Transcriptional control of preadipocyte determination by Zfp423

Zfp423 involved in preadipose cell determination For the past 20 years extensive research from the adipogenesis field has focused almost exclusively on the transcriptional mechanisms governing the differentiation of committed fibroblastic fat cell precursors (preadipocytes) into mature adipocytes. This has led to the identification of a clutch of important regulators of adipocyte differentiation, including PPARγ and various C/EBP family members. Relatively little is known about the transcriptional mechanisms controlling the formation of preadipocytes rather that other fibroblastic cells — the so-called commitment step. Here, the zinc-finger protein Zfp423 is identified as a transcriptional regulator of preadipose cell determination. An understanding of how fat cells (adipocytes) develop will contribute to our understanding of obesity. The differentiation of committed preadipocytes into adipocytes is known to be controlled by PPARγ and several other transcription factors. But what turns a cell into a preadipocyte? Here, the zinc-finger protein Zfp423 is identified as a transcriptional regulator of preadipocyte determination. The worldwide epidemic of obesity has increased the urgency to develop a deeper understanding of physiological systems related to energy balance and energy storage, including the mechanisms controlling the development of fat cells (adipocytes). The differentiation of committed preadipocytes to adipocytes is controlled by PPARγ and several other transcription factors 1 , but the molecular basis for preadipocyte determination is not understood. Using a new method for the quantitative analysis of transcriptional components, we identified the zinc-finger protein Zfp423 as a factor enriched in preadipose versus non-preadipose fibroblasts. Ectopic expression of Zfp423 in non-adipogenic NIH 3T3 fibroblasts robustly activates expression of Pparg in undifferentiated cells and permits cells to undergo adipocyte differentiation under permissive conditions. Short hairpin RNA (shRNA)-mediated reduction of Zfp423 expression in 3T3-L1 cells blunts preadipocyte Pparg expression and diminishes the ability of these cells to differentiate. Furthermore, both brown and white adipocyte differentiation is markedly impaired in Zfp423 -deficient mouse embryos. Zfp423 regulates Pparg expression, in part, through amplification of the BMP signalling pathway, an effect dependent on the SMAD-binding capacity of Zfp423. This study identifies Zfp423 as a transcription