Literature DB >> 2559760

Primary structure and functional expression of a mammalian skeletal muscle sodium channel.

J S Trimmer1, S S Cooperman, S A Tomiko, J Y Zhou, S M Crean, M B Boyle, R G Kallen, Z H Sheng, R L Barchi, F J Sigworth.   

Abstract

We describe the isolation and characterization of a cDNA encoding the alpha subunit of a new voltage-sensitive sodium channel, microI, from rat skeletal muscle. The 1840 amino acid microI peptide is homologous to alpha subunits from rat brain, but, like the protein from eel electroplax, lacks an extended (approximately 200) amino acid segment between homologous domains I and II. Northern blot analysis indicates that the 8.5 kb microI transcript is preferentially expressed in skeletal muscle. Sodium channels expressed in Xenopus oocytes from synthetic RNA encoding microI are blocked by tetrodotoxin and mu-conotoxin at concentrations near 5 nM. The expressed sodium channels have gating kinetics similar to the native channels in rat muscle fibers, except that inactivation occurs more slowly.

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Year:  1989        PMID: 2559760     DOI: 10.1016/0896-6273(89)90113-x

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  190 in total

1.  Voltage-dependent sodium channel function is regulated through membrane mechanics.

Authors:  A Shcherbatko; F Ono; G Mandel; P Brehm
Journal:  Biophys J       Date:  1999-10       Impact factor: 4.033

2.  Effects of channel cytoplasmic regions on the activation mechanisms of cardiac versus skeletal muscle Na(+) channels.

Authors:  E S Bennett
Journal:  Biophys J       Date:  1999-12       Impact factor: 4.033

3.  A single residue differentiates between human cardiac and skeletal muscle Na+ channel slow inactivation.

Authors:  Y Y Vilin; E Fujimoto; P C Ruben
Journal:  Biophys J       Date:  2001-05       Impact factor: 4.033

4.  Structural determinants of slow inactivation in human cardiac and skeletal muscle sodium channels.

Authors:  Y Y Vilin; N Makita; A L George; P C Ruben
Journal:  Biophys J       Date:  1999-09       Impact factor: 4.033

5.  A point mutation in domain 4-segment 6 of the skeletal muscle sodium channel produces an atypical inactivation state.

Authors:  J P O'Reilly; S Y Wang; G K Wang
Journal:  Biophys J       Date:  2000-02       Impact factor: 4.033

6.  Novel point mutations in the German cockroach para sodium channel gene are associated with knockdown resistance (kdr) to pyrethroid insecticides.

Authors:  Z Liu; S M Valles; K Dong
Journal:  Insect Biochem Mol Biol       Date:  2000-10       Impact factor: 4.714

7.  Identification of a chloride-formate exchanger expressed on the brush border membrane of renal proximal tubule cells.

Authors:  F Knauf; C L Yang; R B Thomson; S A Mentone; G Giebisch; P S Aronson
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-17       Impact factor: 11.205

8.  Outer and central charged residues in DIVS4 of skeletal muscle sodium channels have differing roles in deactivation.

Authors:  James Groome; Esther Fujimoto; Lisa Walter; Peter Ruben
Journal:  Biophys J       Date:  2002-03       Impact factor: 4.033

9.  Sodium channel mRNAs at the neuromuscular junction: distinct patterns of accumulation and effects of muscle activity.

Authors:  S S Awad; R N Lightowlers; C Young; Z M Chrzanowska-Lightowlers; T Lomo; C R Slater
Journal:  J Neurosci       Date:  2001-11-01       Impact factor: 6.167

10.  Dual tandem promoter elements containing CCAC-like motifs from the tetrodotoxin-resistant voltage-sensitive Na+ channel (rSkM2) gene can independently drive muscle-specific transcription in L6 cells.

Authors:  H Zhang; M N Maldonado; R L Barchi; R G Kallen
Journal:  Gene Expr       Date:  1999
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