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超分辨率显微镜揭示了哺乳动物中心体亚基附属物与远侧附属物之间的耦合。

Super-resolution microscopy reveals coupling between mammalian centriole subdistal appendages and distal appendages.

机构信息

Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei, Taiwan.

Institute of Biochemistry and Molecular Biology, National Yang Ming University, Taipei, Taiwan.

出版信息

Elife. 2020 Apr 3;9:e53580. doi: 10.7554/eLife.53580.

Abstract

Subdistal appendages (sDAPs) are centriolar elements that are observed proximal to the distal appendages (DAPs) in vertebrates. Despite the obvious presence of sDAPs, structural and functional understanding of them remains elusive. Here, by combining super-resolved localization analysis and CRISPR-Cas9 genetic perturbation, we find that although DAPs and sDAPs are primarily responsible for distinct functions in ciliogenesis and microtubule anchoring, respectively, the presence of one element actually affects the positioning of the other. Specifically, we find dual layers of both ODF2 and CEP89, where their localizations are differentially regulated by DAP and sDAP integrity. DAP depletion relaxes longitudinal occupancy of sDAP protein ninein to cover the DAP region, implying a role of DAPs in sDAP positioning. Removing sDAPs alter the distal border of centrosomal γ-tubulins, illustrating a new role of sDAPs. Together, our results provide an architectural framework for sDAPs that sheds light on functional understanding, surprisingly revealing coupling between DAPs and sDAPs.

摘要

次远端附属物(sDAPs)是位于脊椎动物远端附属物(DAPs)近端的中心粒元件。尽管 sDAPs 明显存在,但对其结构和功能的理解仍然难以捉摸。在这里,我们通过结合超分辨定位分析和 CRISPR-Cas9 基因干扰,发现尽管 DAPs 和 sDAPs 分别主要负责纤毛发生和微管锚定的不同功能,但一个元件的存在实际上会影响另一个元件的定位。具体来说,我们发现 ODF2 和 CEP89 都存在双层结构,它们的定位受 DAP 和 sDAP 完整性的差异调控。DAP 缺失会放松 sDAP 蛋白 ninein 的纵向占据,以覆盖 DAP 区域,这表明 DAPs 在 sDAP 定位中起作用。去除 sDAPs 会改变中心体 γ-微管蛋白的远端边界,说明了 sDAPs 的新作用。总之,我们的结果为 sDAPs 提供了一个结构框架,为功能理解提供了线索,令人惊讶地揭示了 DAPs 和 sDAPs 之间的耦合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf5/7173962/da03b69f60b4/elife-53580-fig1.jpg

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