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  • Adams MD, Celniker SE, Holt RA, Evans CA, Gocayne JD, Amanatides PG, Scherer SE, Li PW, Hoskins RA, Galle RF, George RA et al . (2000) The genome sequence of Drosophila melanogaster. Science 5461, 21852195.
  • Bassett D, Currie PD (2004) Identification of a zebrafish model of muscular dystrophy. Clin. Exp. Pharmacol. Physiol. 8, 537540.
  • Bessou C, Giugia JB, Franks CJ, Holden-Dye L, Segalat L (1998) Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hyperactivity and suggest a link with cholinergic transmission. Neurogenetics 2, 6172.
  • Bier E (2005) Drosophila, the golden bug, emerges as a tool for human genetics. Nat. Rev. Genet. 1, 923.
  • Bier E, Bodmer R (2004) Drosophila, an emerging model for cardiac disease. Gene 342, 111.
  • Blake DJ, Weir A, Newey SE, Davies KE (2002) Function and genetics of dystrophin and dystrophin-related proteins in muscle. Physiol. Rev. 82, 291329.
  • Bodmer R (1993) The gene tinman is required for specification of the heart and visceral muscles in Drosophila. Development 118, 719729.
  • Bodmer R (1995) Heart development in Drosophila and its relationship to vertebrate systems. Trends Cardiovasc. Med. 5, 2127.
  • Bodmer R, Frasch M (1999) Genetic determination of Drosophila heart development. In Heart Development (RosenthalN, HarveyR, eds). San Diego: Academic Press, pp. 6590.
  • Bonini NM, Fortini ME (2003) Human neurodegenerative disease modeling using Drosophila. Annu. Rev. Neurosci. 26, 627656.
  • Bostick B, Yue Y, Long C, Duan D (2008) Prevention of dystrophin-deficient cardiomyopathy in twenty-one-month-old carrier mice by mosaic dystrophin expression or complementary dystrophin/utrophin expression. Circ. Res. 102 [Epub].
  • Brand AH, Perrimon N (1993) Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. Development 118, 401415.
  • Cammarato A, Dambacher CM, Knowles AF, Kronert WA, Bodmer R, Ocorr K, Bernstein SI (2008) Myosin transducer mutations differentially affect motor function, myofibril structure and the performance of skeletal and cardiac muscles. Mol. Biol. Cell 2, 553562.
  • Carre-Pierrat M, Grisoni K, Gieseler K, Mariol MC, Martin E, Jospin M, Allard B, Segalat L (2006) The SLO-1 BK channel of Caenorhabditis elegans is critical for muscle function and is involved in dystrophin-dependent muscle dystrophy. J. Mol. Biol. 358, 387395.
  • Chamberlain JS (2002) Gene therapy of muscular dystrophy. Hum. Mol. Genet. 11, 23552362.
  • Chamberlain JS, Metzger J, Reyes M, Townsend D, Faulkner JA (2007) Dystrophin-deficient mdx mice display a reduced life span and are susceptible to spontaneous rhabdomyosarcoma. FASEB J. 9, 21952204.
  • Connors NC, Kofuji P (2002) Dystrophin Dp71 is critical for the clustered localization of potassium channels in retinal glial cells. J. Neurosci. 22, 43214327.
  • Dekkers LC, Van Der Plas MC, Van Loenen PB, Dunnen JT, Van Ommen GJ, Fradkin LG, Noondermeer JN (2004) Embryonic expression patterns of the Drosophila dystrophin-associated glycoprotein complex orthologs. Gene Expr. Patterns 2, 153159.
  • Emery AE (2002) The muscular dystrophies. Lancet 359, 687695.
  • Fortini ME, Bonini NM (2000) Modeling human neurodegenerative diseases in Drosophila: on a wing and a prayer. Trends Genet. 4, 161167.
  • Franco A Jr, Lansman JB (1990) Stretch-sensitive channels in developing muscle cells from a mouse cell line. J. Physiol. 427, 361380.
  • Gieseler K, Grisoni K, Segalat L (2000) Genetic suppression of phenotypes arising from mutations in dystrophin-related genes in Caenorhabditis elegans. Curr. Biol. 18, 10921097.
  • Goodwin FC, Muntoni F (2005) Cardiac involvement in muscular dystrophies: molecular mechanisms. Muscle Nerve 32, 577588.
  • Grady RM, Merlie JP, Sanes JR (1997) Subtle neuromuscular defects in utrophin-deficient mice. J. Cell Biol. 136, 871882.
  • Grain L, Cortina-Borja M, Forfar C, Hilton-Jones D, Hopkin J, Burch M (2001) Cardiac abnormalities and skeletal muscle weakness in carriers of Duchenne and Becker muscular dystrophies and controls. Neuromuscul. Disord. 11, 186191.
  • Greener MJ, Roberts RG (2000) Conservation of components of the dystrophin complex in Drosophila. FEBS Lett. 1–2, 1318.
  • Haag TA, Haag NP, Lekven AC, Hartenstein V (1999) The role of cell adhesion molecules in Drosophila heart morphogenesis: faint sausage, shotgun/DE-cadherin, and laminin A are required for discrete stages in heart development. Dev. Biol. 1, 5669.
  • Holder E, Maeda RD, Bies RD (1996) Expression and regulation of the dystrophin Purkinge promotor in human skeletal muscle, heart and brain. Hum. Genet. 2, 232239.
  • Johnson E, Sherry T, Ringo J, Dowse H (2002) Modulation of the cardiac pacemaker of Drosophila: cellular mechanisms. J. Comp. Physiol. [B] 3, 227236.
  • Judge LM, Haraguchiln M, Chamberlain JS (2006) Dissecting the signaling and mechanical functions of the dystrophin-glycoprotein complex. J. Cell Sci. 119, 15371546.
  • Koenig M, Monaco AP, Kunkel LM (1988) The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein. Cell 53, 219226.
  • Koh GY, Soonpaa MH, Klug MG (1995) Stable fetal cardiomyocyte grafts in the hearts of dystrophic mice and dogs. J. Clin. Invest. 96, 20342042.
  • Kosman D, Mizutani CM, Lemons D, Cox WG, McGinnis W, Bier E (2004) Multiplex detection of RNA expression in Drosophila embryos. Science 305, 846.
  • Lilly B, Zhao B, Ranganayakulu G, Paterson BM, Schulz RA, Olson EN (1995) Requirement of MADS domain transcription factor D-MEF2 for muscle formation in Drosophila. Science 267, 688693.
  • Mallouk N, Allard B (2000) Stretch-induced activation of Ca(2+)-activated K(+) channels in mouse skeletal muscle fibers. Am. J. Physiol. Cell Physiol. 278, C473C479.
  • Mery A, Taghli-Lamallem O, Clark KA, Beckerle MC, Wu X, Ocorr K, Bodmer R (2008) The Drosophila muscle LIM protein, Mlp84B, is essential for cardiac function. J. Exp Biol. (Pt. 1), 1523.
  • Molina MR, Cripps RM (2001) Ostia, the inflow tracts of the Drosophila heart, develop from a genetically distinct subset of cardial cells. Mech. Dev. 1, 5159.
  • Monier B, Astier M, Semeriva M, Perrin L (2005) Steroid-dependent modification of Hox function drives myocyte reprogramming in the Drosophila heart. Development 23, 52835293.
  • Muntoni F, Torelli S, Ferlini A (2003) Dystrophin and mutations: one gene, several proteins, multiple phenotypes. Lancet Neurol. 2, 731740.
  • Neuman S, Kaban A, Volla T, Yeffe D, Nudel U (2001) The dystrophin/utrophin homologues in Drosophila and sea urchin. Gene 263, 1729.
  • Neuman S, Kovlio M, Yaffe D, Nudel U (2005) The Drosophila homologue of the dystrophin gene – introns containing promoters are the major contributors to the large size of the gene. FEBS Lett. 579, 53655371.
  • Nigro G, Comi LI, Politano L, Bain RJ (1990) The incidence and evolution of cardiomyopathy in Duchenne muscular dystrophy. Int. J. Cardiol. 26, 271277.
  • Ocorr K, Reeves N, Wessells R, Fink M, Chen H-SV, Akasaka T, Yasuda S, Metzger JM, Giles W, Posakony J, Bodmer R (2007) KNCQ potassium channel mutations cause cardiac arrhythmias in Drosophila that mimic the effects of aging. Proc. Natl Acad. Sci. USA 104, 39433948.
  • Paternostro G, Vignola C, Bartsch DU, Omens JH, McCulloch AD, Reed JC (2001) Age-associated cardiac dysfunction in Drosophila melanogaster. Circ. Res. 10, 10531058.
  • Petrof BJ, Shrager JB, Stedman HH, Kelly AM, Sweeney HL (1993) Dystrophin protects the sarcolemma from stress developed during muscle contractions. Proc. Natl. Acad. Sci. USA 90, 37103714.
  • Prall OW, Elliott DA, Harvey RP (2002) Developmental paradigms in heart disease: insights from tinman. Ann. Med. 34, 148156.
  • Qian L, Liu J, Bodmer R (2005) Neuromancer Tbx20-related genes (H15/midline) promote cell fate specification and morphogenesis of the Drosophila heart. Dev. Biol. 279, 509524.
  • Quinlan JG, Hahn HS, Wong BL, Lorenz JN, Wenisch AS, Levin LS (2004) Evolution of the mdx mouse cardiomyopathy: physiological and morphological findings. Neuromuscul. Disord. 14, 491496.
  • Rando TA (2001) Role of nitric oxide in the pathogenesis of muscular dystrophies: a ‘two hit’ hypothesis of the cause of muscle necrosis. Microsc. Res. Tech. 4, 223235.
  • Rohman MS, Emoto N, Takeshima Y, Yokoyama M, Matsuo M (2003) Decreased mAKAP, ryanodine receptor, and SERCA2a gene expression in mdx hearts. Biochem. Biophys. Res. Commun. 310, 228235.
  • Rudge MF, Duncan CJ (1988) Ultrastructural changes in the cardiomyopathy of dystrophic hamsters and mice. Tissue Cell 20, 249253.
  • Saide JD, Chin-Bow S, Hogan-Sheldon J, Busquets-Turner L, Vigoreaux JO, Valgeirsdottir K, Pardue ML (1989) Characterization of components of Z-bands in the fibrillar flight muscle of Drosophila melanogaster. J. Cell Biol. 109, 21572167.
  • Saito M, Kawai H, Akaike M, Adachi K, Nishida Y, Saito S (1996) Cardiac dysfunction with Becker muscular dystrophy. Am. Heart J. 132, 642647.
  • Sanyal S, Jennings T, Dowse H, Ramaswami M (2006) Conditional mutations in SERCA, the sarco-endoplasmic reticulum Ca(2+)-ATPase, alter heart rate and rhythmicity in Drosophila. J. Comp. Physiol. [B] 176, 253263.
  • Schneider M, Khalil AA, Poulton J, Castillejo-Lopez C, Egger-Adam D, Wodarz A, Deng WM, Baumgartner S (2006) Perlecan and dystroglycan act at the basal side of the Drosophila follicular epithelium to maintain epithelial organization. Development 133, 38053815.
  • Shcherbata HR, Yatsenko AS, Patterson L, Sood VD, Nudel U, Yaffe D, Baker D, Ruohola-Baker H (2007) Dissecting muscle and neuronal disorders in a Drosophila model of muscular dystrophy. EMBO J. 2, 481493.
  • Straub V, Rafael JA, Chamberlain JS, Campbell KP (1997) Animal models for muscular dystrophy show different patterns of sarcolemmal disruption. J. Cell Biol. 2, 375385.
  • Sutcliffe JE, Korenjak M, Brehm A (2003) Tumour suppressors – a fly's perspective. Eur. J. Cancer 10, 13551362.
  • Townsend D, Blankinship MJ, Allen JM, Gregorevic P, Chamberlain JS, Metzger JM (2007) Systemic administration of micro-dystrophin restores cardiac geometry and prevents dobutamine-induced cardiac pump failure. Mol. Ther. 15, 10861092.
  • Van der Plas MC, Pilgram GS, Plomp JJ, De Jong A, Fradkin LG, Noordermeer JN (2006) Dystrophin is required for appropriate retrograde control of neurotransmitter release at the Drosophila neuromuscular junction. J. Neurosci. 26, 333344.
  • Venkatesh TV et al . (2000) Cardiac enhancer activity of the homeobox gene tinman depends on CREB consensus binding sites in Drosophila. Genesis 1, 5566.
  • Watchko J, O'Day T, Wang B, Zhou L, Tang Y, Li J, Xiao X (2002) Adeno-associated virus vector-mediated minidystrophin gene therapy improves dystrophic muscle contractile function in mdx mice. Hum. Gene Ther. 12, 14511460.
  • Wehling-Henricks M, Jordan MC, Roos KP, Deng B, Tidball JG (2005) Cardiomyopathy in dystrophin-deficient hearts is prevented by expression of a neuronal nitric oxide synthase transgene in the myocardium. Hum. Mol. Genet. 14, 19211933.
  • Wessells RJ, Bodmer R (2004) Screening assays for heart function mutants in Drosophila. Biotechniques 37, 5860.
  • Wessells RJ, Fitzgerald E, Cypser JR, Tatar M, Bodmer R (2004) Insulin regulation of heart function in aging fruit flies. Nat. Genet. 36, 12751281.
  • Williams IA, Allen DG (2007) Intracellular calcium handling in ventricular myocytes from mdx mice. Am. J. Physiol. Heart Circ. Physiol. 292, H846H855.
  • Wolf MJ, Amrein H, Izatt JA, Choma MA, Reedy MC, Rockman HA (2006) Drosophila as a model for the identification of genes causing adult human heart disease. Proc. Natl. Acad. Sci. USA 103, 13941399.
  • Yasuda S, Townsend D, Michele DE, Favre EG, Day SM, Metzger JM (2005) Dystrophic heart failure blocked by membrane sealant poloxamer. Nature 436, 10251029.
  • Yue Y, Li Z, Harper SQ, Davisson RL, Chamberlain JS, Duan DR (2003) Microdystrophins gene therapy of cardiomyopathy restores dystrophin-glycoprotein complex and improves sarcolemma integrity in the mdx mouse heart. Circulation 108, 16261632.
  • Zaffran S, Frasch M (2002) Early signals in cardiac development. Circ. Res. 91, 457469.
  • Zaffran S, Astier M, Gratecos D, Sémériva M (1997) The held out wings (how) Drosophila gene encodes a putative RNA-binding protein involved in the control of muscular and cardiac activity. Development 124, 20872098.