期刊
BIOCHEMICAL JOURNAL
卷 419, 期 -, 页码 229-236出版社
PORTLAND PRESS LTD
DOI: 10.1042/BJ20081973
关键词
membrane traffic; recycling; Saccharomyces cerevisiae; soluble N-ethlylmaleimide-sensitive fusion protein attachment protein receptor (SNARE); transport vesicle; TVP23 gene
SNARE (soluble N-ethylmaleimide-sensitive fusion protein-attachment protein receptor) proteins contribute to Specific recognition between transport vesicles and target membranes and are required for fusion of membranes. The SNARE Vti1p is required for several transport steps between late Golgi, endosomes and the vacuole in the yeast Saccharomyces cerevisiae. Here, we identified the late Golgi membrane protein TVP23 as a multicopy Suppressor of the growth defect in vti1-2 cells. By contrast, the growth defect in vti1-11 cells was not suppressed by TVP23 overexpression. Deletion of TVP23 aggravated the growth defect in vti1-2 cells. Genetic interactions between TVP23 and vti1-2 were not found in transport from the late Golgi via the late endosome to the vacuole or in transport from file Golgi directly to the vacuole. These results Suggest that Tvp23p is not involved in forward transport from the late Golgi. Therefore retrograde traffic to the late Golgi was analysed. vti1-2 cells accumulated GFP (green fluorescent protein)-Snc 1p within the cell, indicating that retrograde transport From tire early endosome to the late Golgi Was defective in these cells. Deletion of TVP23 in vti1-2 cells resulted in a synthetic defect in GFP-Snc 1p recycling, whereas tvp23 Delta cells had a slight defect. These results indicate that Tvp23p performs a partially redundant function in retrograde transport from the early endosome to the late Golgi. This transport step was unaffected in vit1-11 cells. providing an explanation for the allele-specific multicopy suppression by TVP23.
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