Characterization of the IL-6 responsive elements in the γ fibrinogen gene promoter

Z. Zhang, N. L. Fuentes, G. M. Fuller

Research output: Contribution to journalArticle

88 Scopus citations

Abstract

Fibrinogen, a hepatically derived class II acute phase protein, is the product of three separate genes, (Aα, Bβ, and γ). The fibrinogen genes are expressed constitutively; however, their transcription can he significantly up-regulated by interleukin-6 (IL-6) and glucocorticoid. Inspection of the promoter region of the fibrinogen γ gene revealed three hexanucleotide clusters of CTGGGA that are recognized as class II IL-6 responsive elements. Functional analyses of these regions (designated here as site I, site II, and site III according to their position in the promoter) were performed using luciferase reporter constructs and show a hierarchy of IL-6 response in which site II was the preferred functional site, site I was the next important site, and site III was the site least responsive to IL-6. Gel mobility shift assays using 25-base pair oligonucleotide probes derived from these three regions with the CTGGGA positioned in the middle and nuclear extracts from IL-6-treated primary hepatocytes reveal the presence of IL-6-induced high molecular weight complexes appearing 5 min after cytokine treatment. Supershift assays using anti-Stat3 antibody indicate that Stat3 is part of the IL-6-induced complex formed on the three γ chain probes. The binding of Stat3 to the IL-6 responsive elements of the y probes is significantly weaker than to an α2-macroglobulin probe. These findings show for the first time that Stat3 is involved in associating with the IL-6 responsive elements of fibrinogen γ chain, a class II acute phase gene other than α2- macroglobulin.

Original languageEnglish (US)
Pages (from-to)24287-24291
Number of pages5
JournalJournal of Biological Chemistry
Volume270
Issue number41
DOIs
StatePublished - 1995

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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