Literature DB >> 16650823

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

Lu Cheng1, Xiao-fang Guo, Xue-yan Yang, Mei Chong, Jing Cheng, Ge Li, Yong-hao Gui, Da-ru Lu.   

Abstract

Delta-sarcoglycan, one member of the sarcoglycan complex, is a very conservative muscle-specific protein exclusively expressed in the skeletal and cardiac muscles of vertebrates. Mutations in sarcoglycans are known to be involved in limb-girdle muscular dystrophy (LGMD) and dilated cardiomyopathy (DCM) in humans. To address the role of delta-sarcoglycan gene in zebrafish development, we have studied expression pattern of delta-sarcoglycan in zebrafish embryos and examined the role of delta-sarcoglycan in zebrafish embryonic development by morpholino. Strong expression of delta-sarcoglycan was observed in various muscles including those of the segment, heart, eye, jaw, pectoral fin, branchial arches, and swim bladder in zebrafish embryo. Delta-sarcoglycan was also expressed in midbrain and retina. Knockdown of delta-sarcoglycan resulted in severe abnormality in both the cardiac and skeletal muscles. Some severe ones displayed serious morphological abnormality such as hypoplastic head, linear heart, very weak heartbeats, and runtish trunk, all dead within 5 dpf. Whole-mount in situ hybridization analysis showed that adaxial cells and muscle pioneers were affected in delta-sarcoglycan knockdown embryos. In addition, absence of delta-sarcoglycan protein severely delayed the cardiac development and influenced the differentiation of cardiac muscle, and the cardiac left-right asymmetry was dramatically changed in morpholino-treated embryos. These data together suggest that delta-sarcoglycan plays an important role in early heart and muscle development.

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Year:  2006        PMID: 16650823     DOI: 10.1016/j.bbrc.2006.03.234

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  15 in total

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3.  Lack of Apobec2-related proteins causes a dystrophic muscle phenotype in zebrafish embryos.

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5.  Specific knockdown of delta-sarcoglycan gene in C2C12 in vitro causes post-translational loss of other sarcoglycans without mechanical stress.

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8.  Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin.

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Review 9.  Neuromuscular disorders in zebrafish: state of the art and future perspectives.

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Review 10.  Zebrafish models flex their muscles to shed light on muscular dystrophies.

Authors:  Joachim Berger; Peter D Currie
Journal:  Dis Model Mech       Date:  2012-11       Impact factor: 5.758

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