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

1992 ◽  
Vol 182 (2) ◽  
pp. 794-801 ◽  
Author(s):  
Jianzhou Wang ◽  
Cecilia V. Rojas ◽  
Jianhua Zhou ◽  
Lisa S. Schwartz ◽  
Hugh Nicholas ◽  
...  
Genomics ◽  
1991 ◽  
Vol 9 (3) ◽  
pp. 555-556 ◽  
Author(s):  
Alfred L. George ◽  
H. David Ledbetter ◽  
Roland G. Kallen ◽  
Robert L. Barchi

1999 ◽  
Vol 56 (6) ◽  
pp. 692 ◽  
Author(s):  
Ryogen Sasaki ◽  
Hiroki Takano ◽  
Keiko Kamakura ◽  
Kenichi Kaida ◽  
Akira Hirata ◽  
...  

1995 ◽  
Vol 82 (5) ◽  
pp. 1097-1103 ◽  
Author(s):  
Gary M. Vita ◽  
Antonel Olckers ◽  
Anne E. Jedlicka ◽  
Alfred L. George ◽  
Terry Heiman-Patterson ◽  
...  

Background Succinylcholine-induced masseter muscle rigidity (MMR) is a potentially life-threatening complication of anesthesia and is closely correlated with the heterogeneous disorder malignant hyperthermia (MH) susceptibility. MMR also is identified with a variety of neuromuscular disorders, including the myotonias, that are associated with abnormal in vitro contracture test (IVCT) results. Recently, mutations in the adult skeletal muscle sodium channel alpha-subunit gene (SCN4A) have been shown to cause generalized nondystrophic myotonias, some of which are associated with mild nonspecific symptoms. The purpose of the current investigation was to begin to evaluate the molecular genetic relationship between known mutations in the SCN4A gene, MMR, and the results of the IVCT used to diagnose MH-susceptibility. Methods A single extended pedigree of 16 individuals was ascertained through a proband who experienced MMR and whole-body rigidity after succinylcholine administration. Subsequently, four individuals were shown to have a mild form of myotonia on clinical and laboratory examination. IVCT was carried out according to standardized protocols. Mutations in the SCN4A gene were sought in exons 22 and 24 using single-strand conformational analyses. Variability in the SCN4A gene sequence was confirmed by direct DNA sequence analyses. Results Four individuals with myotonia were shown to carry a guanine-to-cytosine mutation at nucleotide position 3917 of the reported SCN4A sequence. This DNA mutation was coinherited with MMR and an abnormal IVCT result in this family. Previous studies have demonstrated that the glycine1306-to-alanine substitution is associated with a mild clinical syndrome referred to as myotonia fluctuans. Conclusions The current report provides direct evidence that succinylcholine-induced MMR, whole-body rigidity, and an abnormal IVCT result are associated with a mutation in the SCN4A gene.


1992 ◽  
Vol 1 (7) ◽  
pp. 521-527 ◽  
Author(s):  
Andrea I.McClatchey ◽  
Carol S.Lin ◽  
Jianzhou Wang ◽  
Eric P.Hoffman ◽  
Cecilia Rojas ◽  
...  

2014 ◽  
Vol 116 (5) ◽  
pp. 926-935 ◽  
Author(s):  
Mirca Marini ◽  
Stefano Ambrosini ◽  
Erica Sarchielli ◽  
Giorgia Donata Zappoli Thyrion ◽  
Laura Bonaccini ◽  
...  

2005 ◽  
Vol 126 (2) ◽  
pp. 161-172 ◽  
Author(s):  
Gregory N. Filatov ◽  
Martin J. Pinter ◽  
Mark M. Rich

Normal muscle has a resting potential of −85 mV, but in a number of situations there is depolarization of the resting potential that alters excitability. To better understand the effect of resting potential on muscle excitability we attempted to accurately simulate excitability at both normal and depolarized resting potentials. To accurately simulate excitability we found that it was necessary to include a resting potential–dependent shift in the voltage dependence of sodium channel activation and fast inactivation. We recorded sodium currents from muscle fibers in vivo and found that prolonged changes in holding potential cause shifts in the voltage dependence of both activation and fast inactivation of sodium currents. We also found that altering the amplitude of the prepulse or test pulse produced differences in the voltage dependence of activation and inactivation respectively. Since only the Nav1.4 sodium channel isoform is present in significant quantity in adult skeletal muscle, this suggests that either there are multiple states of Nav1.4 that differ in their voltage dependence of gating or there is a distribution in the voltage dependence of gating of Nav1.4. Taken together, our data suggest that changes in resting potential toward more positive potentials favor states of Nav1.4 with depolarized voltage dependence of gating and thus shift voltage dependence of the sodium current. We propose that resting potential–induced shifts in the voltage dependence of sodium channel gating are essential to properly regulate muscle excitability in vivo.


Neuron ◽  
1992 ◽  
Vol 8 (5) ◽  
pp. 891-897 ◽  
Author(s):  
Louis J. Ptáček ◽  
Alfred L. George ◽  
Robert L. Barchi ◽  
Robert C. Griggs ◽  
Jack E. Riggs ◽  
...  

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