Technology Report
Cdx1::Cre allele for gene analysis in the extraembryonic ectoderm and the three germ layers of mice at mid-gastrulation
Article first published online: 23 FEB 2009
DOI: 10.1002/dvg.20484
Copyright © 2009 Wiley-Liss, Inc.
Additional Information
How to Cite
Hierholzer, A. and Kemler, R. (2009), Cdx1::Cre allele for gene analysis in the extraembryonic ectoderm and the three germ layers of mice at mid-gastrulation. Genesis, 47: 204–209. doi: 10.1002/dvg.20484
Publication History
- Issue published online: 23 MAR 2009
- Article first published online: 23 FEB 2009
- Manuscript Accepted: 14 NOV 2008
- Manuscript Revised: 30 SEP 2008
- Manuscript Received: 7 MAY 2008
Funded by
- Max-Planck Society
- Abstract
- References
- Cited By
Keywords:
- Cre recombinase;
- Cdx1 expression;
- trophectoderm;
- primitive streak;
- placental development
Abstract
Transgenic mice with a defined cell- or tissues-specific expression of Cre-recombinase are essential tools to study gene function. Here we report the generation and analysis of a transgenic mouse line (Cdx1::Cre) with restricted Cre-expression from Cdx1 regulatory elements. The expression of Cre-recombinase mimicked the endogenous expression pattern of Cdx1 at midgastrulation (from E7.5 to early headfold stage) inducing recombination in the three germlayers of the primitive streak region throughout the posterior embryo and caudal to the heart. This enables gene modifications to investigate patterning of the caudal embryo during and after gastrulation. Interestingly, we identified Cdx1 expression in the trophectoderm (TE) of blastocyst stage embryos. Concordantly, we detected extensive Cre-mediated recombination in the polar TE and, although to lesser extent, in the mural TE. In E7.5 postimplantation embryos, almost all cells of the extraembryonic ectoderm (ExE), which are derived from the polar TE, are recombined although the ExE itself is negative for Cdx1 and Cre at this stage. These results indicate that Cdx1::Cre mice are also a valuable tool to study gene function in tissues essential for placental development. genesis 47:204–209, 2009. © 2009 Wiley-Liss, Inc.

1526-968X/asset/olbannerleft.gif?v=1&s=14e801d29ba3c663d9859c91f5826e31e3ea8063)
1526-968X/asset/olbannerright.gif?v=1&s=5ad74ac8c249b6349487f1be3fab63c52c1fc451)
