A Yeast t-SNARE Involved in Endocytosis

Author:

Séron Karin1,Tieaho Ville2,Prescianotto-Baschong Cristina3,Aust Thomas3,Blondel Marie-Odile1,Guillaud Philippe1,Devilliers Ginette1,Rossanese Olivia W.4,Glick Benjamin S.4,Riezman Howard3,Keränen Sirkka2,Haguenauer-Tsapis Rosine1

Affiliation:

1. Institut Jacques Monod, Centre National de la Recherche Scientifique-UMRC7592, Université Paris 7-Denis Diderot, Paris Cedex 05, France;

2. VTT Biotechnology and Food Research, FIN-02044 VTT, Finland;

3. Biozentrum, University of Basel, CH-4056 Basel, Switzerland; and

4. Department of Molecular Genetics and Cell Biology, The University of Chicago, Chicago, Illinois 60637

Abstract

The ORF YOL018c (TLG2) of Saccharomyces cerevisiae encodes a protein that belongs to the syntaxin protein family. The proteins of this family, t-SNAREs, are present on target organelles and are thought to participate in the specific interaction between vesicles and acceptor membranes in intracellular membrane trafficking. TLG2 is not an essential gene, and its deletion does not cause defects in the secretory pathway. However, its deletion in cells lacking the vacuolar ATPase subunit Vma2p leads to loss of viability, suggesting that Tlg2p is involved in endocytosis. In tlg2Δ cells, internalization was normal for two endocytic markers, the pheromone α-factor and the plasma membrane uracil permease. In contrast, degradation of α-factor and uracil permease was delayed intlg2Δ cells. Internalization of positively charged Nanogold shows that the endocytic pathway is perturbed in the mutant, which accumulates Nanogold in primary endocytic vesicles and shows a greatly reduced complement of early endosomes. These results strongly suggest that Tlg2p is a t-SNARE involved in early endosome biogenesis.

Publisher

American Society for Cell Biology (ASCB)

Subject

Cell Biology,Molecular Biology

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