Differentiation potential of primary myogenic cells derived from skeletal muscle of dystonia musculorum mice

Differentiation

Volumn 70, Issue 6, 2002, Pages 247-256

  Boudreau Larivière, Céline ^a,b   Kothary, Rashmi ^a,b  

^a OTTAWA HOSPITAL RESEARCH INSTITUTE   (Canada)

^b UNIVERSITY OF OTTAWA   (Canada)

Author keywords

Bullous pemphigoid antigen 1; dystonia musculorum; Dystonin; Myf 5; MyoD; Myogenin; Plakin; Skeletal muscle

Indexed keywords

BROXURIDINE; ISOPROTEIN; MYOSIN; PLECTIN; PROTEIN; AUTOANTIGEN; CARRIER PROTEIN; COLLAGEN; COLLAGEN TYPE 17; CYTOSKELETON PROTEIN; DIFFERENTIATION ANTIGEN; DST PROTEIN, MOUSE; INTERMEDIATE FILAMENT PROTEIN; MUSCLE PROTEIN; MYOSIN HEAVY CHAIN; NERVE PROTEIN; NONFIBRILLAR COLLAGEN; PLEC1 PROTEIN, MOUSE;

ANIMAL CELL; ARTICLE; CELL CULTURE; CELL DIFFERENTIATION; CELL GROWTH; CROSS LINKING; CYTOARCHITECTURE; DYSTONIA; GENE MUTATION; GENETIC CODE; IMMUNOFLUORESCENCE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; REGULATORY MECHANISM; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SKELETAL MUSCLE; WILD TYPE; ANIMAL; ANIMAL MODEL; BIOSYNTHESIS; CELL DIVISION; CELL LINEAGE; CHEMISTRY; CYTOSKELETON; GENE EXPRESSION PROFILING; GENETICS; METABOLISM; MORPHOGENESIS; MOUSE; MULTIGENE FAMILY; PATHOLOGY; PHYSIOLOGY; TORSION DYSTONIA; ULTRASTRUCTURE;

ANIMALIA;

ANIMALS; ANTIGENS, DIFFERENTIATION; AUTOANTIGENS; CARRIER PROTEINS; CELL DIFFERENTIATION; CELL DIVISION; CELL LINEAGE; CELLS, CULTURED; COLLAGEN; CYTOSKELETAL PROTEINS; CYTOSKELETON; DYSTONIA MUSCULORUM DEFORMANS; GENE EXPRESSION PROFILING; INTERMEDIATE FILAMENT PROTEINS; MICE; MODELS, ANIMAL; MORPHOGENESIS; MULTIGENE FAMILY; MUSCLE PROTEINS; MUSCLE, SKELETAL; MYOSIN HEAVY CHAINS; NERVE TISSUE PROTEINS; NON-FIBRILLAR COLLAGENS; PLECTIN; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION;

EID: 0036688682     PISSN: 03014681     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1432-0436.2002.700603.x     Document Type: Article

References (39)

1. Andra, K., Lassmann, H., Bittner, R., Shorny, S., Fassler, R., Propst, F. and Wiche, G. (1997) Targeted inactivation of plectin reveals essential function in maintaining the integrity of skin, muscle, and heart cytoarchitecture. Genes Dev 11:3143-3156.
2. Bernier, G., De Repentigny, Y., Mathieu, M., David, S. and Kothary, R. (1998) Dystonin is an essential component of the Schwann cell cytoskeleton at the time of myelination. Development 125:2135-2148.
3. Bernier, G., Mathieu, M., De Repentigny, Y., Vidal, S.M. and Kothary, R. (1996) Cloning and characterization of mouse ACF7, a novel member of the dystonin subfamily of actin binding proteins. Genomics 38:19-29.
4. Bernier, G., Pool, M., Kilcup, M., Alfoldi, J., De Repentigny, Y. and Kothary, R. (2000) Acf7 (MACF) is an actin and microtubule linker protein whose expression predominates in neural, muscle, and lung development. Dev Dyn 219:216-225.
5. Brown, A., Bernier, G., Mathieu, M., Rossant, J. and Kothary, R. (1995a) The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1. Nat Genet 10:301-306.
6. Brown, A., Copeland, N.G., Gilbert, D.J., Jenkins, N.A., Rossant, J. and Kothary, R. (1994) The genomic structure of an insertional mutation in the dystonia musculorum locus. Genomics 20:371-376.
7. Brown, A., Dalpé, G., Mathieu, M. and Kothary, R. (1995b) Cloning and characterization of the neural isoforms of human dystonin. Genomics 29:777-780.
8. Chavanas, S., Pulkkinen, L., Gache, Y., Smith, F.J., McLean, W.H., Uitto, J., Ortonne, J.P. and Meneguzzi,, G. (1996) A homozygous nonsense mutation in the PLEC1 gene in patients with epidermolysis bullosa simplex with muscular dystrophy. J Clin Invest 98:2196-2200.
9. Dalpé, G., Mathieu, M., Comtois, A., Zhu, E., Wasiak, S., De Repentigny, Y., Leclerc, N. and Kothary, R. (1999) Dystonin-deficient mice exhibit an intrinsic muscle weakness and an instability of skeletal muscle cytoarchitecture. Dev Biol 210:367-380.
10. Duchen, L.W. (1976) Dystonia musculorum - an inherited disease of the nervous system in the mouse. Adv Neurol 14:353-365.
11. Duchen, L.W., Falconer, D.S. and Strich, S.J. (1963) Dystonia Musculorum. A hereditary neuropathy of mice affecting mainly sensory pathways. J Physiol 165:7-9.
12. Duchen, L.W. and Strich, S.J. (1964) Clinical and pathological studies of an hereditary neuropathy in mice. Brain 87:367-378.
13. Elliott, C.E., Becker, B., Oehler, S., Castanon, M.J., Hauptmann, R. and Wiche, G. (1997) Plectin transcript diversity: identification and tissue distribution of variants with distinct first coding exons and rodless isoforms. Genomics 42:115-125.
14. Errante, L.D., Wiche, G. and Shaw, G. (1994) Distribution of plectin, an intermediate filament-associated protein, in the adult rat central nervous system. J Neurosci Res 37:515-528.
15. Fuchs, E. and Karakesisoglou, I. (2001) Bridging cytoskeletal intersections. Genes Dev 15:1-14.
16. Gache, Y., Chavanas, S., Lacour, J.P., Wiche, G., Owaribe, K., Meneguzzi, G. and Ortonne, J.P. (1996) Defective expression of plectin/HD1 in epidermolysis bullosa simplex with muscular dystrophy. J Clin Invest 97:2289-2298.
17. Granger, B.L. and Lazarides, E. (1979) Desmin and vimentin coexist at the periphery of the myofibril Z disc. Cell 18:1053-1063.
18. Green, K.J., Stappenbeck, T.S., Parry, D.A. and Virata, M.L. (1992) Structure of desmoplakin and its association with intermediate filaments. J Dermatol 19:765-769.
19. Guo, L., Degenstein, L., Dowling, J., Yu, Q.C., Wollmann, R., Perman, B. and Fuchs, E. (1995) Gene targeting of BPAG1: abnormalities in mechanical strength and cell migration in stratified epithelia and neurologic degeneration. Cell 81:233-243.
20. Hartmann, N., Martrette, J.M., Strazielle, C. and Westphal, A. (1999) Dystonia musculorum mutation and myosin heavy chain expression in skeletal and cardiac muscles. J Cell Biochem 74:90-98.
21. Janota, I. (1972) Ultrastructural studies of an hereditary sensory neuropathy in mice (dystonia musculorum). Brain 95:529-536.
22. Karakesisoglou, I., Yang, Y. and Fuchs, E. (2000) An epidermal plakin that integrates actin and microtubule networks at cellular junctions. J Cell Biol 149:195-208.
23. Kothary, R., Clapoff, S., Brown, A., Campbell, R., Peterson, A. and Rossant, J. (1988) A transgene containing lacZ inserted into the dystonia locus is expressed in neural tube. Nature 335:435-437.
24. Leung, C.L., Sun, D., Zheng, M., Knowles, D.R. and Liem, R.K. (1999) Microtubule actin cross-linking factor (MACF): a hybrid of dystonin and dystrophin that can interact with the actin and microtubule cytoskeletons. J Cell Biol 147:1275-1286.
25. Leung, C.L., Zheng, M., Prater, S.M. and Liem, R.K. (2001) The BPAG1 locus: alternative splicing produces multiple isoforms with distinct cytoskeletal linker domains, including predominant isoforms in neurons and muscles. J Cell Biol 154:691-698.
26. McLean, W.H., Pulkkinen, L., Smith, F.J., Rugg, E.L., Lane, E.B., Bullrich, F., Burgeson, R.E., Amano, S., Hudson, D.L., Owaribe, K., McGrath, J.A., McMillan, J.R., Eady, R.A., Leigh, I.M., Christiano, A.M. and Uitto, J. (1996) Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization. Genes Dev 10:1724-1735.
27. Milner, D.J., Mavroidis, M., Weisleder, N. and Capetanaki, Y. (2000) Desmin cytoskeleton linked to muscle mitochondrial distribution and respiratory function. J Cell Biol 150:1283-1298.
28. Milner, D.J., Weitzer, G., Tran, D., Bradley, A. and Capetanaki, Y. (1996) Disruption of muscle architecture and myocardial degeneration in mice lacking desmin. J Cell Biol 134:1255-1270.
29. Pulkkinen, L., Smith, F.J., Shimizu, H., Murata, S., Yaoita, H., Hachisuka, H., Nishikawa, T., McLean, W.H. and Uitto, J. (1996) Homozygous deletion mutations in the plectin gene (PLEC1) in patients with epidermolysis bullosa simplex associated with late-onset muscular dystrophy. Hum Mol Genet 5:1539-1546.
30. Ruhrberg, C., Hajibagheri, M.A., Simon, M., Dooley, T.P. and Watt, F.M. (1996) Envoplakin, a novel precursor of the cornified envelope that has homology to desmoplakin. J Cell Biol 134:715-729.
31. Ruhrberg, C. and Watt, F.M. (1997) The plakin family: versatile organizers of cytoskeletal architecture. Curr Opin Genet Dev 7:392-397.
32. Sabourin, L.A., Girgis-Gabardo, A., Seale, P., Asakura, A. and Rudnicki, M.A. (1999) Reduced differentiation potential of primary MyoD-/-myogenic cells derived from adult skeletal muscle. J Cell Biol 144:631-643.
33. Smith, F.J., Eady, R.A., Leigh, I.M., McMillan, J.R., Rugg, E.L., Kelsell, D.P., Bryant, S.P., Spurr, N.K., Geddes, J.F., Kirtschig, G., Milana, G., de, Bono, A.G., Owaribe, K., Wiche, G., Pulkkinen, L., Uitto, J., McLean, W.H. and Lane, E.B. (1996) Plectin deficiency results in muscular dystrophy with epidermolysis bullosa. Nat Genet 13:450-457.
34. Sun, D., Leung, C.L. and Liem, R.K. (2001) Characterization of the microtubule binding domain of microtubule actin cross-linking factor (MACF): identification of a novel group of microtubule associated proteins. J Cell Sci 114:161-172.
35. Tokuyasu, K.T., Dutton, A.H. and Singer, S.J. (1983) Immunoelectron microscopic studies of desmin (skeletin) localization and intermediate filament organization in chicken cardiac muscle. J Cell Biol 96:1736-1742.
36. Virata, M.L., Wagner, R.M., Parry, D.A. and Green, K.J. (1992) Molecular structure of the human desmoplakin I and II amino terminus. Proc Natl Acad Sci U S A 89:544-548.
37. Wiche, G. (1998) Role of plectin in cytoskeleton organization and dynamics. J Cell Sci 111:2477-2486.
38. Wiche, G., Herrmann, H., Leichtfried, F. and Pytela, R. (1982) Plectin: a high-molecular-weight cytoskeletal polypeptide component that copurifies with intermediate filaments of the vimentin type. Cold Spring Harb Symp Quant Biol 46:475-482.
39. Yang, Y., Dowling, J., Yu, Q.C., Kouklis, P., Cleveland, D.W. and Fuchs, E. (1996) An essential cytoskeletal linker protein connecting actin microfilaments to intermediate filaments. Cell 86:655-665.