Mizuta Yoko, Tsuda Katsutoshi
Precursory Research for Embryonic Science and Technology (PRESTO), Japan Science and Technology Agency (JST), Nagoya, Aichi, Japan.
Institute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Nagoya, Aichi, Japan.
Methods Mol Biol. 2018;1830:257-268. doi: 10.1007/978-1-4939-8657-6_15.
In plants, transcription factors often act as cell-to-cell trafficking mobile proteins and specify cell fate. Thus, to visualize spatiotemporal expression pattern and localization of transcription factors are essential to understand their functions during development. Several protocols have been developed to observe fluorescent protein. However, plant-specific autofluorescent compounds and various tissue components with different refractive indexes interfere with detection of fluorescent signals of your interest. Furthermore, cell fate specification often occurs in a limited number of cells covered by lateral/layers of organs. To overcome those issues, the plant clearing method, ClearSee, was recently developed for high-resolution imaging inside tissues by making background transparent. In this chapter, we provide three-dimensional imaging of fluorescent-protein-fused transcription factors by two-photon excitation microscopy in Arabidopsis and rice. Complex cell patterning with gene expression could be observed from any direction three-dimensionally. This method could be applicable to visualize any protein of your interest or it can readily be adapted in various other plants.
在植物中,转录因子通常作为细胞间运输的移动蛋白并决定细胞命运。因此,可视化转录因子的时空表达模式和定位对于理解其在发育过程中的功能至关重要。已经开发了几种用于观察荧光蛋白的方法。然而,植物特有的自发荧光化合物和具有不同折射率的各种组织成分会干扰对目标荧光信号的检测。此外,细胞命运决定通常发生在被器官侧面/层覆盖的有限数量的细胞中。为了克服这些问题,最近开发了一种植物透明化方法ClearSee,通过使背景透明来实现组织内部的高分辨率成像。在本章中,我们通过双光子激发显微镜对拟南芥和水稻中荧光蛋白融合的转录因子进行三维成像。可以从任何方向三维观察具有基因表达的复杂细胞模式。该方法可用于可视化任何目标蛋白,也可以很容易地应用于其他各种植物。