Human PLU-1 Has Transcriptional Repression Properties and Interacts with the Developmental Transcription Factors BF-1 and PAX9
pmid: 12657635
Human PLU-1 Has Transcriptional Repression Properties and Interacts with the Developmental Transcription Factors BF-1 and PAX9
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-X4-Val-Pro-X8-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 co-repressor 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.
- Kings College London, University of London United Kingdom
- Lincoln's Inn United Kingdom
- King's College London United Kingdom
- Guy's and St Thomas' NHS Foundation Trust United Kingdom
- Imperial College London United Kingdom
Transcriptional Activation, 570, Jumonji Domain-Containing Histone Demethylases, Binding Sites, Molecular Sequence Data, Nuclear Proteins, Polycomb-Group Proteins, Nerve Tissue Proteins, Kidney, Cell Line, Neoplasm Proteins, DNA-Binding Proteins, Gene Expression Regulation, Neoplastic, Repressor Proteins, 616, Basic Helix-Loop-Helix Transcription Factors, Mutagenesis, Site-Directed, Humans, Amino Acid Sequence, PAX9 Transcription Factor, Conserved Sequence, Transcription Factors
Transcriptional Activation, 570, Jumonji Domain-Containing Histone Demethylases, Binding Sites, Molecular Sequence Data, Nuclear Proteins, Polycomb-Group Proteins, Nerve Tissue Proteins, Kidney, Cell Line, Neoplasm Proteins, DNA-Binding Proteins, Gene Expression Regulation, Neoplastic, Repressor Proteins, 616, Basic Helix-Loop-Helix Transcription Factors, Mutagenesis, Site-Directed, Humans, Amino Acid Sequence, PAX9 Transcription Factor, Conserved Sequence, Transcription Factors
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