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Sinha, D.K.* ; Neveu, P.* ; Gagey, N.* ; Aujard, I.* ; Le Saux, T.* ; Rampon, C.* ; Gauron, C.* ; Kawakami, K.* ; Leucht, C. ; Bally-Cuif, L. ; Volovitch, M.* ; Bensimon, D.* ; Jullien, L.* ; Vriz, S.*

Photoactivation of the CreER T² recombinase for conditional site-specific recombination with high spatiotemporal resolution.

Zebrafish 7, 199-204 (2010)
DOI PMC
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
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).
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Transgenic zebrafish; Mice; Expression; System; Tool
ISSN (print) / ISBN 1545-8547
e-ISSN 1557-8542
Zeitschrift Zebrafish
Quellenangaben Band: 7, Heft: 2, Seiten: 199-204 Artikelnummer: , Supplement: ,
Verlag Mary Ann Liebert
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed