Binding of C/EBP and RBP (CBF1) to Overlapping Sites Regulates Interleukin-6 Gene Expression*

  1. Erika M. Friedl
  1. From the Department of Biochemistry, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway, New Jersey 08854-5635

Abstract

The ILRE (interleukin response element) contained within the promoter of the interleukin-6 (IL-6) gene is defined as the site recognized by the p65 NF-κB transcriptional activator and is crucial for activation of the IL-6 gene. The region of the promoter containing the ILRE is complex containing a CCAAT enhancer-binding protein (C/EBP) site immediately upstream of the ILRE, which is required for optimal activation of the IL-6 gene. Additionally, the ILRE overlaps a site that is recognized by the mammalian transcriptional repressor RBP (CBF-1), and RBP binding within the ILRE region represses activated IL-6 expression. In this study, the complexity of this region is further revealed by the identification of a second nested C/EBP site, which overlaps that of RBP and therefore also the ILRE. Optimal activation requires both the upstream and newly identified C/EBP sites in conjunction with the p65 NF-κB binding site. We previously reported that RBP represses IL-6 activation but does not target p65. We extend these analyses here to show that RBP binding does not occlude p65 from binding but instead directly overlaps the newly identified downstream C/EBP site, thereby impeding p65-C/EBP-mediated co-activation. This result suggests a role for RBP in the repression of other genes containing a C/EBP site that exhibits sequence overlap with the RBP site.

  • Abbreviations:
    IL
    interleukin
    ILRE
    interleukin response element
    C/EBP
    CCAAT enhancer-binding protein
    EBPM
    mutation in C/EBP DNA-binding site
    RBPM
    mutation in RBP DNA-binding site
    AdMLP
    adenovirus major late promoter
    CMV
    cytomegalovirus
    EMSA
    electrophoretic mobility shift assay
    nt
    nucleotide(s)
    • Received July 22, 2002.
    • Revision received August 27, 2002.
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    This Article

    1. The Journal of Biological Chemistry 277, 42438-42446.
    1. All Versions of this Article:
      1. M207363200v1
      2. 277/45/42438 (most recent)

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