The regulation of hepatic glucose metabolism has a key role in whole-body energy metabolism, since the liver is able to store (glycogen synthesis, lipogenesis) and to produce (glycogenolysis, gluconeogenesis) glucose. These pathways are regulated at several levels, including a transcriptional level, since many of the metabolism-related genes are expressed according to the quantity and quality of nutrients. Recent advances have been made in the understanding of the regulation of hepatic glycolytic, lipogenic and gluconeogenic gene expression by pancreatic hormones, insulin and glucagon and glucose. Here we review the role of the transcription factors forkhead and sterol regulatory element binding protein-1c in the inductive and repressive effects of insulin on hepatic gene expression, and the pathway that leads from glucose to gene regulation with the recently discovered carbohydrate response element binding protein. We discuss how these transcription factors are integrated in a regulatory network that allows a fine tuning of hepatic glucose storage or production, and their potential importance in metabolic diseases.
- carbohydrate response element binding protein
Abbreviations used: ACC, acetyl-CoA carboxylase; AMPK, AMP-activated protein kinase; bHLH-LZ, basic domain helix–loop–helix leucine zipper; CHO, Chinese-hamster ovary; ChoRE, carbohydrate response element; ChREBP, carbohydrate response element binding protein; DN-SREBP-1c, dominant negative form of SREBP-1c; DP-SREBP-1c, dominant positive form of SREBP-1c; EMSA, electrophoretic mobility shift assay; ER, endoplasmic reticulum; FAS, fatty acid synthase; FKHR, forkhead-related protein; GK, glucokinase; GKRP, glucokinase regulatory protein; Glc-6-Pase, glucose-6-phosphatase; GlRE, glucose response element; IGFBP-1, insulin-like growth factor binding protein-1; IRE, insulin response element; IRS, insulin receptor substrate; L-PK, liver pyruvate kinase; LXR, liver X receptor; MAP kinase, mitogen-activated protein kinase; PEPCK, phosphoenolpyruvate carboxykinase; PI 3-kinase, phosphoinositide 3-kinase; PKA, protein kinase A; PKB, protein kinase B; SCAP, SREBP cleavage activating protein; Snf1, sucrose non-fermenting; S1P/S2P, site-1/site-2 protease; SRE, sterol regulatory element; SREBP, sterol regulatory element binding protein; TAT, tyrosine aminotransferase; USF, upstream stimulatory factor.
- The Biochemical Society, London ©2002