Centriole and transition zone structures in photoreceptor cilia revealed by cryo-electron tomography.

IF 3.3 2区 生物学 Q1 BIOLOGY
Life Science Alliance Pub Date : 2024-01-05 Print Date: 2024-03-01 DOI:10.26508/lsa.202302409
Zhixian Zhang, Abigail R Moye, Feng He, Muyuan Chen, Melina A Agosto, Theodore G Wensel
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引用次数: 0

Abstract

Primary cilia mediate sensory signaling in multiple organisms and cell types but have structures adapted for specific roles. Structural defects in them lead to devastating diseases known as ciliopathies in humans. Key to their functions are structures at their base: the basal body, the transition zone, the "Y-shaped links," and the "ciliary necklace." We have used cryo-electron tomography with subtomogram averaging and conventional transmission electron microscopy to elucidate the structures associated with the basal region of the "connecting cilia" of rod outer segments in mouse retina. The longitudinal variations in microtubule (MT) structures and the lumenal scaffold complexes connecting them have been determined, as well as membrane-associated transition zone structures: Y-shaped links connecting MT to the membrane, and ciliary beads connected to them that protrude from the cell surface and form a necklace-like structure. These results represent a clearer structural scaffold onto which molecules identified by genetics, proteomics, and superresolution fluorescence can be placed in our emerging model of photoreceptor sensory cilia.

低温电子断层扫描揭示感光细胞纤毛的中心粒和过渡区结构
初级纤毛在多种生物和细胞类型中介导感觉信号,但其结构适应于特定的作用。纤毛的结构缺陷会导致毁灭性疾病,人类称之为纤毛疾病。纤毛功能的关键在于其基部的结构:基底体、过渡区、"Y 形连接 "和 "纤毛项链"。我们利用低温电子断层扫描与子图平均法和传统透射电子显微镜阐明了小鼠视网膜视杆细胞外节 "连接纤毛 "基部的相关结构。研究人员确定了微管(MT)结构的纵向变化和连接它们的管腔支架复合物,以及与膜相关的过渡区结构:连接MT和膜的Y形链和与之相连的纤毛珠突出于细胞表面,形成项链状结构。这些结果代表了一个更清晰的结构支架,通过遗传学、蛋白质组学和超分辨率荧光鉴定的分子可以被置于我们正在建立的感光器感觉纤毛模型中。
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
Life Science Alliance
Life Science Alliance Agricultural and Biological Sciences-Plant Science
CiteScore
5.80
自引率
2.30%
发文量
241
审稿时长
10 weeks
期刊介绍: Life Science Alliance is a global, open-access, editorially independent, and peer-reviewed journal launched by an alliance of EMBO Press, Rockefeller University Press, and Cold Spring Harbor Laboratory Press. Life Science Alliance is committed to rapid, fair, and transparent publication of valuable research from across all areas in the life sciences.
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