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Updated: Dec 30, 2025

A Method for Characterizing Embryogenesis in Arabidopsis
Published on: August 4, 2017
Visualizing Protein Associations in Living Arabidopsis Embryo
Yuchen Long1, Yvonne Stahl2, Stefanie Weidtkamp-Peters3
1Laboratoire Reproduction et Développement des Plantes (RDP), Univ Lyon, ENS de Lyon, UCB Lyon 1, CNRS, INRA, Lyon, France.
Abstract:
Protein-protein interactions (PPI) are essential for a plethora of biological processes. These interactions can be visualized and quantified with spatial resolution using Förster resonance energy transfer (FRET) measured by fluorescence lifetime imaging microscopy (FLIM) technology. Currently, FRET-FLIM is routinely used in cell biology, and it has become a powerful tool to map protein interactions in native environments. However, implementing this technology in living multicellular organism remains challenging, especially when dealing with developing plant embryos where tissues are confined in multiple cell layers preventing direct imaging. In this chapter, we describe a step-by-step protocol for studying PPI using FRET-FLIM of the two transcription factors SCARECROW and SHORTROOT in Arabidopsis embryos. We provide a detailed description from embryo isolation to data analysis and representation.
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