State Key Laboratory of Hybrid Rice, Hunan Hybrid Rice Research Center, Changsha, China.
International Rice Research Institute, Metro Manila, Philippines.
Nat Plants. 2024 Jun;10(6):994-1004. doi: 10.1038/s41477-024-01694-z. Epub 2024 Jun 4.
Blast disease caused by the fungus Magnaporthe oryzae is one of the most devastating rice diseases. Disease resistance genes such as Pi-ta or Pi-ta2 are critical in protecting rice production from blast. Published work reports that Pi-ta codes for a nucleotide-binding and leucine-rich repeat domain protein (NLR) that recognizes the fungal protease-like effector AVR-Pita by direct binding. However, this model was challenged by the recent discovery that Pi-ta2 resistance, which also relies on AVR-Pita detection, is conferred by the unconventional resistance gene Ptr, which codes for a membrane protein with a cytoplasmic armadillo repeat domain. Here, using NLR Pi-ta and Ptr RNAi knockdown and CRISPR/Cas9 knockout mutant rice lines, we found that AVR-Pita recognition relies solely on Ptr and that the NLR Pi-ta has no role in it, indicating that it is not the Pi-ta resistance gene. Different alleles of Ptr confer different recognition specificities. The A allele of Ptr (PtrA) detects all natural sequence variants of the effector and confers Pi-ta2 resistance, while the B allele of Ptr (PtrB) recognizes a restricted set of AVR-Pita alleles and, thereby, confers Pi-ta resistance. Analysis of the natural diversity in AVR-Pita and of mutant and transgenic strains identified one specific polymorphism in the effector sequence that controls escape from PtrB-mediated resistance. Taken together, our work establishes that the M. oryzae effector AVR-Pita is detected in an allele-specific manner by the unconventional rice resistance protein Ptr and that the NLR Pi-ta has no function in Pi-ta resistance and the recognition of AVR-Pita.
稻瘟病是由真菌稻瘟病菌引起的,是最具破坏性的水稻病害之一。Pi-ta 或 Pi-ta2 等抗病基因对于保护水稻免受稻瘟病至关重要。已发表的研究报告称,Pi-ta 编码一种核苷酸结合和富含亮氨酸重复结构域蛋白(NLR),该蛋白通过直接结合识别真菌蛋白酶样效应因子 AVR-Pita。然而,最近的发现挑战了这一模型,即 Pi-ta2 抗性也依赖于 AVR-Pita 的检测,它是由非常规抗病基因 Ptr 赋予的,Ptr 编码一种具有细胞质卷曲螺旋重复结构域的膜蛋白。在这里,我们使用 NLR Pi-ta 和 Ptr RNAi 敲低和 CRISPR/Cas9 敲除突变体水稻系,发现 AVR-Pita 的识别仅依赖于 Ptr,而 NLR Pi-ta 在此过程中不起作用,表明它不是 Pi-ta 抗性基因。Ptr 的不同等位基因赋予不同的识别特异性。Ptr 的 A 等位基因(PtrA)检测效应物的所有天然序列变体,并赋予 Pi-ta2 抗性,而 Ptr 的 B 等位基因(PtrB)识别受限制的 AVR-Pita 等位基因,从而赋予 Pi-ta 抗性。对 AVR-Pita 的自然多样性以及突变和转基因株系的分析确定了效应物序列中的一个特定多态性,该多态性控制了对 PtrB 介导的抗性的逃逸。总之,我们的工作表明,稻瘟病菌效应因子 AVR-Pita 被非常规水稻抗病蛋白 Ptr 以等位基因特异性的方式检测到,而 NLR Pi-ta 在 Pi-ta 抗性和 AVR-Pita 的识别中没有功能。