Coordinating gene expression during the cell cycle

被引:105
|
作者
Fischer, Martin [1 ]
Schade, Amy E. [2 ,3 ]
Branigan, Timothy B. [3 ,4 ,5 ]
Mueller, Gerd A. [6 ]
DeCaprio, James A. [3 ,4 ,5 ]
机构
[1] FLI, Computat Biol Grp, Leibniz Inst Aging, D-07745 Jena, Germany
[2] Brigham & Womens Hosp, Dept Med, Div Genet, Boston, MA 02115 USA
[3] Harvard Med Sch, Boston, MA 02115 USA
[4] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02215 USA
[5] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[6] Univ Calif Santa Cruz, Dept Chem & Biochem, Santa Cruz, CA 95064 USA
关键词
S-M CHECKPOINT; DREAM COMPLEX; TRANSCRIPTION FACTOR; PROTEIN COMPLEX; REPRESS TRANSCRIPTION; MOLECULAR-MECHANISMS; REPLICATION STRESS; TUMOR-SUPPRESSOR; MUVB COMPLEX; B-MYB;
D O I
10.1016/j.tibs.2022.06.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
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页码:1009 / 1022
页数:14
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