Key result
HNF-4α promotes ChREBP-α and ChREBP-β transcription in response to glucose by directly binding to cis-elements in the ChREBP gene.
p-value: p=<0.05
HNF-4α is identified as a key transcription factor that promotes ChREBP expression in response to glucose, providing novel insights into metabolic gene regulation.
Extends glucose-responsive gene regulation insights in animals; leaves open human cardiometabolic relevance pending further study.
Transcription factor carbohydrate responsive element binding protein (ChREBP) promotes glycolysis and lipogenesis in metabolic tissues and cancer cells. ChREBP-α and ChREBP-β, two isoforms of ChREBP transcribed from different promoters, are both transcriptionally induced by glucose. However, the mechanism by which glucose increases ChREBP mRNA levels remains unclear. Here we report that hepatocyte nuclear factor 4 alpha (HNF-4α) is a key transcription factor for glucose-induced ChREBP-α and ChREBP-β expression. Ectopic HNF-4α expression increased ChREBP transcription while knockdown of HNF-4α greatly reduced ChREBP mRNA levels in liver cancer cells and mouse primary hepatocytes. HNF-4α not only directly bound to an E-box-containing region in intron 12 of the ChREBP gene, but also promoted ChREBP-β transcription by directly binding to two DR1 sites and one E-box-containing site of the ChREBP-β promoter. Moreover, HNF-4α interacted with ChREBP-α and synergistically promoted ChREBP-β transcription. Functionally, HNF-4α suppression reduced glucose-dependent ChREBP induction. Increased nuclear abundance of HNF-4α and its binding to cis-elements of ChREBP gene in response to glucose contributed to glucose-responsive ChREBP transcription. Taken together, our results not only revealed the novel mechanism by which HNF-4α promoted ChREBP transcription in response to glucose, but also demonstrated that ChREBP-α and HNF-4α synergistically increased ChREBP-β transcription.
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Meng et al. (2016) studied this question. HNF-4α overexpression or knockdown and glucose treatment vs. Control (empty vector, non-targeting siRNA, or 0 mM glucose) was evaluated on ChREBP-α and ChREBP-β mRNA and protein expression (p=<0.05). HNF-4α promotes ChREBP-α and ChREBP-β transcription in response to glucose by directly binding to cis-elements in the ChREBP gene.
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