Laboratoire Reproduction et Développement des Plantes (RDP), Univ Lyon, ENS de Lyon, UCB Lyon 1, CNRS, INRA, Lyon, France.
Methods Mol Biol. 2020;2094:79-89. doi: 10.1007/978-1-0716-0183-9_9.
Visualizing the distribution of hormone signaling activity such as auxin and cytokinins is of key importance for understanding regulation of plant development and physiology. Live imaging and genetically encoded hormone biosensors and reporters allow monitoring the spatial and temporal distribution of these phytohormones. Here, we describe how to cultivate live shoot apical meristems after dissection for observation under the confocal microscope for up to 4 days. The shoot apical meristems are maintained on an appropriate medium allowing them to grow and initiate new organs at a frequency similar to plants grown on soil. Meristems expressing hormone biosensors and reporters allows following hormone signaling activity distribution at high spatiotemporal resolution without chemical fixation, an approach that that can also be applied to follow the dynamics of expression in vivo of any fluorescent marker.
可视化激素信号活性(如生长素和细胞分裂素)的分布对于理解植物发育和生理学的调控至关重要。活细胞成像和遗传编码的激素生物传感器和报告器可用于监测这些植物激素的时空分布。在这里,我们描述了如何在共聚焦显微镜下观察后培养活体茎尖分生组织,时间最长可达 4 天。将茎尖分生组织置于适当的培养基上,使其以类似于在土壤中生长的植物的频率生长并启动新器官。表达激素生物传感器和报告器的分生组织允许以高时空分辨率跟踪激素信号活性的分布,而无需化学固定,这种方法也可用于跟踪任何荧光标记物在体内的表达动态。