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Tension directly stabilizes reconstituted kinetochore-microtubule attachments

机译:张力直接稳定重建的动粒体-微管附件

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摘要

Kinetochores are macromolecular machines that couple chromosomes to dynamic microtubule tips during cell division, thereby generating force to segregate the chromosomes. Accurate segregation depends on selective stabilization of correct 'bi-oriented' kinetochore-microtubule attachments, which come under tension as the result of opposing forces exerted by microtubules. Tension is thought to stabilize these bi-oriented attachments indirectly, by suppressing the destabilizing activity of a kinase, Aurora B. However, a complete mechanistic understanding of the role of tension requires reconstitution of kinetochore-microtubule attachments for biochemical and biophysical analyses in vitro. Here we show that native kinetochore particles retaining the majority of kinetochore proteins can be purified from budding yeast and used to reconstitute dynamic microtubule attachments. Individual kinetochore particles maintain load-bearing associations with assembling and disassembling ends of single microtubules for >30min, providing a close match to the persistent coupling seen in vivo between budding yeast kinetochores and single microtubules. Moreover, tension increases the lifetimes of the reconstituted attachments directly, through a catch bond-like mechanism that does not require Aurora B. On the basis of these findings, we propose that tension selectively stabilizes proper kinetochore-microtubule attachments in vivo through a combination of direct mechanical stabilization and tension-dependent phosphoregulation.
机译:动植物是在细胞分裂过程中将染色体连接到动态微管末端的大分子机器,从而产生分离染色体的作用力。正确的隔离取决于正确的“双向”动球体-微管附件的选择性稳定化,由于微管施加相反的力,这些附件会承受张力。人们认为张力可以通过抑制激酶Aurora B的去稳定化活性来间接稳定这些双向连接。但是,对张力作用的完整机械理解需要重建动线体-微管连接,以便进行体外生化和生物物理分析。在这里,我们显示可以从发芽的酵母中纯化保留大部分线粒体蛋白的天然线粒体颗粒,并用于重建动态微管附件。单个动粒体颗粒与单个微管的组装和拆卸末端保持承重关联> 30分钟,这与发芽的酵母动植物和单个微管之间的体内持久耦合紧密匹配。此外,张力通过不需要Aurora B的类捕集键机制直接延长了重组附件的寿命。基于这些发现,我们建议通过结合以下方式在体内选择性地稳定适当的动粒微管附件直接机械稳定和张力依赖性磷酸化。

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  • 来源
    《Nature》 |2010年第7323期|p.576-579|共4页
  • 作者单位

    Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA Molecular and Cellular Biology Program, University of Washington, Seattle, Washington 98195, USA;

    rnDepartment of Physiology & Biophysics, University of Washington, Seattle, Washington 98195, USA;

    rnDepartment of Physiology & Biophysics, University of Washington, Seattle, Washington 98195, USA;

    rnDivision of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA;

    rnDepartment of Biochemistry, University of Washington, Seattle, Washington 98195, USA;

    Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA Molecular and Cellular Biology Program, University of Washington, Seattle, Washington 98195, USA Department of Physiology & Biophysics, University of Washington, Seattle, Washington 98195, USA;

    rnDepartment of Biochemistry, University of Washington, Seattle, Washington 98195, USA Howard Hughes Medical Institute, University of Washington, Seattle, Washington 98195, USA;

    rnlnstitute for Systems Biology, Seattle, Washington 98103, USA;

    Department of Physiology & Biophysics, University of Washington, Seattle, Washington 98195, USA;

    rnDivision of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 02:55:20

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