The structure of basal body inner junctions from Tetrahymena revealed by electron cryo-tomography.

IF 9.4 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Sam Li, Jose-Jesus Fernandez, Marisa D Ruehle, Rachel A Howard-Till, Amy Fabritius, Chad G Pearson, David A Agard, Mark E Winey
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引用次数: 0

Abstract

The cilium is a microtubule-based eukaryotic 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 cryo-electron tomography, we obtained structures of the inner junction in three regions of the cilium from Tetrahymena: the proximal, the central core of the basal body, and the axoneme. We identified several protein components in the basal body. While a few proteins are distributed throughout the entire length of the organelle, many are restricted to specific regions, forming intricate local interaction networks in the inner junction and bolstering local structural stability. By examining the inner junction in a POC1 knockout mutant, we found the triplet microtubule 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 the inner junctions, underscoring its precise spatial regulation.

纤毛是一种基于微管的真核生物细胞器,对许多细胞功能至关重要。纤毛的组装始于基部体,然后以轴丝的形式伸出细胞外,形成功能性纤毛。这一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还很有限。通过应用低温电子断层扫描技术,我们获得了四膜虫纤毛器三个区域的内部连接结构:近端、基体的中央核心和轴丝。我们在基体中发现了几种蛋白质成分。少数蛋白质分布于整个细胞器,而许多蛋白质则局限于特定区域,在内部连接处形成错综复杂的局部相互作用网络,并增强了局部结构的稳定性。通过研究POC1基因敲除突变体的内部连接,我们发现三重微管的稳定性被破坏,从而导致结构缺陷。令人惊讶的是,我们发现有几种轴突特异性成分 "渗入 "了突变体的基底体。我们的发现从分子角度揭示了纤毛在内部连接处的组装,强调了其精确的空间调控。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
EMBO Journal
EMBO Journal 生物-生化与分子生物学
CiteScore
18.90
自引率
0.90%
发文量
246
审稿时长
1.5 months
期刊介绍: The EMBO Journal has stood as EMBO's flagship publication since its inception in 1982. Renowned for its international reputation in quality and originality, the journal spans all facets of molecular biology. It serves as a platform for papers elucidating original research of broad general interest in molecular and cell biology, with a distinct focus on molecular mechanisms and physiological relevance. With a commitment to promoting articles reporting novel findings of broad biological significance, The EMBO Journal stands as a key contributor to advancing the field of molecular biology.
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