Literature DB >> 9240931

Mechanisms by which carbohydrates regulate expression of genes for glycolytic and lipogenic enzymes.

J Girard1, P Ferré, F Foufelle.   

Abstract

Regulation of gene expression by nutrients is an important mechanism in the adaptation of mammals to their nutritional environment. This is especially true for enzymes involved in the storage of energy, such as the lipogenic and glycolytic enzymes in liver and adipose tissue. Transcription of the genes for lipogenic and glycolytic enzymes is stimulated by glucose in adipose tissue, liver, and pancreatic beta-cells. Several lines of evidence suggest that glucose must be metabolized to glucose-6-phosphate to stimulate gene transcription. In adipose tissue, insulin increases the expression of lipogenic enzymes indirectly by stimulating glucose uptake. In the liver, insulin also acts indirectly by stimulating the expression of glucokinase and, hence, by increasing glucose metabolism. Glucose response elements have been characterized for the L-pyruvate kinase and S14 genes. They have in common the presence of a sequence 5'-CACGTG-3', which binds a transcription factor called USF (upstream stimulatory factor). Another glucose response element, which uses a transcription factor named Sp1, has been characterized in the gene for the acetyl-coenzyme A carboxylase. The mechanisms linking glucose-6-phosphate to the glucose-responsive transcription complex are largely unknown.

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Year:  1997        PMID: 9240931     DOI: 10.1146/annurev.nutr.17.1.325

Source DB:  PubMed          Journal:  Annu Rev Nutr        ISSN: 0199-9885            Impact factor:   11.848


  69 in total

1.  Transcriptional regulation of the human asparagine synthetase gene by carbohydrate availability.

Authors:  I P Barbosa-Tessmann; V L Pineda; H S Nick; S M Schuster; M S Kilberg
Journal:  Biochem J       Date:  1999-04-01       Impact factor: 3.857

Review 2.  Glucose and cAMP: adversaries in the regulation of hepatic gene expression.

Authors:  H C Towle
Journal:  Proc Natl Acad Sci U S A       Date:  2001-11-20       Impact factor: 11.205

3.  Spot 14 protein interacts and co-operates with chicken ovalbumin upstream promoter-transcription factor 1 in the transcription of the L-type pyruvate kinase gene through a specificity protein 1 (Sp1) binding site.

Authors:  E Compe; G de Sousa; K François; R Roche; R Rahmani; J Torresani; M Raymondjean; R Planells
Journal:  Biochem J       Date:  2001-08-15       Impact factor: 3.857

Review 4.  New perspectives in the regulation of hepatic glycolytic and lipogenic genes by insulin and glucose: a role for the transcription factor sterol regulatory element binding protein-1c.

Authors:  Fabienne Foufelle; Pascal Ferré
Journal:  Biochem J       Date:  2002-09-01       Impact factor: 3.857

5.  Nucleocytoplasmic shuttling of hexokinase II in a cancer cell.

Authors:  Catherine L Neary; John G Pastorino
Journal:  Biochem Biophys Res Commun       Date:  2010-03-24       Impact factor: 3.575

6.  Postprandial molecular responses in the liver of the barramundi, Lates calcarifer.

Authors:  Nicholas M Wade; Sandrine Skiba-Cassy; Karine Dias; Brett D Glencross
Journal:  Fish Physiol Biochem       Date:  2013-08-30       Impact factor: 2.794

7.  Overexpression of c-myc in diabetic mice restores altered expression of the transcription factor genes that regulate liver metabolism.

Authors:  Efren Riu; Tura Ferre; Alex Mas; Antonio Hidalgo; Sylvie Franckhauser; Fatima Bosch
Journal:  Biochem J       Date:  2002-12-15       Impact factor: 3.857

8.  PGC-1β and ChREBP partner to cooperatively regulate hepatic lipogenesis in a glucose concentration-dependent manner.

Authors:  Kari T Chambers; Zhouji Chen; Ling Lai; Teresa C Leone; Howard C Towle; Anastasia Kralli; Peter A Crawford; Brian N Finck
Journal:  Mol Metab       Date:  2013-05-09       Impact factor: 7.422

9.  A novel high-throughput screening assay for putative antidiabetic agents through PPARalpha interactions.

Authors:  Heather A Hostetler; Lindsay R Syler; Lindy N Hall; Guan Zhu; Friedhelm Schroeder; Ann B Kier
Journal:  J Biomol Screen       Date:  2008-09-23

10.  Farnesoid X receptor inhibits the transcriptional activity of carbohydrate response element binding protein in human hepatocytes.

Authors:  Sandrine Caron; Carolina Huaman Samanez; Hélène Dehondt; Maheul Ploton; Olivier Briand; Fleur Lien; Emilie Dorchies; Julie Dumont; Catherine Postic; Bertrand Cariou; Philippe Lefebvre; Bart Staels
Journal:  Mol Cell Biol       Date:  2013-03-25       Impact factor: 4.272

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