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pubmed-article:10385523pubmed:abstractTextVacuole SNAREs, including the t-SNAREs Vam3p and Vam7p and the v-SNARE Nyv1p, are found in a multisubunit "cis" complex on isolated organelles. We now identify the v-SNAREs Vti1p and Ykt6p by mass spectrometry as additional components of the immunoisolated vacuolar SNARE complex. Immunodepletion of detergent extracts with anti-Vti1p removes all the Ykt6p that is in a complex with Vam3p, immunodepletion with anti-Ykt6p removes all the Vti1p that is complexed with Vam3p, and immunodepletion with anti-Nyv1p removes all the Ykt6p in complex with other SNAREs, demonstrating that they are all together in the same cis multi-SNARE complex. After priming, which disassembles the cis-SNARE complex, antibodies to any of the five SNARE proteins still inhibit the fusion assay until the docking stage is completed, suggesting that each SNARE plays a role in docking. Furthermore, vti1 temperature-sensitive alleles cause a synthetic fusion-defective phenotype in our reaction. Our data show that vacuole-vacuole fusion requires a cis-SNARE complex of five SNAREs, the t-SNAREs Vam3p and Vam7p and the v-SNAREs Nyv1p, Vti1p, and Ykt6p.lld:pubmed
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pubmed-article:10385523pubmed:authorpubmed-author:WicknerWWlld:pubmed
pubmed-article:10385523pubmed:authorpubmed-author:StevensT HTHlld:pubmed
pubmed-article:10385523pubmed:authorpubmed-author:JensenO NONlld:pubmed
pubmed-article:10385523pubmed:authorpubmed-author:MargolisNNlld:pubmed
pubmed-article:10385523pubmed:authorpubmed-author:von...lld:pubmed
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