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STAM adaptor proteins interact with COPII complexes and function in ER-to-Golgi trafficking.

Signal-transducing adaptor molecules (STAMs) are involved in growth factor and cytokine signaling as well as receptor degradation, and they form complexes with a number of endocytic proteins, including Hrs and Eps15. In this study, we demonstrate that STAM proteins also localize prominently to early exocytic compartments and profoundly regulate Golgi morphology. Upon STAM overexpression in cells, the Golgi apparatus becomes extensively fragmented and dispersed, but when STAMs are depleted, the Golgi becomes highly condensed. Under both scenarios, vesicular stomatitis virus G protein-green fluorescent protein trafficking to the plasma membrane is markedly inhibited, and recovery of Golgi morphology after Brefeldin A treatment is substantially impaired in STAM-depleted cells. Furthermore, STAM proteins interact with coat protein II (COPII) proteins, probably at endoplasmic reticulum (ER) exit sites, and Sar1 activity is required to maintain the localization of STAMs at discrete sites. Thus, in addition to their roles in signaling and endocytosis, STAMs function prominently in ER-to-Golgi trafficking, most likely through direct interactions with the COPII complex.

Pubmed ID: 19054391 RIS Download

Mesh terms: Adaptor Proteins, Signal Transducing | COP-Coated Vesicles | Endoplasmic Reticulum | Endosomal Sorting Complexes Required for Transport | Exocytosis | GTP-Binding Proteins | Gene Deletion | Gene Expression Regulation | Golgi Apparatus | HeLa Cells | Humans | Microscopy, Electron | Phenotype | Phosphoproteins | Protein Binding | Protein Transport | RNA, Small Interfering | Time Factors | Vesicular Transport Proteins

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Associated grants

  • Agency: Intramural NIH HHS, Id: Z01 NS002992-06

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