Coordinating gene expression during the cell cycle

Martin Fischer(Leibniz Institute on Aging - Fritz Lipmann Institute (FLI)), Amy E. Schade(Brigham and Women's Hospital), Timothy B. Branigan(Brigham and Women's Hospital), Gerd A. Müller(University of California, Santa Cruz), James A. DeCaprio(Brigham and Women's Hospital)
Trends in Biochemical Sciences
July 11, 2022
Cited by 232Open Access
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Abstract

Cell cycle-dependent gene transcription is tightly controlled by the retinoblastoma (RB):E2F and DREAM complexes, which repress all cell cycle genes during quiescence. Cyclin-dependent kinase (CDK) phosphorylation of RB and DREAM allows for the expression of two gene sets. The first set of genes, with peak expression in G1/S, is activated by E2F transcription factors (TFs) and is required for DNA synthesis. The second set, with maximum expression during G2/M, is required for mitosis and is coordinated by the MuvB complex, together with B-MYB and Forkhead box M1 (FOXM1). In this review, we summarize the key findings that established the distinct control mechanisms regulating G1/S and G2/M gene expression in mammals and discuss recent advances in the understanding of the temporal control of these genes.


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