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Role of the dynamin-related protein 2 family and SH3P2 in clathrin-mediated endocytosis in Arabidopsis thaliana.
Gnyliukh, Nataliia; Johnson, Alexander; Nagel, Marie-Kristin; Monzer, Aline; Babic, David; Hlavata, Annamaria; Alotaibi, Saqer S; Isono, Erika; Loose, Martin; Friml, Jirí.
Affiliation
  • Gnyliukh N; Institute of Science and Technology Austria (ISTA), 3400 Klosterneuburg, Austria.
  • Johnson A; Division of Anatomy, Centre for Anatomy & Cell Biology, Medical University of Vienna, 1090 Vienna, Austria.
  • Nagel MK; Department of Biology, University of Konstanz, 78464 Konstanz, Germany.
  • Monzer A; Institute of Science and Technology Austria (ISTA), 3400 Klosterneuburg, Austria.
  • Babic D; Institute of Science and Technology Austria (ISTA), 3400 Klosterneuburg, Austria.
  • Hlavata A; Institute of Science and Technology Austria (ISTA), 3400 Klosterneuburg, Austria.
  • Alotaibi SS; Department of Biotechnology, College of Science, Taif University, Taif 21944, Saudi Arabia.
  • Isono E; Department of Biology, University of Konstanz, 78464 Konstanz, Germany.
  • Loose M; Institute of Science and Technology Austria (ISTA), 3400 Klosterneuburg, Austria.
  • Friml J; Institute of Science and Technology Austria (ISTA), 3400 Klosterneuburg, Austria.
J Cell Sci ; 137(8)2024 04 15.
Article de En | MEDLINE | ID: mdl-38506228
ABSTRACT
Clathrin-mediated endocytosis (CME) is vital for the regulation of plant growth and development through controlling plasma membrane protein composition and cargo uptake. CME relies on the precise recruitment of regulators for vesicle maturation and release. Homologues of components of mammalian vesicle scission are strong candidates to be part of the scission machinery in plants, but the precise roles of these proteins in this process are not fully understood. Here, we characterised the roles of the plant dynamin-related protein 2 (DRP2) family (hereafter DRP2s) and SH3-domain containing protein 2 (SH3P2), the plant homologue to recruiters of dynamins, such as endophilin and amphiphysin, in CME by combining high-resolution imaging of endocytic events in vivo and characterisation of the purified proteins in vitro. Although DRP2s and SH3P2 arrive similarly late during CME and physically interact, genetic analysis of the sh3p123 triple mutant and complementation assays with non-SH3P2-interacting DRP2 variants suggest that SH3P2 does not directly recruit DRP2s to the site of endocytosis. These observations imply that, despite the presence of many well-conserved endocytic components, plants have acquired a distinct mechanism for CME.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Arabidopsis / Protéines d'Arabidopsis / Dynamines / Endocytose Langue: En Journal: J Cell Sci / J. cell. sci / Journal of cell science Année: 2024 Type de document: Article Pays d'affiliation: Autriche Pays de publication: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Arabidopsis / Protéines d'Arabidopsis / Dynamines / Endocytose Langue: En Journal: J Cell Sci / J. cell. sci / Journal of cell science Année: 2024 Type de document: Article Pays d'affiliation: Autriche Pays de publication: Royaume-Uni