Biochemical evidence for association of dystrobrevin with the sarcoglycan-sarcospan complex as a basis for understanding sarcoglycanopathy

Human Molecular Genetics

Volumn 9, Issue 7, 2000, Pages 1033-1040

  Yoshida, Mikiharu ^a   Hama, Hiroshi ^a   Ishikawa Sakurai, Michiko ^a   Imamura, Michihiro ^a   Mizuno, Yuji ^a   Araishi, Kenji ^a   Wakabayashi Takai, Eriko ^a   Noguchi, Satoru ^a,b   Sasaoka, Toshikuni ^a   Ozawa, Eijiro ^a  

^a NATIONAL INSTITUTE OF NEUROSCIENCE   (Japan)

^b JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

DYSTROBREVIN; DYSTROGLYCAN; MUSCLE PROTEIN; NITRIC OXIDE SYNTHASE; PROTEIN; SARCOGLYCAN; SARCOSPAN; SYNTROPHIN; UNCLASSIFIED DRUG;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; COMPLEX FORMATION; CONTROLLED STUDY; KNOCKOUT MOUSE; MOUSE; MUSCULAR DYSTROPHY; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; SARCOGLYCANOPATHY; SIGNAL TRANSDUCTION; SKELETAL MUSCLE;

ANIMALIA;

EID: 17344382194     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/9.7.1033     Document Type: Article

References (42)

1. Yoshida, M., Suzuki, A., Yamamoto, H., Noguchi, S., Mizuno, Y. and Ozawa, E. (1994) Dissociation of the complex of dystrophin and its associated proteins into several unique groups by n-octyl β-D-glucoside. Eur. J. Biochem., 222, 1055-1061.
2. Ibraghimov-Beskrovnaya, O., Ervasti, J.M., Leveille, C.J., Slaughter, C.A., Sernett, S.W. and Campbell, K.P. (1992) Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix. Nature, 355, 696-702.
3. Suzuki, A., Yoshida, M., Hayashi, K., Mizuno, Y., Hagiwara, Y. and Ozawa, E. (1994) Molecular-organization at the glycoprotein-complex-binding site of dystrophin. Three dystrophin-associated proteins bind directly to the carboxy-terminal portion of dystrophin. Eur. J. Biochem., 220, 283-292.
4. Ozawa, E., Hagiwara, Y. and Yoshida, M. (1999) Creatine kinase, cell membrane and Duchenne muscular dystrophy. Mol. Cell. Biochem., 190, 143-145.
5. Ozawa, E., Noguchi, S., Mizuno, Y., Hagiwara, Y. and Yoshida, M. (1998) From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy. Muscle Nerve, 21, 421-438.
6. Ozawa, E., Yoshida, M., Suzuki, A., Mizuno, Y., Hagiwara, Y. and Noguchi, S. (1995) Dystrophin-associated proteins in muscular-dystrophy. Hum. Mol. Genet., 4, 1711-1716.
7. Duclos, F., Straub, V., Moore, S.A., Venzke, D.P., Hrstka, R.F., Crosbie, R.H., Durbeej, M., Lebakken, C.S., Ettinger, A.J., van der Meulen, J. et al. (1998) Progressive muscular dystrophy in α-sarcoglycan-deficient mice. J. Cell Biol., 142, 1461-1471.
8. Araishi, K., Sasaoka, T., Imamura, M., Noguchi, S., Hama, H., Wakabayashi, E., Yoshida, M., Hori, T. and Ozawa, E. (1999) Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in β-sarcoglycan-deficient mice. Hum. Mol. Genet., 8, 1589-1598.
9. Iwata, Y., Nakamura, H., Mizuno, Y., Yoshida, M., Ozawa, E. and Shigekawa, M. (1993) Defective association of dystrophin with sarcolemmal glycoproteins in the cardiomyopathic hamster heart. FEBS Lett., 329, 227-231.
10. Roberds, S.L., Ervasti, J.M., Anderson, R.D., Ohlendieck, K., Kahl, S.D., Zoloto, D. and Campbell, K.P. (1993) Disruption of the dystrophin-glycoprotein complex in the cardiomyopathic hamster. J. Biol. Chem., 268, 11496-11499.
11. McNally, E.M., Duggan, D., Gorospe, J.R., Bönnemann, C.G., Fanin, M., Pegoraro, E., Lidov, H.G., Noguchi, S., Ozawa, E., Finkel, R.S. et al. (1996) Mutations that disrupt the carboxyl-terminus of γ-sarcoglycan cause muscular dystrophy. Hum. Mol. Genet., 5, 1841-1847.
12. Brenman, J.E., Chao, D.S., Gee, S.H., McGee, A.W., Craven, S.E., Santillano, D.R., Wu, Z., Huang, F., Xia, H., Peters, M.F. et al. (1996) Interaction of nitric oxide synthase with the postsynaptic density protein PSD-95 and α1-syntrophin mediated by PDZ domains. Cell, 84, 757-767.
13. Grady, R.M., Grange, R.W., Lau, K.S., Maimone, M.M., Nichol, M.C., Stull, J.T. and Sanes, J.R. (1999) Role for α-dystrobrevin in the pathogenesis of dystrophin-dependent muscular dystrophies. Nature Cell Biol., 1, 215-220.
14. Crosbie, R.H., Lebakken, C.S., Holt, K.H., Venzke, D.P., Straub, V., Lee, J.C., Grady, R.M., Chamberlain, J.S., Sanes, J.R. and Campbell, K.P. (1999) Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex. J. Cell Biol., 145, 153-165.
15. Suzuki, A., Yoshida, M., Yamamoto, H. and Ozawa, E. (1992) Glycoprotein-binding site of dystrophin is confined to the cysteine-rich domain and the first half of the carboxy-terminal domain. FEBS Lett., 308, 154-160.
16. Nawrotzki, R., Loh, N.Y., Ruegg, M.A., Davies, K.E. and Blake, D.J. (1998) Characterisation of α-dystrobrevin in muscle. J. Cell Sci., 111, 2595-2605.
17. Puca, A.A., Nigro, V., Piluso, G., Belsito, A., Sampaolo, S., Quaderi, N., Rossi, E., Di Iorio, G., Ballabio, A. and Franco, B. (1998) Identification and characterization of a novel member of the dystrobrevin gene family. FEBS Lett., 425, 7-13.
18. Peters, M., O'Brien, K., Sadoulet-Puccio, H., Kunkel, L., Adams, M. and Froehner, S. (1997) β-dystrobrevin, a new member of the dystrophin family. Identification, cloning, and protein associations. J. Biol. Chem., 272, 31561-31569.
19. Blake, D.J., Nawrotzki, R., Loh, N.Y., Gorecki, D.C. and Davies, K.E. (1998) β-Dystrobrevin, a member of the dystrophin-related protein family. Proc. Natl Acad Sci. USA, 95, 241-246.
20. Sadoulet-Puccio, H.M., Rajala, M. and Kunkel, L.M. (1997) Dystrobrevin and dystrophin: an interaction through coiled-coil motifs. Proc. Natl Acad. Sci. USA, 94, 12413-12418.
21. Blake, D.J., Nawrotzki, R., Peters, M.F., Froehner, S.C. and Davies, K.E. (1996) Isoform diversity of dystrobrevin, the murine 87-kDa postsynaptic protein. J. Biol. Chem., 271, 7802-7810.
22. Sadoulet-Puccio, H.M., Khurana, T.S., Cohen, J.B. and Kunkel, L.M. (1996) Cloning and characterization of the human homologue of a dystrophin related phosphoprotein found at the Torpedo electric organ postsynaptic membrane. Hum. Mol. Genet., 5, 489-496.
23. Yamamoto, H., Hagiwara, Y., Mizuno, Y., Yoshida, M. and Ozawa, E. (1993) Heterogeneity of dystrophin-associated proteins. J. Biochem. (Tokyo), 114, 132-139.
24. Noguchi, S., Wakabayashi, E., Imamura, M., Yoshida, M. and Ozawa, E. (2000) Formation of sarcoglycan complex with differentiation in cultured myocytes. Eur. J. Biochem., 267, 640-648.
25. Crosbie, R.H., Heighway, J., Venzke, D.P., Lee, J.C. and Campbell, K.P. (1997) Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex. J. Biol. Chem., 272, 31221-31224.
26. Metzinger, L., Blake, D.J., Squier, M.V., Anderson, L.V., Deconinck, A.E., Nawrotzki, R., Hilton-Jones, D. and Davies, K.E. (1997) Dystrobrevin deficiency at the sarcolemma of patients with muscular dystrophy. Hum. Mol. Genet., 6, 1185-1191.
27. Rafael, J., Cox, G., Corrado, K., Jung, D., Campbell, K. and Chamberlain, J. (1996) Forced expression of dystrophin deletion constructs reveals structure-function correlations. J. Cell Biol., 134, 93-102.
28. Ahn, A.H. and Kunkel, L.M. (1995) Syntrophin binds to an alternatively spliced exon of dystrophin. J. Cell Biol., 128, 363-371.
29. Suzuki, A., Yoshida, M. and Ozawa, E. (1995) Mammalian α1-and β1-syntrophin bind to the alternative splice-prone region of the dystrophin COOH terminus. J. Cell Biol., 128, 373-381.
30. Yang, B., Jung, D., Rafael, J.A., Chamberlain, J.S. and Campbell, K.P. (1995) Identification of α-syntrophin binding to syntrophin triplet, dystrophin, and utrophin. J. Biol. Chem., 270, 4975-4978.
31. Sakamoto, A., Ono, K., Abe, M., Jasmin, G., Eki, T., Murakami, Y., Masaki, T., Toyo-oka, T. and Hanaoka, F. (1997) Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, δ-sarcoglycan, in hamster: an animal model of disrupted dystrophin-associated glycoprotein complex. Proc. Natl Acad. Sci. USA, 94, 13873-13878.
32. Chan, Y.-M., Bönnemann, C., Lidov, H.G.W. and Kunkel, L.M. (1998) Molecular organization of sarcoglycan complex in mouse myotubes in culture. J. Cell Biol., 143, 2033-2044.
33. Dwyer, T.M. and Froehner, S.C. (1995) Direct binding of Torpedo syntrophin to dystrophin and the 87 kDa dystrophin homolog. FEBS Lett., 375, 91-94.
34. Ahn, A.H. and Kunkel, L.M. (1995) Syntrophin binds to an alternatively spliced exon of dystrophin. J. Cell Biol., 128, 363-371.
35. Brenman, J.E., Chao, D.S., Xia, H., Aldape, K. and Bredt, D.S. (1995) Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy. Cell, 82, 743-752.
36. Thomas, G.D., Sander, M., Lau, K.S., Huang, P.L., Stull, J.T. and Victor, R.G. (1998) impaired metabolic modulation of alpha-adrenergic vasoconstriction in dystrophin-deficient skeletal muscle. Proc. Natl Acad. Sci. USA, 95, 15090-15095.
37. Kameya, S., Miyagoe, Y., Nonaka, I., Ikemoto, T., Endo, M., Hanaoka, K., Nabeshima, Y. and Takeda, S. (1999) α1-syntrophin gene disruption results in the absence of neuronal-type nitric-oxide synthase at the sarcolemma but does not induce muscle degeneration. J. Biol. Chem., 274, 2193-2200.
38. Venema, V.J., Ju, H., Zou, R. and Venema, R.C. (1997) Interaction of neuronal nitric-oxide synthase with caveolin-3 in skeletal muscle. Identification of a novel caveolin scaffolding/inhibitory domain. J. Biol. Chem., 272, 28187-28190.
39. Minetti, C., Sotgia, F., Bruno, C., Scartezzini, P., Broda, P., Bado, M., Masetti, E., Mazzocco, M., Egeo, A., Donati, M.A. et al. (1998) Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy. Nature Genet., 18, 365-368.
40. McNally, E.M., de Sá Moreira, E., Duggan, D.J., Bönnemann, C., Lisanti, M.P., Lidov, H.G.W., Vainzof, M., Passos-Bueno, M.R., Hoffman, E.P., Zatz, M. and Kunkel, L.M. (1998) Caveolin-3 in muscular dystrophy. Hum. Mol. Genet., 7, 871-877.
41. Heighway, J., Betticher, D.C., Hoban, P.R., Altermatt, H.J. and Cowen, R. (1996) Coamplification in tumors of KRAS2, type 2 inositol 1,4,5 triphosphate receptor gene, and a novel human gene, KRAG. Genomics, 35, 207-214.
42. Ahn, A., Yoshida, M., Anderson, M., Feener, C., Selig, S., Hagiwara, Y., Ozawa, E. and Kunkel, L. (1994) Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24. Proc. Natl Acad. Sci. USA, 91, 4446-4450.