Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis

Silvia Corrochano, Roope Männikkö, Peter I. Joyce, Philip McGoldrick, Jessica Wettstein, Glenda Lassi, Dipa L Raja Rayan, Gonzalo Blanco, Colin Quinn, Andrianos Liavas, Arimantas Lionikas, Neta Amior, James Dick, Estelle G. Healy, Michelle Stewart, Sarah Carter, Marie Hutchinson, Liz Bentley, Pietro Fratta, Andrea CorteseRoger Cox, D. Steve, Valter Tucci, Henning Wackerhage, Anthony A. Amato, Linda Greensmith, Martin Koltzenburg, Michael G. Hanna, Abraham Acevedo-Arozena

Research output: Contribution to journalArticle

Abstract

Mutations in the skeletal muscle channel (SCN4A), encoding the Nav1.4 voltage-gated sodium channel, are causative of a variety of muscle channelopathies, including non-dystrophic myotonias and periodic paralysis. The effects of many of these mutations on channel function have been characterized both in vitro and in vivo. However, little is known about the consequences of SCN4A mutations downstream from their impact on the electrophysiology of the Nav1.4 channel. Here we report the discovery of a novel SCN4A mutation (c.1762A>G; p.I588V) in a patient with myotonia and periodic paralysis, located within the S1 segment of the second domain of the Nav1.4 channel. Using N-ethyl-N-nitrosourea mutagenesis, we generated and characterized a mouse model (named draggen), carrying the equivalent point mutation (c.1744A>G; p.I582V) to that found in the patient with periodic paralysis and myotonia. Draggen mice have myotonia and suffer from intermittent hind-limb immobility attacks. In-depth characterization of draggen mice uncovered novel systemic metabolic abnormalities in Scn4a mouse models and provided novel insights into disease mechanisms. We discovered metabolic alterations leading to lean mice, as well as abnormal AMP-activated protein kinase activation, which were associated with the immobility attacks and may provide a novel potential therapeutic target.

Original languageEnglish
Pages (from-to)3171-3185
Number of pages15
JournalBrain
Volume137
Issue number12
DOIs
Publication statusPublished - Dec 1 2014

Fingerprint

Myotonia
AMP-Activated Protein Kinases
Paralysis
Mutation
NAV1.4 Voltage-Gated Sodium Channel
Channelopathies
Ethylnitrosourea
Electrophysiology
Point Mutation
Mutagenesis
Skeletal Muscle
Extremities
Mouse
Muscles

Keywords

  • AMPK
  • Mice
  • Myotonia
  • Periodic paralysis
  • SCN4A

ASJC Scopus subject areas

  • Clinical Neurology
  • Arts and Humanities (miscellaneous)

Cite this

Corrochano, S., Männikkö, R., Joyce, P. I., McGoldrick, P., Wettstein, J., Lassi, G., ... Acevedo-Arozena, A. (2014). Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis. Brain, 137(12), 3171-3185. https://doi.org/10.1093/brain/awu292

Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis. / Corrochano, Silvia; Männikkö, Roope; Joyce, Peter I.; McGoldrick, Philip; Wettstein, Jessica; Lassi, Glenda; Rayan, Dipa L Raja; Blanco, Gonzalo; Quinn, Colin; Liavas, Andrianos; Lionikas, Arimantas; Amior, Neta; Dick, James; Healy, Estelle G.; Stewart, Michelle; Carter, Sarah; Hutchinson, Marie; Bentley, Liz; Fratta, Pietro; Cortese, Andrea; Cox, Roger; Steve, D.; Tucci, Valter; Wackerhage, Henning; Amato, Anthony A.; Greensmith, Linda; Koltzenburg, Martin; Hanna, Michael G.; Acevedo-Arozena, Abraham.

In: Brain, Vol. 137, No. 12, 01.12.2014, p. 3171-3185.

Research output: Contribution to journalArticle

Corrochano, S, Männikkö, R, Joyce, PI, McGoldrick, P, Wettstein, J, Lassi, G, Rayan, DLR, Blanco, G, Quinn, C, Liavas, A, Lionikas, A, Amior, N, Dick, J, Healy, EG, Stewart, M, Carter, S, Hutchinson, M, Bentley, L, Fratta, P, Cortese, A, Cox, R, Steve, D, Tucci, V, Wackerhage, H, Amato, AA, Greensmith, L, Koltzenburg, M, Hanna, MG & Acevedo-Arozena, A 2014, 'Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis', Brain, vol. 137, no. 12, pp. 3171-3185. https://doi.org/10.1093/brain/awu292
Corrochano S, Männikkö R, Joyce PI, McGoldrick P, Wettstein J, Lassi G et al. Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis. Brain. 2014 Dec 1;137(12):3171-3185. https://doi.org/10.1093/brain/awu292
Corrochano, Silvia ; Männikkö, Roope ; Joyce, Peter I. ; McGoldrick, Philip ; Wettstein, Jessica ; Lassi, Glenda ; Rayan, Dipa L Raja ; Blanco, Gonzalo ; Quinn, Colin ; Liavas, Andrianos ; Lionikas, Arimantas ; Amior, Neta ; Dick, James ; Healy, Estelle G. ; Stewart, Michelle ; Carter, Sarah ; Hutchinson, Marie ; Bentley, Liz ; Fratta, Pietro ; Cortese, Andrea ; Cox, Roger ; Steve, D. ; Tucci, Valter ; Wackerhage, Henning ; Amato, Anthony A. ; Greensmith, Linda ; Koltzenburg, Martin ; Hanna, Michael G. ; Acevedo-Arozena, Abraham. / Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis. In: Brain. 2014 ; Vol. 137, No. 12. pp. 3171-3185.
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abstract = "Mutations in the skeletal muscle channel (SCN4A), encoding the Nav1.4 voltage-gated sodium channel, are causative of a variety of muscle channelopathies, including non-dystrophic myotonias and periodic paralysis. The effects of many of these mutations on channel function have been characterized both in vitro and in vivo. However, little is known about the consequences of SCN4A mutations downstream from their impact on the electrophysiology of the Nav1.4 channel. Here we report the discovery of a novel SCN4A mutation (c.1762A>G; p.I588V) in a patient with myotonia and periodic paralysis, located within the S1 segment of the second domain of the Nav1.4 channel. Using N-ethyl-N-nitrosourea mutagenesis, we generated and characterized a mouse model (named draggen), carrying the equivalent point mutation (c.1744A>G; p.I582V) to that found in the patient with periodic paralysis and myotonia. Draggen mice have myotonia and suffer from intermittent hind-limb immobility attacks. In-depth characterization of draggen mice uncovered novel systemic metabolic abnormalities in Scn4a mouse models and provided novel insights into disease mechanisms. We discovered metabolic alterations leading to lean mice, as well as abnormal AMP-activated protein kinase activation, which were associated with the immobility attacks and may provide a novel potential therapeutic target.",
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AU - Corrochano, Silvia

AU - Männikkö, Roope

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AU - Wettstein, Jessica

AU - Lassi, Glenda

AU - Rayan, Dipa L Raja

AU - Blanco, Gonzalo

AU - Quinn, Colin

AU - Liavas, Andrianos

AU - Lionikas, Arimantas

AU - Amior, Neta

AU - Dick, James

AU - Healy, Estelle G.

AU - Stewart, Michelle

AU - Carter, Sarah

AU - Hutchinson, Marie

AU - Bentley, Liz

AU - Fratta, Pietro

AU - Cortese, Andrea

AU - Cox, Roger

AU - Steve, D.

AU - Tucci, Valter

AU - Wackerhage, Henning

AU - Amato, Anthony A.

AU - Greensmith, Linda

AU - Koltzenburg, Martin

AU - Hanna, Michael G.

AU - Acevedo-Arozena, Abraham

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N2 - Mutations in the skeletal muscle channel (SCN4A), encoding the Nav1.4 voltage-gated sodium channel, are causative of a variety of muscle channelopathies, including non-dystrophic myotonias and periodic paralysis. The effects of many of these mutations on channel function have been characterized both in vitro and in vivo. However, little is known about the consequences of SCN4A mutations downstream from their impact on the electrophysiology of the Nav1.4 channel. Here we report the discovery of a novel SCN4A mutation (c.1762A>G; p.I588V) in a patient with myotonia and periodic paralysis, located within the S1 segment of the second domain of the Nav1.4 channel. Using N-ethyl-N-nitrosourea mutagenesis, we generated and characterized a mouse model (named draggen), carrying the equivalent point mutation (c.1744A>G; p.I582V) to that found in the patient with periodic paralysis and myotonia. Draggen mice have myotonia and suffer from intermittent hind-limb immobility attacks. In-depth characterization of draggen mice uncovered novel systemic metabolic abnormalities in Scn4a mouse models and provided novel insights into disease mechanisms. We discovered metabolic alterations leading to lean mice, as well as abnormal AMP-activated protein kinase activation, which were associated with the immobility attacks and may provide a novel potential therapeutic target.

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