Literature DB >> 19118277

Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis.

E Matthews1, R Labrum, M G Sweeney, R Sud, A Haworth, P F Chinnery, G Meola, S Schorge, D M Kullmann, M B Davis, M G Hanna.   

Abstract

BACKGROUND: Several missense mutations of CACNA1S and SCN4A genes occur in hypokalemic periodic paralysis. These mutations affect arginine residues in the S4 voltage sensors of the channel. Approximately 20% of cases remain genetically undefined.
METHODS: We undertook direct automated DNA sequencing of the S4 regions of CACNA1S and SCN4A in 83 cases of hypokalemic periodic paralysis.
RESULTS: We identified reported CACNA1S mutations in 64 cases. In the remaining 19 cases, mutations in SCN4A or other CACNA1S S4 segments were found in 10, including three novel changes and the first mutations in channel domains I (SCN4A) and III (CACNA1S).
CONCLUSIONS: All mutations affected arginine residues, consistent with the gating pore cation leak hypothesis of hypokalemic periodic paralysis. Arginine mutations in S4 segments underlie 90% of hypokalemic periodic paralysis cases.

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Year:  2008        PMID: 19118277      PMCID: PMC2848101          DOI: 10.1212/01.wnl.0000342387.65477.46

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  20 in total

1.  Voltage sensors in domains III and IV, but not I and II, are immobilized by Na+ channel fast inactivation.

Authors:  A Cha; P C Ruben; A L George; E Fujimoto; F Bezanilla
Journal:  Neuron       Date:  1999-01       Impact factor: 17.173

2.  New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis.

Authors:  S Vicart; D Sternberg; E Fournier; F Ochsner; P Laforet; T Kuntzer; B Eymard; B Hainque; B Fontaine
Journal:  Neurology       Date:  2004-12-14       Impact factor: 9.910

Review 3.  Pathomechanisms in channelopathies of skeletal muscle and brain.

Authors:  Stephen C Cannon
Journal:  Annu Rev Neurosci       Date:  2006       Impact factor: 12.449

4.  Sodium channel inactivation defects are associated with acetazolamide-exacerbated hypokalemic periodic paralysis.

Authors:  S Bendahhou; T R Cummins; R C Griggs; Y H Fu; L J Ptácek
Journal:  Ann Neurol       Date:  2001-09       Impact factor: 10.422

5.  Sodium channel gene mutations in hypokalemic periodic paralysis: an uncommon cause in the UK.

Authors:  N P Davies; L H Eunson; M Samuel; M G Hanna
Journal:  Neurology       Date:  2001-10-09       Impact factor: 9.910

6.  A novel mutation in the gene for the adult skeletal muscle sodium channel alpha-subunit (SCN4A) that causes paramyotonia congenita of von Eulenburg.

Authors:  R Sasaki; H Takano; K Kamakura; K Kaida; A Hirata; M Saito; H Tanaka; S Kuzuhara; S Tsuji
Journal:  Arch Neurol       Date:  1999-06

7.  Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current.

Authors:  K Jurkat-Rott; N Mitrovic; C Hang; A Kouzmekine; P Iaizzo; J Herzog; H Lerche; S Nicole; J Vale-Santos; D Chauveau; B Fontaine; F Lehmann-Horn
Journal:  Proc Natl Acad Sci U S A       Date:  2000-08-15       Impact factor: 11.205

8.  Gating pore current in an inherited ion channelopathy.

Authors:  Stanislav Sokolov; Todd Scheuer; William A Catterall
Journal:  Nature       Date:  2007-03-01       Impact factor: 49.962

9.  Histidine scanning mutagenesis of basic residues of the S4 segment of the shaker k+ channel.

Authors:  D M Starace; F Bezanilla
Journal:  J Gen Physiol       Date:  2001-05       Impact factor: 4.086

10.  Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita.

Authors:  L J Ptácek; A L George; R L Barchi; R C Griggs; J E Riggs; M Robertson; M F Leppert
Journal:  Neuron       Date:  1992-05       Impact factor: 17.173

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  66 in total

Review 1.  Mechanism of thyrotoxic periodic paralysis.

Authors:  Shih-Hua Lin; Chou-Long Huang
Journal:  J Am Soc Nephrol       Date:  2012-03-29       Impact factor: 10.121

Review 2.  Mutations of SCN4A gene cause different diseases: 2 case reports and literature review.

Authors:  Xiao-li Liu; Xiao-jun Huang; Xing-hua Luan; Hai-yan Zhou; Tian Wang; Jing-yi Wang; Sheng-di Chen; Hui-dong Tang; Li Cao
Journal:  Channels (Austin)       Date:  2015       Impact factor: 2.581

3.  Dihydropyridine Receptor Congenital Myopathy In A Consangineous Turkish Family.

Authors:  Uluç Yiş; Semra Hiz; Sezgin Güneş; Gülden Diniz; Figen Baydan; Ana Töpf; Ece Sonmezler; Hanns Lochmüller; Rita Horvath; Yavuz Oktay
Journal:  J Neuromuscul Dis       Date:  2019

4.  Leaky sodium channels from voltage sensor mutations in periodic paralysis, but not paramyotonia.

Authors:  David G Francis; Volodymyr Rybalchenko; Arie Struyk; Stephen C Cannon
Journal:  Neurology       Date:  2011-04-13       Impact factor: 9.910

Review 5.  Extracellular potassium homeostasis: insights from hypokalemic periodic paralysis.

Authors:  Chih-Jen Cheng; Elizabeth Kuo; Chou-Long Huang
Journal:  Semin Nephrol       Date:  2013-05       Impact factor: 5.299

6.  A sodium channel knockin mutant (NaV1.4-R669H) mouse model of hypokalemic periodic paralysis.

Authors:  Fenfen Wu; Wentao Mi; Dennis K Burns; Yu Fu; Hillery F Gray; Arie F Struyk; Stephen C Cannon
Journal:  J Clin Invest       Date:  2011-09-01       Impact factor: 14.808

Review 7.  Voltage-sensor mutations in channelopathies of skeletal muscle.

Authors:  Stephen C Cannon
Journal:  J Physiol       Date:  2010-02-15       Impact factor: 5.182

8.  Genetic epidemiology of malignant hyperthermia in the UK.

Authors:  D M Miller; C Daly; E M Aboelsaod; L Gardner; S J Hobson; K Riasat; S Shepherd; R L Robinson; J G Bilmen; P K Gupta; M-A Shaw; P M Hopkins
Journal:  Br J Anaesth       Date:  2018-08-17       Impact factor: 9.166

9.  Bumetanide prevents transient decreases in muscle force in murine hypokalemic periodic paralysis.

Authors:  Fenfen Wu; Wentao Mi; Stephen C Cannon
Journal:  Neurology       Date:  2013-02-20       Impact factor: 9.910

10.  Functional analysis of three Nav1.6 mutations causing early infantile epileptic encephalopathy.

Authors:  Laura Solé; Jacy L Wagnon; Michael M Tamkun
Journal:  Biochim Biophys Acta Mol Basis Dis       Date:  2020-09-08       Impact factor: 5.187

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