A novel Golgi membrane protein is part of a GTPase‐binding protein complex involved in vesicle targeting

Through two‐hybrid interactions, protein affinity and localization studies, we previously identified Yip1p, an integral yeast Golgi membrane protein able to bind the Ras‐like GTPases Ypt1p and Ypt31p in their GDP‐bound conformation. In a further two‐hybrid screen, we identified Yif1p as an interacting factor of Yip1p. We show that Yif1p is an evolutionarily conserved, essential 35.5 kDa transmembrane protein that forms a tight complex with Yip1p on Golgi membranes. The hydrophilic N‐terminal half of Yif1p faces the cytosol, and according to two‐hybrid analyses can interact with the transport GTPases Ypt1p, Ypt31p and Sec4p, but in contrast to Yip1p, this interaction is dispensable for Yif1 protein function. Loss of Yif1p function in conditional‐lethal mutants results in a block of endoplasmic reticulum (ER)‐to‐Golgi protein transport and in an accumulation of ER membranes and 40–50 nm vesicles. Genetic analyses suggest that Yif1p acts downstream of Yip1p. It is inferred that Ypt GTPase binding to the Yip1p–Yif1p complex is essential for and precedes vesicle docking and fusion.

[1]  E. Craig,et al.  Genomic libraries and a host strain designed for highly efficient two-hybrid selection in yeast. , 1996, Genetics.

[2]  T. Südhof,et al.  Membrane fusion and exocytosis. , 1999, Annual review of biochemistry.

[3]  T. Südhof,et al.  A conformational switch in syntaxin during exocytosis: role of munc18 , 1999, The EMBO journal.

[4]  D. Robinson,et al.  Two GTPase isoforms, Ypt31p and Ypt32p, are essential for Golgi function in yeast. , 1996, The EMBO journal.

[5]  T. Ito,et al.  Toward a protein-protein interaction map of the budding yeast: A comprehensive system to examine two-hybrid interactions in all possible combinations between the yeast proteins. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[6]  J. Rayner,et al.  A novel SNARE complex implicated in vesicle fusion with the endoplasmic reticulum , 1997, The EMBO journal.

[7]  R. Sternglanz,et al.  Perinuclear localization of chromatin facilitates transcriptional silencing , 1998, Nature.

[8]  J. Mulholland,et al.  Two New Ypt GTPases Are Required for Exit From the Yeast trans-Golgi Compartment , 1997, The Journal of cell biology.

[9]  R. Schekman,et al.  Distinct sets of SEC genes govern transport vesicle formation and fusion early in the secretory pathway , 1990, Cell.

[10]  S. Pfeffer,et al.  Identification of a GDI displacement factor that releases endosomal Rab GTPases from Rab–GDI , 1997, The EMBO journal.

[11]  A. Wach PCR‐synthesis of marker cassettes with long flanking homology regions for gene disruptions in S. cerevisiae , 1996, Yeast.

[12]  D. Gallwitz,et al.  Specific binding to a novel and essential Golgi membrane protein (Yip1p) functionally links the transport GTPases Ypt1p and Ypt31p , 1998, The EMBO journal.

[13]  Reinhard Jahn,et al.  Crystal structure of a SNARE complex involved in synaptic exocytosis at 2.4 Å resolution , 1998, Nature.

[14]  H. Pelham,et al.  Localization of Sed5, a putative vesicle targeting molecule, to the cis- Golgi network involves both its transmembrane and cytoplasmic domains , 1994, The Journal of cell biology.

[15]  J. Rothman,et al.  Mechanisms of intracellular protein transport , 1994, Nature.

[16]  R. Schekman,et al.  Order of events in the yeast secretory pathway , 1981, Cell.

[17]  H. Riezman,et al.  The Golgi-localization of yeast Emp47p depends on its di-lysine motif but is not affected by the ret1-1 mutation in alpha-COP , 1995, The Journal of cell biology.

[18]  J. Rothman,et al.  A rab protein is required for the assembly of SNARE complexes in the docking of transport vesicles , 1994, Cell.

[19]  S. Hinton,et al.  New mutations in cloned Escherichia coli umuDC genes: novel phenotypes of strains carrying a umuC125 plasmid. , 1991, Mutation research.

[20]  S. Munro,et al.  Multi‐protein complexes in the cis Golgi of Saccharomyces cerevisiae with α‐1,6‐mannosyltransferase activity , 1998, The EMBO journal.

[21]  M. Götte,et al.  Vesicular transport: how many Ypt/Rab-GTPases make a eukaryotic cell? , 1997, Trends in biochemical sciences.

[22]  D. Gallwitz,et al.  High‐affinity binding of the yeast cis‐Golgi t‐SNARE, Sed5p, to wild‐type and mutant Sly1p, a modulator of transport vesicle docking , 1997, FEBS letters.

[23]  M. Zerial,et al.  The diversity of Rab proteins in vesicle transport. , 1997, Current opinion in cell biology.

[24]  R. Scheller,et al.  Nsec1 Binds a Closed Conformation of Syntaxin1a , 2000, The Journal of cell biology.

[25]  D. Gallwitz,et al.  Mutational analysis of the putative effector domain of the GTP‐binding Ypt1 protein in yeast suggests specific regulation by a novel GAP activity. , 1991, The EMBO journal.

[26]  C. Barlowe,et al.  Initial docking of ER‐derived vesicles requires Uso1p and Ypt1p but is independent of SNARE proteins , 1998, The EMBO journal.

[27]  C. Barlowe,et al.  Asymmetric Requirements for a Rab Gtpase and Snare Proteins in Fusion of Copii Vesicles with Acceptor Membranes , 2000, The Journal of cell biology.

[28]  D. Gallwitz,et al.  Identification and structure of four yeast genes (SLY) that are able to suppress the functional loss of YPT1, a member of the RAS superfamily , 1991, Molecular and cellular biology.

[29]  D. Gallwitz,et al.  Evidence for Overlapping and Distinct Functions in Protein Transport of Coat Protein Sec24p Family Members* , 2000, The Journal of Biological Chemistry.

[30]  S. Pfeffer Transport-vesicle targeting: tethers before SNAREs , 1999, Nature Cell Biology.

[31]  G. Fink,et al.  Methods in yeast genetics , 1979 .

[32]  R. Schekman,et al.  Identification of 23 complementation groups required for post-translational events in the yeast secretory pathway , 1980, Cell.

[33]  Ira Mellman,et al.  The Road Taken: Past and Future Review Foundations of Membrane Traffic , 2000 .