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Publication : In vitro differentiated adipocytes from a Foxc2 reporter knock-in mouse as screening tool.

First Author  Cederberg A Year  2009
Journal  Transgenic Res Volume  18
Issue  6 Pages  889-97
PubMed ID  19475495 Mgi Jnum  J:155032
Mgi Id  MGI:4412164 Doi  10.1007/s11248-009-9280-1
Citation  Cederberg A, et al. (2009) In vitro differentiated adipocytes from a Foxc2 reporter knock-in mouse as screening tool. Transgenic Res 18(6):889-97
abstractText  We have developed a generic model for in vitro high-throughput screening for agents regulating transcription of genes in the mouse genome here exemplified by Foxc2, a forkhead transcription factor involved in regulation of adipocyte metabolism. We made a Foxc2-LacZ reporter 'knock-in' mouse in which one of the two Foxc2 alleles has been inactivated and replaced by a LacZ reporter gene. Mouse embryonic fibroblasts, derived from such mice, were differentiated in vitro to adipocytes and used in cell-based screens. Forskolin as well as 12-O-tetradecanoylphorbol-13-acetate (TPA) increased levels of Foxc2nLacZ fusion protein. We could also demonstrate that this was paralleled by an increase in Foxc2 mRNA, transcribed from the wild type allele. This generic method offers a novel way of identifying both positive and negative upstream regulators of a gene, using high-throughput screening methodology. In a cell-based screen using such methodology we demonstrate efficacy by identifying NKH477 as a Foxc2 activating compound.
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