Ziqing Winston Zhao1,3, Melanie D White1,3, Yanina D Alvarez1-3, Jennifer Zenker1,3, Stephanie Bissiere1 & Nicolas Plachta1.
1 Institute of Molecular and Cell Biology (IMCB), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
2 Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina.
3 These authors contributed equally to this work.
Correspondence should be addressed to N.P. (email@example.com).
Published online in Nature Protocols on 29 June 2017.
Probing transcription factor (TF)–DNA interactions remains challenging in complex in vivo systems such as mammalian embryos, especially when TF copy numbers and fluorescence background are high. To address this difficulty, fluorescence correlation spectroscopy (FCS ) can be combined with the use of photoactivatable fluorescent proteins to achieve selective photoactivation of a subset of tagged TF molecules. This approach, termed paFCS , enables FCS measurements within single cell nuclei inside live embryos, and obtains autocorrelation data of a quality previously only attainable in simpler in vitro cell culture systems. Here, we present a protocol demonstrating the applicability of paFCS in developing mouse embryos by outlining its implementation on a commercial laser-scanning microscope. We also provide procedures for optimizing the photoactivation and acquisition parameters and determining key parameters describing TF–DNA binding. The entire procedure can be performed within ~2 d (excluding embryo culture time), although the acquisition of each paFCS data set takes only ~10 min. This protocol can be used to noninvasively reveal cell-to-cell variation in TF dynamics, as well as critical, fate-predicting changes over the course of early embryonic development.
Binding of transcription factors to DNA is highly dynamics. New techniques enable measurement of these dynamic interactions in single cells of developing mouse embryos.
For more information on Nicolas PLACHTA's lab, please click here.