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冷冻电子断层扫描揭示纤毛内部连接的结构

The Structure of Cilium Inner Junctions Revealed by Electron Cryo-tomography.

作者信息

Li Sam, Fernandez Jose-Jesus, Ruehle Marisa D, Howard-Till Rachel A, Fabritius Amy, Pearson Chad G, Agard David A, Winey Mark E

机构信息

Department of Biochemistry and Biophysics, University of California San Francisco, San Francisco, CA 94158, USA.

Nanomaterials and Nanotechnology Research Center (CINN-CSIC), Health Research Institute of Asturias (ISPA), 33011 Oviedo, Spain.

出版信息

bioRxiv. 2024 Sep 9:2024.09.09.612100. doi: 10.1101/2024.09.09.612100.

Abstract

The cilium is a microtubule-based organelle critical for many cellular functions. Its assembly initiates at a basal body and continues as an axoneme that projects out of the cell to form a functional cilium. This assembly process is tightly regulated. However, our knowledge of the molecular architecture and the mechanism of assembly is limited. By applying electron cryotomography and subtomogram averaging, we obtained subnanometer resolution structures of the inner junction in three distinct regions of the cilium: the proximal region of the basal body, the central core of the basal body, and the flagellar axoneme. The structures allowed us to identify several basal body and axoneme components. While a few proteins are distributed throughout the entire length of the organelle, many are restricted to particular regions of the cilium, forming intricate local interaction networks and bolstering local structural stability. Finally, by knocking out a critical basal body inner junction component Poc1, we found the triplet MT was destabilized, resulting in a defective structure. Surprisingly, several axoneme-specific components were found to "infiltrate" into the mutant basal body. Our findings provide molecular insight into cilium assembly at its inner Junctions, underscoring its precise spatial regulation.

摘要

纤毛是一种基于微管的细胞器,对许多细胞功能至关重要。其组装起始于基体,并作为轴丝持续延伸,轴丝从细胞中伸出形成功能性纤毛。这个组装过程受到严格调控。然而,我们对其分子结构和组装机制的了解有限。通过应用电子冷冻断层扫描和亚断层平均技术,我们获得了纤毛三个不同区域内连接的亚纳米分辨率结构:基体的近端区域、基体的中心核心以及鞭毛轴丝。这些结构使我们能够鉴定出几种基体和轴丝成分。虽然有一些蛋白质分布在细胞器的整个长度上,但许多蛋白质被限制在纤毛的特定区域,形成复杂的局部相互作用网络并增强局部结构稳定性。最后,通过敲除关键的基体内部连接成分Poc1,我们发现三联微管不稳定,导致结构缺陷。令人惊讶的是,发现几种轴丝特异性成分“渗入”到突变的基体中。我们的研究结果为纤毛内部连接的组装提供了分子层面的见解,强调了其精确的空间调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a4c/11419100/bd18e9c496a9/nihpp-2024.09.09.612100v1-f0001.jpg

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