Fine mapping and identification of causal alleles at the Ur-11 locus controlling rust resistance in common bean (Phaseolus vulgaris L.)

被引:0
作者
Erfatpour, Mohammad [1 ,2 ]
Simons, Kristin J. [3 ]
Roy, Jayanta [1 ]
Figueroa-Cerna, Jose C. [1 ]
Lee, Rian [1 ]
Beaver, James [4 ]
Mcclean, Phillip E. [1 ]
Osorno, Juan M. [1 ]
机构
[1] North Dakota State Univ, Dept Plant Sci, Fargo, ND 58108 USA
[2] Univ Guelph, Dept Plant Agr, Guelph, ON N1G 2W1, Canada
[3] North Dakota State Univ, Carrington Res Extens Ctr, Carrington, ND 58421 USA
[4] Univ Puerto Rico, Dept Agroenvironm Sci, Mayaguez, PR 00680 USA
关键词
CULTIVAR OURO NEGRO; ASSISTED SELECTION; GERMPLASM LINES; GENE PRESENT; PROTEIN; BINDING; PATHOGEN; REGISTRATION; DOMAINS; ARABIDOPSIS;
D O I
10.1007/s00122-025-04836-9
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
The Middle American rust resistance gene Ur-11 present in common bean (Phaseolus vulgaris L.) confers resistance to all but one known race of the pathogen Uromyces appendiculatus (Pers.) Unger. Even though progress has been made in understanding the host-pathogen interactions between common bean and U. appendiculatus, the causal alleles of the majority of rust resistance loci, including Ur-11, remain unknown. A genome-wide association study (GWAS) was conducted to identify genomic regions associated with resistance to the U. appendiculatus race 31-22, which is avirulent to Ur-11 but virulent to other Middle American rust resistance genes. GWAS using genotypic data consisting of approximately 70,959 SNP markers and phenotypic data based on the median reaction type (1-9 scale) of a panel of 357 Middle American breeding lines and cultivars, plus 5 germplasm lines with the Ur-11 locus derived from PI 181996, located Ur-11 on chromosome Pv11. Twenty-seven SNP markers clustered in the 55.16-55.56 Mb region of the P. vulgaris UI111 reference. Multiple DNA sequence alignments detected a missense mutation [c.1,328A > G] in the PvUI111.11G202400 gene model that encodes a leucine-rich repeat-containing protein in response to race 31-22. A PCR allele competitive extension marker (PACE) was developed and tested across a panel of similar to 700 Middle American dry bean genotypes. No recombination event was observed for the PACE marker among the tested genotypes; suggesting that the polymorphism on which it is based is very close to or in the Ur-11 gene. This PACE marker will be a useful and reliable marker for marker-assisted selection of Ur-11-based resistance to bean rust.
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页数:14
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