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

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Jordan,  Mareike A
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Viar,  Gonzalo Alvarez
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Pigino,  Gaia
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Citation

Hoek, H. v. d., Klena, N., Jordan, M. A., Viar, G. A., Righetto, R. D., Schaffer, M., et al. (2022). In situ architecture of the ciliary base reveals the stepwise assembly of intraflagellar transport trains. Science (New York, N.Y.), 377(6605), 543-548. doi:10.1126/science.abm6704.


Cite as: https://hdl.handle.net/21.11116/0000-000C-7453-4
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.