Transcriptional and epigenetic control of adipocyte remodeling during obesity

The rising prevalence of obesity over the past decades coincides with the rising awareness that a detailed understanding of both adipose tissue biology and obesity-associated remodeling is crucial for developing therapeutic and preventive strategies. Substantial progress has been made in identifying the signaling pathways and transcriptional networks that orchestrate alterations of adipocyte gene expression linked to diverse phenotypes. Owing to recent advances in epigenomics, we also gained a better appreciation for the fact that different environmental cues can epigenetically reprogram adipocyte fate and function, mainly by altering DNA methylation and histone modification patterns. Intriguingly, it appears that transcription factors and chromatin-modifying coregulator complexes are the key regulatory components that coordinate both signaling-induced transcriptional and epigenetic alterations in adipocytes. In this review, we summarize and discuss current molecular insights into how these alterations and the involved regulatory components trigger adipogenesis and adipose tissue remodeling in response to energy surplus.

Automated summary

The rising prevalence of obesity has highlighted the importance of understanding adipose tissue biology and obesity-associated remodeling in developing therapeutic strategies. Recent advances in epigenomics have shown that environmental cues can epigenetically reprogram adipocyte fate and function. Transcription factors and chromatin-modifying coregulator complexes are key components in coordinating transcriptional and epigenetic alterations in adipocytes.