Spindle checkpoint silencing requires association of PP1 to both Spc7 and kinesin-8 motors.
Spindle checkpoint silencing requires association of PP1 to both Spc7 and kinesin-8 motors.
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DOI:
10.1016/j.devcel.2011.05.008
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发表时间:
2011-06-14
影响因子:
11.8
通讯作者:
Millar, Jonathan B. A.
中科院分区:
文献类型:
--
作者:
Meadows, John C.;Shepperd, Lindsey A.;Vanoosthuyse, Vincent;Lancaster, Theresa C.;Sochaj, Alicja M.;Buttrick, Graham J.;Hardwick, Kevin G.;Millar, Jonathan B. A.
The spindle checkpoint is the prime cell cycle control mechanism that ensures sister chromatids are bi-oriented before anaphase takes place. Aurora B kinase, the catalytic subunit of the chromosome passenger complex, both destabilises kinetochore attachments that do not generate tension and simultaneously maintains the spindle checkpoint signal. However, it is unclear how the checkpoint is silenced following chromosome bi-orientation. We demonstrate that association of type 1 phosphatase (PP1Dis2) to both the N-terminus of Spc7 and the non-motor domains of the Klp5-Klp6 (Kinesin-8) complex are necessary to counteract Aurora B kinase to efficiently silence the spindle checkpoint. The role of Klp5 and Klp6 in checkpoint silencing is specific to this class of kinesin and independent of their motor activities. These data demonstrate that at least two distinct pools of PP1, one kinetochore associated and the other motor associated, are needed to silence the spindle checkpoint.
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DOI:
10.1016/j.cub.2009.06.043
发表时间:
2009-07-28
期刊:
Current biology : CB
影响因子:
--
作者:
Pinsky BA;Nelson CR;Biggins S
通讯作者:
Biggins S
影响因子:
21.3
作者:
Gupta, Mohan L., Jr.;Carvalho, Pedro;Pellman, David
通讯作者:
Pellman, David
影响因子:
10.5
作者:
Gassmann, Reto;Holland, Andrew J.;Desai, Arshad
通讯作者:
Desai, Arshad
影响因子:
9.2
作者:
Mayr, Monika I.;Huemmer, Stefan;Mayer, Thomas U.
通讯作者:
Mayer, Thomas U.
DOI:
10.1083/jcb.201001006
发表时间:
2010-03-22
期刊:
The Journal of cell biology
影响因子:
--
作者:
Liu D;Vleugel M;Backer CB;Hori T;Fukagawa T;Cheeseman IM;Lampson MA
通讯作者:
Lampson MA