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

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

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

2020
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Overview
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.