Literature DB >> 8132677

Definition of the carbohydrate response element of the rat S14 gene. Context of the CACGTG motif determines the specificity of carbohydrate regulation.

H Shih1, H C Towle.   

Abstract

Transcription of the S14 gene in primary hepatocytes is stimulated in response to increased carbohydrate metabolism. We have demonstrated previously that a 30-base pair (bp) segment of the S14 gene from -1457 to -1428 is a carbohydrate response element (ChoRE). This element contains a (5')CACGTG motif that is essential for control. DNase I footprinting experiments with liver nuclear extract revealed two factors binding within the S14 ChoRE. In transient transfection experiments, mutation of the upstream site between -1457 and -1450 did not affect the response to elevated glucose, whereas the downstream 21-bp site between -1448 and -1428 was sufficient to mediate the glucose induction. Electrophoretic mobility shift assays indicated that the hepatic factor binding to this site in vitro is closely related or identical to the major late transcription factor (MLTF). However, replacement of the 21-bp S14 ChoRE with the authentic MLTF binding site from the adenovirus major late promoter failed to elicit the glucose response. By systematically exchanging bases between the functional S14 and nonresponsive adenovirus sites, the sequence (5')CACGTGNNNGCC was found to be essential for carbohydrate regulation. A segment containing this specific motif from the rat fatty acid synthase gene, another carbohydrate-responsive gene in hepatocytes, conferred a carbohydrate response when linked to the S14 promoter. Thus, the context of the CACGTG motif provides the specificity for regulation by carbohydrate metabolism.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 8132677

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  23 in total

Review 1.  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

2.  Transcriptional regulation of the rat fatty acid synthase gene: identification and functional analysis of positive and negative effectors of basal transcription.

Authors:  B Oskouian; V S Rangan; S Smith
Journal:  Biochem J       Date:  1996-07-01       Impact factor: 3.857

3.  Identification of upstream stimulatory factor as transcriptional activator of the liver promoter of the glucokinase gene.

Authors:  P B Iynedjian
Journal:  Biochem J       Date:  1998-08-01       Impact factor: 3.857

4.  Regulation of rat hepatic L-pyruvate kinase promoter composition and activity by glucose, n-3 polyunsaturated fatty acids, and peroxisome proliferator-activated receptor-alpha agonist.

Authors:  Jinghua Xu; Barbara Christian; Donald B Jump
Journal:  J Biol Chem       Date:  2006-04-27       Impact factor: 5.157

5.  Induction of fatty acid synthase and S14 gene expression by glucose, xylitol and dihydroxyacetone in cultured rat hepatocytes is closely correlated with glucose 6-phosphate concentrations.

Authors:  F Mourrieras; F Foufelle; M Foretz; J Morin; S Bouche; P Ferre
Journal:  Biochem J       Date:  1997-09-01       Impact factor: 3.857

6.  Activation and repression of glucose-stimulated ChREBP requires the concerted action of multiple domains within the MondoA conserved region.

Authors:  Michael N Davies; Brennon L O'Callaghan; Howard C Towle
Journal:  Am J Physiol Endocrinol Metab       Date:  2010-08-03       Impact factor: 4.310

7.  Dual DNA binding specificity of ADD1/SREBP1 controlled by a single amino acid in the basic helix-loop-helix domain.

Authors:  J B Kim; G D Spotts; Y D Halvorsen; H M Shih; T Ellenberger; H C Towle; B M Spiegelman
Journal:  Mol Cell Biol       Date:  1995-05       Impact factor: 4.272

8.  Functional synergism in the carbohydrate-induced activation of liver-type pyruvate kinase gene expression.

Authors:  Z Liu; H C Towle
Journal:  Biochem J       Date:  1995-05-15       Impact factor: 3.857

9.  ChREBP regulates Pdx-1 and other glucose-sensitive genes in pancreatic β-cells.

Authors:  Gabriela da Silva Xavier; Gao Sun; Qingwen Qian; Guy A Rutter; Isabelle Leclerc
Journal:  Biochem Biophys Res Commun       Date:  2010-10-08       Impact factor: 3.575

10.  Regulation of mammalian pyruvate dehydrogenase alpha subunit gene expression by glucose in HepG2 cells.

Authors:  J Tan; H S Yang; M S Patel
Journal:  Biochem J       Date:  1998-11-15       Impact factor: 3.857

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.