Abstract
The small GTPase Rab6a is involved in the regulation of membrane traffic from the Golgi apparatus towards the endoplasmic reticulum (ER) in a coat complex coatomer protein I (COPI)-independent pathway. Here, we used a yeast two-hybrid approach to identify binding partners of Rab6a. In particular, we identified the dynein-dynactin-binding protein Bicaudal-D1 (BICD1), one of the two mammalian homologues of Drosophila Bicaudal-D. BICD1 and BICD2 colocalize with Rab6a on the trans-Golgi network (TGN) and on cytoplasmic vesicles, and associate with Golgi membranes in a Rab6-dependent manner. Overexpression of BICD1 enhances the recruitment of dynein-dynactin to Rab6a-containing vesicles. Conversely, overexpression of the carboxy-terminal domain of BICD, which can interact with Rab6a but not with cytoplasmic dynein, inhibits microtubule minus-end-directed movement of green fluorescent protein (GFP)-Rab6a vesicles and induces an accumulation of Rab6a and COPI-independent ER cargo in peripheral structures. These data suggest that coordinated action between Rab6a, BICD and the dynein-dynactin complex controls COPI-independent Golgi-ER transport.
Original language | English |
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Pages (from-to) | 986-92 |
Number of pages | 7 |
Journal | Nature Cell Biology |
Volume | 4 |
Issue number | 12 |
DOIs | |
Publication status | Published - Dec 2002 |
Keywords
- Animals
- Biological Transport
- COS Cells
- Coat Protein Complex I
- Coatomer Protein
- Drosophila Proteins
- Dyneins
- Endoplasmic Reticulum
- Golgi Apparatus
- HeLa Cells
- Humans
- Microtubule-Associated Proteins
- Molecular Motor Proteins
- Molecular Sequence Data
- rab GTP-Binding Proteins