 50.20% for average IT. Markers Xgwm389 and Xbarc238 flanking the major QTL should be useful in breeding for obtaining durable and high-level resistance by combinations with other non-race-specific resistance genes.

Technical Abstract: Stripe rust is one of major diseases in wheat production worldwide. The best economic and efficient method is to utilize resistant varieties. Alturas has high-temperature adult-plant resistance. In order to determine stripe rust resistance characteristics, resistance gene combination and molecular map of the resistance gene(s), Alturas was crossed with Chinese susceptible cultivar Taichung29. The parents, F1, F2 progenies were tested with Chinese predominant mixed races CYR31, CYR32 and CYR33 in field experiments in 2010 and F3 progenies were evaluated at one site in Beijing, the other site in Langfang, Hebei Province. Infection type (IT) and disease severity (DS) were recorded three times for each plant for F1 and F2, and each progeny for F3 during each growing season. The DS data were used to calculate relative area under the disease progress curve (AUDPC) values. Both IT and AUDPC data showed continuous distributions, indicating that the Alturas HTAP resistance was controlled by quantitative trait loci (QTLs). A major HTAP QTL, designated as QYrAlt.syau-3BS, was consistently detected across environments and was located on chromosome 3BS. The gene contributed to 34.28 % of the phenotypic variation for average AUDPC and 50.20 % for average IT. Markers Xgwm389 and Xbarc238 flanking the major QTL, should be useful in breeding for obtaining durable and high-level resistance by combinations with other non-race-specific resistance genes.