C/EBP transcription factors regulate SREBP1c gene expression during adipogenesis

Abstract

The transcription factor SREBP1c (sterol-regulatory-element-binding protein 1c) is highly expressed in adipose tissue and plays a central role in several aspects of adipocyte development including the induction of PPARγ (peroxisome-proliferator-activated receptor γ), the generation of an endogenous PPARγ ligand and the expression of several genes critical for lipid biosynthesis. Despite its significance, the regulation of SREBP1c expression during adipogenesis is not well characterized. We have noted that in several models of adipogenesis, SREBP1c expression closely mimics that of known C/EBPβ (CCAAT/enhancer-binding protein β) targets. Inhibition of C/EBP activity during adipogenesis by expressing either the dominant-negative C/EBPβ LIP (liver-enriched inhibitory protein) isoform, the co-repressor ETO (eight-twenty one/MTG8) or using siRNAs (small interfering RNAs) targeting either C/EBPβ or C/EBPδ significantly impaired early SREBP1c induction. Furthermore, ChIP (chromatin immunoprecipitation) assays identified specific sequences in the SREBP1c promoter to which C/EBPβ and C/EBPδ bind in intact cells, demonstrating that these factors may directly regulate SREBP1c expression. Using cells in which C/EBPα expression is inhibited using shRNA (short hairpin RNA) and ChIP assays we show that C/EBPα replaces C/EBPβ and C/EBPδ as a regulator of SREBP1c expression in maturing adipocytes. These results provide novel insight into the induction of SREBP1c expression during adipogenesis. Moreover, the findings of the present study identify an important additional mechanism via which the C/EBP transcription factors may control a network of gene expression regulating adipogenesis, lipogenesis and insulin sensitivity.

Insulin induction of SREBP-1c in rodent liver requires LXRα-C/EBPβ complex

“…Based on previous data implicating C/EBPβ in promoting the transcription of SREBP-1c in adipocytes and liver (11,13,14),…”

Tribbles-1 regulates hepatic lipogenesis through posttranscriptional regulation of C/EBPα

“…Motif analysis at sites with stronger C/EBPα binding in the Trib1_LSKO mice revealed robust enrichment for the canonical C/EBP motif (Figure 7B), and gene-set enrichment analysis of these peaks showed major enrichment of genes involved in lipid metabolism as one of the top findings (Supplemental Figure 6A). Moreover, differ- thesis, such as ChREBP, LXR, and SREBP1, the latter of which C/EBPα is reported to regulate the transcription of in adipose (8). C/EBPα protein abundance in liver is regulated by TRIB1, and thus the TRIB1-C/EBPα axis may be an underappreciated moderator of human hepatic lipogenesis.…”

Adipogenesis at a glance

“…Among the targets of C/EBP and C/EBPd are the promoters of the genes encoding the key adipogenic transcription factors C/EBP and PPARg and the regulator of lipogenic genes SREBP1 (for sterol-regulatory-element-binding protein 1) (Payne et al, 2010;Rosen and MacDougald, 2006;White and Stephens, 2010). PPARg activates the promoter of the gene encoding C/EBP and vice versa, creating a positive-feedback loop.…”