Literature DB >> 7894483

Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx mice.

D S Greenberg1, Y Sunada, K P Campbell, D Yaffe, U Nudel.   

Abstract

Dp71 is a non-muscle product of the Duchenne muscular dystrophy gene. It consists of the cysteine-rich and C-terminal domains of dystrophin. We have generated transgenic mdx mice which do not have dystrophin but express Dp71 in their muscle. In these mice, Dp71 was localized to the plasma membrane and restored normal levels of dystrophin associated proteins (DAPs), indicating that Dp71 is capable of interacting with the DAPs in a similar manner to dystrophin. However, the presence of Dp71 and DAPs in the muscle fibres of mdx mice was not sufficient to alleviate symptoms of muscle degeneration.

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Year:  1994        PMID: 7894483     DOI: 10.1038/ng1294-340

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  32 in total

1.  The dystrophin-associated glycoprotein complex: what parts can you do without?

Authors:  H L Sweeney; E R Barton
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-05       Impact factor: 11.205

Review 2.  Gene replacement therapies for duchenne muscular dystrophy using adeno-associated viral vectors.

Authors:  Jane T Seto; Julian N Ramos; Lindsey Muir; Jeffrey S Chamberlain; Guy L Odom
Journal:  Curr Gene Ther       Date:  2012-06       Impact factor: 4.391

Review 3.  The membrane-cytoskeleton interface: the role of dystrophin and utrophin.

Authors:  S J Winder
Journal:  J Muscle Res Cell Motil       Date:  1997-12       Impact factor: 2.698

4.  Expression of the dystrophin isoform Dp116 preserves functional muscle mass and extends lifespan without preventing dystrophy in severely dystrophic mice.

Authors:  Luke M Judge; Andrea L H Arnett; Glen B Banks; Jeffrey S Chamberlain
Journal:  Hum Mol Genet       Date:  2011-09-23       Impact factor: 6.150

5.  Preventing phosphorylation of dystroglycan ameliorates the dystrophic phenotype in mdx mouse.

Authors:  Gaynor Miller; Chris J Moore; Rebecca Terry; Tracy La Riviere; Andrew Mitchell; Robert Piggott; T Neil Dear; Dominic J Wells; Steve J Winder
Journal:  Hum Mol Genet       Date:  2012-07-18       Impact factor: 6.150

6.  Functional protection of dystrophic mouse (mdx) muscles after adenovirus-mediated transfer of a dystrophin minigene.

Authors:  N Deconinck; T Ragot; G Maréchal; M Perricaudet; J M Gillis
Journal:  Proc Natl Acad Sci U S A       Date:  1996-04-16       Impact factor: 11.205

Review 7.  Creatine kinase, cell membrane and Duchenne muscular dystrophy.

Authors:  E Ozawa; Y Hagiwara; M Yoshida
Journal:  Mol Cell Biochem       Date:  1999-01       Impact factor: 3.396

Review 8.  Dystrophin Dp71: the smallest but multifunctional product of the Duchenne muscular dystrophy gene.

Authors:  Ramin Tadayoni; Alvaro Rendon; L E Soria-Jasso; Bulmaro Cisneros
Journal:  Mol Neurobiol       Date:  2011-11-22       Impact factor: 5.590

9.  Mechanical and non-mechanical functions of Dystrophin can prevent cardiac abnormalities in Drosophila.

Authors:  Ouarda Taghli-Lamallem; Krzysztof Jagla; Jeffrey S Chamberlain; Rolf Bodmer
Journal:  Exp Gerontol       Date:  2013-11-12       Impact factor: 4.032

10.  Unique expression of cytoskeletal proteins in human soft palate muscles.

Authors:  Farhan Shah; Diana Berggren; Thorbjörn Holmlund; Eva Levring Jäghagen; Per Stål
Journal:  J Anat       Date:  2015-11-24       Impact factor: 2.610

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