An inducible 50-kilodalton NPκB-like protein and a constitutive protein both bind the acute-phase response element of the angiotensinogen gene

David Ron, Allan R. Brasier, Kathy A. Wright, James E. Tate, Joel F. Habener

Research output: Contribution to journalArticle

70 Citations (Scopus)

Abstract

The rat angiotensinogen gene is induced in the course of the hepatic acute-phase response. We demonstrate that monocyte conditioned medium can stimulate transcription of a stably introduced reporter construct driven by 615 base pairs of the angiotensinogen 5′-flanking sequence, as well as the endogenous gene, in Reuber H35 cells. Point mutations of cis-acting element, located 545 base pairs from the transcription start site and sharing sequence identity with known nuclear factor kappa B (NFκB)-binding sites, led to loss of cytokine inducibility. When cloned upstream of a minimal promoter, this cis-acting element imparted transcriptional inducibility by monocyte conditioned medium, interleukin-1, and tumor necrosis factor on a luciferase reporter gene in HepG2 cells. Two distinct proteins bound this element in vitro: a heat-stable, constitutively present, hepatic nuclear protein that gave rise to a DNase I-protected footprint covering the functionally defined element; and a binding protein of different mobility, induced by monocyte conditioned medium, which also recognized the NFκB-binding site of the murine kappa light-chain enhancer. UV cross-linking showed this inducible protein to have an apparent molecular mass of 50 kilodaltons, similar to that described for NFκB and distinct from the constitutively present protein that was shown by Southwestern (DNA-protein) blot to have a molecular mass of 32 kilodaltons. Methylation interference analysis showed that the induced species made contact points with guanine residues in the NFκB consensus sequence typical of NFκB. Induction of this binding activity did not require new protein synthesis, and 12-O-tetradecanoylphorbol-13-acetate could mimic the induction by cytokines. We thus provide direct evidence for involvement of NFκB or a similar factor in the hepatic acute-phase response and discuss the potential role of the presence of a constitutive nuclear factor binding the same cis element.

Original languageEnglish (US)
Pages (from-to)1023-1032
Number of pages10
JournalMolecular and Cellular Biology
Volume10
Issue number3
StatePublished - 1990
Externally publishedYes

Fingerprint

Angiotensinogen
Acute-Phase Reaction
NF-kappa B
Response Elements
Conditioned Culture Medium
Genes
Monocytes
Proteins
Base Pairing
Liver
Binding Sites
Cytokines
5' Flanking Region
Transcription Initiation Site
Deoxyribonuclease I
Consensus Sequence
Hep G2 Cells
Guanine
Tetradecanoylphorbol Acetate
Nuclear Proteins

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cell Biology

Cite this

An inducible 50-kilodalton NPκB-like protein and a constitutive protein both bind the acute-phase response element of the angiotensinogen gene. / Ron, David; Brasier, Allan R.; Wright, Kathy A.; Tate, James E.; Habener, Joel F.

In: Molecular and Cellular Biology, Vol. 10, No. 3, 1990, p. 1023-1032.

Research output: Contribution to journalArticle

Ron, David ; Brasier, Allan R. ; Wright, Kathy A. ; Tate, James E. ; Habener, Joel F. / An inducible 50-kilodalton NPκB-like protein and a constitutive protein both bind the acute-phase response element of the angiotensinogen gene. In: Molecular and Cellular Biology. 1990 ; Vol. 10, No. 3. pp. 1023-1032.
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