Literature DB >> 7511375

Localization of sequences for the basal and insulin-like growth factor-I inducible activity of the fatty acid synthase promoter in 3T3-L1 fibroblasts.

S Misra1, K Sakamoto, N Moustaïd, H S Sul.   

Abstract

Fatty acid synthase (FAS) plays a central role in fatty acid synthesis and its expression is under nutritional and hormonal control. We have investigated insulin-like growth factor-I (IGF-I) regulation of FAS by transfecting into 3T3-L1 fibroblasts chimeric genes comprising the 5'-flanking region of the FAS gene linked to a luciferase (LUC) reporter gene. First, the basal promoter activity of the 5' serial deletions from nucleotides -318 to -19 of the FAS gene were compared. Deletions of the promoter sequences from -136 to -19 resulted in a step-wise decrease in the promoter activity, with the -67 LUC and -19 LUC plasmids retaining 40% and 16% of the luciferase activity of -136 LUC. Regulatory sequences important for the FAS basal promoter activity in 3T3-L1 fibroblasts are, therefore, located within the -136 to -19 region. Treatment with 10 mM IGF-I also increased luciferase activity 1.8 +/- 0.2-, 1.8 +/- 0.3- and 2.5 +/- 0.1-fold in 3T3-L1 fibroblasts transiently transfected with -136 LUC, -110 LUC and -67 LUC plasmids, respectively. Deletion of sequences from -67 to -19 resulted in the loss of responsiveness to IGF-I. Physiological doses of insulin (10 nM), however, did not increase luciferase activity in 3T3-L1 fibroblasts transfected with any of the above plasmids. Only upon treatment with pharmacological doses of insulin (1 microM), probably through IGF-I receptor, did luciferase activity increase 4.3 +/- 0.4-, 3.2 +/- 0.4- and 3.5 +/- 0.5-fold when transfected with -136 LUC, -110 LUC and -67 LUC plasmids, respectively; there was no increase with -19 LUC. The half-maximal effect of IGF-I on FAS promoter activity was observed at 3 nM and a maximal effect was reached at 10 nM. These results indicate that the increased promoter activities observed are probably mediated through the IGF-I receptor. Furthermore, sequences responsible for IGF-I regulation of the FAS gene are located within the proximal promoter between nucleotides -67 and -19 of the FAS gene.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7511375      PMCID: PMC1137897          DOI: 10.1042/bj2980575

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  23 in total

1.  The fatty acid synthase gene in avian liver. Two mRNAs are expressed and regulated in parallel by feeding, primarily at the level of transcription.

Authors:  D W Back; M J Goldman; J E Fisch; R S Ochs; A G Goodridge
Journal:  J Biol Chem       Date:  1986-03-25       Impact factor: 5.157

2.  Insulin-like growth factor-I is an essential regulator of the differentiation of 3T3-L1 adipocytes.

Authors:  P J Smith; L S Wise; R Berkowitz; C Wan; C S Rubin
Journal:  J Biol Chem       Date:  1988-07-05       Impact factor: 5.157

3.  A rapid, sensitive, and versatile assay for protein using Coomassie brilliant blue G250.

Authors:  J J Sedmak; S E Grossberg
Journal:  Anal Biochem       Date:  1977-05-01       Impact factor: 3.365

4.  Interaction of insulin-like growth factors with a nonfusing mouse muscle cell line: binding, action, and receptor down-regulation.

Authors:  M A de Vroede; J A Romanus; M L Standaert; R J Pollet; S P Nissley; M M Rechler
Journal:  Endocrinology       Date:  1984-05       Impact factor: 4.736

Review 5.  The insulin-like growth factors (IGF) of human serum: chemical and biological characterization and aspects of their possible physiological role.

Authors:  J Zapf; E R Froesch; R E Humbel
Journal:  Curr Top Cell Regul       Date:  1981

6.  Characterization of the insulin and insulin-like growth factor receptors and responsitivity of a fibroblast/adipocyte cell line before and after differentiation.

Authors:  M Shimizu; F Torti; R A Roth
Journal:  Biochem Biophys Res Commun       Date:  1986-05-29       Impact factor: 3.575

7.  Control of the synthesis of fatty-acid synthetase in rat liver by insulin, glucagon, and adenosine 3':5' cyclic monophosphate.

Authors:  M R Lakshmanan; C M Nepokroeff; J W Porter
Journal:  Proc Natl Acad Sci U S A       Date:  1972-12       Impact factor: 11.205

8.  Nutritionally-induced changes in hepatic insulin-like growth factor I (IGF-I) gene expression in rats.

Authors:  C A Emler; D S Schalch
Journal:  Endocrinology       Date:  1987-02       Impact factor: 4.736

9.  DNA sequencing with chain-terminating inhibitors.

Authors:  F Sanger; S Nicklen; A R Coulson
Journal:  Proc Natl Acad Sci U S A       Date:  1977-12       Impact factor: 11.205

10.  Cloning and expression of mouse fatty acid synthase and other specific mRNAs. Developmental and hormonal regulation in 3T3-L1 cells.

Authors:  J D Paulauskis; H S Sul
Journal:  J Biol Chem       Date:  1988-05-25       Impact factor: 5.157

View more
  2 in total

1.  Nutritional regulation of the fatty acid synthase promoter in vivo: sterol regulatory element binding protein functions through an upstream region containing a sterol regulatory element.

Authors:  M J Latasa; Y S Moon; K H Kim; H S Sul
Journal:  Proc Natl Acad Sci U S A       Date:  2000-09-12       Impact factor: 11.205

2.  Insulin-like growth factor I and insulin induce adipogenic-related gene expression in fetal brown adipocyte primary cultures.

Authors:  T Teruel; A M Valverde; M Benito; M Lorenzo
Journal:  Biochem J       Date:  1996-10-15       Impact factor: 3.857

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.