Literature DB >> 2481825

Dystrophin distribution in heterozygote MDX mice.

S C Watkins1, E P Hoffman, H S Slayter, L M Kunkel.   

Abstract

The distribution of dystrophin in myofibers from normal, mdx hemizygous, and mdx heterozygous mice was studied at various times in development. While normal mice exhibit dystrophin immunostaining around the entire fiber periphery regardless of age, mdx hemizygous mice exhibit no staining (0-35 days). In contrast, young (10 day) heterozygous mdx mice showed neighboring dystrophin-negative and dystrophin-positive fibers as well as fibers with a discontinuous or patchy dystrophin labelling. Older heterozygotes displayed very few negative fibers, with most fibers exhibiting apparently complete dystrophin immunostaining. This, coupled with the absence of muscle fiber degeneration at any age point, and the apparently normal levels of dystrophin in older heterozygous mice, indicates that myonuclei containing the dystrophin gene can compensate for myonuclei which do not contain the dystrophin gene within the same myofiber.

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Year:  1989        PMID: 2481825     DOI: 10.1002/mus.880121013

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  11 in total

1.  Inhibition of myosatellite cell proliferation by gamma irradiation does not prevent the age-related increase of the number of dystrophin-positive fibers in soleus muscles of mdx female heterozygote mice.

Authors:  B Weller; G Karpati; S Lehnert; S Carpenter; B Ajdukovic; P Holland
Journal:  Am J Pathol       Date:  1991-06       Impact factor: 4.307

2.  A model to estimate the expression of the dystrophin gene in muscle from female Becker muscular dystrophy carriers.

Authors:  M Vainzof; M R Passos-Bueno; R C Pavanello; R Schreiber; M Zatz
Journal:  J Med Genet       Date:  1992-07       Impact factor: 6.318

3.  Lack of myoblasts migration between transplanted and host muscles of mdx and normal mice.

Authors:  P D Moens; M C Van-Schoor; G Maréchal
Journal:  J Muscle Res Cell Motil       Date:  1996-02       Impact factor: 2.698

4.  Characterization and localization of a 77 kDa protein related to the dystrophin gene family.

Authors:  E Fabbrizio; U Nudel; G Hugon; A Robert; F Pons; D Mornet
Journal:  Biochem J       Date:  1994-04-15       Impact factor: 3.857

5.  Detection of new paternal dystrophin gene mutations in isolated cases of dystrophinopathy in females.

Authors:  E Pegoraro; R N Schimke; K Arahata; Y Hayashi; H Stern; H Marks; M R Glasberg; J E Carroll; J W Taber; H B Wessel
Journal:  Am J Hum Genet       Date:  1994-06       Impact factor: 11.025

6.  Full-length dystrophin expression in half of the heart cells ameliorates beta-isoproterenol-induced cardiomyopathy in mdx mice.

Authors:  Yongping Yue; Jeffrey W Skimming; Mingju Liu; Tammy Strawn; Dongsheng Duan
Journal:  Hum Mol Genet       Date:  2004-06-09       Impact factor: 6.150

Review 7.  Determining the role of skewed X-chromosome inactivation in developing muscle symptoms in carriers of Duchenne muscular dystrophy.

Authors:  Emanuela Viggiano; Manuela Ergoli; Esther Picillo; Luisa Politano
Journal:  Hum Genet       Date:  2016-04-21       Impact factor: 4.132

8.  Normal myogenic cells from newborn mice restore normal histology to degenerating muscles of the mdx mouse.

Authors:  J E Morgan; E P Hoffman; T A Partridge
Journal:  J Cell Biol       Date:  1990-12       Impact factor: 10.539

9.  Blastocyst injection of wild type embryonic stem cells induces global corrections in mdx mice.

Authors:  Elizabeth Stillwell; Joseph Vitale; Qingshi Zhao; Amanda Beck; Joel Schneider; Farah Khadim; Genie Elson; Aneela Altaf; Ghassan Yehia; Jia-hui Dong; Jing Liu; Willie Mark; Mantu Bhaumik; Robert Grange; Diego Fraidenraich
Journal:  PLoS One       Date:  2009-03-11       Impact factor: 3.240

10.  Connexin-43 reduction prevents muscle defects in a mouse model of manifesting Duchenne muscular dystrophy female carriers.

Authors:  Julie Nouet; Eric Himelman; Kevin C Lahey; Qingshi Zhao; Diego Fraidenraich
Journal:  Sci Rep       Date:  2020-03-30       Impact factor: 4.379

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