Skip NavigationSkip to Content

C/Ebp-Alpha Is a Regulator of the Udp Glucuronosyltransferase Ugt2b1 Gene

  1. Author:
    Hansen, A. J.
    Lee, Y. H.
    Sterneck, E.
    Gonzalez, F. J.
    Mackenzie, P. I.
    1. Year: 1998
  1. Journal: Molecular Pharmacology
    1. 53
    2. 6
    3. Pages: 1027-1033
  2. Type of Article: Article
  1. Abstract:

    The rat UDP glucuronosyltransferase, UGT2B1, is expressed in the liver where it glucuronidates steroids, environmental toxins, and carcinogens. A region between -88 and -111 base pairs upstream from the UGT2B1 gene transcription start site contains a CCAAT enhancer binding protein (C/EBP)-like element and was previously shown by Dnase I footprint analysis to bind to proteins in both rat liver and human hepatoma (HepG2) cell nuclear extracts. In this study, the importance of this region in the regulation of the UGT2B1 gene was assessed by functional and DNA binding assays. Varying lengths of the UGT2B1 gene promoter, with and without the C/EBP-like element, were fused to the chloramphenicol acetyltransferase reporter gene and transfected into HepG2 cells. Transcriptional activity of the UGT2B1 promoter construct containing the C/EBP-like element was strongly elevated in the presence of a cotransfected C/EBP alpha expression vector. In contrast, no change was observed when an expression vector encoding C/EBP beta was cotransfected with the UGT2B1 promoter constructs. Introduction of point mutations into the C/EBP-like element prevented any C/EBP alpha-mediated increase in chloramphenicol acetyltransferase activity. Gel shift analyses demonstrated that the C/EBP-like element binds a complex of nuclear proteins present in both HepG2 cells and rat liver. The presence of C/EBP alpha in this complex was confirmed by supershift analysis with antiserum to this factor. These data strongly suggest that the liver-enriched factor C/EBP alpha binds to, and activates, the UGT2B1 gene promoter. The importance of C/EBP alpha in the regulation of the homologous mouse UGT2B1 gene was also assessed in vivo. Transcripts homologous to UGT2B1 were detected in the livers of mice containing intact c/ebp alpha and c/ebp beta genes and in mice containing a homozygous null mutation in the c/ebp beta gene. In contrast, these transcripts were not detected in mice with a disrupted hepatic c/ebp alpha gene. These data extend the findings with the rat UGT2B1 gene promoter and establish that C/EBP alpha, but not C/EBP beta, is an essential transcriptional regulator of the homologous UGT2B1 gene in the mouse. [References: 35]

    See More

External Sources

  1. No sources found.

Library Notes

  1. No notes added.
NCI at Frederick

You are leaving a government website.

This external link provides additional information that is consistent with the intended purpose of this site. The government cannot attest to the accuracy of a non-federal site.

Linking to a non-federal site does not constitute an endorsement by this institution or any of its employees of the sponsors or the information and products presented on the site. You will be subject to the destination site's privacy policy when you follow the link.

ContinueCancel