Dystroglycan Organizes Axon Guidance Cue Localization and Axonal Pathfinding

Precise patterning of axon guidance cue distribution is critical for nervous system development. Using a murine forward genetic screen for novel determinants of axon guidance, we identified B3gnt1 and ISPD as required for the glycosylation of dystroglycan in vivo. Analysis of B3gnt1, ISPD, and dystroglycan mutant mice revealed a critical role for glycosylated dystroglycan in the development of several longitudinal axon tracts. Remarkably, the axonal guidance defects observed in B3gnt1, ISPD, and dystroglycan mutants resemble several of the axon guidance defects found in mice lacking the axon guidance cue Slit and its receptor Robo. This similarity is explained by our observations that dystroglycan binds directly to Slit and is required for proper Slit localization within the basement membrane and floor plate in vivo. These findings establish a novel role for glycosylated dystroglycan as a key determinant of axon guidance cue distribution and function in the mammalian nervous system.

[1]  Marc Tessier-Lavigne,et al.  Diversity and Specificity of Actions of Slit2 Proteolytic Fragments in Axon Guidance , 2001, The Journal of Neuroscience.

[2]  K. Daniels,et al.  Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice. , 1997, Human molecular genetics.

[3]  Eric A. Vitriol,et al.  Growth Cone Travel in Space and Time: the Cellular Ensemble of Cytoskeleton, Adhesion, and Membrane , 2012, Neuron.

[4]  M. Tessier-Lavigne,et al.  The role of the floor plate in axon guidance. , 1995, Annual review of neuroscience.

[5]  A. Kolodkin,et al.  Mechanisms and molecules of neuronal wiring: a primer. , 2011, Cold Spring Harbor perspectives in biology.

[6]  K. Campbell,et al.  Dystroglycan: from biosynthesis to pathogenesis of human disease , 2006, Journal of Cell Science.

[7]  D. V. Vactor,et al.  Axonal Heparan Sulfate Proteoglycans Regulate the Distribution and Efficiency of the Repellent Slit during Midline Axon Guidance , 2004, Current Biology.

[8]  Xinhua Lin,et al.  Shaping morphogen gradients by proteoglycans. , 2009, Cold Spring Harbor perspectives in biology.

[9]  M. Tessier-Lavigne,et al.  Autocrine/juxtaparacrine regulation of axon fasciculation by Slit-Robo signaling , 2012, Nature Neuroscience.

[10]  R. Timpl,et al.  Binding of the G domains of laminin α1 and α2 chains and perlecan to heparin, sulfatides, α‐dystroglycan and several extracellular matrix proteins , 1999 .

[11]  Alexander F Schier,et al.  Extracellular movement of signaling molecules. , 2011, Developmental cell.

[12]  G. Comi,et al.  Congenital muscular dystrophies with defective glycosylation of dystroglycan , 2009, Neurology.

[13]  D. Cane,et al.  Kinetic analysis of Escherichia coli 2-C-methyl-D-erythritol-4-phosphate cytidyltransferase, wild type and mutants, reveals roles of active site amino acids. , 2004, Biochemistry.

[14]  Yassir A. Ahmed,et al.  A Molecular Mechanism for the Heparan Sulfate Dependence of Slit-Robo Signaling* , 2006, Journal of Biological Chemistry.

[15]  M. Tessier-Lavigne,et al.  Mammalian Brain Morphogenesis and Midline Axon Guidance Require Heparan Sulfate , 2003, Science.

[16]  Y. Rao,et al.  The mouse SLIT family: secreted ligands for ROBO expressed in patterns that suggest a role in morphogenesis and axon guidance. , 1999, Developmental biology.

[17]  D. Price,et al.  Heparan Sulphation Patterns Generated by Specific Heparan Sulfotransferase Enzymes Direct Distinct Aspects of Retinal Axon Guidance at the Optic Chiasm , 2006, The Journal of Neuroscience.

[18]  R. Timpl,et al.  Binding of the G domains of laminin alpha1 and alpha2 chains and perlecan to heparin, sulfatides, alpha-dystroglycan and several extracellular matrix proteins. , 1999, The EMBO journal.

[19]  M. Tessier-Lavigne,et al.  Collaborative and Specialized Functions of Robo1 and Robo2 in Spinal Commissural Axon Guidance , 2010, The Journal of Neuroscience.

[20]  J. Hewitt Abnormal glycosylation of dystroglycan in human genetic disease. , 2009, Biochimica et biophysica acta.

[21]  Francesco Muntoni,et al.  ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome , 2012, Nature Genetics.

[22]  Hao Wang,et al.  Netrin-1 Is Required for Commissural Axon Guidance in the Developing Vertebrate Nervous System , 1996, Cell.

[23]  J. Ervasti,et al.  Crystal structure and cell surface anchorage sites of laminin alpha1LG4-5. , 2007, The Journal of biological chemistry.

[24]  M. Fukuda,et al.  Tumor suppressor function of laminin-binding α-dystroglycan requires a distinct β3-N-acetylglucosaminyltransferase , 2009, Proceedings of the National Academy of Sciences.

[25]  Huaiyu Hu Cell-surface heparan sulfate is involved in the repulsive guidance activities of Slit2 protein , 2001, Nature Neuroscience.

[26]  J. Rubenstein,et al.  Intermediate targets in formation of topographic projections: inputs from the thalamocortical system , 2004, Trends in Neurosciences.

[27]  Rebecca K. Chance,et al.  The Adam family metalloprotease Kuzbanian regulates the cleavage of the roundabout receptor to control axon repulsion at the midline , 2010, Development.

[28]  A. Chédotal Further tales of the midline , 2011, Current Opinion in Neurobiology.

[29]  P. Carmeliet,et al.  VEGF Mediates Commissural Axon Chemoattraction through Its Receptor Flk1 , 2011, Neuron.

[30]  Takashi Fujikado,et al.  Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation , 2008, Nature Neuroscience.

[31]  T. Südhof,et al.  A stoichiometric complex of neurexins and dystroglycan in brain , 2001, The Journal of cell biology.

[32]  C. Goodman,et al.  Slit Proteins Bind Robo Receptors and Have an Evolutionarily Conserved Role in Repulsive Axon Guidance , 1999, Cell.

[33]  C. Chien,et al.  When sugars guide axons: insights from heparan sulphate proteoglycan mutants , 2004, Nature Reviews Genetics.

[34]  Marc Tessier-Lavigne,et al.  Anterior-Posterior Guidance of Commissural Axons by Wnt-Frizzled Signaling , 2003, Science.

[35]  C. Goodman,et al.  Conserved Roles for Slit and Robo Proteins in Midline Commissural Axon Guidance , 2004, Neuron.

[36]  A. Kolodkin,et al.  A Forward Genetic Screen in Mice Identifies Sema3AK108N, which Binds to Neuropilin-1 but Cannot Signal , 2010, The Journal of Neuroscience.

[37]  K. Campbell,et al.  Brain and Eye Malformations Resembling Walker–Warburg Syndrome Are Recapitulated in Mice by Dystroglycan Deletion in the Epiblast , 2008, Journal of Neuroscience.

[38]  T. Abe,et al.  Draxin, a Repulsive Guidance Protein for Spinal Cord and Forebrain Commissures , 2009, Science.

[39]  Marc Tessier-Lavigne,et al.  Squeezing Axons Out of the Gray Matter A Role for Slit and Semaphorin Proteins from Midline and Ventral Spinal Cord , 2000, Cell.

[40]  K. Campbell,et al.  Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy , 2002, Nature.

[41]  C. Petito,et al.  Walker-Warburg syndrome: neurologic features and muscle membrane structure. , 1998, Pediatric neurology.

[42]  O. Hobert,et al.  Extracellular Sugar Modifications Provide Instructive and Cell-Specific Information for Axon-Guidance Choices , 2008, Current Biology.

[43]  A. McMahon,et al.  The Morphogen Sonic Hedgehog Is an Axonal Chemoattractant that Collaborates with Netrin-1 in Midline Axon Guidance , 2003, Cell.

[44]  J. Ervasti,et al.  Crystal Structure and Cell Surface Anchorage Sites of Laminin α1LG4-5* , 2007, Journal of Biological Chemistry.

[45]  T. Toda,et al.  Mislocalization of Fukutin Protein by Disease-causing Missense Mutations Can Be Rescued with Treatments Directed at Folding Amelioration* , 2012, The Journal of Biological Chemistry.

[46]  S. Carbonetto,et al.  Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor. , 1994, Cell.

[47]  H. Baier,et al.  Assembly of Lamina-Specific Neuronal Connections by Slit Bound to Type IV Collagen , 2011, Cell.

[48]  Christian Gilissen,et al.  Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan , 2012, Nature Genetics.

[49]  E. Engle,et al.  Human genetic disorders of axon guidance. , 2010, Cold Spring Harbor perspectives in biology.

[50]  Yutaka Yoshida,et al.  A midline switch of receptor processing regulates commissural axon guidance in vertebrates. , 2010, Genes & development.

[51]  K. Campbell,et al.  Glycomic Analyses of Mouse Models of Congenital Muscular Dystrophy* , 2011, The Journal of Biological Chemistry.

[52]  S. Carbonetto,et al.  Dystroglycan-α, a dystrophin-associated glycoprotein, is a functional agrin receptor , 1994, Cell.

[53]  C. Goodman,et al.  Genetic analysis of Laminin A in Drosophila: extracellular matrix containing laminin A is required for ocellar axon pathfinding. , 1996, Development.

[54]  K. Campbell,et al.  Distinct Functions of Glial and Neuronal Dystroglycan in the Developing and Adult Mouse Brain , 2010, The Journal of Neuroscience.

[55]  K. Jagla,et al.  Genetic control of cell morphogenesis during Drosophila melanogaster cardiac tube formation , 2008, The Journal of cell biology.

[56]  H. Jäckle,et al.  Heparan Sulfate Proteoglycan Syndecan Promotes Axonal and Myotube Guidance by Slit/Robo Signaling , 2004, Current Biology.

[57]  Liping Yu,et al.  Dystroglycan Function Requires Xylosyl- and Glucuronyltransferase Activities of LARGE , 2012, Science.