Shi Hui, Shen Xing, Liu Renlu, Xue Chang, Wei Ning, Deng Xing Wang, Zhong Shangwei
State Key Laboratory of Protein and Plant Gene Research, Peking-Tsinghua Center for Life Sciences, School of Advanced Agricultural Sciences and School of Life Sciences, Peking University, Beijing 100871, China.
Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT 06520, USA.
Dev Cell. 2016 Dec 5;39(5):597-610. doi: 10.1016/j.devcel.2016.10.020. Epub 2016 Nov 23.
Plants germinating under subterranean darkness assume skotomorphogenesis, a developmental program strengthened by ethylene in response to mechanical pressure of soil. Upon reaching the surface, light triggers a dramatic developmental transition termed de-etiolation that requires immediate termination of ethylene responses. Here, we report that light activation of photoreceptor phyB results in rapid degradation of EIN3, the master transcription factor in the ethylene signaling pathway. As a result, light rapidly and efficiently represses ethylene actions. Specifically, phyB directly interacts with EIN3 in a light-dependent manner and also physically associates with F box protein EBFs. The light-activated association of phyB, EIN3, and EBF1/EBF2 proteins stimulates robust EIN3 degradation by SCF E3 ligases. We reveal that phyB manipulates substrate-E3 ligase interactions in a light-dependent manner, thus directly controlling the stability of EIN3. Our findings illustrate a mechanistic model of how plants transduce light information to immediately turn off ethylene signaling for de-etiolation initiation.
在地下黑暗环境中萌发的植物呈现出暗形态建成,这是一种由乙烯强化的发育程序,以响应土壤的机械压力。一旦到达地表,光照会触发一种称为去黄化的显著发育转变,这需要立即终止乙烯反应。在此,我们报道光感受器phyB的光激活导致EIN3快速降解,EIN3是乙烯信号通路中的主转录因子。结果,光照迅速且有效地抑制乙烯作用。具体而言,phyB以光依赖的方式直接与EIN3相互作用,并且还与F盒蛋白EBFs发生物理关联。phyB、EIN3和EBF1/EBF2蛋白的光激活关联通过SCF E3连接酶刺激EIN3的强烈降解。我们揭示phyB以光依赖的方式操纵底物-E3连接酶相互作用,从而直接控制EIN3的稳定性。我们的研究结果阐明了一个机制模型,即植物如何转导光信息以立即关闭乙烯信号从而启动去黄化过程。