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控制中心体数量:许可与阻碍。

Controlling centrosome number: licenses and blocks.

作者信息

Tsou Meng-Fu Bryan, Stearns Tim

机构信息

Department of Biological Sciences, Stanford University, Stanford, California 94305, USA.

出版信息

Curr Opin Cell Biol. 2006 Feb;18(1):74-8. doi: 10.1016/j.ceb.2005.12.008. Epub 2005 Dec 19.

Abstract

Centrosomes organize microtubule structures in animal cells. The centrosome duplicates once per cell cycle in most dividing cells via a pathway that relies on a pre-existing centrosome. The molecular mechanism of this 'once and only once' control is not understood, and recent results show that centrosomes can also be assembled by a de novo pathway that bypasses this control. These results require a rethinking of how proper centrosome number is maintained. We propose that the engagement of centrioles with each other normally blocks centrosome re-duplication, and that disengagement of centrioles from each other at the end of mitosis licenses them for duplication in the subsequent cell cycle.

摘要

中心体在动物细胞中组织微管结构。在大多数分裂细胞中,中心体在每个细胞周期通过依赖于预先存在的中心体的途径复制一次。这种“一次且仅一次”控制的分子机制尚不清楚,最近的研究结果表明,中心体也可以通过一种绕过这种控制的从头途径组装。这些结果需要重新思考如何维持适当的中心体数量。我们提出,中心粒彼此结合通常会阻止中心体再次复制,而在有丝分裂末期中心粒彼此脱离会使它们在随后的细胞周期中进行复制。

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