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纺锤体组装以及微管相关蛋白(MAPs)和Stathmin/Op18调控微管动力学的机制

Spindle assembly and the art of regulating microtubule dynamics by MAPs and Stathmin/Op18.

作者信息

Andersen S S

机构信息

Dept of Biology, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0357, USA.

出版信息

Trends Cell Biol. 2000 Jul;10(7):261-7. doi: 10.1016/s0962-8924(00)01786-4.

Abstract

The way that microtubules reorganize from their long, stable interphase configuration to form the mitotic spindle remains a challenging and unsolved question. It is now widely recognized that microtubule polymerization during the cell cycle is regulated by a balance between microtubule-stabilizing and-destabilizing factors. Stabilizing factors include a large group of microtubule-associated proteins (MAPs; e.g. MAP4, XMAP215, XMAP230/XMAP4 and XMAP310) and the destabilizing factors are a growing family of proteins (e.g. Stathmin/Op18 and XKCM1). Recent studies have allowed a mechanistic dissection of how these stabilizing and destabilizing factors regulate microtubule dynamics and spindle assembly.

摘要

微管如何从其长而稳定的间期构型重新组织以形成有丝分裂纺锤体仍然是一个具有挑战性且尚未解决的问题。现在人们普遍认识到,细胞周期中的微管聚合是由微管稳定因子和去稳定因子之间的平衡调节的。稳定因子包括一大类微管相关蛋白(MAPs;例如MAP4、XMAP215、XMAP230/XMAP4和XMAP310),而去稳定因子是一个不断增加的蛋白质家族(例如Stathmin/Op18和XKCM1)。最近的研究使得对这些稳定和去稳定因子如何调节微管动力学和纺锤体组装进行了机制剖析。

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