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Ndc80复合体连接两个Dam1复合体环。

The Ndc80 complex bridges two Dam1 complex rings.

作者信息

Kim Jae Ook, Zelter Alex, Umbreit Neil T, Bollozos Athena, Riffle Michael, Johnson Richard, MacCoss Michael J, Asbury Charles L, Davis Trisha N

机构信息

Department of Biochemistry, University of Washington, Seattle, United States.

Department of Genome Sciences, University of Washington, Seattle, United States.

出版信息

Elife. 2017 Feb 13;6:e21069. doi: 10.7554/eLife.21069.

Abstract

Strong kinetochore-microtubule attachments are essential for faithful segregation of sister chromatids during mitosis. The Dam1 and Ndc80 complexes are the main microtubule binding components of the kinetochore. Cooperation between these two complexes enhances kinetochore-microtubule coupling and is regulated by Aurora B kinase. We show that the Ndc80 complex can simultaneously bind and bridge across two Dam1 complex rings through a tripartite interaction, each component of which is regulated by Aurora B kinase. Mutations in any one of the Ndc80p interaction regions abrogates the Ndc80 complex's ability to bind two Dam1 rings in vitro, and results in kinetochore biorientation and microtubule attachment defects in vivo. We also show that an extra-long Ndc80 complex, engineered to space the two Dam1 rings further apart, does not support growth. Taken together, our work suggests that each kinetochore in vivo contains two Dam1 rings and that proper spacing between the rings is vital.

摘要

在有丝分裂过程中,牢固的动粒-微管附着对于姐妹染色单体的准确分离至关重要。Dam1和Ndc80复合体是动粒的主要微管结合成分。这两个复合体之间的协同作用增强了动粒-微管的耦合,并受极光B激酶调节。我们发现,Ndc80复合体可通过三方相互作用同时结合并横跨两个Dam1复合体环,其中每个成分都受极光B激酶调节。Ndc80p相互作用区域中任何一个区域的突变都会消除Ndc80复合体在体外结合两个Dam1环的能力,并在体内导致动粒双定向和微管附着缺陷。我们还发现,经过改造使两个Dam1环间距更远的超长Ndc80复合体无法支持细胞生长。综上所述,我们的研究表明,体内每个动粒都包含两个Dam1环,且环之间的适当间距至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca8e/5354518/cf4c94d66f2b/elife-21069-fig1.jpg

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