Kinetochores generate microtubules with distal plus ends: their roles and limited lifetime in mitosis.
Kinetochores generate microtubules with distal plus ends: their roles and limited lifetime in mitosis.
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DOI:
10.1016/j.devcel.2009.12.018
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发表时间:
2010-02-16
影响因子:
11.8
通讯作者:
Tanaka TU
中科院分区:
文献类型:
--
作者:
Kitamura E;Tanaka K;Komoto S;Kitamura Y;Antony C;Tanaka TU
In early mitosis, microtubules can be generated at kinetochores as well as at spindle poles. However, the role and regulation of kinetochore-derived microtubules have been unclear. In general, metaphase spindle microtubules are oriented such that their plus ends bind to kinetochores. However, we now have evidence that, during early mitosis in budding yeast, microtubules are generated at kinetochores with distal plus ends. These kinetochore-derived microtubules interact along their length with microtubules that extend from a spindle pole, facilitating kinetochore loading onto the lateral surface of spindle pole microtubules. Once kinetochores are loaded, microtubules are no longer generated at kinetochores, and those that remain disappear rapidly and do not contribute to the metaphase spindle. Stu2 (the ortholog of vertebrate XMAP215/ch-TOG) localizes to kinetochores and plays a central role in regulating kinetochore-derived microtubules. Our work provides insight into microtubule generation at kinetochores and the mechanisms that facilitate initial kinetochore interaction with spindle pole microtubules. ► A short-lived population of kinetochore-derived microtubules (MTs) has distal plus ends ► These MTs are generated in early mitosis and regulated by Stu2 ► They interact with spindle pole-derived MTs before kinetochore attachment ► Once kinetochores attach to spindle-pole MTs, the short-lived MT population disappears
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DOI:
10.1083/jcb.84.1.151
发表时间:
1980-01
期刊:
The Journal of cell biology
影响因子:
--
作者:
Bergen LG;Kuriyama R;Borisy GG
通讯作者:
Borisy GG
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:
7.5
作者:
Schiebel, E
通讯作者:
Schiebel, E
影响因子:
11.4
作者:
Maekawa, H;Usui, T;Schiebel, E
通讯作者:
Schiebel, E
影响因子:
64.8
作者:
Tanaka, K;Mukae, N;Tanaka, TU
通讯作者:
Tanaka, TU