The molecular mechanisms underlying early/recycling endosomes-to-TGN transport are still not understood. We identified interactions between the TGN-localized putative t-SNAREs syntaxin 6, syntaxin 16, and Vti1a, and two early/recycling endosomal v-SNAREs, VAMP3/cellubrevin, and VAMP4. Using a novel permeabilized cell system, these proteins were functionally implicated in the post-Golgi retrograde transport step. The function of Rab6a' was also required, whereas its closely related isoform, Rab6a, has previously been implicated in Golgi-to-endoplasmic reticulum transport. Thus, our study shows that membrane exchange between the early endocytic and the biosynthetic/secretory pathways involves specific components of the Rab and SNARE machinery, and suggests that retrograde transport between early/recycling endosomes and the endoplasmic reticulum is critically dependent on the sequential action of two members of the Rab6 subfamily.
Early/recycling endosomes-to-TGN transport involves two SNARE complexes and a Rab6 isoform
F. Mallard and B.L. Tang contributed equally to this work.
W. Hong, B. Goud, and L. Johannes were principal investigators.
Abbreviations used in this paper: EE, early endosome; NEM, N-ethylmaleimide; NSF, NEM-sensitive soluble factor; PAPS, 3′-phosphoadenosine 5′-phosphosulfate; RE, recycling endosome; SLO, streptolysin O; SNAP, soluble NSF attachment protein; SNARE, SNAP receptor; STxB, Shiga toxin; Syn, syntaxin; TeNT, tetanus neurotoxin; TGN, trans-Golgi network; VAMP, vesicle associated membrane protein.
Frédéric Mallard, Bor Luen Tang, Thierry Galli, Danièle Tenza, Agnès Saint-Pol, Xu Yue, Claude Antony, Wanjin Hong, Bruno Goud, Ludger Johannes; Early/recycling endosomes-to-TGN transport involves two SNARE complexes and a Rab6 isoform . J Cell Biol 18 February 2002; 156 (4): 653–664. doi: https://doi.org/10.1083/jcb.200110081
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