USDA ARS Dale Bumpers National Rice Research Center, Stuttgart, AR, 72160, USA.
University of Arkansas Rice Research and Extension Center, Stuttgart, AR, 72160, USA.
Nat Commun. 2018 May 23;9(1):2039. doi: 10.1038/s41467-018-04369-4.
Plant resistance genes typically encode proteins with nucleotide binding site-leucine rich repeat (NLR) domains. Here we show that Ptr is an atypical resistance gene encoding a protein with four Armadillo repeats. Ptr is required for broad-spectrum blast resistance mediated by the NLR R gene Pi-ta and by the associated R gene Pi-ta2. Ptr is expressed constitutively and encodes two isoforms that are mainly localized in the cytoplasm. A two base pair deletion within the Ptr coding region in the fast neutron-generated mutant line M2354 creates a truncated protein, resulting in susceptibility to M. oryzae. Targeted mutation of Ptr in a resistant cultivar using CRISPR/Cas9 leads to blast susceptibility, further confirming its resistance function. The cloning of Ptr may aid in the development of broad spectrum blast resistant rice.
植物抗性基因通常编码具有核苷酸结合位点-亮氨酸丰富重复(NLR)结构域的蛋白质。在这里,我们展示了 Ptr 是一个非典型的抗性基因,编码具有四个 Armadillo 重复的蛋白质。Ptr 是由 NLR R 基因 Pi-ta 和相关的 R 基因 Pi-ta2 介导的广谱稻瘟病抗性所必需的。Ptr 组成型表达,并编码两种主要定位于细胞质中的同工型。在快速中子产生的突变体系 M2354 中 Ptr 编码区的两个碱基对缺失导致截短蛋白的产生,从而导致对 M. oryzae 的敏感性。使用 CRISPR/Cas9 在抗性品种中靶向突变 Ptr 导致稻瘟病敏感性,进一步证实了其抗性功能。Ptr 的克隆可能有助于开发广谱稻瘟病抗性水稻。