The transcriptional co-repressor c-terminal binding protein (CtBP) associates with centrosomes during mitosis
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作者:
Spyer, Moira
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Univ London Imperial Coll Sci Technol & Med, Fac Med, Dept Virol, London W2 1PG, EnglandUniv London Imperial Coll Sci Technol & Med, Fac Med, Dept Virol, London W2 1PG, England
Spyer, Moira
[1
]
Allday, Martin J.
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Univ London Imperial Coll Sci Technol & Med, Fac Med, Dept Virol, London W2 1PG, EnglandUniv London Imperial Coll Sci Technol & Med, Fac Med, Dept Virol, London W2 1PG, England
Allday, Martin J.
[1
]
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[1] Univ London Imperial Coll Sci Technol & Med, Fac Med, Dept Virol, London W2 1PG, England
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 organizing 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.