http://www.cnr.it/ontology/cnr/individuo/prodotto/ID23690
Expression and location of myotonic dystrophy protein kinase in human skeletal muscle cells determined with a novel antibody: possible role of the protein in cytokeletal rearrangement during differentation (Articolo in rivista)
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- Expression and location of myotonic dystrophy protein kinase in human skeletal muscle cells determined with a novel antibody: possible role of the protein in cytokeletal rearrangement during differentation (Articolo in rivista) (literal)
- Anno
- 2005-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/J.CELLBI.2005.05.011 (literal)
- Alternative label
Beffy, P.a; Barsanti, C.b; Del Carratore, R.a; Simi, S.a; Benedetti, P.A.c; Benzi, L.d; Prelle, A.e; Ciscato, P.e; Simili, M.a (2005)
Expression and location of myotonic dystrophy protein kinase in human skeletal muscle cells determined with a novel antibody: possible role of the protein in cytokeletal rearrangement during differentation
in Cell biology international (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Beffy, P.a; Barsanti, C.b; Del Carratore, R.a; Simi, S.a; Benedetti, P.A.c; Benzi, L.d; Prelle, A.e; Ciscato, P.e; Simili, M.a (literal)
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- In: \"Cell Biol Int \"29,2005,9,742-753 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Note
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- a Institute of Clinical Physiology, C.N.R., Research Area, Via Moruzzi n.1, 56100 Pisa, Italy
b Department of Physiology and Biochemistry, University of Pisa, Pisa, Italy
c Institute for Chemical and Physical Processes, C.N.R, Pisa, Italy
d Department of Endocrinology and Metabolism, University of Pisa, Pisa, Italy
e Ospedale Maggiore, Department of Neuroscience, University of Milan, Italy (literal)
- Titolo
- Expression and location of myotonic dystrophy protein kinase in human skeletal muscle cells determined with a novel antibody: possible role of the protein in cytokeletal rearrangement during differentation (literal)
- Abstract
- Myotonic dystrophy is a multisystemic disorder, due to a CTG triplet expansion at the 3'UTR of the DM1 gene encoding for myotonic dystrophy protein kinase. Recent studies indicate that decreased DMPK levels could account for part of the symptoms suggesting a role of this protein in skeletal muscle differentiation. To investigate this aspect, polyclonal antibodies were raised against two peptides of the catalytic domain and against the human full-length DMPK (DMFL). In western blots, anti-hDMFL antibody was able to detect low amounts of purified human recombinant protein and recognized the splicing isoforms in heart and stomach of overexpressing mice. In human muscle extracts, this antibody specifically recognized a protein of apparent molecular weight of 85 kDa and it specifically stained neuromuscular junctions in skeletal muscle sections. In contrast, both anti-peptide antibodies demonstrated low specificity for either denatured or native DMPK, suggesting that these two epitopes are probably cryptic sites. Using anti-hDMFL, the expression and localization of DMPK was studied in human skeletal muscle cells (SkMC). Western blot analysis indicated that the antibody recognizes a main protein of apparent MW of 75 kDa, which appears to be expressed during differentiation into myotubes. Immunolocalization showed low levels of DMPK in the cytoplasm of undifferentiated cells; during differentiation the staining became more intense and was localized to the terminal part of the cells, suggesting that DMPK might have a role in cell elongation and fusion. (literal)
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