TY - JOUR
T1 - The Importance of Kinase-Phosphatase Integration
T2 - Lessons from Mitosis
AU - Gelens, Lendert
AU - Qian, Junbin
AU - Bollen, Mathieu
AU - Saurin, Adrian T.
N1 - The ATS lab is funded by Cancer Research UK (Programme Foundation Award; C47320/A21229), Tenovus Scotland, and the Ninewells Cancer Campaign. L.G. acknowledges support from the research foundation Flanders (FWO-Vlaanderen) and the research coordination office of the KU Leuven. J.Q. and M.B. were supported by the Fund for Scientific Research-Flanders (Grant G0B9917N), a Flemish Concerted Research Action (GOA/15/016), and the Belgian Foundation against Cancer.
PY - 2018/1
Y1 - 2018/1
N2 - 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.
AB - 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.
U2 - 10.1016/j.tcb.2017.09.005
DO - 10.1016/j.tcb.2017.09.005
M3 - Review article
C2 - 29089159
SN - 0962-8924
VL - 28
SP - 6
EP - 21
JO - Trends in Cell Biology
JF - Trends in Cell Biology
IS - 1
ER -