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PMID: 17661401 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

Foxl1-Cre BAC transgenic mice: a new tool for gene ablation in the gastrointestinal mesenchyme.

Genesis (New York, N.Y. : 2000) ·Vol. 45 ·No. 8 ·2007-08-00 ·Pages 518-22

Sackett SD, Fulmer JT, Friedman JR, Kaestner KH

Abstract

The use of Cre-loxP technology for the purpose of cell type-specific gene ablation has revolutionized developmental biology and biomedicine. Several transgenic mouse lines have been developed for the analysis of gene function in the gastrointestinal tract, but in all of these the expression of Cre is limited to the epithelial cell layer. No Cre- expressing transgenic mouse lines ("Cre lines") exist for the deletion of loxP-flanked genes specifically in gut mesoderm. To address this deficiency, we have derived a bacterial artificial chromosome based transgenic mouse line in which the Cre gene is controlled by the Foxl1 promoter and enhancer elements. X-Gal staining of Foxl1-Cre; Rosa26R bi-transgenic lines confirm that Foxl1-Cre results in recombination specifically in the gastrointestinal mesenchyme. The Foxl1-Cre line will facilitate the dissection of mesenchymal to epithelial signaling that is known to play a major role in the patterning and function of the gastrointestinal tract.

MeSH Terms
Animals Cell Survival Chromosomes, Artificial, Bacterial Embryo, Mammalian/cytology,metabolism Female Forkhead Transcription Factors/genetics Gastrointestinal Tract/cytology,metabolism Gene Deletion Integrases/genetics Male Mesoderm/cytology,metabolism Mice Mice, Knockout Mice, Transgenic
Chemicals
Forkhead Transcription Factors Foxl1 protein, mouse Cre recombinase Integrases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Sackett Sara D
Department of Genetics, University of Pennsylvania School of Medicine, 415 Curie Boulevard, Philadelphia, PA 19104, USA.
Fulmer James T
Friedman Joshua R
Kaestner Klaus H
Article Info
Journal
Genesis (New York, N.Y. : 2000)
Abbr.
Genesis
ISSN
1526-954X
Published
2007-08-00
Pages
518-22
Language
English
Region
United States
NLM ID
100931242
Subset
IM
Grants
NIDDK NIH HHS · P30 DK50305 · United States
NIDDK NIH HHS · R01 DK 053839 · United States
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