- V.A. Lombardo
- A. Sporbert
- S. Abdelilah-Seyfried
- Journal of Visualized Experiments
- J Vis Exp (67): e4350
Embryogenesis is a dynamic process that is best studied by using techniques that allow the documentation of developmental changes in vivo. The use of genetically-encoded fluorescent proteins has proven a valuable strategy for elucidating dynamic morphogenetic processes as they occur in the intact organism. During the past decade, the development of photoactivatable and photoconvertible fluorescent proteins has opened the possibility to investigate the fate of discrete subpopulations of tagged proteins(1). Unlike photoactivatable proteins, photoconvertible fluorescent proteins (PCFPs) are readily tracked and imaged in their native emission state prior to photoconversion, making it easier to identify and select regions by optical inspection. PCFPs, such as Kaede(2), KikGR(3), Dendra(4) and EosFP(5), can be shifted from green to red upon exposure to UV or blue light due to a His-Tyr-Gly tripeptide sequence which forms a green chromophore that can be photoconverted to a red one by a light-catalyzed beta-elimination and subsequent extension of a π-conjugated system(3). PCFPs and their monomeric variants are useful tools for tracking cells(6-10) and studying protein dynamics(11-14), respectively. During recent years, PCFPs have been expressed in different animal model, such as zebrafish(6), chicken(7,8) and mouse(9,10) for cell fate tracking. Here we report a protocol for cell-specific photoconversion of PCFPs in the living zebrafish embryo and further tracking of photoconverted proteins at later developmental stages. This methodology allows studying, in a tissue-specific manner, cell biological events underlying morphogenesis in the zebrafish animal model.