Abstract
The incubation of HeLa cells at 15°C induces the formation of Golgi tubules, which contain glycosylation enzymes but neither cargo nor matrix proteins. We now show by immunofluorescence and immunoelectron microscopy that these tubules are enriched in a specific set of SNARE and Rab proteins mediating intra-Golgi transport (Gos28, GS15 and Rab6) but excluded others involved in endoplasmic reticulum-Golgi trafficking (Sec22, membrin, Rab 1 and Rab2). In vivo experiments using cyan fluorescent protein-tagged galactosyltransferase showed that most of these tubules are dynamic transient membranes that grow to the cell periphery but then decrease until disappearing into the perinuclear area. Interestingly, in experiments carried out with cells cultured under physiological conditions, Golgi tubules containing Gos28, GS15, Rab6 and glycosylation enzymes and showing in vivo dynamics identical to that detected in low-temperature-cultured cells were observed. Together, our results support that low-temperature-induced tubules may be representatives of the carriers mediating intra-Golgi recycling of enzymes. © 2007 The Authors Journal compilation.
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Martínez-Alonso, E., Ballesta, J., & Martínez-Menárguez, J. A. (2007). Low-temperature-induced Golgi tubules are transient membranes enriched in molecules regulating intra-Golgi transport. Traffic, 8(4), 359–368. https://doi.org/10.1111/j.1600-0854.2006.00533.x
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