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Literature DB >> 7607329

Dystrophin-associated protein A0 is a homologue of the Torpedo 87K protein.

M Yoshida¹, H Yamamoto, S Noguchi, Y Mizuno, Y Hagiwara, E Ozawa.

Abstract

We raised a monoclonal antibody, MA0, which reacts with A0, a 94-kDa rabbit skeletal muscle dystrophin-associated protein (DAP) bound to the syntrophin-binding domain of dystrophin. The antibody also reacted with the 62-kDa DAP which was moved to the locus close to beta-syntrophins by 2-dimensional PAGE, but the DAP did not coincide with any known beta-syntrophins. We have cloned a fragment of cDNA which codes the protein reacting with MA0 from a neonatal rabbit heart cDNA library. Based on the coincidence of cDNA sequences and the similarity in molecular mass, we concluded that the proteins reacting with MA0 are rabbit homologues of the Torpedo 87K protein.

Entities: Chemical Gene Species

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Year: 1995 PMID： 7607329 DOI： 10.1016/0014-5793(95)00574-s

Source DB: PubMed Journal: FEBS Lett ISSN： 0014-5793 Impact factor: 4.124

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Cited

12 in total

1. Desmuslin, an intermediate filament protein that interacts with alpha -dystrobrevin and desmin.

Authors: Y Mizuno; T G Thompson; J R Guyon; H G Lidov; M Brosius; M Imamura; E Ozawa; S C Watkins; L M Kunkel
Journal: Proc Natl Acad Sci U S A Date: 2001-05-15 Impact factor: 11.205

2. Dystrobrevin increases dystrophin's binding to the dystrophin-glycoprotein complex and provides protection during cardiac stress.

Authors: Jana Strakova; Jon D Dean; Katharine M Sharpe; Tatyana A Meyers; Guy L Odom; DeWayne Townsend
Journal: J Mol Cell Cardiol Date: 2014-08-24 Impact factor: 5.000

Dystrophin-associated protein A0 is a homologue of the Torpedo 87K protein.

1. Desmuslin, an intermediate filament protein that interacts with alpha -dystrobrevin and desmin.

2. Dystrobrevin increases dystrophin's binding to the dystrophin-glycoprotein complex and provides protection during cardiac stress.

3. Dystrobrevin and dystrophin: an interaction through coiled-coil motifs.

Review 4. The membrane-cytoskeleton interface: the role of dystrophin and utrophin.

Review 5. Creatine kinase, cell membrane and Duchenne muscular dystrophy.

6. Muscle degeneration without mechanical injury in sarcoglycan deficiency.

7. NO production results in suspension-induced muscle atrophy through dislocation of neuronal NOS.

8. Interaction of α-catulin with dystrobrevin contributes to integrity of dystrophin complex in muscle.

9. Differential membrane localization and intermolecular associations of alpha-dystrobrevin isoforms in skeletal muscle.

10. Assembly of the dystrophin-associated protein complex does not require the dystrophin COOH-terminal domain.