ArticleBMC cell biology2003
Chlamydomonas fla mutants reveal a link between deflagellation and intraflagellar transport.
Article in BMC cell biology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.
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Who cites it
23 citing papers in PubMed.
- Primary cilium disassembly - from mechanisms to roles in physiology and disease.Journal of cell science · 2026Review
- Distribution and bulk flow analyses of the intraflagellar transport (IFT) motor kinesin-2 support an "on-demand" model for Chlamydomonas ciliary length control.Cytoskeleton (Hoboken, N.J.) · 2024Article
- Review
- The retrograde IFT dynein is required for normal function of diverse mechanosensory cilia inFrontiers in molecular neuroscience · 2023Article
- Primary cilium loss in mammalian cells occurs predominantly by whole-cilium shedding.PLoS biology · 2019Article
- Acute Inhibition of Heterotrimeric Kinesin-2 Function Reveals Mechanisms of Intraflagellar Transport in Mammalian Cilia.Current biology : CB · 2019Article
- Mechanism of ciliary disassembly.Cellular and molecular life sciences : CMLS · 2016Review
- New mutations in flagellar motors identified by whole genome sequencing in Chlamydomonas.Cilia · 2013Article
- Calmodulin activation of Aurora-A kinase (AURKA) is required during ciliary disassembly and in mitosis.Molecular biology of the cell · 2012Article
- A chemical screen identifies class a g-protein coupled receptors as regulators of cilia.ACS chemical biology · 2012Article
- Stages of ciliogenesis and regulation of ciliary length.Differentiation; research in biological diversity · 2012Review
- Centrioles are freed from cilia by severing prior to mitosis.Cytoskeleton (Hoboken, N.J.) · 2010Article
- Intraflagellar transport particle size scales inversely with flagellar length: revisiting the balance-point length control model.The Journal of cell biology · 2009Article
- A microtubule depolymerizing kinesin functions during both flagellar disassembly and flagellar assembly in Chlamydomonas.Proceedings of the National Academy of Sciences of the United States of America · 2009Article
- Katanin knockdown supports a role for microtubule severing in release of basal bodies before mitosis in Chlamydomonas.Molecular biology of the cell · 2009Article
- Primary cilia and the cell cycle.Methods in cell biology · 2009Article
- Members of the NIMA-related kinase family promote disassembly of cilia by multiple mechanisms.Molecular biology of the cell · 2006Article
- Intraflagellar transport (IFT) during assembly and disassembly of Chlamydomonas flagella.The Journal of cell biology · 2005Article
- Cilia and the cell cycle?The Journal of cell biology · 2005Review
- The FLA3 KAP subunit is required for localization of kinesin-2 to the site of flagellar assembly and processive anterograde intraflagellar transport.Molecular biology of the cell · 2005Article
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2 authors.
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No grant is acknowledged in the PubMed record.
Abstract
backgroundCilia and flagella are often lost in anticipation of mitosis or in response to stress. There are two ways that a cell can lose its flagella: resorption or deflagellation. Deflagellation involves active severing of the axoneme at the base of the flagellum; this process is defective in Chlamydomonas fa mutants. In contrast, resorption has been thought to occur as a consequence of constitutive disassembly at the tip in the absence of continued assembly, which requires intraflagellar transport (IFT). Chlamydomonas fla mutants are unable to build and maintain flagella due to defects in IFT.
resultsfla10 cells, which are defective in kinesin-II, the anterograde IFT motor, resorb their flagella at the restrictive temperature (33 degrees C), as previously reported. We find that in standard media containing approximately 300 microM calcium, fla10 cells lose flagella by deflagellation at 33 degrees C. This temperature-induced deflagellation of a fla mutant is not predicted by the IFT-based model for flagellar length control. Other fla mutants behave similarly, losing their flagella by deflagellation instead of resorption, if adequate calcium is available. These data suggest a new model whereby flagellar resorption involves active disassembly at the base of the flagellum via a mechanism with components in common with the severing machinery of deflagellation. As predicted by this model, we discovered that deflagellation stimuli induce resorption if deflagellation is blocked either by mutation in a FA gene or by lack of calcium. Further support for this model comes from our discovery that fla10-fa double mutants resorb their flagella more slowly than fla10 mutants.
conclusionsDeflagellation of the fla10 mutant at the restrictive temperature is indicative of an active disassembly signal, which can manifest as either resorption or deflagellation. We propose that when IFT is halted by either an inactivating mutation or a cellular signal, active flagellar disassembly is initiated. This active disassembly is distinct from the constitutive disassembly which plays a role in flagellar length control.
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