Sec 15 interacts with Rab 11 via a novel domain and affects Rab 11 localization in vivo

Sec15, a component of the exocyst, recognizes vesicle-associated Rab GTPases, helps target transport vesicles to the budding sites in yeast and is thought to recruit other exocyst proteins. Here we report the characterization of a 35-kDa fragment that comprises most of the C-terminal half of Drosophila melanogaster Sec15. This C-terminal domain was found to bind a subset of Rab GTPases, especially Rab11, in a GTP-dependent manner. We also provide evidence that in fly photoreceptors Sec15 colocalizes with Rab11 and that loss of Sec15 affects rhabdomere morphology. Determination of the 2.5-Å crystal structure of the C-terminal domain revealed a novel fold consisting of ten a-helices equally distributed between two subdomains (N and C subdomains). We show that the C subdomain, mainly via a single helix, is sufficient for Rab binding.

[1]  Sunil Q. Mehta,et al.  Sec15, a component of the exocyst, promotes notch signaling during the asymmetric division of Drosophila sensory organ precursors. , 2005, Developmental cell.

[2]  Sunil Q. Mehta,et al.  Mutations in Drosophila sec15 Reveal a Function in Neuronal Targeting for a Subset of Exocyst Components , 2005, Neuron.

[3]  D. Ready,et al.  Rab11 mediates post-Golgi trafficking of rhodopsin to the photosensitive apical membrane of Drosophila photoreceptors , 2005, Development.

[4]  C. Mitchell,et al.  Sec15 Is an Effector for the Rab11 GTPase in Mammalian Cells* , 2004, Journal of Biological Chemistry.

[5]  Guangpu Li,et al.  Structural basis of Rab5-Rabaptin5 interaction in endocytosis , 2004, Nature Structural &Molecular Biology.

[6]  J. Cherfils,et al.  The Structural GDP/GTP Cycle of Rab11 Reveals a Novel Interface Involved in the Dynamics of Recycling Endosomes* , 2004, Journal of Biological Chemistry.

[7]  C. Yeaman,et al.  Mechanism of recruiting Sec6/8 (exocyst) complex to the apical junctional complex during polarization of epithelial cells , 2004, Journal of Cell Science.

[8]  I. Mellman,et al.  The Rab8 GTPase selectively regulates AP-1B–dependent basolateral transport in polarized Madin-Darby canine kidney cells , 2003, The Journal of cell biology.

[9]  S. Munro,et al.  Structural basis for Arl1-dependent targeting of homodimeric GRIP domains to the Golgi apparatus. , 2003, Molecular cell.

[10]  M. N. Vyas,et al.  Crystal structure of M tuberculosis ABC phosphate transport receptor: specificity and charge compensation dominated by ion-dipole interactions. , 2003, Structure.

[11]  M. Fukuda Distinct Rab Binding Specificity of Rim1, Rim2, Rabphilin, and Noc2 , 2003, The Journal of Biological Chemistry.

[12]  Alan R. Saltiel,et al.  The exocyst complex is required for targeting of Glut4 to the plasma membrane by insulin , 2003, Nature.

[13]  Mala Murthy,et al.  Mutations in the Exocyst Component Sec5 Disrupt Neuronal Membrane Traffic, but Neurotransmitter Release Persists , 2003, Neuron.

[14]  Zhaohong Yi,et al.  The Rab27a/Granuphilin Complex Regulates the Exocytosis of Insulin-Containing Dense-Core Granules , 2002, Molecular and Cellular Biology.

[15]  R. Cohen,et al.  Rab11 polarization of the Drosophila oocyte: a novel link between membrane trafficking, microtubule organization, and oskar mRNA localization and translation. , 2002, Development.

[16]  J. Pereira-Leal,et al.  Evolution of the Rab family of small GTP-binding proteins. , 2001, Journal of molecular biology.

[17]  N. Segev Ypt and Rab GTPases: insight into functions through novel interactions. , 2001, Current opinion in cell biology.

[18]  Irving E. Vega,et al.  The Exocyst Complex Associates with Microtubules to Mediate Vesicle Targeting and Neurite Outgrowth , 2001, The Journal of Neuroscience.

[19]  R. Buscà,et al.  Rab27a: A key to melanosome transport in human melanocytes. , 2001, The Journal of cell biology.

[20]  A. Chakraborty,et al.  Small Gtpase rab3A is associated with melanosomes in melanoma cells. , 2000, Pigment cell research.

[21]  N. Copeland,et al.  A mutation in Rab27a causes the vesicle transport defects observed in ashen mice. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[22]  A. Fischer,et al.  Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome , 2000, Nature Genetics.

[23]  P. Verstreken,et al.  A Genome-Wide Search for Synaptic Vesicle Cycle Proteins in Drosophila , 2000, Neuron.

[24]  P. Novick,et al.  The exocyst is an effector for Sec4p, targeting secretory vesicles to sites of exocytosis , 1999, The EMBO journal.

[25]  A. Brunger,et al.  Structural Basis of Rab Effector Specificity Crystal Structure of the Small G Protein Rab3A Complexed with the Effector Domain of Rabphilin-3A , 1999, Cell.

[26]  R J Read,et al.  Crystallography & NMR system: A new software suite for macromolecular structure determination. , 1998, Acta crystallographica. Section D, Biological crystallography.

[27]  R. Scheller,et al.  Sec6/8 Complex Is Recruited to Cell–Cell Contacts and Specifies Transport Vesicle Delivery to the Basal-Lateral Membrane in Epithelial Cells , 1998, Cell.

[28]  Peter Novick,et al.  Sec3p Is a Spatial Landmark for Polarized Secretion in Budding Yeast , 1998, Cell.

[29]  Philippe Soriano,et al.  The secretory protein Sec8 is required for paraxial mesoderm formation in the mouse. , 1997, Developmental biology.

[30]  H. Horvitz,et al.  Caenorhabditis elegans rab-3 Mutant Synapses Exhibit Impaired Function and Are Partially Depleted of Vesicles , 1997, The Journal of Neuroscience.

[31]  Thomas C. Südhof,et al.  Rim is a putative Rab3 effector in regulating synaptic-vesicle fusion , 1997, Nature.

[32]  P. Novick,et al.  The Exocyst is a multiprotein complex required for exocytosis in Saccharomyces cerevisiae. , 1996, The EMBO journal.

[33]  C. Wollheim,et al.  Expression, localization and functional role of small GTPases of the Rab3 family in insulin-secreting cells. , 1996, Journal of cell science.

[34]  J. H. Chou,et al.  Rab3 reversibly recruits rabphilin to synaptic vesicles by a mechanism analogous to raf recruitment by ras. , 1996, The EMBO journal.

[35]  C. Sander,et al.  Dali: a network tool for protein structure comparison. , 1995, Trends in biochemical sciences.

[36]  P. Novick,et al.  Sec6, Sec8, and Sec15 are components of a multisubunit complex which localizes to small bud tips in Saccharomyces cerevisiae , 1995, The Journal of cell biology.

[37]  R. Scheller,et al.  The molecular machinery for secretion is conserved from yeast to neurons. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[38]  J. Zou,et al.  Improved methods for building protein models in electron density maps and the location of errors in these models. , 1991, Acta crystallographica. Section A, Foundations of crystallography.

[39]  T. Südhof,et al.  rab3 is a small GTP-binding protein exclusively localized to synaptic vesicles. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[40]  S. Zipursky,et al.  Analysis of mutants in chaoptin, a photoreceptor cell-specific glycoprotein in Drosophila, reveals its role in cellular morphogenesis , 1988, Cell.

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

[42]  John B. Anderson,et al.  CDD: a curated Entrez database of conserved domain alignments , 2003, Nucleic Acids Res..

[43]  Z. Otwinowski,et al.  Processing of X-ray diffraction data collected in oscillation mode. , 1997, Methods in enzymology.

[44]  D. Deretic Rab proteins and post‐Golgi trafficking of rhodopsin in photoreceptor cells , 1997, Electrophoresis.