Cyclin B is a central regulator of transition from the G2 phase of the cell cycle to mitosis. In mammalian cells two B-type cyclins have been characterised, cyclin B1 and B2. Both are expressed with a maximum in G2 and their synthesis is mainly regulated on the transcriptional level. We show that a single cell cycle genes homology region, lacking a functional cell cycle-dependent element in tandem with it, contributes most of the cell cycle-dependent transcription from the cyclin B1 promoter. The coactivator p300 binds to the cyclin B1 promoter and synergises with the transcription factor NF-Y in activating transcription of cyclin B1.

Cyclin B1 transcription is enhanced by the p300 coactivator and regulated during the cell cycle by a CHR-dependent repression mechanism / M. Wasner, K. Tschöp, K. Spiesbach, U. Haugwitz, C. Johne, J. Mössner, R. Mantovani, K. Engeland. - In: FEBS LETTERS. - ISSN 0014-5793. - 536:1-3(2003), pp. 66-70.

Cyclin B1 transcription is enhanced by the p300 coactivator and regulated during the cell cycle by a CHR-dependent repression mechanism

R. Mantovani
Penultimo
;
2003

Abstract

Cyclin B is a central regulator of transition from the G2 phase of the cell cycle to mitosis. In mammalian cells two B-type cyclins have been characterised, cyclin B1 and B2. Both are expressed with a maximum in G2 and their synthesis is mainly regulated on the transcriptional level. We show that a single cell cycle genes homology region, lacking a functional cell cycle-dependent element in tandem with it, contributes most of the cell cycle-dependent transcription from the cyclin B1 promoter. The coactivator p300 binds to the cyclin B1 promoter and synergises with the transcription factor NF-Y in activating transcription of cyclin B1.
Cancer; Cell cycle-dependent element/cell cycle genes homology region; Cell cycle-dependent transcription; Cell division cycle; Chromatin immunoprecipitation; Histone acetyltransferase
Settore BIO/18 - Genetica
2003
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/49434
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