Guiding Mitotic Progression by Crosstalk between Post-translational Modifications

被引:41
|
作者
Cuijpers, Sabine A. G. [1 ]
Vertegaal, Alfred C. O. [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Mol Cell Biol, NL-2333 ZA Leiden, Netherlands
基金
欧洲研究理事会;
关键词
ANAPHASE-PROMOTING COMPLEX/CYCLOSOME; TRCP-DEPENDENT DEGRADATION; SISTER-CHROMATID COHESION; AURORA-B; CELL-CYCLE; HISTONE H3; CHROMOSOME CONDENSATION; CENP-A; SIGNALING NETWORKS; PROTEOMIC ANALYSIS;
D O I
10.1016/j.tibs.2018.02.004
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 division is tightly regulated to disentangle copied chromosomes in an orderly manner and prevent loss of genome integrity. During mitosis, transcriptional activity is limited and post-translational modifications (PTMs) are responsible for functional protein regulation. Essential mitotic regulators, including polo-like kinase 1 (PLK1) and cyclin-dependent kinases (CDK), as well as the anaphase-promoting complex/cyclosome (APC/C), are members of the enzymatic machinery responsible for protein modification. Interestingly, communication between PTMs ensures the essential tight and timely control during all consecutive phases of mitosis. Here, we present an overview of current concepts and understanding of crosstalk between PTMs regulating mitotic progression.
引用
收藏
页码:251 / 268
页数:18
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