CRL4Cdt2 Master coordinator of cell cycle progression and genome stability

被引:120
作者
Abbas, Tarek [1 ]
Dutta, Anindya [1 ]
机构
[1] Univ Virginia, Dept Biochem & Mol Genet, Charlottesville, VA 22903 USA
关键词
ubiquitylation; cullins; Cul4; Cdt2; DTL; CRLs; cancer; cell cycle; CUL4-DDB1 UBIQUITIN LIGASE; MATRIX-ASSOCIATED PROTEIN; DNA-DAMAGE RESPONSE; S-PHASE; REGULATED NUCLEAR; CDT1; PROTEOLYSIS; RIBONUCLEOTIDE REDUCTASE; PREVENTS REREPLICATION; WD40-REPEAT PROTEINS; HISTONE-METHYLATION;
D O I
10.4161/cc.10.2.14530
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Polyubiquitin-mediated degradation of proteins plays an essential role in various physiological processes including cell cycle progression, transcription and DNA replication and repair. Increasing evidence supports a vital role for the E3 ubiquitin ligase cullin-4, in conjunction with the substrate recognition factor Cdt2 (CRL4(Cdt2)), for the degradation of multiple cell cycle-regulated proteins to prevent genomic instability. In addition, it is critical for normal cell cycle progression by ensuring the timely destruction of various cell cycle proteins whose deregulated expression impairs cell cycle progression. Here, we summarize our current knowledge about the various roles of the CRL4(Cdt2) E3 ubiquitin ligase, and how its activity contributes both to the preservation of genome integrity and to normal cell cycle progression, and how its deregulation may contribute to human cancer.
引用
收藏
页码:241 / 249
页数:9
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