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      CP110 and CEP135 Localize Near the Proximal Centriolar Remnants of Mice Spermatozoa

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      microPublication Biology
      Caltech Library

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          Abstract

          Centrioles form centrosomes that organize microtubules, assist in cell structure, and nucleate cilia that provide motility and sensation. Within the sperm, the centrosome consists of two centrioles (proximal and distal centriole) and a pericentriolar material known as the striated column and capitulum. The distal centriole nucleates the flagellum. Mice spermatozoa, unlike other mammal spermatozoa (e.g., human and bovine), have no ultra-structurally recognizable centrioles, but their neck has the centriolar proteins POC1B and FAM161A, suggesting mice spermatozoa have remnant centrioles. Here, we examine whether other centriolar proteins, CP110 and CEP135, found in the human and bovine spermatozoa centrioles are also found in the mouse spermatozoa neck. CP110 is a tip protein controlling ciliogenesis, and CEP135 is a centriole-specific structural protein in the centriole base of canonical centrioles found in most cell types. Here, we report that CP110 and CEP135 were both located in the mice spermatozoa neck around the proximal centriolar remnants labeled by POC1B, increasing the number of centriolar proteins found in the mice spermatozoa neck, further supporting the hypothesis that a remnant proximal centriole is present in mice.

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          Most cited references47

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          The vertebrate primary cilium in development, homeostasis, and disease.

          Cilia are complex structures that have garnered interest because of their roles in vertebrate development and their involvement in human genetic disorders. In contrast to multicellular invertebrates in which cilia are restricted to specific cell types, these organelles are found almost ubiquitously in vertebrate cells, where they serve a diverse set of signaling functions. Here, we highlight properties of vertebrate cilia, with particular emphasis on their relationship with other subcellular structures, and explore the physiological consequences of ciliary dysfunction.
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            Plk4-induced centriole biogenesis in human cells.

            We show that overexpression of Polo-like kinase 4 (Plk4) in human cells induces centrosome amplification through the simultaneous generation of multiple procentrioles adjoining each parental centriole. This provided an opportunity for dissecting centriole assembly and characterizing assembly intermediates. Critical components were identified and ordered into an assembly pathway through siRNA and localized through immunoelectron microscopy. Plk4, hSas-6, CPAP, Cep135, gamma-tubulin, and CP110 were required at different stages of procentriole formation and in association with different centriolar structures. Remarkably, hSas-6 associated only transiently with nascent procentrioles, whereas Cep135 and CPAP formed a core structure within the proximal lumen of both parental and nascent centrioles. Finally, CP110 was recruited early and then associated with the growing distal tips, indicating that centrioles elongate through insertion of alpha-/beta-tubulin underneath a CP110 cap. Collectively, these data afford a comprehensive view of the assembly pathway underlying centriole biogenesis in human cells.
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              Overview of structure and function of mammalian cilia.

              Cilia are membrane-bounded, centriole-derived projections from the cell surface that contain a microtubule cytoskeleton, the ciliary axoneme, surrounded by a ciliary membrane. Axonemes in multiciliated cells of mammalian epithelia are 9 + 2, possess dynein arms, and are motile. In contrast, single nonmotile 9 + 0 primary cilia are found on epithelial cells, such as those of the kidney tubule, but also on nonepithelial cells, such as chondrocytes, fibroblasts, and neurons. The ciliary membranes of all cilia contain specific receptors and ion channel proteins that initiate signaling pathways controlling motility and/or linking mechanical or chemical stimuli, including sonic hedgehog and growth factors, to intracellular transduction cascades regulating differentiation, migration, and cell growth during development and in adulthood. Unique motile 9 + 0 cilia, found during development at the embryonic node, determine left-right asymmetry of the body.
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                Author and article information

                Journal
                MicroPubl Biol
                MicroPubl Biol
                microPublication Biology
                Caltech Library
                2578-9430
                29 January 2024
                2024
                : 2024
                : 10.17912/micropub.biology.001083
                Affiliations
                [1 ] University of Toledo, Toledo, Ohio, United States
                Author notes
                [§ ] Correspondence to: Tomer Avidor-Reiss ( Tomer.AvidorReiss@ 123456utoledo.edu )

                The authors declare that there are no conflicts of interest present.

                Article
                10.17912/micropub.biology.001083
                10862134
                38351906
                3b17874c-486c-4277-ae14-5c561a1a8e17
                Copyright: © 2024 by the authors

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 5 December 2023
                : 17 January 2024
                : 18 January 2024
                Funding
                Funded by: Eunice Kennedy Shriver National Institute of Child Health and Human Development (United States), https://ror.org/04byxyr05;
                Award ID: 1R15HD110863
                Award Recipient : Tomer Avidor-Reiss
                Funded by: University of Toledo (United States), https://ror.org/01pbdzh19;
                Award ID: Undergraduate Summer Research and Creative Activity Program
                Award Recipient : Abirami Subbiah
                Categories
                New Finding
                Expression Data
                Mouse

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