Decision for cell fate: deubiquitinating enzymes in cell cycle checkpoint

被引:37
|
作者
Lim, Key-Hwan [1 ]
Song, Myoung-Hyun [1 ]
Baek, Kwang-Hyun [1 ]
机构
[1] CHA Univ, Dept Biomed Sci, 335 Pangyo Ro, Songnam 463400, Gyeonggi Do, South Korea
基金
新加坡国家研究基金会;
关键词
Cell cycle; Deubiquitinating enzyme; DNA damage; Ubiquitination; SMALL-MOLECULE INHIBITOR; E3 UBIQUITIN LIGASE; NUCLEOTIDE EXCISION-REPAIR; STRAND BREAK REPAIR; UV-DAMAGED DNA; HISTONE H2A; FANCONI-ANEMIA; MULTIPLE-MYELOMA; TUMOR-SUPPRESSOR; BRCA1-ASSOCIATED PROTEIN-1;
D O I
10.1007/s00018-015-2129-2
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
All organs consisting of single cells are consistently maintaining homeostasis in response to stimuli such as free oxygen, DNA damage, inflammation, and microorganisms. The cell cycle of all mammalian cells is regulated by protein expression in the right phase to respond to proliferation and apoptosis signals. Post-translational modifications (PTMs) of proteins by several protein-editing enzymes are associated with cell cycle regulation by their enzymatic functions. Ubiquitination, one of the PTMs, is also strongly related to cell cycle regulation by protein degradation or signal transduction. The importance of deubiquitinating enzymes (DUBs), which have a reversible function for ubiquitination, has recently suggested that the function of DUBs is also important for determining the fate of proteins during cell cycle processing. This article reviews and summarizes the diverse roles of DUBs, including DNA damage, cell cycle processing, and regulation of histone proteins, and also suggests the possibility for therapeutic targets.
引用
收藏
页码:1439 / 1455
页数:17
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