Home LiteratureArticle Details
PMID: 11050169 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Role of C/EBP homologous protein (CHOP-10) in the programmed activation of CCAAT/enhancer-binding protein-beta during adipogenesis.

Tang QQ, Lane MD

Abstract

Hormone induction of growth-arrested preadipocytes triggers mitotic clonal expansion followed by expression of CCAAT/enhancer-binding protein (C/EBP)alpha and differentiation into adipocytes. The order of these events is critical because C/EBPalpha is antimitotic and its expression prematurely would block the mitotic clonal expansion required for differentiation. C/EBPbeta, a transcriptional activator of the C/EBPalpha gene, is expressed early in the differentiation program, but lacks DNA-binding activity and fails to localize to centromeres until preadipocytes traverse the G(1)-S checkpoint of mitotic clonal expansion. Evidence is presented that dominant-negative CHOP-10 expressed by growth-arrested preadipocytes transiently sequesters C/EBPbeta by heterodimerization. As preadipocytes reach S phase, CHOP-10 is down-regulated, apparently releasing C/EBPbeta from inhibitory constraint and allowing transactivation of the C/EBPalpha gene. In support of these findings, up-regulation of CHOP-10 with the protease inhibitor N-acetyl-Leu-Leu-norleucinal prevents activation of C/EBPbeta, expression of C/EBPalpha, and adipogenesis.

MeSH Terms
3T3 Cells Adipocytes/cytology,metabolism Animals CCAAT-Enhancer-Binding Protein-alpha/genetics,metabolism CCAAT-Enhancer-Binding Protein-beta/metabolism CCAAT-Enhancer-Binding Proteins/genetics,metabolism,physiology Cell Differentiation Centromere/metabolism DNA/metabolism Down-Regulation Mice Phenotype Trans-Activators/metabolism Transcription Factor CHOP Transcription Factors/genetics,metabolism,physiology Up-Regulation
Chemicals
CCAAT-Enhancer-Binding Protein-alpha CCAAT-Enhancer-Binding Protein-beta CCAAT-Enhancer-Binding Proteins Ddit3 protein, mouse Trans-Activators Transcription Factors Transcription Factor CHOP DNA
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Tang Q Q
Department of Biological Chemistry, The Johns Hopkins University School of Medicine, Baltimore, MD 21209, USA. qqtang@welchlink.welch.jhu.edu
Lane M D
References (19)
19 references, click to expand
  1. Phosphorylation of rat serine 105 or mouse threonine 217 in C/EBP beta is required for hepatocyte proliferation induced by TGF alpha.
    Mol Cell. 1999 Dec;4(6):1087-92 PMID: 10635333
  2. CCAAT-enhancer binding protein: a component of a differentiation switch.
    Science. 1991 Jan 18;251(4991):288-92 PMID: 1987644
  3. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.
    Anal Biochem. 1987 Apr;162(1):156-9 PMID: 2440339
  4. CCAAT/enhancer binding protein gene promoter: binding of nuclear factors during differentiation of 3T3-L1 preadipocytes.
    Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2593-7 PMID: 2006196
  5. Regulated expression of three C/EBP isoforms during adipose conversion of 3T3-L1 cells.
    Genes Dev. 1991 Sep;5(9):1538-52 PMID: 1840554
  6. CHOP, a novel developmentally regulated nuclear protein that dimerizes with transcription factors C/EBP and LAP and functions as a dominant-negative inhibitor of gene transcription.
    Genes Dev. 1992 Mar;6(3):439-53 PMID: 1547942
  7. Antisense CCAAT/enhancer-binding protein RNA suppresses coordinate gene expression and triglyceride accumulation during differentiation of 3T3-L1 preadipocytes.
    Genes Dev. 1992 Apr;6(4):533-44 PMID: 1373117
  8. A 30-kDa alternative translation product of the CCAAT/enhancer binding protein alpha message: transcriptional activator lacking antimitotic activity.
    Proc Natl Acad Sci U S A. 1993 Oct 15;90(20):9606-10 PMID: 8415748
  9. Regulation of adipocyte development.
    Annu Rev Nutr. 1994;14:99-129 PMID: 7946535
  10. Cascade regulation of terminal adipocyte differentiation by three members of the C/EBP family of leucine zipper proteins.
    Genes Dev. 1995 Jan 15;9(2):168-81 PMID: 7531665
  11. Impaired energy homeostasis in C/EBP alpha knockout mice.
    Science. 1995 Aug 25;269(5227):1108-12 PMID: 7652557
  12. Transcriptional regulation of gene expression during adipocyte differentiation.
    Annu Rev Biochem. 1995;64:345-73 PMID: 7574486
  13. CCAAT/enhancer-binding protein alpha (C/EBP alpha) inhibits cell proliferation through the p21 (WAF-1/CIP-1/SDI-1) protein.
    Genes Dev. 1996 Apr 1;10(7):804-15 PMID: 8846917
  14. Repression of transcription mediated by dual elements in the CCAAT/enhancer binding protein alpha gene.
    Proc Natl Acad Sci U S A. 1997 Dec 9;94(25):13571-5 PMID: 9391067
  15. CCAAT enhancer- binding protein beta is required for normal hepatocyte proliferation in mice after partial hepatectomy.
    J Clin Invest. 1998 Sep 1;102(5):996-1007 PMID: 9727068
  16. Role of calpain in adipocyte differentiation.
    Proc Natl Acad Sci U S A. 1999 Feb 16;96(4):1279-84 PMID: 9990015
  17. Repressive effect of Sp1 on the C/EBPalpha gene promoter: role in adipocyte differentiation.
    Mol Cell Biol. 1999 Jul;19(7):4855-65 PMID: 10373535
  18. Activation and centromeric localization of CCAAT/enhancer-binding proteins during the mitotic clonal expansion of adipocyte differentiation.
    Genes Dev. 1999 Sep 1;13(17):2231-41 PMID: 10485846
  19. Evidence for an increase in transcription of specific mRNAs during differentiation of 3T3-L1 preadipocytes.
    J Biol Chem. 1985 May 10;260(9):5563-7 PMID: 3988766
Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
2000-11-07
Pages
12446-50
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC18783
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com