Author:

Keywords:

Science & Technology, Multidisciplinary Sciences, Science & Technology - Other Topics, TRANSCRIPTION FACTOR E4F1, CELL-CYCLE ARREST, GROWTH, DIFFERENTIATION, IDENTIFICATION, LIPOGENESIS, ACTIVATION, REGULATOR, P120(E4F), REVEALS, Adipocytes, Adipose Tissue, Adult, Aged, Animals, Body Mass Index, Fatty Acids, Monounsaturated, Female, Gene Expression Regulation, Humans, Insulin Resistance, Lipid Metabolism, Male, Mice, Mice, Knockout, Middle Aged, Obesity, Repressor Proteins, Signal Transduction, Stearoyl-CoA Desaturase, Tumor Suppressor Protein p53, Ubiquitin-Protein Ligases

Abstract:

Growing evidence supports the importance of the p53 tumor suppressor in metabolism but the mechanisms underlying p53-mediated control of metabolism remain poorly understood. Here, we identify the multifunctional E4F1 protein as a key regulator of p53 metabolic functions in adipocytes. While E4F1 expression is upregulated during obesity, E4f1 inactivation in mouse adipose tissue results in a lean phenotype associated with insulin resistance and protection against induced obesity. Adipocytes lacking E4F1 activate a p53-dependent transcriptional program involved in lipid metabolism. The direct interaction between E4F1 and p53 and their co-recruitment to the Steaoryl-CoA Desaturase-1 locus play an important role to regulate monounsaturated fatty acids synthesis in adipocytes. Consistent with the role of this E4F1-p53-Steaoryl-CoA Desaturase-1 axis in adipocytes, p53 inactivation or diet complementation with oleate partly restore adiposity and improve insulin sensitivity in E4F1-deficient mice. Altogether, our findings identify a crosstalk between E4F1 and p53 in the control of lipid metabolism in adipocytes that is relevant to obesity and insulin resistance.