College of Agronomy & Center for Crop Genome Engineering, Henan Agricultural University, Zhengzhou 450046, Henan, China.
College of Agronomy & Center for Crop Genome Engineering, Henan Agricultural University, Zhengzhou 450046, Henan, China.
Plant Physiol Biochem. 2024 Dec;217:109295. doi: 10.1016/j.plaphy.2024.109295. Epub 2024 Nov 14.
Bacterial wilt (BW) caused by Ralstonia solanacearum severely impacts the yield and quality of peanut (Arachis hypogaea L.), a globally cultivated industrial crop. Despite the abscisic acid (ABA) signaling pathway have been identified as key factors in peanut resistance to BW, the molecular mechanism remains unclear. Through systematic identification, it was discovered that the peanut genome contains 18 ABA receptor pyrabactin resistance 1-like (PYL) family genes, which show conservation with other plant species. Among these PYL genes in peanut (referred to as AhPYL), AhPYL6 and AhPYL16 showed significant up-regulation in response to salicylic acid, jasmonic acid, ABA treatments, and R. solanacearum infection. Subsequently, the full-length AhPYL6 was cloned and functionally characterized. The fusion protein AhPYL6-YFP was predominantly expressed in the cytoplasm and nucleus of tobacco leaves, and overexpression of AhPYL6 notably enhanced resistance against R. solanacearum. Expression analysis revealed that the expression levels defense -related genes including NbNPR1, NbPR2, NbPR3, NbHRS203, NbEFE26, and NbNDR1 were significantly up-regulated by the overexpression of AhPYL6, which suggested that AhPYL6 confers the resistance to R. solanacearum through promoting expression of defense -related genes. These findings highlight the potential roles of PYL ABA receptors in the plant defense response to bacterial pathogens.
青枯病(BW)由青枯雷尔氏菌引起,严重影响了全球种植的工业作物花生(Arachis hypogaea L.)的产量和质量。尽管脱落酸(ABA)信号通路已被确定为花生对 BW 抗性的关键因素,但分子机制尚不清楚。通过系统鉴定,发现花生基因组含有 18 个 ABA 受体吡喃并[2,3-d]嘧啶 1 样(PYL)家族基因,与其他植物物种具有保守性。在这些花生 PYL 基因(称为 AhPYL)中,AhPYL6 和 AhPYL16 对水杨酸、茉莉酸、ABA 处理和青枯雷尔氏菌感染的响应表现出显著的上调。随后,克隆并功能表征了全长 AhPYL6。AhPYL6-YFP 融合蛋白主要在烟草叶片的细胞质和细胞核中表达,过表达 AhPYL6 显著增强了对青枯雷尔氏菌的抗性。表达分析显示,防御相关基因 NbNPR1、NbPR2、NbPR3、NbHRS203、NbEFE26 和 NbNDR1 的表达水平在 AhPYL6 的过表达下显著上调,这表明 AhPYL6 通过促进防御相关基因的表达赋予对青枯雷尔氏菌的抗性。这些发现强调了 PYL ABA 受体在植物对细菌病原体防御反应中的潜在作用。