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SPACA9 is a lumenal protein of human ciliary singlet and doublet microtubules.
Gui, Miao; Croft, Jacob T; Zabeo, Davide; Acharya, Vajradhar; Kollman, Justin M; Burgoyne, Thomas; Höög, Johanna L; Brown, Alan.
Affiliation
  • Gui M; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115.
  • Croft JT; Department of Chemistry and Molecular Biology, University of Gothenburg, Gothenburg 41390, Sweden.
  • Zabeo D; Department of Biochemistry, University of Washington, Seattle, WA 98195.
  • Acharya V; Department of Chemistry and Molecular Biology, University of Gothenburg, Gothenburg 41390, Sweden.
  • Kollman JM; Department of Chemistry and Molecular Biology, University of Gothenburg, Gothenburg 41390, Sweden.
  • Burgoyne T; Department of Biochemistry, University of Washington, Seattle, WA 98195.
  • Höög JL; Royal Brompton Hospital, Guy's and St Thomas' NHS Foundation Trust, London SW3 6NP, United Kingdom.
  • Brown A; Institute of Ophthalmology, University College London, London EC1V 9EL, United Kingdom.
Proc Natl Acad Sci U S A ; 119(41): e2207605119, 2022 10 11.
Article in En | MEDLINE | ID: mdl-36191189
The cilium-centrosome complex contains triplet, doublet, and singlet microtubules. The lumenal surfaces of each microtubule within this diverse array are decorated by microtubule inner proteins (MIPs). Here, we used single-particle cryo-electron microscopy methods to build atomic models of two types of human ciliary microtubule: the doublet microtubules of multiciliated respiratory cells and the distal singlet microtubules of monoflagellated human spermatozoa. We discover that SPACA9 is a polyspecific MIP capable of binding both microtubule types. SPACA9 forms intralumenal striations in the B tubule of respiratory doublet microtubules and noncontinuous spirals in sperm singlet microtubules. By acquiring new and reanalyzing previous cryo-electron tomography data, we show that SPACA9-like intralumenal striations are common features of different microtubule types in animal cilia. Our structures provide detailed references to help rationalize ciliopathy-causing mutations and position cryo-EM as a tool for the analysis of samples obtained directly from ciliopathy patients.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Semen / Ciliopathies Limits: Animals / Humans / Male Language: En Journal: Proc Natl Acad Sci U S A Year: 2022 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Semen / Ciliopathies Limits: Animals / Humans / Male Language: En Journal: Proc Natl Acad Sci U S A Year: 2022 Type: Article