Phosphorylation of the C Terminus of RHD3 Has a Critical Role in Homotypic ER Membrane Fusion in Arabidopsis

• Published in: Plant physiology (Bethesda) 2016-02, Vol.170 (2), p.867-880
• Main Authors: Ueda, Haruko, Yokota, Etsuo, Kuwata, Keiko, Kutsuna, Natsumaro, Mano, Shoji, Shimada, Tomoo, Tamura, Kentaro, Stefano, Giovanni, Fukao, Yoichiro, Brandizzi, Federica, Shimmen, Teruo, Nishimura, Mikio, Hara-Nishimura, Ikuko
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Arabidopsis - metabolism; Arabidopsis Proteins - chemistry; Arabidopsis Proteins - metabolism; Biological Assay; CELL BIOLOGY; Endoplasmic Reticulum - metabolism; Endoplasmic Reticulum - ultrastructure; GTP-Binding Proteins - chemistry; GTP-Binding Proteins - metabolism; Guanosine Triphosphate - metabolism; Intracellular Membranes - metabolism; Intracellular Membranes - ultrastructure; Membrane Fusion; Molecular Sequence Data; Phosphopeptides - chemistry; Phosphopeptides - metabolism; Phosphorylation; Protein Kinases - metabolism; Protein Multimerization; Serine - metabolism
• ISSN: 0032-0889; 1532-2548
• DOI: 10.1104/pp.15.01172

The endoplasmic reticulum (ER) consists of dynamically changing tubules and cisternae. In animals and yeast, homotypic ER membrane fusion is mediated by fusogens (atlastin and Sey1p, respectively) that are membrane-associated dynamin-like GTPases. In Arabidopsis (Arabidopsis thaliana), another dynamin-like GTPase, ROOT HAIR DEFECTIVE3 (RHD3), has been proposed as an ER membrane fusogen, but direct evidence is lacking. Here, we show that RHD3 has an ER membrane fusion activity that is enhanced by phosphorylation of its C terminus. The ER network was RHD3-dependently reconstituted from the cytosol and microsome fraction of tobacco (Nicotiana tabacum) cultured cells by exogenously adding GTP, ATP, and F-actin.We next established an in vitro assay system of ER tubule formation with Arabidopsis ER vesicles, in which addition of GTP caused ER sac formation from the ER vesicles. Subsequent application of a shearing force to this system triggered the formation of tubules from the ER sacs in an RHD-dependent manner. Unexpectedly, in the absence of a shearing force, Ser/Thr kinase treatment triggered RHD3-dependent tubule formation. Mass spectrometry showed that RHD3 was phosphorylated at multiple Ser and Thr residues in the C terminus. An antibody against the RHD3 C-terminal peptide abolished kinase-triggered tubule formation.When the Ser cluster was deleted or when the Ser residues were replaced with Ala residues, kinase treatment had no effect on tubule formation. Kinase treatment induced the oligomerization of RHD3. Neither phosphorylation-dependentmodulation of membrane fusion nor oligomerization has been reported for atlastin or Sey1p. Taken together, we propose that phosphorylation-stimulated oligomerization of RHD3 enhances ER membrane fusion to formthe ER network.