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Ca 2+ elevations disrupt interactions between intraflagellar transport and the flagella membrane in Chlamydomonas

Ca 2+ elevations disrupt interactions between intraflagellar transport and the flagella membrane in Chlamydomonas
Ca 2+ elevations disrupt interactions between intraflagellar transport and the flagella membrane in Chlamydomonas

The movement of ciliary membrane proteins is directed by transient interactions with intraflagellar transport (IFT) trains. The green alga Chlamydomonas has adapted this process for gliding motility, using retrograde IFT motors to move adhesive glycoproteins in the flagella membrane. Ca 2+signalling contributes directly to the gliding process, although uncertainty remains over the mechanism through which it acts. Here, we show that flagella Ca 2+elevations initiate the movement of paused retrograde IFT trains, which accumulate at the distal end of adherent flagella, but do not influence other IFT processes. On highly adherent surfaces, flagella exhibit highfrequency Ca 2+elevations that prevent the accumulation of paused retrograde IFT trains. Flagella Ca 2+elevations disrupt the IFTdependent movement of microspheres along the flagella membrane, suggesting that Ca 2+acts by directly disrupting an interaction between retrograde IFT trains and flagella membrane glycoproteins. By regulating the extent to which glycoproteins on the flagella surface interact with IFT motor proteins on the axoneme, this signalling mechanism allows precise control of traction force and gliding motility in adherent flagella.

Ca signalling, Chlamydomonas, Intraflagellar transport
0021-9533
Fort, Cecile
7d2c4022-da68-4eb8-8f03-01b6ed727dde
Collingridge, Peter
b7b8b73b-815d-48af-a637-c0b10f2b55b4
Brownlee, Colin
2af37c1c-b2bf-4832-8370-d9c35e7b3385
Wheeler, Glen
70608a88-45d6-4d42-968d-00e15c800fd5
Fort, Cecile
7d2c4022-da68-4eb8-8f03-01b6ed727dde
Collingridge, Peter
b7b8b73b-815d-48af-a637-c0b10f2b55b4
Brownlee, Colin
2af37c1c-b2bf-4832-8370-d9c35e7b3385
Wheeler, Glen
70608a88-45d6-4d42-968d-00e15c800fd5

Fort, Cecile, Collingridge, Peter, Brownlee, Colin and Wheeler, Glen (2021) Ca 2+ elevations disrupt interactions between intraflagellar transport and the flagella membrane in Chlamydomonas. Journal of Cell Science, 134 (3), [jcs253492]. (doi:10.1242/jcs.253492).

Record type: Article

Abstract

The movement of ciliary membrane proteins is directed by transient interactions with intraflagellar transport (IFT) trains. The green alga Chlamydomonas has adapted this process for gliding motility, using retrograde IFT motors to move adhesive glycoproteins in the flagella membrane. Ca 2+signalling contributes directly to the gliding process, although uncertainty remains over the mechanism through which it acts. Here, we show that flagella Ca 2+elevations initiate the movement of paused retrograde IFT trains, which accumulate at the distal end of adherent flagella, but do not influence other IFT processes. On highly adherent surfaces, flagella exhibit highfrequency Ca 2+elevations that prevent the accumulation of paused retrograde IFT trains. Flagella Ca 2+elevations disrupt the IFTdependent movement of microspheres along the flagella membrane, suggesting that Ca 2+acts by directly disrupting an interaction between retrograde IFT trains and flagella membrane glycoproteins. By regulating the extent to which glycoproteins on the flagella surface interact with IFT motor proteins on the axoneme, this signalling mechanism allows precise control of traction force and gliding motility in adherent flagella.

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More information

Accepted/In Press date: 5 January 2021
e-pub ahead of print date: 11 February 2021
Published date: February 2021
Keywords: Ca signalling, Chlamydomonas, Intraflagellar transport

Identifiers

Local EPrints ID: 449087
URI: http://eprints.soton.ac.uk/id/eprint/449087
ISSN: 0021-9533
PURE UUID: a6aa49e7-952b-4b27-9b2a-d14cee40562e

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Date deposited: 17 May 2021 16:32
Last modified: 16 Mar 2024 11:48

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Contributors

Author: Cecile Fort
Author: Peter Collingridge
Author: Colin Brownlee
Author: Glen Wheeler

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