The complexities of dystroglycan

Trends in Biochemical Sciences

Volumn 26, Issue 2, 2001, Pages 118-124

  Winder, Steven J ^a  

^a UNIVERSITY OF GLASGOW   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DYSTROBREVIN; DYSTROGLYCAN; DYSTROPHIN; LAMININ BINDING PROTEIN; PERLECAN; RAPSYN; SARCOGLYCAN; SYNTROPHIN; UTROPHIN;

BINDING AFFINITY; CAENORHABDITIS ELEGANS; COMPLEX FORMATION; CYTOSKELETON; MOLECULAR INTERACTION; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; REVIEW; SIGNAL TRANSDUCTION;

ANIMALS; CELL ADHESION; CELL DIVISION; CYTOSKELETAL PROTEINS; CYTOSKELETON; DYSTROGLYCANS; LAMININ; MEMBRANE GLYCOPROTEINS; MODELS, MOLECULAR; PROTEIN BINDING; PROTEIN STRUCTURE, TERTIARY; SIGNAL TRANSDUCTION;

CAENORHABDITIS ELEGANS;

EID: 0035252649     PISSN: 09680004     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0004(00)01731-X     Document Type: Review

References (62)

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2. Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle
3. Cranin a laminin-binding protein of cell membranes
4. Laminin-binding protein 120 from brain is closely related to the dystrophin-associated glycoprotein, dystroglycan, and binds with high affinity to the major heparin binding domain of laminin
5. Purification of cranin, a laminin-binding membrane-protein - Identity with dystroglycan and reassessment of its carbohydrate moieties
6. Primary structure of dystrophin-related protein
7. Dystroglycan in development and disease
8. Crystal structure of the actin-binding region of utrophin reveals a head-to-tail dimer
9. The structure of the N-terminal actin-binding domain of human dystrophin and how mutations in this domain may cause Duchenne or Becker muscular dystrophy
10. Structure of the utrophin actin-binding domain bound to F-actin reveals binding by an induced fit mechanism
11. Structure of a WW domain containing fragment of dystrophin in complex with β-dystroglycan
12. Structure of the C-terminal laminin G-like domain pair of the laminin α2 chain harbouring binding sites for α-dystroglycan and heparin
13. The membrane-cytoskeleton interface: The role of dystrophin and utrophin
14. Exploring the molecular-basis for variability among patients with Becker muscular-dystrophy - Dystrophin gene and protein studies
15. Three muscular dystrophies: Loss of cytoskeleton-extracellular matrix linkage
16. Dystroglycan is essential for early embryonic development: Disruption of Reichert's membrane in Dag1-null mice
17. Chimeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses
18. A new model for the interaction of dystrophin with F-actin
19. Structure and function of the WW domain
20. Adhesion-dependent tyrosine phosphorylation of β-dystroglycan regulates its interaction with utrophin
21. Identification and characterization of the dystrophin anchoring site on β-dystroglycan
22. The WW domain of dystrophin requires EF-hands region to interact with β-dystroglycan
23. The crystal structure of a laminin G-like module reveals the molecular basis of α-dystroglycan binding to laminin, perlecan and agrin
24. A role for the dystrophin glycoprotein complex as a transmembrane linker between laminin and actin
25. Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan. The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with laminin
26. 4 masked by sialic acid modification
27. The small leucine-rich repeat proteoglycan biglycan binds to α-dystroglycan and is upregulated in dystrophic muscle
28. A role for dystroglycan in basement membrane assembly
29. Dystroglycan and laminins: Glycoconjugates involved in branching epithelial morphogenesis
30. Dystrophic phenotype induced in vitro by blockade of muscle α-dystroglycan-laminin interaction
31. Neural regulation of α-dystroglycan biosynthesis and glycosylation in skeletal muscle
32. Laminin polymerisation induces a receptor-cytoskeleton network
33. Building synapses: Agrin and dystroglycan stick together
34. Dystrophin-associated proteins and synapse formation: Is α-dystroglycan the agrin receptor?
35. Dystroglycan - An extracellular-matrix receptor-linked to the cytoskeleton
36. Failure of postsynaptic specialisation to develop at neuromuscular junctions of rapsyn-deficient mice
37. Maturation and maintenance of the neuromuscular synapse: Genetic evidence for roles of the dystrophin-glycoprotein complex
38. Caveolin-3 directly interacts with the c-terminal tail of β-dystroglycan: Identification of a central WW-like domain within caveolin family members
39. Transgenic overexpression of caveolin-3 in skeletal muscle fibers induces a Duchenne-like muscular dystrophy phenotype
40. Knocking signalling out of the dystrophin complex
41. Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins
42. Bidirectional signaling between sarcoglycans and the integrin adhesion system in cultured L6 myoblasts
43. Association of the dystroglycan complex isolated from bovine brain synaptosomes with proteins involved in signal transduction
44. SH3 domain-mediated interaction of dystroglycan and Grb2
45. Localization of utrophin and aciculin at sites of cell-matrix and cell-cell adhesion in cultured cells
46. Localization of cranin (dystroglycan) at sites of call-matrix and cell-cell contact: Recruitment to focal adhesions is dependent upon extracellular ligands
47. Utrophin-dystroglycan complex in membranes of adherent cultured cells
48. Association of TM4SF proteins with integrins: Relevance to cancer
49. Sarcospan, the 25 kDa transmembrane component of the dystrophin-glycoprotein complex
50. Role of dystrophin isoforms and associated proteins in muscular dystrophy
51. Muscular dystrophy associated with β-dystroglycan deficiency
52. Role of α-dystroglycan as a Schwann cell receptor for Mycobacterium leprae
53. Identification of α-dystroglycan as a receptor for lymphocytic choriomeningitis virus and Lassa fever virus
54. The sarcoglycan complex in limb-girdle muscular dystrophy
55. A PDZ-containing scaffold related to the dystrophin complex at the basolateral membrane of epithelial cells
56. Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene
57. The SH2 and SH3 domain containing protein GRB2 links receptor tyrosine kinases to ras signaling
58. Formation of the neuromuscular junction - Agrin and its unusual receptors
59. Form and function: The laminin family of heterotrimers
60. Matrix proteoglycans: From molecular design to cellular function
61. Biosynthesis of dystroglycan: Processing of a precursor propeptide
62. Electron microscopic evidence for a mucin-like region in chick muscle α-dystroglycan