Ultrastructural localization of adhalin in normal murine skeletal myofiber

Annals of Neurology

Volumn 39, Issue 2, 1996, Pages 217-223

  Wakayama, Yoshihiro ^a   Inoue, Masahiko ^a   Murahashi, Makoto ^a   Shibuya, Seiji ^a   Jimi, Takahiro ^a   Kojima, Hiroko ^a   Oniki, Hiroaki ^a  

^a SHOWA UNIVERSITY FUJIGAOKA HOSPITAL   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADHALIN; DYSTROPHIN; SPECTRIN;

ANIMAL CELL; ANIMAL TISSUE; ANTIBODY LABELING; ARTICLE; CARBOXY TERMINAL SEQUENCE; CELL MEMBRANE; CELL ULTRASTRUCTURE; CYTOSKELETON; IMMUNOBLOTTING; IMMUNOGOLD STAINING; IMMUNOHISTOCHEMISTRY; MOUSE; MUSCLE FIBER MEMBRANE; MUSCLE FIBRIL; NONHUMAN; PRIORITY JOURNAL; PROTEIN LOCALIZATION; SARCOPLASM; SKELETAL MUSCLE;

ANIMALS; BLOTTING, WESTERN; CYTOSKELETAL PROTEINS; DYSTROGLYCANS; DYSTROPHIN; IMMUNOHISTOCHEMISTRY; MEMBRANE GLYCOPROTEINS; MICE; MICE, INBRED C57BL; MICROSCOPY, IMMUNOELECTRON; MUSCLE FIBERS; MUSCLE, SKELETAL; REFERENCE VALUES; SARCOGLYCANS; SPECTRIN; TISSUE DISTRIBUTION;

EID: 0030030297     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410390211     Document Type: Article

References (34)

1. Roberds SL, Anderson RD, Ibraghimov-Beskrovnaya O, Campbell KP. Primary structure and muscle-specific expression of the 50-kDa dystrophin-associated glycoprotein (adhalin). J Biol Chem 1993;268:23739-23742
2. Ervasti JM, Campbell KP. Membrane organization of the dystrophin-glycoprotein complex. Cell 1991;66:1121-1131
3. Yamamoto H, Hagiwara Y, Mizuno Y, et al. Heterogeneity of dystrophin-associated proteins. J Biochem 1993;114:132-139
4. Ibraghimov-Beskrovnaya O, Milatovich A, Ozcelik T, et al. Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization. Hum Mol Genet 1993;2:1651-1657
5. Ahn AH, Kunkel LM. Syntrophin binds to an alternatively spliced exon of dystrophin. J Cell Biol 1995;128:363-371
6. Suzuki A, Yoshida M, Ozawa E. Mammalian α1- and β1-syntrophin bind to the alternative splice-prone region of the dystrophin COOH terminus. J Cell Biol 1995;128:373-381
7. Suzuki A, Yoshida M, Hayashi K, et al. 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 1994;220:283-292
8. Wakayama Y, Jimi T, Takeda A, et al. Immunoelectron microscopic localization of C-terminus of 43-kDa dystrophin-associated glycoprotein in normal human skeletal myofibers. J Electron Microsc 1994;43:327-331
9. Wakayama Y, Shibuya S, Takeda A, et al. Ultrastructural localization of the C-terminus of the 43-kd dystrophin-associated glycoprotein and its relation to dystrophin in normal murine skeletal myofiber. Am J Pathol 1995;146:189-196
10. Ibraghimov-Beskrovnaya O, Ervasti JM, Leveille CJ, et al. Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix. Nature 1992;355:696-702
11. Ervasti JM, Campbell KP. A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin. J Cell Biol 1993;122:809-823
12. Hemmings L, Kuhlman PA, Critchley DR. Analysis of the actin-binding domain of α-actinin by mutagenesis and demonstration that dystrophin contains a functionally homologous domain. J Cell Biol 1992;116:1369-1380
13. Yoshida M, Mizuno Y, Nonaka I, Ozawa E. A dystrophin-associated glycoprotein, A3a (one of 43 DAG doublets), is retained in Duchenne muscular dystrophy muscle. J Biochem 1993;114:634-639
14. Mizuno Y, Yoshida M, Nonaka I, et al. Expression of utrophin (dystrophin-related protein) and dystrophin-associated glycoproteins in muscles from patients with Duchenne muscular dystrophy. Muscle Nerve 1994;17:206-216
15. Jimi T, Wakayama Y, Takeda A, et al. Altered distribution of β-dystroglycan in sarcolemma of human dystrophic muscles: an immunohistochemical study. Muscle Nerve 1995;18:910-913
16. Yamamoto H, Mizuno Y, Hayashi K, et al. Expression of dys trophin-associated protein 35 DAG (A4) and 50 DAG (A2) is confined to striated muscles. J Biochem 1994;115:162-167
17. Matsumura K, Tomé FMS, Collin H, et al. Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy. Nature 1992;359:320-322
18. Roberds SL, Leturcq F, Allamand V, et al. Missense mutations in the adhalin gene linked to autosomal recesssive muscular dystrophy. Cell 1994;78:625-633
19. Ljunggren A, Duggan D, McNally E, et al. Primary adhalin deficiency as a cause of muscular dystrophy in patients with normal dystrophin. Ann Neurol 1995;38:367-372
20. Campbell KP. Adhalin gene mutations and autosomal recessive limb-girdle muscular dystrophy. Ann Neurol 1995;38:353-354
21. Roberds SL, Ervasti JM, Anderson RD, et al. Disruption of the dystrophin-glycoprotein complex in the cardiomyopathic hamster. J Biol Chem 1993;268:11496-11499
22. Mizuno Y, Noguchi S, Yamamoto H, et al. Sarcoglycan complex is selectively lost in dystrophic hamster muscle. Am J Pathol 1995;146:530-536
23. McNally EM, Yoshida M, Mizuno Y, et al. Human adhalin is alternatively spliced and the gene is located on chromosome 17q21. Proc Natl Acad Sci USA 1994;91:9690-9694
24. Azibi K, Bachner L, Beckmann JS, et al. Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12. Hum Mol Genet 1993;2:1423-1428
25. Wakayama Y, Jimi T, Takeda A, et al. Immunoreactivity of antibodies raised against synthetic peptide fragments predicted from mid-portions of dystrophin cDNA. J Neurol Sci 1990; 97:241-250
26. Byers TJ, Kunkel LM, Watkins SC. The subcellular distribution of dystrophin in mouse skeletal, cardiac, and smooth muscle. J Cell Biol 1991;115:411-421
27. Lidov HGW, Byers TJ, Watkins SC, Kunkel LM. Localization of dystrophin to postsynaptic regions of central nervous system cortical neurons. Nature 1990;348:725-728
28. Cullen MJ, Walsh J, Nicholson LVB. Immunogold localization of the 43-kDa dystroglycan at the plasma membrane in control and dystrophic human muscle. Acta Neuropathol 1994;87: 349-354
29. Porter GA, Dmytrenko GM, Winkelmann JC, Bloch RJ. Dystrophin colocalizes with β-spectrin in distinct subsarcolemmal domains in mammalian skeletal muscle. J Cell Biol 1992;117: 997-1005
30. Masuda T, Fujimaki N, Ozawa E, Ishikawa H. Confocal laser microscopy of dystrophin localization in guinea pig skeletal muscle fibers. J Cell Biol 1992;119:543-548
31. Minetti C, Beltrame F, Marcenaro G, Bonilla E. Dystrophin at the plasma membrane of human muscle fibers shows a costameric localization. Neuromusc Disord 1992;2:99-109
32. Straub V, Bittner RE, Léger JJ, Voit T. Direct visualization of the dystrophin network on skeletal muscle fiber membrane. J Cell Biol 1992;119:1183-1191
33. Pardo JV, Siliciano JD, Craig SW. A vinculin-containing cortical lattice in skeletal muscle: transverse lattice elements ("costameres") mark sites of attachment between myofibrils and sarcolemma. Proc Natl Acad Sci USA 1983;80:1008-1012
34. Mizuno Y, Yoshida M, Yamamoto H, et al. Distribution of dystrophin isoforms and dystrophin-associated proteins 43 DAG (A3a) and 50 DAG (A2) in various monkey tissues. J Biochem 1993;114:936-941