Literature DB >> 1310396

Sequence and genomic structure of the human adult skeletal muscle sodium channel alpha subunit gene on 17q.

J Z Wang1, C V Rojas, J H Zhou, L S Schwartz, H Nicholas, E P Hoffman.   

Abstract

The amino acid sequence of the sodium channel alpha subunit from adult human skeletal muscle has been deduced by cross-species PCR-mediated cloning and sequencing of the cDNA. The protein consists of 1836 amino acid residues. The amino acid sequence shows 93% identity to the alpha subunit from rat adult skeletal muscle and 70% identity to the alpha subunit from other mammalian tissues. A 500 kb YAC clone containing the complete coding sequence and two overlapping lambda clones covering 68% of the cDNA were used to estimate the gene size at 35 kb. The YAC clone proved crucial for gene structure studies as the high conservation between ion channel genes made hybridization studies with total genomic DNA difficult. Our results provide valuable information for the study of periodic paralysis and paramyotonia congenita, two inherited neurological disorders which are caused by point mutations within this gene.

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Year:  1992        PMID: 1310396     DOI: 10.1016/0006-291x(92)91802-w

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  8 in total

1.  Molecular genetic and genetic correlations in sodium channelopathies: lack of founder effect and evidence for a second gene.

Authors:  J Wang; J Zhou; S M Todorovic; W G Feero; F Barany; R Conwit; I Hausmanowa-Petrusewicz; A Fidzianska; K Arahata; H B Wessel
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

2.  Biophysical costs associated with tetrodotoxin resistance in the sodium channel pore of the garter snake, Thamnophis sirtalis.

Authors:  Chong Hyun Lee; David K Jones; Christopher Ahern; Maen F Sarhan; Peter C Ruben
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2010-09-07       Impact factor: 1.836

Review 3.  Sodium channelopathies of skeletal muscle result from gain or loss of function.

Authors:  Karin Jurkat-Rott; Boris Holzherr; Michael Fauler; Frank Lehmann-Horn
Journal:  Pflugers Arch       Date:  2010-03-17       Impact factor: 3.657

4.  Functional expression and properties of the human skeletal muscle sodium channel.

Authors:  M Chahine; P B Bennett; A L George; R Horn
Journal:  Pflugers Arch       Date:  1994-05       Impact factor: 3.657

5.  Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families.

Authors:  A Elbaz; J Vale-Santos; K Jurkat-Rott; P Lapie; R A Ophoff; B Bady; T P Links; C Piussan; A Vila; N Monnier
Journal:  Am J Hum Genet       Date:  1995-02       Impact factor: 11.025

6.  A Sodium Channel Myotonia Presenting with Intermittent Dysphagia as a Manifestation of a Rare SCN4A Variant.

Authors:  Jihane N Benhammou; Jennifer Phan; Hane Lee; Kevin Ghassemi; William Parsons; Wayne W Grody; Joseph R Pisegna
Journal:  J Mol Neurosci       Date:  2016-12-23       Impact factor: 3.444

7.  RNA metabolism in myotonic dystrophy: patient muscle shows decreased insulin receptor RNA and protein consistent with abnormal insulin resistance.

Authors:  A Morrone; E Pegoraro; C Angelini; E Zammarchi; G Marconi; E P Hoffman
Journal:  J Clin Invest       Date:  1997-04-01       Impact factor: 14.808

8.  RNA sequencing reveals region-specific molecular mechanisms associated with epileptogenesis in a model of classical hippocampal sclerosis.

Authors:  A S Vieira; A H de Matos; A M do Canto; C S Rocha; B S Carvalho; V D B Pascoal; B Norwood; S Bauer; F Rosenow; R Gilioli; F Cendes; I Lopes-Cendes
Journal:  Sci Rep       Date:  2016-03-03       Impact factor: 4.379

  8 in total

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