Laudes, MatthiasChristodoulides, ConstantinosSewter, CiaranRochford, Justin J.Considine, Robert V.Sethi, Jaswinder K.Vidal-Puig, AntonioO’Rahilly, Stephen2016-03-072016-03-072004-03-19Laudes, M., Christodoulides, C., Sewter, C., Rochford, J. J., Considine, R. V., Sethi, J. K., … O’Rahilly, S. (2004). Role of the POZ Zinc Finger Transcription Factor FBI-1 in Human and Murine Adipogenesis. The Journal of Biological Chemistry, 279(12), 11711–11718. http://doi.org/10.1074/jbc.M310240200https://hdl.handle.net/1805/8743Poxvirus zinc finger (POZ) zinc finger domain transcription factors have been shown to play a role in the control of growth arrest and differentiation in several types of mesenchymal cells but not, as yet, adipocytes. We found that a POZ domain protein, factor that binds to inducer of short transcripts-1 (FBI-1), was induced during both murine and human preadipocyte differentiation with maximal expression levels seen at days 2-4. FBI-1 mRNA was expressed in human adipose tissue with the highest levels found in samples from morbidly obese subjects. Murine cell lines constitutively expressing FBI-1 showed evidence for accelerated adipogenesis with earlier induction of markers of differentiation and enhanced lipid accumulation, suggesting that FBI-1 may be an active participant in the differentiation process. Consistent with the properties of this family of proteins in other cell systems, 3T3L1 cells stably overexpressing FBI-1 showed reduced DNA synthesis and reduced expression of cyclin A, cyclin-dependent kinase 2, and p107, proteins known to be involved in the regulation of mitotic clonal expansion. In addition, FBI-1 reduced the transcriptional activity of the cyclin A promoter. Thus, FBI-1, a POZ zinc finger transcription factor, is induced during the early phases of human and murine preadipocyte differentiation where it may contribute to adipogenesis through influencing the switch from cellular proliferation to terminal differentiation.en-USPublisher Policy3T3-L1 CellsAdipose Tissue -- CytologyAdipose Tissue -- MetabolismAnimalsBase SequenceCloning, MolecularDNA PrimersDNA-Binding Proteins -- PhysiologyHumansMiceMitosisOligonucleotide Array Sequence AnalysisRepressor Proteins -- PhysiologyReverse Transcriptase Polymerase Chain ReactionTranscription Factors -- PhysiologyZinc FingersArticle