The transcriptional co-repressor C-terminal binding protein (CtBP) associates with centrosomes during mitosis.

CtBP is a corepressor of transcription that acts by inhibiting coactivators and recruiting to promoter control elements (via interactions with DNA-binding transcription factors) a complex of proteins that modify histones, repress transcription and silence gene expression. There are two highly homologous genes, CtBP1 and CtBP2 that encode CtBP. In addition, ...
a CtBP1-related protein has been described that has 11 fewer amino acids at its N-terminus than CtBP1. This variant of CtBP1--known as CtBP3 or BARS [Brefeldin A (BFA) ribosylated substrate]--plays a critical role in the fragmentation of the Golgi complex at the onset of mitosis. Although there are some reports of CtBP with a cytoplasmic distribution after transfection, it is unclear how in normal cells a nuclear corepressor regulates the behavior of the Golgi complex at the onset of mitosis. Using polyclonal rabbit antibodies that were raised against a human CtBP1-GST fusion-protein, here we show by immunofluorescence laser-scanning confocal microscopy that in mitotic cells a species of CtBP becomes associated with the centrosomes at the onset of prophase and then throughout mitosis. The association can be seen in both cycling mitotic cells and nocodazole-arrested cells. The interaction was confirmed by coimmunoprecipitation and centrosome isolation. Since centrosomes are considered to be the organising centre for Golgi morphogenesis, the interaction demonstrated here may explain how a nuclear corepressor of transcription can exert a regulatory effect on the Golgi complex at a specific stage of the cell cycle.
Mesh Terms:
Alcohol Oxidoreductases, Cell Cycle Proteins, Cell Nucleus, Cells, Cultured, Centrosome, DNA-Binding Proteins, Humans, Immunoprecipitation, Interphase, Mitosis, Nocodazole, Phosphoproteins, Protein Transport, Protein-Serine-Threonine Kinases, Proto-Oncogene Proteins, Recombinant Fusion Proteins, Repressor Proteins, Reproducibility of Results, Transcription, Genetic, Tubulin
Cell Cycle
Date: Mar. 01, 2006
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