Abstract
The dimerization partner, RB-like, E2F and multi-vulval class B (DREAM) complex provides a previously unsuspected unifying role in the cell cycle by directly linking p130, p107, E2F, BMYB and forkhead box protein M1. DREAM mediates gene repression during the G0 phase and coordinates periodic gene expression with peaks during the G1/S and G2/M phases. Perturbations in DREAM complex regulation shift the balance from quiescence towards proliferation and contribute to the increased mitotic gene expression levels that are frequently observed in cancers with a poor prognosis.
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Change history
23 August 2013
On page 593 of this Opinion article, a citation to a key reference (Flowers. S., Beck, G. R. Jr & Moran, E. Tissue-specific gene targeting by the multiprotein mammalian DREAM complex. J. Biol. Chem. 286, 27867–27871 (2011)) was not included. This reference should have been cited at the end of the following sentence: "Perhaps isolation of the DREAM and the BMYB–MuvB complexes from distinct mammalian tissues will reveal functions in addition to cell cycle control130,131". This has now been corrected online.
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Acknowledgements
The authors gratefully acknowledge the many helpful discussions about DREAM with L. Litovchick, N. Dyson, M. Botchan and K. Engeland. This work was supported in part by US Public Health Service grants P01CA050661 and R01CA63113 to J.A.D.
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Sadasivam, S., DeCaprio, J. The DREAM complex: master coordinator of cell cycle-dependent gene expression. Nat Rev Cancer 13, 585–595 (2013). https://doi.org/10.1038/nrc3556
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DOI: https://doi.org/10.1038/nrc3556
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