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Rice blast, caused by the fungal pathogen Magnaporthe oryzae , is one of the most important diseases of rice. Utilization of blast-resistance genes is the most economical, effective, and environmentally friendly way to control the disease. However, genetic resources with broad-spectrum resistance (BSR) that is effective throughout the rice growth period are rare. In this work, using a genome-wide association study, we identify a new blast-resistance gene, Pijx , which encodes a typical CC-NBS-LRR protein. Pijx is derived from a wild rice species and confers BSR to M. oryzae at both the seedling and panicle stages. The functions of the resistant haplotypes of Pijx are confirmed by gene knockout and overexpression experiments. Mechanistically, the LRR domain in Pijx interacts with and promotes the degradation of the ATP synthase β subunit (ATPb) via the 26S proteasome pathway. ATPb acts as a negative regulator of Pijx- mediated panicle blast resistance, and interacts with OsRbohC to promote its degradation. Consistently, loss of ATPb function causes an increase in NAPDH content and ROS burst. Remarkably, when Pijx is introgressed into two japonica rice varieties, the introgression lines show BSR and increased yields that are approximately 51.59% and 79.31% higher compared with those of their parents in a natural blast disease nursery. In addition, we generate PPL Pijx Pigm and PPL Pijx Piz-t pyramided lines and these lines also have higher BSR to panicle blast compared with Pigm- or Piz-t- containing rice plants. Collectively, this study demonstrates that Pijx not only confers BSR to M. oryzae but also maintains high and stable rice yield, providing new genetic resources and molecular targets for breeding rice varieties with broad-spectrum blast resistance. Mechanism of Pijx-conferred blast resistance Using a genome-wide association study, a new blast resistance gene, Pijx , that encodes a typical CC-NBS-LRR protein, was identified in this work. Mechanistically, Pijx interacts with ATPb and promotes the degradation of ATPb through the 26S proteasome pathway, causing OsRbohC accumulation to produce the ROS burst and ultimately leading to broad-spectrum seedling and panicle blast resistance. [ABSTRACT FROM AUTHOR]