The distribution and phosphorylation of the microtubule-associated protein MAP 1B in growth cones (original) (raw)

References

• Aletta, J. M., Lewis, S. A., Cowan, N. J. &Greene, L. A. (1988) Nerve growth factor regulates both the phosphorylation and steady-state levels of microtubule associated protein 1.2 (MAP 1.2).Journal of Cell Biology 106, 1573–81.
  Google Scholar
• Asai, D. J., Thompson, W. C., Wilson, L., Dresden, C. F., Schulman, H. &Purich, D. L. (1985). Microtubule associated proteins (MAPs): a monoclonal antibody to MAP 1 decorates microtubules_in vitro_ but stains stress fibres and not microtubules_in vivo_.Proceedings of the National Academy of Science (USA) 82, 1434–8.
  Google Scholar
• Baas, P. W., White, L. A. &Heidemann, S. R. (1987) Microtubule polarity reversal accompanies regrowth of amputated neurites.Proceedings of the National Academy of Science (USA) 84, 5272–6.
  Google Scholar
• Bamburg, J. R., Bray, D. &Chapman, K. (1986) Assembly of microtubules at the tip of growing axons.Nature 321, 788–90.
  PubMed Google Scholar
• Bartlett, W. P. &Banker, G. A. (1984) An electron microscopic study of the development of axons and dendrites by hippocampal neurons in culture I. Cells which develop without intercellular contacts.Journal of Neuroscience 4, 1944–53.
  PubMed Google Scholar
• Bloom, G. S., Luca, F. C. &Vallee, R. B. (1985a) Identification of high molecular weight microtubule associated proteins in anterior pituitary tissue and cells using taxol dependent purification combined with microtubule associated protein specific antibodies.Biochemistry 24, 4185–91.
  PubMed Google Scholar
• Bloom, G. S., Luca, F. C. &Vallee, R. B. (1985b) Microtubule associated protein 1B: identification of a major component of the neuronal cytoskeleton.Proceedings of the National Academy of Science (USA) 82, 5404–8.
  Google Scholar
• Bloom, G. S., Schoenfield, T. A. &Vallee, R. B. (1984) Widespread distribution of the major polypeptide component of MAP 1 (Microtubule associated protein 1) in the nervous system.Journal of Cell Biology 98, 320–30.
  PubMed Google Scholar
• Bradford, M. M. (1976) A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein dye-binding.Analytical Biochemistry 72, 248–54.
  PubMed Google Scholar
• Brugg, B. &Matus, A. (1988) PC12 cells express juvenile microtubule-associated proteins during nerve factorinduced neurite outgrowth.Journal of Cell Biology 107, 643–50.
  Google Scholar
• Calvert, R. &Anderton, B. H. (1985) A microtubule associated protein MAP 1 which is expressed at elevated levels during development of rat cerebellum.EMBO Journal 4, 1171–6.
  PubMed Google Scholar
• Daniels, M. (1972) Colchicine inhibition of nerve fiber formation_in vitro_.Journal of Cell Biology 53, 164–76.
  Google Scholar
• Diaz-Nido, J., Armas-Potela, R., Martinez, A., Rocha, M. &Avila, J. (1991) Role of microtubules in neurite outgrowth. In_The Nerve Growth Cone_ (edited byKater, S. B., Letourneau, P. C. &Macagno, E. R.) New York: Raven Press, in press.
  Google Scholar
• Diaz-Nido, J. &Avila, J. (1989) Characterization of proteins immunologically related to brain microtubule associated protein MAP 1B in non-neuronal cells.Journal of Cell Science 92, 607–20.
  PubMed Google Scholar
• Diaz-Nido, J., Serrano, L., Hernandez, M. A. &Avila, J. (1990) Phosphorylation of microtubule proteins in rat brain at different developmental stages: comparison with that found in neural cultures.Journal of Neurochemistry 54, 211–22.
  PubMed Google Scholar
• Diaz-Nido, J., Serrano, L., Mendez, E. &Avila, J. (1988) A casein kinase II-related activity is involved in phosphorylation of microtubule associated protein MAP 1B during neuroblastoma cell differentiation.Journal of Cell Biology 106, 2057–65.
  Google Scholar
• Dodd, J. &Jessell, T. M. (1988) Axonal guidance and the patterning of neuronal projections in vertebrates.Science 242, 692–9.
  PubMed Google Scholar
• Drubin, D. G., Feinstein, S., Shooter, E. &Kirschner, M. (1985) Nerve growth factor induced outgrowth in PC12 cells involves the coordinate induction of microtubule assembly and assembly promoting factors.Journal of Cell Biology 101, 1799–1807.
  Google Scholar
• Fairbanks, G., Steck, N. C. &Wallach, D. F. (1981) Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane.Biochemistry 10, 2606–17.
  Google Scholar
• Fischer, I. &Romano-Clarke, G. (1990). Changes in microtubule-associated protein MAP 1B phosphorylation during rat brain development.Journal of Neurochemistry 55, 328–33.
  PubMed Google Scholar
• Fried, R. C. &Blaustein, M. P. (1978) Retrieval and recycling of synaptic vesicle membrane in pinched-off nerve terminals (synaptosomes).Journal of Cell Biology 78, 685–700.
  PubMed Google Scholar
• Gard, D. L. &Kirschner, M. W. (1985) A polymerdependent increase in phosphorylation of β-tubulin accompanies differentiation of a neuroblastoma cell line.Journal of Cell Biology 100, 764–74.
  PubMed Google Scholar
• Garner, C. C., Garner, A., Huber, G., Kozak, C. &Matus, A. (1990) Molecular cloning of MAP 1 (MAP 1A) and MAP 5 (MAP 1B): identification of distinct genes and their differential expression in developing brain.Journal of Neurochemistry 55, 146–54.
  PubMed Google Scholar
• Garner, C. C., Matus, A., Anderton, B. &Calvert, R. (1989) Microtubule-associated proteins MAP 5 and MAP 1x: closely related components of the neuronal cytoskeleton with different cytoplasmic distribution in the developing brain.Molecular Brain Research 5, 85–92.
  PubMed Google Scholar
• Girault, J. A., Hemmings, H. C. Jr., Williams, K. R., Nairn, A. C. &Greengard, P. (1989) Phosphorylation of DARPP-32, a dopamine- and cAMP-regulated phosphoprotein by casein kinase II.Journal of Biological Chemisfry 264, 21748–59.
  Google Scholar
• Girault, J. A., Hemmings, H. C. Jr., Zorn, S. H., Gustafson, E. L. &Greengard, P. (1990) Characterization in mammalian brain of a DARPP-32 serine kinase identical to casein kinase II.Journal of Neurochemistry 55, 1772–83.
  PubMed Google Scholar
• Gogstad, G. O. &Krutnes, M. -B. (1982) Measurement of protein in cell suspensions using the Coomassie Brilliant Blue dye-binding assay.Analytical Biochemistry 126, 355–9.
  PubMed Google Scholar
• Gordon-Weeks, P. R. (1987) The cytoskeletons of isolated, neuronal growth cones.Neuroscience 21, 977–89.
  PubMed Google Scholar
• Gordon-Weeks, P. R. (1991) Growth cones: the mechanism of neurite advance.BioEssays 13, 235–9.
  PubMed Google Scholar
• Gordon-Weeks, P. R. &Lang, R. D. A. (1988) The α-tubulin of the growth cone is predominantly in the tyrosinated form.Developmental Brain Research 42, 156–60.
  Google Scholar
• Gordon-Weeks, P. R. &Lockerbie, R. O. (1984) Isolation and partial characterization of neuronal growth cones from neonatal rat forebrain.Neuroscience 13, 119–36.
  PubMed Google Scholar
• Gordon-Weeks, P. R. &Mansfield, S. G. (1991) The assembly of microtubules in growth cones: the role of microtubule-associated proteins. In_The Nerve Growth Cone_ (edited byKater, S. B., Letourneau, P. C. &Macagno, E. R.). New York: Raven Press, in press.
  Google Scholar
• Gordon-Weeks, P. R., Mansfield, S. G. &Curran, I. (1989) Direct visualization of the soluble pool of tubulin in the neuronal growth cone: immunofluorescence studies following taxol polymerisation.Developmental Brain Research 49, 305–10.
  PubMed Google Scholar
• Goslin, K., Schreyer, D. J., Skene, J. H. P. &Banker, G. A. (1988) Development of neuronal polarity: GAP-43 distinguishes axonal from dendritic growth cones.Nature 336, 672–4.
  PubMed Google Scholar
• Greene, L. A., Liem, R. K. H. &Shelanski, M. L. (1983) Regulation of a high molecular weight microtubule associated protein in PC12 cells by nerve growth factor.Journal of Cell Biology 96, 76–83.
  Google Scholar
• Gundersen, G. G., Kalnoski, M. H. &Bulinski, J. C. (1984) Distinct populations of microtubules: tyrosinated and nontyrosinated alpha-tubulins are distributed differently in vivo.Cell 38, 779–89.
  PubMed Google Scholar
• Hasegawa, M., Arai, T. &Ihara, Y. (1990) Immunochemical evidence that fragments of phosphorylated MAP5 (MAP 1B) are bound to neurofibrillary tangles in Alzheimer's disease.Neuron 4, 909–18.
  PubMed Google Scholar
• Hoshi, M., Nishida, E., Inagaki, M., Gotoh, Y. &Sakai, H. (1990) Activation of a serine/-threonine kinase that phosphorylates microtubule-associated protein 1B_in vitro_ by growth factors and phorbol esters in quiescent rat fibroblastic cells.European Journal of Biochemistry 193, 513–19.
  PubMed Google Scholar
• Iimoto, D. S., Masliah, E., Deteresa, R., Terry, R. D. &Saitoh, T. (1989) Aberrant casein kinase II in Alzheimer's disease.Brain Research 507, 273–80.
  Google Scholar
• Kilmartin, J. V., Wright, B. &Milstein, C. (1982) Rat monoclonal antitubulin antibodies derived using a new non-secreting rat cell line.Journal of Cell Biology 93, 576–82.
  PubMed Google Scholar
• Kuznetsov, S. A., &Gelfand, V. I. (1987) 18kDa microtubule associated protein: identification as a new light chain (LC-3) of microtubule associated protein 1 (MAP 1).FEBS Letters 212, 145–8.
  PubMed Google Scholar
• Laemmli, U. K. (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4.Nature 227, 680–5.
  PubMed Google Scholar
• Letourneau, P. C. &Ressler, A. H. (1984) Inhibition of neurite initiation and growth by taxol.Journal of Cell Biology 98, 1355–62.
  Google Scholar
• Levi, G., Aloisi, F., Ciotti, M. T. &Gallo, V. (1984) Autoradiographic localisation and depolarisation-induced release of acidic amino acids in differentiating cerebellar granule cell cultures.Brain Research 290, 77–86.
  PubMed Google Scholar
• Lindwall, G. &Cole, R. D. (1984) Phosphorylation affects the ability of tau protein to promote microtubule assembly.Journal of Cell Biological Chemistry 259, 5301–5.
  Google Scholar
• Lockerbie, R. O. (1987) The neuronal growth cone: a review of its locomotory, navigational and target recognition capabilities.Neuroscience 20, 719–29.
  PubMed Google Scholar
• Mansfield, S. G. &Gordon-Weeks, P. R. (1990) Post-translational modification of tubulin in rat cerebral cortical neurons extending neurites in culture: effects of taxol.Journal of Physiology 426, 118P.
  Google Scholar
• Mansfield, S. G. &Gordon-Weeks, P. R. (1991) Dynamic post-translational modification of tubulin in rat cerebral cortical neurons extending neurites in culture: effects of taxol.Journal of Neurocytology 20, 654–66.
  Google Scholar
• Matus, A. (1988) Microtubule-associated proteins: their potential role in determining neuronal morphology.Annual Review of Neuroscience 11, 29–44.
  PubMed Google Scholar
• Meiri, K. &Gordon-Weeks, P. R. (1990) GAP-43 in growth cones is associated with areas of membrane that are tightly bound to substrate, and is a component of a membrane skeleton subcellular fraction.Journal of Neuroscience 10, 256–66.
  PubMed Google Scholar
• Murthy, A. &Flavin, M. (1983) Microtubule assembly using the microtubule associated protein MAP 2 prepared in defined states of phosphorylation with protein kinase and phosphatase.European Journal of Biochemistry 137, 37–46.
  PubMed Google Scholar
• Noble, M., Lewis, S. A. &Cowan, N. J. (1989) The microtubule binding domain of microtubule associated protein MAP 1B contains a repeated sequence motif unrelated to that of MAP 2 and tau.Journal of Cell Biology 109, 3367–76.
  PubMed Google Scholar
• Olmsted, J. B. (1986) Microtubule-associated proteins.Annual Review of Neuroscience 11, 29–44.
  Google Scholar
• Pfenninger, K. H., Ellis, L., Johnson, M. P., Friedman, L. B., &Somlo, S. (1983) Nerve growth cones isolated from fetal rat brain. Subcellular fractionation and characterization.Cell 35, 573–84.
  PubMed Google Scholar
• Pisano, M. R., Hegazy, M. G., Reimann, E. M. &Lokas, L. A. (1988) Phosphorylation of protein B-50 (GAP-43) from adult rat brain cortex by casein kinase II.Biochemical and Biophysical Research Communications 155, 1207–1212.
  PubMed Google Scholar
• Ramón Y Cajal, S. (1890) A quelle époque apparaissent les expensions des cellules nerveuses de la môlle épinière du populet?Anatomischer Anzeiger 21, 609–13, 631–9.
  Google Scholar
• Read, S. M. &Northcote, D. H. (1981) Minimisation of variation in the response to different proteins of the Coomassie Blue G dye-binding assay for protein.Analytical Biochemistry 116, 53–64.
  PubMed Google Scholar
• Riederer, B., Cohen, R. &Matus, A. (1986) MAP 5: a novel microtubule associated protein under strong developmental regulation.Journal of Neurocytology 15, 763–75.
  Google Scholar
• Riederer, B. M., Guadano-Ferraz, A. &Innocenti, G. M. (1990) Difference in distribution of microtubule-associated proteins 5a and 5b during the development of cerebral cortex and corpus callosum in cats: dependence on phosphorylation.Developmental Brain Research 56, 235–43.
  PubMed Google Scholar
• Sargent, P. B. (1990) What distinguishes axons from dendrites? Neurons know more than we do.Trends in Neuroscience 12, 203–5.
  Google Scholar
• Sato-Yoshitake, R., Shiomura, Y., Miyasaka, H. &Hirokawa, N. (1989) Microtubule associated protein 1B: molecular structure, localization and phosphorylation-dependent expression in developing neurons.Neuron 3, 229–38.
  PubMed Google Scholar
• Schiff, P. B., Fant, J. &Howitz, S. B. (1979) Promotion of microtubule assembly_in vitro_ by taxol.Nature 277, 665–7.
  PubMed Google Scholar
• Schoenfeld, J. A., Mckerracher, L., Obar, R. &Vallee, R. B. (1989) MAP 1A and MAP 1B are structurally related microtubule associated proteins with distinct developmental patterns in the CNS.Journal of Neuroscience 9, 1712–30.
  PubMed Google Scholar
• Serrano, L., Hernandez, M. A., Diaz-Nido, J. &Avila, J. (1989) Association of casein kinase II with microtubules.Experimental Cell Research 181, 263–72.
  PubMed Google Scholar
• Tsao, H., Aletta, J. M. &Greene, L. A. (1990) Nerve Growth Factor and Fibroblast Growth Factor selectively activate a protein kinase that phosphorylates high molecular weight microtubule-associated proteins.Journal of Biological Chemistry 265, 15471–80.
  PubMed Google Scholar
• Viereck, C. &Matus, A. (1990) The expression of phosphorylated and non-phosphorylated forms of MAP 5 in the amphibian CNS.Brain Research 508, 257–64.
  PubMed Google Scholar
• Viereck, C., Tucker, R. P. &Matus, A. (1989) The adult rat olfactory system expresses microtubule-associated proteins found in the developing brain.Journal of Neuroscience 9, 3547–57.
  Google Scholar
• Wiche, G., Oberkanins, C. &Himmler, A. (1991) Molecular structure and function of microtubule-associated proteins.International Review of Cytology 124, 217–73.
  PubMed Google Scholar
• Yamada, K. M., Spooner, B. S. &Wessells, N. K. (1970) Axon growth: roles of microfilaments and microtubules.Proceedings of the National Academy of Science (USA) 66, 1206–12.
  Google Scholar

Download references