Liu Qiulin, Wang Tianyu, Ke Meiyu, Qian Chongzhen, Li Jiejie, Huang Xi, Gao Zhen, Chen Xu, Tu Tianli
Fujian Provincial Key Laboratory of Haixia Applied Plant Systems Biology, College of Life Science, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
Horticultural Plant Biology and Metabolomics Center, Haixia Institute of Science and Technology, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
Plants (Basel). 2024 Jun 1;13(11):1536. doi: 10.3390/plants13111536.
While it is well known that plants interpret UV-B as an environmental cue and a potential stressor influencing their growth and development, the specific effects of UV-B-induced oxidative stress on the dynamics of membrane lipids and proteins remain underexplored. Here, we demonstrate that UV-B exposure notably increases the formation of ordered lipid domains on the plasma membrane (PM) and significantly alters the behavior of the nodule autoregulation receptor kinase (GmNARK) protein in leaves. The GmNARK protein was located on the PM and accumulated as small particles in the cytoplasm. We found that UV-B irradiation interrupted the lateral diffusion of GmNARK proteins on the PM. Furthermore, UV-B light decreases the efficiency of surface molecule internalization by clathrin-mediated endocytosis (CME). In brief, UV-B irradiation increased the proportion of the ordered lipid phase and disrupted clathrin-dependent endocytosis; thus, the endocytic trafficking and lateral mobility of GmNARK protein on the plasma membrane are crucial for nodule formation tuning. Our results revealed a novel role of low-intensity UV-B stress in altering the organization of the plasma membrane and the dynamics of membrane-associated proteins.
虽然众所周知植物将UV-B视为一种环境信号以及影响其生长发育的潜在应激源,但UV-B诱导的氧化应激对膜脂和膜蛋白动态变化的具体影响仍未得到充分研究。在此,我们证明UV-B照射显著增加了质膜(PM)上有序脂域的形成,并显著改变了叶片中结节自调控受体激酶(GmNARK)蛋白的行为。GmNARK蛋白位于质膜上,并在细胞质中以小颗粒形式积累。我们发现UV-B辐射中断了GmNARK蛋白在质膜上的侧向扩散。此外,UV-B光降低了网格蛋白介导的内吞作用(CME)介导的表面分子内化效率。简而言之,UV-B照射增加了有序脂相的比例并破坏了网格蛋白依赖性内吞作用;因此,GmNARK蛋白在质膜上的内吞运输和侧向移动对于根瘤形成的调节至关重要。我们的结果揭示了低强度UV-B胁迫在改变质膜组织和膜相关蛋白动态变化方面的新作用。