The Importance of Kinase-Phosphatase Integration: Lessons from Mitosis

被引:71
作者
Gelens, Lendert [1 ]
Qian, Junbin [2 ]
Bollen, Mathieu [2 ]
Saurin, Adrian T. [3 ,4 ]
机构
[1] Univ Leuven, Dept Cellular & Mol Med, Lab Dynam Biol Syst, B-3000 Leuven, Belgium
[2] Univ Leuven, KU Leuven Dept Cellular & Mol Med, Lab Biosignaling & Therapeut, Leuven, Belgium
[3] Ninewells Hosp, Jacqui Wood Canc Ctr, Sch Med, Div Canc Res, Dundee DD1 9SY, Scotland
[4] Univ Dundee, Med Sch, Dundee DD1 9SY, Scotland
关键词
CHROMOSOME BI-ORIENTATION; SPINDLE ASSEMBLY CHECKPOINT; KINETOCHORE-MICROTUBULE ATTACHMENTS; SISTER-CHROMATID COHESION; CELL-CYCLE TRANSITIONS; AURORA-B; MULTISITE PHOSPHORYLATION; SUBSTRATE DEPHOSPHORYLATION; POSITIVE FEEDBACK; MITOTIC EXIT;
D O I
10.1016/j.tcb.2017.09.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Kinases and phosphatases work antagonistically to control the behaviour of individual substrate molecules. This can be incorrectly extrapolated to imply that they also work antagonistically on the signals or processes that these molecules control. In fact, in many situations kinases and phosphatases work together to positively drive signal responses. We explain how this `cooperativity' is critical for setting the amplitude, localisation, timing, and shape of phosphorylation signals. We use mitosis to illustrate why these properties are important for controlling mitotic entry, sister chromatid cohesion, kinetochore-microtubule attachments, the spindle assembly checkpoint, mitotic spindle elongation, and mitotic exit. These examples provide a rationale to explain how complex signalling behaviour could rely on similar types of integration within many other biological processes.
引用
收藏
页码:6 / 21
页数:16
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