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PMID: 7822291 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Insulin regulates transcription of the CCAAT/enhancer binding protein (C/EBP) alpha, beta, and delta genes in fully-differentiated 3T3-L1 adipocytes.

The Journal of biological chemistry ·Vol. 270 ·No. 2 ·1995-01-13 ·Pages 647-54

MacDougald OA, Cornelius P, Liu R, Lane MD

Abstract

The effect of insulin on expression of CCAAT/enhancer binding protein (C/EBP) alpha, beta, and delta was investigated in fully-differentiated 3T3-L1 adipocytes. Treatment of adipocytes with insulin stimulated rapid dephosphorylation of C/EBP alpha, and repressed the expression of C/EBP alpha within 2-4 h, with > 90% suppression occurring at 24 h. While insulin induced expression of C/EBP beta and C/EBP delta within 1 h and caused a > 20-fold increase by 4 h, expression returned to nearly pretreatment levels by 24 h. The insulin concentration dependence of these effects was consistent with involvement of the insulin receptor. Gel shift analysis revealed that 6 h of insulin treatment decreased the binding of nuclear C/EBP alpha while increasing binding of nuclear C/EBP beta and C/EBP delta. The reciprocal effects of insulin on the steady-state levels of C/EBP transcription factors can be accounted for kinetically and quantitatively by changes in their mRNA levels, which can be accounted for by effects on gene transcription. The effects of insulin on adipocyte gene transcription (e.g. GLUT4) may be mediated, at least in part, by down-regulation of C/EBP alpha and/or its dephosphorylation.

Related Genes
MeSH Terms
3T3 Cells Adipocytes/cytology,metabolism Amino Acid Sequence Animals CCAAT-Enhancer-Binding Proteins Cell Differentiation DNA-Binding Proteins/genetics Down-Regulation Gene Expression Regulation Glucose Transporter Type 4 Insulin/physiology Mice Molecular Sequence Data Monosaccharide Transport Proteins/genetics Muscle Proteins Nuclear Proteins/genetics Oligonucleotides/metabolism Protein Binding RNA, Messenger/genetics,metabolism Transcription, Genetic
Chemicals
CCAAT-Enhancer-Binding Proteins DNA-Binding Proteins Glucose Transporter Type 4 Insulin Monosaccharide Transport Proteins Muscle Proteins Nuclear Proteins Oligonucleotides RNA, Messenger Slc2a4 protein, mouse
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
MacDougald O A
Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Cornelius P
Liu R
Lane M D
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1995-01-13
Pages
647-54
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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