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有丝分裂期间动粒构型的调控。

Regulation of kinetochore configuration during mitosis.

作者信息

Dhatchinamoorthy Karthik, Mattingly Mark, Gerton Jennifer L

机构信息

Stowers Institute for Medical Research, Kansas City, USA.

The Open Univeristy, Milton Keynes, England, UK.

出版信息

Curr Genet. 2018 Dec;64(6):1197-1203. doi: 10.1007/s00294-018-0841-9. Epub 2018 Apr 27.

Abstract

Successful proliferation and function of an organism relies on the equal segregation of its genetic material during cell division. Duplicate sister chromatids need to accurately segregate at mitosis. Precise segregation depends on a multicomplex protein structure called the kinetochore. The kinetochore assembles at centromeres and attaches to microtubules to segregate sister chromatids. Even though the kinetochore structure was first observed nearly a century ago, many aspects of the regulation, function and assembly of this large 100 + protein structure remain to be determined. Improved microscopy and proteomics techniques over the years have helped to reveal the structure, composition and localization of sub-modules of the kinetochore. Recent work suggests that the configuration of the kinetochore is plastic, with extra submodules being added during anaphase to support microtubule tracking and chromosome segregation. We discuss our perspective of how this process might be regulated.

摘要

生物体的成功增殖和功能依赖于其遗传物质在细胞分裂过程中的均等分离。复制后的姐妹染色单体需要在有丝分裂时精确分离。精确分离依赖于一种称为动粒的多复合体蛋白质结构。动粒在着丝粒处组装,并附着于微管以分离姐妹染色单体。尽管动粒结构在近一个世纪前就首次被观察到,但这个由100多种蛋白质组成的大型结构的调控、功能和组装的许多方面仍有待确定。多年来改进的显微镜技术和蛋白质组学技术有助于揭示动粒亚模块的结构、组成和定位。最近的研究表明,动粒的构型是可变的,在后期会添加额外的亚模块以支持微管追踪和染色体分离。我们讨论了我们对这一过程可能如何调控的观点。

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