A novel direct interaction of endoplasmic reticulum with microtubules

The positioning and dynamics of organelles in eukaryotic cells critically depend on membrane–cytoskeleton interactions. Motor proteins play an important role in the directed movement of organelle membranes along microtubules, but the basic mechanism by which membranes stably interact with the microtubule cytoskeleton is largely unknown. Here we report that p63, an integral membrane protein of the reticular subdomain of the rough endoplasmic reticulum (ER), binds microtubules in vivo and in vitro. Overexpression of p63 in cell culture led to a striking rearrangement of the ER and to concomitant bundling of microtubules along the altered ER. Mutational analysis of the cytoplasmic domain of p63 revealed two determinants responsible for these changes: an ER rearrangement determinant near the N‐terminus and a central microtubule‐binding region. The two determinants function independently of one another as indicated by deletion experiments. A peptide corresponding to the cytoplasmic tail of p63 promoted microtubule polymerization in vitro. p63 is the first identified integral membrane protein that can link a membrane organelle directly to microtubules. By doing so, it may contribute to the positioning of the ER along microtubules.

[1]  M. Yanagida,et al.  Dissection of fission yeast microtubule associating protein p93Dis1: regions implicated in regulated localization and microtubule interaction , 1996, Genes to cells : devoted to molecular & cellular mechanisms.

[2]  R. Vallee,et al.  Targeting of Motor Proteins , 1996, Science.

[3]  T. Kreis,et al.  CLIPs for organellemicrotubule interactions , 1996 .

[4]  R. Pepperkok,et al.  Molecular characterization of two functional domains of CLIP-170 in vivo. , 1994, Journal of cell science.

[5]  J. Rohrer,et al.  Retention of p63 in an ER-Golgi intermediate compartment depends on the presence of all three of its domains and on its ability to form oligomers , 1994, The Journal of cell biology.

[6]  B. Dahllöf,et al.  The endoplasmic reticulum retention signal of the E3/19K protein of adenovirus-2 is microtubule binding. , 1991, The Journal of biological chemistry.

[7]  V. Allan,et al.  Protein phosphatase 1 regulates the cytoplasmic dynein-driven formation of endoplasmic reticulum networks in vitro , 1995, The Journal of cell biology.

[8]  M. Koonce,et al.  Identification of a Microtubule-binding Domain in a Cytoplasmic Dynein Heavy Chain* , 1997, The Journal of Biological Chemistry.

[9]  J. Thyberg,et al.  Microtubules and the organization of the Golgi complex. , 1985, Experimental cell research.

[10]  P. L. Jørgensen,et al.  Purification and characterization of (Na+ plus K+ )-ATPase. 3. Purification from the outer medulla of mammalian kidney after selective removal of membrane components by sodium dodecylsulphate. , 1974, Biochimica et biophysica acta.

[11]  S. Lewis,et al.  Microtubule-associated protein MAP2 shares a microtubule binding motif with tau protein , 1988, Science.

[12]  J. Burkhardt In search of membrane receptors for microtubule-based motors - is kinectin a kinesin receptor? , 1996, Trends in cell biology.

[13]  S. Dabora,et al.  The microtubule-dependent formation of a tubulovesicular network with characteristics of the ER from cultured cell extracts , 1988, Cell.

[14]  H. Hauri,et al.  Expression and intracellular transport of microvillus membrane hydrolases in human intestinal epithelial cells , 1985, The Journal of cell biology.

[15]  Richard B. Vallee,et al.  An extended microtubule-binding structure within the dynein motor domain , 1997, Nature.

[16]  Jennifer Lippincott-Schwartz,et al.  ER-to-Golgi transport visualized in living cells , 1997, Nature.

[17]  C. I. Zeeuw,et al.  CLIP-115, a Novel Brain-Specific Cytoplasmic Linker Protein, Mediates the Localization of Dendritic Lamellar Bodies , 1997, Neuron.

[18]  E. Salmon,et al.  Membrane/microtubule tip attachment complexes (TACs) allow the assembly dynamics of plus ends to push and pull membranes into tubulovesicular networks in interphase Xenopus egg extracts , 1995, The Journal of cell biology.

[19]  T. Takenawa,et al.  β-Tubulin Binds Src Homology 2 Domains through a Region Different from the Tyrosine-phosphorylated Protein-recognizing Site* , 1996, The Journal of Biological Chemistry.

[20]  J. Bulinski,et al.  Non-neuronal 210 x 10(3) Mr microtubule-associated protein (MAP4) contains a domain homologous to the microtubule-binding domains of neuronal MAP2 and tau. , 1991, Journal of cell science.

[21]  J. Rohrer,et al.  A reversibly palmitoylated resident protein (p63) of an ER-Golgi intermediate compartment is related to a circulatory shock resuscitation protein. , 1993, Journal of cell science.

[22]  T. Kreis,et al.  CLIPs for organelle-microtubule interactions. , 1996, Trends in cell biology.

[23]  C. Deutschman,et al.  Molecular biology of circulatory shock. Part II. Expression of four groups of hepatic genes is enhanced after resuscitation from cardiogenic shock. , 1990, Surgery.

[24]  T. Kreis,et al.  Motor protein independent binding of endocytic carrier vesicles to microtubules in vitro. , 1991, The Journal of biological chemistry.

[25]  N. Hirokawa,et al.  Kinesin and dynein superfamily proteins and the mechanism of organelle transport. , 1998, Science.

[26]  T. Schroer,et al.  Chapter 3 Interactions between Microtubules and Intracellular Membranes: The Roles of Microtubule-Based Motors and Accessory Proteins , 1996 .

[27]  H. Hauri,et al.  The isolated ER-Golgi intermediate compartment exhibits properties that are different from ER and cis-Golgi , 1991, The Journal of cell biology.

[28]  Stephen J. Smith,et al.  Tubulovesicular processes emerge from trans-Golgi cisternae, extend along microtubules, and interlink adjacent trans-Golgi elements into a reticulum , 1990, Cell.

[29]  M. Sheetz,et al.  Kinectin, a major kinesin-binding protein on ER , 1992, The Journal of cell biology.

[30]  Extracts , 1869, The Indian medical gazette.

[31]  G K Lewis,et al.  Isolation of monoclonal antibodies specific for human c-myc proto-oncogene product , 1985, Molecular and cellular biology.

[32]  M. Kirschner,et al.  Properties of the depolymerization products of microtubules from mammalian brain. , 1974, Biochemistry.

[33]  R. Vale,et al.  Formation of membrane networks in vitro by kinesin-driven microtubule movement , 1988, The Journal of cell biology.

[34]  C. Echeverri,et al.  Molecular characterization of the 50-kD subunit of dynactin reveals function for the complex in chromosome alignment and spindle organization during mitosis , 1996, The Journal of cell biology.

[35]  D. Mundy Protein palmitoylation in membrane trafficking. , 1995, Biochemical Society transactions.

[36]  M. Jackson,et al.  An N‐terminal double‐arginine motif maintains type II membrane proteins in the endoplasmic reticulum. , 1994, The EMBO journal.

[37]  M. Noble,et al.  The microtubule binding domain of microtubule-associated protein MAP1B contains a repeated sequence motif unrelated to that of MAP2 and tau , 1989, The Journal of cell biology.

[38]  Ronald D Vale,et al.  Microtubule Interaction Site of the Kinesin Motor , 1997, Cell.

[39]  L. Chen,et al.  Dynamic behavior of endoplasmic reticulum in living cells , 1988, Cell.

[40]  V. Allan Membrane traffic motors , 1995, FEBS letters.

[41]  M. Kirschner,et al.  The primary structure and heterogeneity of tau protein from mouse brain. , 1988, Science.

[42]  J. Lippincott-Schwartz,et al.  Organization of organelles and membrane traffic by microtubules. , 1995, Current opinion in cell biology.

[43]  M. Sheetz,et al.  Cytoplasmic microtubule-associated motors. , 1993, Annual review of biochemistry.

[44]  R. Vallee,et al.  DYNEINS: molecular structure and cellular function. , 1994, Annual review of cell biology.

[45]  K. Fujiwara,et al.  Microtubules and the endoplasmic reticulum are highly interdependent structures , 1986, The Journal of cell biology.

[46]  M. Caplan,et al.  Monoclonal antibody to Na,K-ATPase: immunocytochemical localization along nephron segments. , 1985, Kidney international.

[47]  J. Lippincott-Schwartz,et al.  Golgi dispersal during microtubule disruption: regeneration of Golgi stacks at peripheral endoplasmic reticulum exit sites. , 1996, Molecular biology of the cell.

[48]  T. Kreis,et al.  CLIP-170 links endocytic vesicles to microtubules , 1992, Cell.

[49]  Robert Presley,et al.  Evolutionary biology: Pelvic problems for mammals , 1997, Nature.

[50]  C. Echeverri,et al.  Overexpression of the Dynamitin (p50) Subunit of the Dynactin Complex Disrupts Dynein-dependent Maintenance of Membrane Organelle Distribution , 1997, The Journal of cell biology.

[51]  G. Warren,et al.  Mitosis and inhibition of intracellular transport stimulate palmitoylation of a 62-kD protein , 1992, The Journal of cell biology.

[52]  B. Cullen Use of eukaryotic expression technology in the functional analysis of cloned genes. , 1987, Methods in enzymology.

[53]  T. Huffaker,et al.  Stu2p: A Microtubule-Binding Protein that Is an Essential Component of the Yeast Spindle Pole Body , 1997, The Journal of cell biology.

[54]  H. Goodson,et al.  Motors and membrane traffic. , 1997, Current opinion in cell biology.

[55]  H. Hauri,et al.  Characterization of a novel 63 kDa membrane protein. Implications for the organization of the ER-to-Golgi pathway. , 1993, Journal of cell science.

[56]  A. Linstedt,et al.  Giantin, a novel conserved Golgi membrane protein containing a cytoplasmic domain of at least 350 kDa. , 1993, Molecular biology of the cell.

[57]  R. Vallee Purification of brain microtubules and microtubule-associated protein 1 using taxol. , 1986, Methods in enzymology.

[58]  J. Slot,et al.  Reassessment of the subcellular localization of p63. , 1995, Journal of cell science.

[59]  T. Kreis,et al.  Microtubules containing detyrosinated tubulin are less dynamic. , 1987, The EMBO journal.

[60]  A. Matus,et al.  Functional analysis of the MAP2 repeat domain. , 1996, Journal of cell science.