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Mech Dev. 2002 Oct;118(1-2):91-8.

I-SceI meganuclease mediates highly efficient transgenesis in fish.

Author information

1
INRA Junior Group, UPR2197, Institut de Neurobiologie A. Fessard, CNRS, Avenue de la Terrasse, 91 198 Gif-Sur-Yvette, France.

Erratum in

  • Mech Dev. 2003 Feb;120(2):267.

Abstract

The widespread use of fish as model systems is still limited by the mosaic distribution of cells transiently expressing transgenes leading to a low frequency of transgenic fish. Here we present a strategy that overcomes this problem. Transgenes of interest were flanked by two I-SceI meganuclease recognition sites, and co-injected together with the I-SceI meganuclease enzyme into medaka embryos (Oryzias latipes) at the one-cell stage. First, the promoter dependent expression was strongly enhanced. Already in F0, 76% of the embryos exhibited uniform promoter dependent expression compared to 26% when injections were performed without meganuclease. Second, the transgenesis frequency was raised to 30.5%. Even more striking was the increase in the germline transmission rate. Whereas in standard protocols it does not exceed a few percent, the number of transgenic F1 offspring of an identified founder fish reached the optimum of 50% in most lines resulting from meganuclease co-injection. Southern blot analysis showed that the individual integration loci contain only one or few copies of the transgene in tandem. At a lower rate this method also leads to enhancer trapping effects, novel patterns that are likely due to the integration of the transgene in the vicinity of enhancer elements. Meganuclease co-injection thus provides a simple and highly efficient tool to improve transgenesis by microinjection.

PMID:
12351173
DOI:
10.1016/s0925-4773(02)00218-6
[Indexed for MEDLINE]
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