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The SNARE Ykt6 mediates protein palmitoylation during an early stage of homotypic vacuole fusion.

ABSTRACT: The NSF homolog Sec18 initiates fusion of yeast vacuoles by disassembling cis-SNARE complexes during priming. Sec18 is also required for palmitoylation of the fusion factor Vac8, although the acylation machinery has not been identified. Here we show that the SNARE Ykt6 mediates Vac8 palmitoylation and acts during a novel subreaction of vacuole fusion. This subreaction is controlled by a Sec17-independent function of Sec18. Our data indicate that Ykt6 presents Pal-CoA via its N-terminal longin domain to Vac8, while transfer to Vac8's SH4 domain occurs spontaneously and not enzymatically. The conservation of Ykt6 and its localization to several organelles suggest that its acyltransferase activity may also be required in other intracellular fusion events.

SUBMITTER: Dietrich LE

PROVIDER: S-EPMC1271655 | biostudies-literature | 2004 Jan

REPOSITORIES: biostudies-literature

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The SNARE Ykt6 mediates protein palmitoylation during an early stage of homotypic vacuole fusion.

Dietrich Lars E P LE Gurezka Rolf R Veit Michael M Ungermann Christian C

The EMBO journal 20031211 1

The NSF homolog Sec18 initiates fusion of yeast vacuoles by disassembling cis-SNARE complexes during priming. Sec18 is also required for palmitoylation of the fusion factor Vac8, although the acylation machinery has not been identified. Here we show that the SNARE Ykt6 mediates Vac8 palmitoylation and acts during a novel subreaction of vacuole fusion. This subreaction is controlled by a Sec17-independent function of Sec18. Our data indicate that Ykt6 presents Pal-CoA via its N-terminal longin do ...[more]

PMID: 14685280

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