Oct-2 regulates CD36 gene expression via a consensus octamer, which excludes the co-activator OBF-1

Paul Shore, Wendy Dietrich, Lynn M. Corcoran

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The POU domain transcription factor, Oct-2, is essential for the B cell-specific expression of CD36 in mouse B cells. In order to determine how Oct-2 mediates expression of CD36 in B cells, we cloned and analysed the mouse CD36 promoter. In contrast to the human CD36 promoter, the mouse promoter contains a consensus octamer element of the type ATGCTAAT. This octamer element can be bound by either Oct-1 or Oct-2 but requires the expression of Oct-2 to activate transcription in B cells. Mutation of the octamer element renders the CD36 promoter refractory to activation by Oct-2. Furthermore, we demonstrate that the CD36 octamer element does not support recruitment of the B cell-specific co-activator OBF-1 and that CD36 expression is unaffected in primary B cells derived from obf-1-/- mice. We conclude that Oct-2 activates CD36 gene expression in mouse B cells via the octamer element in the promoter. Our data also demonstrate that CD36 is the first example of an Oct-2-dependent gene whose expression in B cells is independent of OBF-1. These findings support the notion that Oct-2 regulates gene transcription by both OBF-1-dependent and -independent mechanisms.
    Original languageEnglish
    Pages (from-to)1767-1773
    Number of pages6
    JournalNucleic acids research.
    Volume30
    Issue number8
    DOIs
    Publication statusPublished - 15 Apr 2002

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