Bai Ling, Ma Xiaonan, Zhang Guozeng, Song Shufei, Zhou Yun, Gao Lijie, Miao Yuchen, Song Chun-Peng
Institute of Plant Stress Biology, State Key Laboratory of Cotton Biology, Department of Biology, Henan University, Kaifeng 475001, China.
Institute of Plant Stress Biology, State Key Laboratory of Cotton Biology, Department of Biology, Henan University, Kaifeng 475001, China
Plant Cell. 2014 Apr;26(4):1497-1511. doi: 10.1105/tpc.114.124586. Epub 2014 Apr 25.
Ammonium (NH) is both a necessary nutrient and an important signal in plants, but can be toxic in excess. Ammonium sensing and regulatory mechanisms in plant cells have not been fully elucidated. To decipher the complex network of NH signaling, we analyzed [Ca]-associated protein kinase (CAP) genes, which encode signaling components that undergo marked changes in transcription levels in response to various stressors. We demonstrated that CAP1, a tonoplast-localized receptor-like kinase, regulates root hair tip growth by maintaining cytoplasmic Ca gradients. A CAP1 knockout mutant (cap1-1) produced elevated levels of cytoplasmic NH. Furthermore, root hair growth of cap1-1 was inhibited on Murashige and Skoog medium, but NH depletion reestablished the Ca gradient necessary for normal growth. The lower net NH influx across the vacuolar membrane and relatively alkaline cytosolic pH of cap1-1 root hairs implied that mutation of CAP1 increased NH accumulation in the cytoplasm. Furthermore, CAP1 functionally complemented the npr1 (nitrogen permease reactivator protein) kinase yeast mutant, which is defective in high-affinity NH uptake via MEP2 (methylammonium permease 2), distinguishing CAP1 as a cytosolic modulator of NH levels that participates in NH homeostasis-regulated root hair growth by modulating tip-focused cytoplasmic Ca gradients.
铵(NH)既是植物必需的养分,也是重要的信号分子,但过量时可能有毒。植物细胞中铵的感知和调节机制尚未完全阐明。为了解析复杂的NH信号网络,我们分析了[Ca]相关蛋白激酶(CAP)基因,这些基因编码的信号成分在响应各种应激源时转录水平会发生显著变化。我们证明,液泡膜定位的类受体激酶CAP1通过维持细胞质Ca梯度来调节根毛顶端生长。CAP1基因敲除突变体(cap1-1)的细胞质NH水平升高。此外,cap1-1在Murashige和Skoog培养基上的根毛生长受到抑制,但NH耗尽重新建立了正常生长所需的Ca梯度。cap1-1根毛液泡膜上较低的净NH流入量和相对碱性的细胞质pH值表明,CAP1突变增加了细胞质中NH的积累。此外,CAP1在功能上互补了npr1(氮通透酶激活蛋白)激酶酵母突变体,该突变体通过MEP2(甲基铵通透酶2)进行高亲和力NH摄取存在缺陷,这表明CAP1是一种细胞质NH水平调节剂,通过调节顶端聚焦的细胞质Ca梯度参与NH稳态调节的根毛生长。