Department of Crop Sciences, University of Illinois, 1102 S Goodwin Ave, Urbana, IL, 61801, USA.
Department of Molecular, Cellular and Developmental Biology, Yale University, 260 Whitney Ave # 266, New Haven, CT, 06511, USA.
Plant J. 2023 Mar;113(5):915-933. doi: 10.1111/tpj.16038. Epub 2023 Feb 8.
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.
大豆 Rpp1 基因座赋予了对叶锈病病原菌 Phakopsora pachyrhizi 的抗性,且抗性通常是显性的。然而,当抗性基因型(Rpp1 或 Rpp1b)与感病系 TMG06_0011 杂交时,Rpp1 介导的抗性的显性易感性(DS)就会丢失,而这种 DS 的机制尚不清楚。对 Rpp1 区域进行测序表明,TMG06_0011 的 Rpp1 基因座只有一个核苷酸结合位点富含亮氨酸重复(NBS-LRR)基因(DS-R),而抗性 PI 594760B(Rpp1b)与 PI 200492(Rpp1)相似,且有三个 NBS-LRR 抗性基因候选。DS-R 是 DS 原因的证据反映在 Rpp1b/DS-R 或 Rpp1/DS-R 杂合植物中通过病毒诱导基因沉默 DS-R 后,抗性部分恢复。在 Rpp1b/DS-R 杂合植物中,Rpp1b 候选基因的表达没有明显改变,这表明 DS-R 对转录没有影响。酵母双杂交研究和计算机建模支持 DS-R 蛋白与候选 Rpp1b 抗性蛋白之间的物理相互作用。因此,我们得出结论,抗性的抑制很可能不是在转录水平上发生的,而是很可能在蛋白质水平上发生的,可能是 Rpp1 功能通过与 DS-R 蛋白结合而受到抑制。在其他大豆品系中也发现了 DS-R 基因,在一个多样化的群体中,其等位基因频率估计为 6%,也在野生大豆(Glycine soja)中发现了该基因。显性易感性 NBS-LRR 基因的鉴定为 NBS-LRR 蛋白的行为提供了深入了解,并提醒育种家注意,R 基因的显性可以受到易感性等位基因的影响。