An NBS-LRR protein in the Rpp1 locus negates the dominance of Rpp1-mediated resistance against Phakopsora pachyrhizi in soybean

被引:11
作者
Wei, Wei [1 ]
Wu, Xing [1 ,2 ]
Garcia, Alexandre [3 ]
McCoppin, Nancy [4 ]
Viana, Joao Paulo Gomes [1 ]
Murad, Praerona S. S. [1 ]
Walker, David R. R. [1 ,4 ]
Hartman, Glen L. L. [1 ,4 ]
Domier, Leslie L. L. [1 ,4 ]
Hudson, Matthew E. E. [1 ]
Clough, Steven J. J. [1 ,4 ]
机构
[1] Univ Illinois, Dept Crop Sci, 1102 S Goodwin Ave, Urbana, IL 61801 USA
[2] Yale Univ, Dept Mol Cellular & Dev Biol, 260 Whitney Ave 266, New Haven, CT 06511 USA
[3] Trop Melhoramento & Genet LTDA, Rodovia Celso Garcia Cid,Km 87, BR-86183600 Cambe, PR, Brazil
[4] USDA, Soybean Maize Germplasm Pathol & Genet Res Unit, 1101 W Peabody Dr, Urbana, IL 61801 USA
关键词
dominant susceptible; Glycine max; NBS-LRR; Phakopsora pachyrhizi; plant disease resistance; Rpp1; Rpp1b; soybean rust; RICH REPEAT PROTEIN; DISEASE RESISTANCE; RUST RESISTANCE; ARABIDOPSIS-THALIANA; CONFERS RESISTANCE; GENE-EXPRESSION; PLANT; NLR; SUSCEPTIBILITY; IDENTIFICATION;
D O I
10.1111/tpj.16038
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The soybean Rpp1 locus confers resistance to Phakopsora pachyrhizi, causal agent of rust, and resistance is usually dominant over susceptibility. However, dominance of Rpp1-mediated resistance is lost when a resistant genotype (Rpp1 or Rpp1b) is crossed with susceptible line TMG06_0011, and the mechanism of this dominant susceptibility (DS) is unknown. Sequencing the Rpp1 region reveals that the TMG06_0011 Rpp1 locus has a single nucleotide-binding site leucine-rich repeat (NBS-LRR) gene (DS-R), whereas resistant PI 594760B (Rpp1b) is similar to PI 200492 (Rpp1) and has three NBS-LRR resistance gene candidates. Evidence that DS-R is the cause of DS was reflected in virus-induced gene silencing of DS-R in Rpp1b/DS-R or Rpp1/DS-R heterozygous plants with resistance partially restored. In heterozygous Rpp1b/DS-R plants, expression of Rpp1b candidate genes was not significantly altered, indicating no effect of DS-R on transcription. Physical interaction of the DS-R protein with candidate Rpp1b resistance proteins was supported by yeast two-hybrid studies and in silico modeling. Thus, we conclude that suppression of resistance most likely does not occur at the transcript level, but instead probably at the protein level, possibly with Rpp1 function inhibited by binding to the DS-R protein. The DS-R gene was found in other soybean lines, with an estimated allele frequency of 6% in a diverse population, and also found in wild soybean (Glycine soja). The identification of a dominant susceptible NBS-LRR gene provides insight into the behavior of NBS-LRR proteins and serves as a reminder to breeders that the dominance of an R gene can be influenced by a susceptibility allele.
引用
收藏
页码:915 / 933
页数:19
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