Cited by 78Cellular transport and secretionProtein Kinase Regulation and GTPase SignalingCellular Mechanics and Interactions

Citron-N is a neuronal Rho-associated protein involved in Golgi organization through actin cytoskeleton regulation

Camera, Paola, Da Silva, Jorge Santos, Griffiths, Gareth, Giuffrida, Maria Gabriella, Ferrara, Luciana, Schubert, Vanessa, Imarisio, Sara, Silengo, Lorenzo +2 more·2003·Nature Cell Biology

Abstract

The actin cytoskeleton is best known for its role during cellular morphogenesis. However, other evidence suggests that actin is also crucial for the organization and dynamics of membrane organelles such as endosomes and the Golgi complex. As in morphogenesis, the Rho family of small GTPases are key mediators of organelle actin-driven events, although it is unclear how these ubiquitously distributed proteins are activated to regulate actin dynamics in an organelle-specific manner. Here we show that the brain-specific Rho-binding protein Citron-N is enriched at, and associates with, the Golgi apparatus of hippocampal neurons in culture. Suppression of the whole protein or expression of a mutant form lacking the Rho-binding activity results in dispersion of the Golgi apparatus. In contrast, high intracellular levels induce localized accumulation of RhoA and filamentous actin, protecting the Golgi from the rupture normally produced by actin depolymerization. Biochemical and functional analyses indicate that Citron-N controls actin locally by assembling together the Rho effector ROCK-II and the actin-binding, neuron-specific, protein Profilin-IIa (PIIa). Together with recent data on endosomal dynamics, our results highlight the importance of organelle-specific Rho modulators for actin-dependent organelle organization and dynamics.

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Crossref · 10.1038/ncb1064

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  • Citron N maintains Golgi architecture by modulating local actin polymerization together with ROCK.

    “Citron N is enriched in dendritic spines and is associated with the endomembrane system, in particular the Golgi complex, where it maintains Golgi architecture by modulating local actin polymerization together with ROCK [126,127].”

    From RhoA Signaling in Neurodegenerative Diseases (2022) · cites this paper as [126]

  • Citron N is enriched in dendritic spines and is associated with the endomembrane system, in particular the Golgi complex.

    “Citron N is enriched in dendritic spines and is associated with the endomembrane system, in particular the Golgi complex, where it maintains Golgi architecture by modulating local actin polymerization together with ROCK [126,127].”

    From RhoA Signaling in Neurodegenerative Diseases (2022) · cites this paper as [126]

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Authors
Camera, P., Da Silva, J. S., Griffiths, G., Giuffrida, M. G., Ferrara, L., Schubert, V., Imarisio, S., Silengo, L., Dotti, C. G., & Di Cunto, F.
Affiliations
  • University of Turin (IT)
  • European Molecular Biology Laboratory (DE)
  • National Research Council (IT)
Corresponding author
Dotti, Carlos G.
Venue
Nature Cell Biology
Published
2003-11-02
Volume
5
Issue
12
Pages
1071-1078
ISSN
  • 1465-7392 (ISSN-L)
  • 1476-4679
OpenAlex
W2040577245
Cited by
78
References
1
Citations by year
2026: 3 · 2025: 2 · 2024: 1 · 2022: 2 · 2021: 4 · 2020: 3 · 2019: 5 · 2018: 2 · 2017: 4 · 2016: 3 · 2015: 6 · 2014: 5 · 2013: 2 · 2012: 3
FWCI
1.70
Type
journal article
Language
en
Open access
closed
Locations
  • Nature Cell Biology (publishedVersion)
  • PubMed (publishedVersion)
  • Institutional Research Information System University of Turin (University of Turin) (submittedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
Keywords
actin cytoskeleton, RhoA, ROCK2, hippocampal neurons, actin depolymerization, Rho GTPases
MeSH terms
Actins, Animals, Binding Sites, Cell Differentiation, Cells, Cultured, Contractile Proteins, Fetus, Golgi Apparatus, Hippocampus, Microfilament Proteins, Actin Cytoskeleton, Neurons, Protein Binding, Proteins, Protein Serine-Threonine Kinases, Cell Cycle Proteins, Protein Isoforms, rho GTP-Binding Proteins, rhoA GTP-Binding Protein, Intracellular Signaling Peptides and Proteins, Profilins, Rats, rho-Associated Kinases

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