解析中心体γ- turc的结构组织、募集和激活机制。

Florian W Hofer, Martin Würtz, Qi Gao, Bram J A Vermeulen, Elmar Schiebel, Stefan Pfeffer
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引用次数: 0

摘要

利用低温电子断层成像技术观察人类中心体,揭示了γ-微管蛋白环复合物(γ-TuRCs)的天然结构和分子组织。γ-TuRCs定位于两个不同的中心体池,一个在中心粒周围物质(PCM)中,另一个在有丝分裂过程中释放的中心粒管腔中。所有检测到的γ- turc均与四聚体接头蛋白NEDD1相关。在PCM中,以不同模式结合小头畸形蛋白CDK5RAP2的中心体蛋白(CM1)基序与γ- turc的构象变化相关。在中心粒腔内,augmin复合物将γ- turc锚定在内部支架上。这些观察结果为研究γ- turc的结构组织和调节因子如何共同控制中心体微管成核的时空控制提供了关键的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dissecting the Structural Organization, Recruitment and Activation Mechanisms of Centrosomal γ-TuRCs.

Visualizing human centrosomes using cryo-electron tomography revealed the native structure and molecular organization of γ-tubulin ring complexes (γ-TuRCs). γ-TuRCs localized to two distinct centrosomal pools, one in the pericentriolar material (PCM) and another in the centriole lumen, which is released during mitosis. All detected γ-TuRCs were associated with the tetrameric adaptor protein NEDD1. Within the PCM, binding to the centrosomin (CM1) motif of the microcephaly protein CDK5RAP2 in different patterns correlates with conformational changes of γ-TuRCs. In the centriole lumen, the augmin complex anchors γ-TuRCs to the inner scaffold. These observations provide key insights into how the structural organization of γ-TuRCs and regulatory factors collectively govern the spatial and temporal control of microtubule nucleation in centrosomes.

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