z-logo
open-access-imgOpen Access
Photoactivation of the CreERT2 Recombinase for Conditional Site-Specific Recombination with High Spatiotemporal Resolution
Author(s) -
Deepak K. Sinha,
Pierre Neveu,
Nathalie GageyEilstein,
Isabelle Aujard,
Thomas Le Saux,
Christine Rampon,
Carole Gauron,
Koichi Kawakami,
Christoph Leucht,
Laure BallyCuif,
Michel Volovitch,
David Bensimon,
Ludovic Jullien,
Sophie Vriz
Publication year - 2010
Publication title -
zebrafish
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.722
H-Index - 46
eISSN - 1557-8542
pISSN - 1545-8547
DOI - 10.1089/zeb.2009.0632
Subject(s) - recombinase , cre recombinase , biology , zebrafish , site specific recombination , transgene , microbiology and biotechnology , cre lox recombination , recombination , reporter gene , computational biology , gene , gene expression , genetics , genetically modified mouse
We implemented a noninvasive optical method for the fast control of Cre recombinase in single cells of a live zebrafish embryo. Optical uncaging of the caged precursor of a nonendogeneous steroid by one- or two-photon illumination was used to restore Cre activity of the CreER(T2) fusion protein in specific target cells. This method labels single cells irreversibly by inducing recombination in an appropriate reporter transgenic animal and thereby can achieve high spatiotemporal resolution in the control of gene expression. This technique could be used more generally to investigate important physiological processes (e.g., in embryogenesis, organ regeneration, or carcinogenesis) with high spatiotemporal resolution (single cell and 10-min scales).

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom