In situ architecture of the ciliary base reveals the stepwise assembly of intraflagellar transport trains

Author:

van den Hoek Hugo123ORCID,Klena Nikolai45ORCID,Jordan Mareike A.6ORCID,Alvarez Viar Gonzalo56,Righetto Ricardo D.12ORCID,Schaffer Miroslava3ORCID,Erdmann Philipp S.5ORCID,Wan William7ORCID,Geimer Stefan8ORCID,Plitzko Jürgen M.3ORCID,Baumeister Wolfgang3ORCID,Pigino Gaia56ORCID,Hamel Virginie4ORCID,Guichard Paul4ORCID,Engel Benjamin D.12ORCID

Affiliation:

1. Biozentrum, University of Basel, 4056 Basel, Switzerland.

2. Helmholtz Pioneer Campus, Helmholtz Munich, 85764 Neuherberg, Germany.

3. Department of Molecular Structural Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany.

4. Department of Molecular and Cellular Biology, Section of Biology, University of Geneva, 1211 Geneva, Switzerland.

5. Human Technopole, 20157 Milan, Italy.

6. Max Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany.

7. Department of Biochemistry and Center for Structural Biology, Vanderbilt University, Nashville, TN 37232, USA.

8. Cell Biology and Electron Microscopy, University of Bayreuth, 95447 Bayreuth, Germany.

Abstract

The cilium is an antenna-like organelle that performs numerous cellular functions, including motility, sensing, and signaling. The base of the cilium contains a selective barrier that regulates the entry of large intraflagellar transport (IFT) trains, which carry cargo proteins required for ciliary assembly and maintenance. However, the native architecture of the ciliary base and the process of IFT train assembly remain unresolved. In this work, we used in situ cryo–electron tomography to reveal native structures of the transition zone region and assembling IFT trains at the ciliary base in Chlamydomonas . We combined this direct cellular visualization with ultrastructure expansion microscopy to describe the front-to-back stepwise assembly of IFT trains: IFT-B forms the backbone, onto which bind IFT-A, dynein-1b, and finally kinesin-2 before entry into the cilium.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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