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Skp1p and the F-Box Protein Rcy1p Form a Non-SCF Complex Involved in Recycling of the SNARE Snc1p in Yeast

Galan, Jean-Marc and Wiederkehr, Andreas and Seol, Jae Hong and Haugenauer-Tsapis, Rosine and Deshaies, Raymond J. and Riezman, Howard and Peter, Matthias (2001) Skp1p and the F-Box Protein Rcy1p Form a Non-SCF Complex Involved in Recycling of the SNARE Snc1p in Yeast. Molecular and Cellular Biology, 21 (9). pp. 3105-3117. ISSN 0270-7306. PMCID PMC86938.

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Skp1p-cullin-F-box protein (SCF) complexes are ubiquitin-ligases composed of a core complex including Skp1p, Cdc53p, Hrt1p, the E2 enzyme Cdc34p, and one of multiple F-box proteins which are thought to provide substrate specificity to the complex. Here we show that the F-box protein Rcy1p is required for recycling of the v-SNARE Snc1p in Saccharomyces cerevisiae. Rcy1p localized to areas of polarized growth, and this polarized localization required its CAAX box and an intact actin cytoskeleton. Rcy1p interacted with Skp1p in vivo in an F-box-dependent manner, and both deletion of its F box and loss of Skp1p function impaired recycling. In contrast, cells deficient in Cdc53p, Hrt1p, or Cdc34p did not exhibit recycling defects. Unlike the case for F-box proteins that are known to participate in SCF complexes, degradation of Rcy1p required neither its F box nor functional 26S proteasomes or other SCF core subunits. Importantly, Skp1p was the only major partner that copurified with Rcy1p. Our results thus suggest that a complex composed of Rcy1p and Skp1p but not other SCF components may play a direct role in recycling of internalized proteins.

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Deshaies, Raymond J.0000-0002-3671-9354
Additional Information:© 2001, American Society for Microbiology. Received 31 October 2000/Returned for modification 15 December 2000/Accepted 1 February 2001 We thank M. Lewis, H. Pelham, S. Elledge, and P. Silver for providing antibodies, plasmids, and strains. We are grateful to M. Blondel and W. Krek for helpful suggestions, to N. Perrinjaquet and P. Pagé for excellent technical assistance, to members of our laboratories for discussion, and to R. Iggo for critical reading of the manuscript. Special thanks go to S. Avaro and C. Lafourcade for help and advice during the early stages of this work. J.-M.G. is supported by an EMBO postdoctoral fellowship; M.P. is supported by the Swiss National Science Foundation, the Swiss Cancer League, and a Helmut Horten Incentive Award.
Funding AgencyGrant Number
European Molecular Biology Organization (EMBO)UNSPECIFIED
Swiss National Science Foundation (SNSF)UNSPECIFIED
Swiss Cancer LeagueUNSPECIFIED
Helmut Horten Incentive AwardUNSPECIFIED
Issue or Number:9
PubMed Central ID:PMC86938
Record Number:CaltechAUTHORS:GAImcb01
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Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:4895
Deposited By: Archive Administrator
Deposited On:12 Sep 2006
Last Modified:02 Oct 2019 23:17

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