δ-sarcoglycan is necessary for early heart and muscle development in zebrafish

Biochemical and Biophysical Research Communications

Volumn 344, Issue 4, 2006, Pages 1290-1299

  Cheng, Lu ^a   Guo, Xiao fang ^a   Yang, Xue yan ^a   Chong, Mei ^a   Cheng, Jing ^a   Li, Ge ^a   Gui, Yong hao ^a   Lu, Da ru ^a  

^a FUDAN UNIVERSITY   (China)

Author keywords

Development; Heart; Muscle; Sarcoglycan; Zebrafish

Indexed keywords

DELTA SARCOGLYCAN; SARCOGLYCAN; UNCLASSIFIED DRUG;

ANIMAL EMBRYO; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BLADDER; CELL DIFFERENTIATION; CONTROLLED STUDY; DEVELOPMENTAL GENETICS; EMBRYO; EMBRYO DEVELOPMENT; EYE; FUNCTIONAL PROTEOMICS; GENE MUTATION; GENETIC ASSOCIATION; HEART DEVELOPMENT; HEART DISEASE; HEART MUSCLE CELL; HYPOPLASIA; IN SITU HYBRIDIZATION; JAW; KNOCKOUT GENE; MESENCEPHALON; MUSCLE DEVELOPMENT; MUSCLE MALFORMATION; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN DETERMINATION; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; RETINA; TISSUE DISTRIBUTION; ZEBRA FISH;

ANIMALS; EMBRYO, NONMAMMALIAN; HEART; MUSCLE DEVELOPMENT; MUSCLES; OLIGODEOXYRIBONUCLEOTIDES, ANTISENSE; SARCOGLYCANS; SOMITES; ZEBRAFISH; ZEBRAFISH PROTEINS;

DANIO RERIO; VERTEBRATA;

EID: 33646183010     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2006.03.234     Document Type: Article

References (37)

1. Nigro V., Piluso G., Belsito A., Politano L., Puca A.A., Papparella S., Rossi E., Viglietto G., Esposito M.G., Abbondanza C., Medici N., Molinari A.M., Nigro G., and Puca G.A. Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein. Hum. Mol. Genet. 5 (1996) 1179-1186
2. Jung D., Duclos F., Apostol B., Straub V., Lee J.C., Allamand V., Venzke D.P., Sunada Y., Moomaw C.R., Leveille C.J., Slaughter C.A., Crawford T.O., McPherson J.D., and Campbell K.P. Characterization of δ-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy. J. Biol. Chem. 271 (1996) 32321-32329
3. Yoshida M., Noguchi S., Wakabayashi E., Piluso G., Belsito A., Nigro V., and Ozawa E. The fourth component of the sarcoglycan complex. FEBS Lett. 403 (1997) 143-148
4. Ervasti J.M., Ohlendieck K., Kahl S.D., Gaver M.G., and Campbell K.P. Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle. Nature 345 (1990) 315-319
5. Yoshida M., and Ozawa E. Glycoprotein complex anchoring dystrophin to sarcolemma. J. Biochem. (Tokyo) 108 (1990) 748-752
6. Hack A.A., Groh M.E., and McNally E.M. Sarcoglycans in muscular dystrophy. Microsc. Res. Technol. 48 (2000) 167-180
7. Wheeler M.T., Zarnegar S., and McNally E.M. ζ-sarcoglycan, a novel component of the sarcoglycan complex, is reduced in muscular dystrophy. Hum. Mol. Genet. 11 (2002) 2147-2154
8. Ettinger A.J., Feng G., and Sanes J.R. epsilon-Sarcoglycan, a broadly expressed homologue of the gene mutated in limb-girdle muscular dystrophy 2D. J. Biol. Chem. 272 (1997) 32534-32538
9. Noguchi S., Wakabayashi E., Imamura M., Yoshida M., and Ozawa E. Formation of sarcoglycan complex with differentiation in cultured myocytes. Eur. J. Biochem. 267 (2000) 640-648
10. Shi W., Chen Z., Schottenfeld J., Stahl R.C., Kunkel L.M., and Chan Y.M. Specific assembly pathway of sarcoglycans is dependent on beta- and delta-sarcoglycan. Muscle Nerve 29 (2004) 409-419
11. Hack A.A., Cordier L., Shoturma D.I., Lam M.Y., Sweeney H.L., and McNally E.M. Muscle degeneration without mechanical injury in sarcoglycan deficiency. Proc. Natl. Acad. Sci. USA 96 (1999) 10723-10728
12. Chan Y.M., Bonnemann C.G., Lidov H.G., and Kunkel L.M. Molecular organization of sarcoglycan complex in mouse myotubes in culture. J. Cell. Biol. 143 (1998) 2033-2044
13. Durbeej M., and Campbell K.P. Muscular dystrophies involving the dystrophin-glycoprotein complex: an overview of current mouse models. Curr. Opin. Genet. Dev. 12 (2002) 349-361
14. Nigro V., de Sa Moreira E., Piluso G., Vainzof M., Belsito A., Politano L., Puca A.A., Passos-Bueno M.R., and Zatz M. Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene. Nat. Genet. 14 (1996) 195-198
15. Moreira E.S., Vainzof M., Marie S.K., Nigro V., Zatz M., and Passos-Bueno M.R. A first missense mutation in the δ-sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies. J. Med. Genet. 35 (1998) 951-953
16. Dincer P., Bonnemann C.G., Erdir Aker O., Akcoren Z., Nigro V., Kunkel L.M., and Topalolu H. A homozygous nonsense mutation in delta-sarcoglycan exon 3 in a case of LGMD2F. Neuromuscul. Disord. 10 (2000) 247-250
17. Tsubata S., Bowles K.R., Vatta M., Zintz C., Titus J., Muhonen L., Bowles N.E., and Towbin J.A. Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy. J. Clin. Invest. 106 (2000) 655-662
18. Sakamoto A., Ono K., Abe M., Jasmin G., Eki T., Murakami Y., Masaki T., Toyo-oka T., and Hanaoka F. 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 (1997) 13873-13878
19. Mitsuhashi S., Saito N., Watano K., Igarashi K., Tagami S., Shima H., and Kikuchi K. Defect of δ-sarcoglycan gene is responsible for development of dilated cardiomyopathy of a novel hamster strain, J2N-k: calcineurin/PP2B activity in the heart of J2N-k hamster. J. Biochem. (Tokyo) 134 (2003) 269-276
20. Karkkainen S., Miettinen R., Tuomainen P., Karkkainen P., Helio T., Reissell E., Kaartinen M., Toivonen L., Nieminen M.S., Kuusisto J., Laakso M., and Peuhkurinen K. A novel mutation, Arg71Thr, in the δ-sarcoglycan gene is associated with dilated cardiomyopathy. J. Mol. Med. 81 (2003) 795-800
21. Westerfield M. The Zebrafish Book (1995), Eugene Press, Eugene, Oregon
22. Kimmel C.B., Ballard W.W., Kimmel S.R., Ullmann B., and Schilling T.F. Stages of embryonic development of the zebrafish. Dev. Dyn. 203 (1995) 253-310
23. Dominguez I., Itoh K., and Sokol S.Y. Role of glycogen synthase kinase 3 beta as a negative regulator of dorsoventral axis formation in Xenopus embryos. Proc. Natl. Acad. Sci. USA 92 (1995) 8498-8502
24. Nasevicius A., and Ekker S.C. Effective targeted gene 'knockdown' in zebrafish. Nat. Genet. 26 (2000) 216-220
25. Weinberg E.S., Allende M.L., Kelly C.S., Abdelhamid A., Murakami T., Andermann P., Doerre O.G., Grunwald D.J., and Riggleman B. Developmental regulation of zebrafish MyoD in wild-type, no tail and spadetail embryos. Development 122 (1996) 271-280
26. Nikaido M., Tada M., Saji T., and Ueno N. Conservation of BMP signaling in zebrafish mesoderm patterning. Mech. Dev. 61 (1997) 75-88
27. Berdougo E., Coleman H., Lee D.H., Stainier D.Y., and Yelon D. Mutation of weak atrium/atrial myosin heavy chain disrupts atrial function and influences ventricular morphogenesis in zebrafish. Development 130 (2003) 6121-6129
28. Serbedzija G.N., Chen J.N., and Fishman M.C. Regulation in the heart field of zebrafish. Development 125 (1998) 1095-1101
29. Walsh E.C., and Stainier D.Y. UDP-glucose dehydrogenase required for cardiac valve formation in zebrafish. Science 293 (2001) 1670-1673
30. Chen J.N., van Eeden F.J., Warren K.S., Chin A., Nusslein-Volhard C., Haffter P., and Fishman M.C. Left-right pattern of cardiac BMP4 may drive asymmetry of the heart in zebrafish. Development 124 (1997) 4373-4382
31. Chambers S.P., Anderson L.V., Maguire G.M., Dodd A., and Love D.R. Sarcoglycans of the zebrafish: orthology and localization to the sarcolemma and myosepta of muscle. Biochem. Biophys. Res. Commun. 303 (2003) 488-495
32. Wheeler M.T., Korcarz C.E., Collins K.A., Lapidos K.A., Hack A.A., Lyons M.R., Zarnegar S., Earley J.U., Lang R.M., and McNally E.M. Secondary coronary artery vasospasm promotes cardiomyopathy progression. Am. J. Pathol. 164 (2004) 1063-1071
33. Claudepierre T., Dalloz C., Mornet D., Matsumura K., Sahel J., and Rendon A. Characterization of the intermolecular associations of the dystrophin-associated glycoprotein complex in retinal Muller glial cells. J. Cell Sci. 113 (2000) 3409-3417
34. Dekkers L.C., van der Plas M.C., van Loenen P.B., den Dunnen J.T., van Ommen G.J., Fradkin L.G., and Noordermeer J.N. Embryonic expression patterns of the Drosophila dystrophin-associated glycoprotein complex orthologs. Gene Express Patterns 4 (2004) 153-159
35. Guyon J.R., Mosley A.N., Zhou Y., Davidson A.J., Sheng X., Chiang K., O'Brien K.F., Volinski J.M., Zon L.I., and Kunkel L.M. The dystrophin associated protein complex in zebrafish. Hum. Mol. Genet. 12 (2003) 601-615
36. Parsons M.J., Campos I., Hirst E.M., and Stemple D.L. Removal of dystroglycan causes severe muscular dystrophy in zebrafish embryos. Development 129 (2002) 3505-3512
37. Guyon J.R., Mosley A.N., Jun S.J., Montanaro F., Steffen L.S., Zhou Y., Nigro V., Zon L.I., and Kunkel L.M. δ-sarcoglycan is required for early zebrafish muscle organization. Exp. Cell Res. 304 (2005) 105-115