Human PLU-1 has transcriptional repression properties and interacts with the developmental transcription factors BF-1 and PAX9

K Tan, A L Shaw, B Madsen, K Jensen, J Taylor-Papadimitriou, P S Freemont

    Research output: Contribution to journalArticlepeer-review

    86 Citations (Scopus)

    Abstract

    PLU-1 is a large ( 1544 amino acids) nuclear protein that is highly expressed in breast cancers and is proposed to function as a regulator of gene expression. A yeast two-hybrid screen using PLU-1 as bait has identified two unrelated PLU-1 interacting proteins, namely brain factor-1 (BF-1) and paired box 9 (PAX9), both of which are developmental transcription factors. BF-1 and PAX9 interact with PLU-1 via a novel conserved sequence motif ( Ala-X-Ala-Ala-X-Val-Pro-X-4-Val-Pro-X(8)Pro, termed the VP motif), because deletion or site-directed mutagenesis of this motif in either protein abolishes PLU-1 interaction in vivo. In a reporter assay system, PLU-1 has potent transcriptional repression activity. BF-1 and PAX9 also represses transcription in the same assay, but co-expression of PLU-1 with BF-1 or PAX9 significantly enhances this repression. Mutation of the PLU-1 binding motifs in BF-1 and PAX9 abolishes the observed PLU-1 co-repression activity. These data support a role for PLU-1 acting as a transcriptional corepressor of two unrelated developmental transcription factors. Because both BF-1 and PAX proteins interact with members of the groucho co-repressor family, it is plausible that PLU-1 has a role in groucho-mediated transcriptional repression.
    Original languageEnglish
    Pages (from-to)20507 - 20513
    Number of pages7
    JournalJournal of Biological Chemistry
    Volume278
    Issue number23
    DOIs
    Publication statusPublished - 6 Jun 2003

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