Insights into degradation and targeting of the photoreceptor channelrhodopsin-1.

ARL11 CEP1 Calpain Chlamydomonas cilia cysteine proteases extracellular vesicles photoreceptor endocytosis phototaxis phototropin

Journal

Plant, cell & environment
ISSN: 1365-3040
Titre abrégé: Plant Cell Environ
Pays: United States
ID NLM: 9309004

Informations de publication

Date de publication:
27 Jun 2024
Historique:
revised: 05 06 2024
received: 20 03 2024
accepted: 11 06 2024
medline: 27 6 2024
pubmed: 27 6 2024
entrez: 27 6 2024
Statut: aheadofprint

Résumé

In Chlamydomonas, the directly light-gated, plasma membrane-localized cation channels channelrhodopsins ChR1 and ChR2 are the primary photoreceptors for phototaxis. Their targeting and abundance is essential for optimal movement responses. However, our knowledge how Chlamydomonas achieves this is still at its infancy. Here we show that ChR1 internalization occurs via light-stimulated endocytosis. Prior or during endocytosis ChR1 is modified and forms high molecular mass complexes. These are the solely detectable ChR1 forms in extracellular vesicles and their abundance therein dynamically changes upon illumination. The ChR1-containing extracellular vesicles are secreted via the plasma membrane and/or the ciliary base. In line with this, ciliogenesis mutants exhibit increased ChR1 degradation rates. Further, we establish involvement of the cysteine protease CEP1, a member of the papain-type C1A subfamily. ΔCEP1-knockout strains lack light-induced ChR1 degradation, whereas ChR2 degradation was unaffected. Low light stimulates CEP1 expression, which is regulated via phototropin, a SPA1 E3 ubiquitin ligase and cyclic AMP. Further, mutant and inhibitor analyses revealed involvement of the small GTPase ARL11 and SUMOylation in ChR1 targeting to the eyespot and cilia. Our study thus defines the degradation pathway of this central photoreceptor of Chlamydomonas and identifies novel elements involved in its homoeostasis and targeting.

Identifiants

pubmed: 38935876
doi: 10.1111/pce.15017
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Deutsche Forschungsgemeinschaft
ID : 468480235
Organisme : Deutsche Forschungsgemeinschaft
ID : 426566805
Organisme : Deutsche Forschungsgemeinschaft
ID : 221545957

Informations de copyright

© 2024 The Author(s). Plant, Cell & Environment published by John Wiley & Sons Ltd.

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Auteurs

Michaela Wolfram (M)

Department of Biology, Cell Biology, Friedrich-Alexander Universität, Erlangen-Nürnberg, Germany.

Arne Greif (A)

Department of Biology, Cell Biology, Friedrich-Alexander Universität, Erlangen-Nürnberg, Germany.

Olga Baidukova (O)

Institute of Biology, Experimental Biophysics, Humboldt Universität, Berlin, Germany.

Hildegard Voll (H)

Department of Biology, Cell Biology, Friedrich-Alexander Universität, Erlangen-Nürnberg, Germany.

Sandra Tauber (S)

Department of Biology, Cell Biology, Friedrich-Alexander Universität, Erlangen-Nürnberg, Germany.

Jana Lindacher (J)

Department of Biology, Cell Biology, Friedrich-Alexander Universität, Erlangen-Nürnberg, Germany.

Peter Hegemann (P)

Institute of Biology, Experimental Biophysics, Humboldt Universität, Berlin, Germany.

Georg Kreimer (G)

Department of Biology, Cell Biology, Friedrich-Alexander Universität, Erlangen-Nürnberg, Germany.

Classifications MeSH