© 1993 Oxford University Press
OTHER |
The cloning and expression of a sodium channel ß1-subunit cDNA from human brain
Molecular Neurogenetics Unit, Massachusetts General Hospital and Department of Genetics, Harvard Medical School Charlestown MA 02129 1Howard Hughes Medical Institute and Department of Neurology, Massachusetts General Hospital and Harvard Medical School Boston, MA 02114, USA
* To whom correspondence should be addressed at: Molecular Neurogenetics Unit, Massachusetts General Hospital East, Building 149,13th Street Charlestown, MA 02129, USA
Received February 2, 1993; Revised April 12, 1993; Accepted April 12, 1993
Electrical excitability of neurons and muscle cells is mediated largely through the actions of the voltage-gated sodium channel. Initiation and propagation of the action potential is a direct result of the precisely controlled inward flux of sodium through these channels. Much attention has been paid to the sodium channel
-subunit, the major, pore-forming component. However,
-subunits are associated with one or more smaller ß-subunits, which have been implicated in the critical fine tuning of the gating properties of the channel. To investigate the properties of the ß-subunit, we have isolated a cDNA encoding the human brain ß1-subunit and assigned the corresponding gene to chromosome 19. We have also examined the effects of expressing the brain ß1-subunit on the kinetics of a coexpressed muscle sodium channel
-subunit. Our results underscore the functional importance of the ß1-subunit and imply a conserved mechanism for the interaction of the ß1-subunit with different
-subunits.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
D. Hu, H. Barajas-Martinez, E. Burashnikov, M. Springer, Y. Wu, A. Varro, R. Pfeiffer, T. T. Koopmann, J. M. Cordeiro, A. Guerchicoff, et al. A Mutation in the {beta}3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG Phenotype Circ Cardiovasc Genet, June 1, 2009; 2(3): 270 - 278. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. F. Struyk, V. S. Markin, D. Francis, and S. C. Cannon Gating Pore Currents in DIIS4 Mutations of NaV1.4 Associated with Periodic Paralysis: Saturation of Ion Flux and Implications for Disease Pathogenesis J. Gen. Physiol., October 1, 2008; 132(4): 447 - 464. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Webb and S. C. Cannon Cold-induced defects of sodium channel gating in atypical periodic paralysis plus myotonia Neurology, March 4, 2008; 70(10): 755 - 761. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Medeiros-Domingo, T. Kaku, D. J. Tester, P. Iturralde-Torres, A. Itty, B. Ye, C. Valdivia, K. Ueda, S. Canizales-Quinteros, M. T. Tusie-Luna, et al. SCN4B-Encoded Sodium Channel 4 Subunit in Congenital Long-QT Syndrome Circulation, July 10, 2007; 116(2): 134 - 142. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. F. Struyk and S. C. Cannon A Na+ Channel Mutation Linked to Hypokalemic Periodic Paralysis Exposes a Proton-selective Gating Pore J. Gen. Physiol., July 1, 2007; 130(1): 11 - 20. [Abstract] [Full Text] [PDF] |
||||
![]() |
F.-f. Wu, E. Gordon, E. P. Hoffman, and S. C. Cannon A C-terminal skeletal muscle sodium channel mutation associated with myotonia disrupts fast inactivation J. Physiol., June 1, 2005; 565(2): 371 - 380. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Johnson, M. L. Montpetit, P. J. Stocker, and E. S. Bennett The Sialic Acid Component of the {beta}1 Subunit Modulates Voltage-gated Sodium Channel Function J. Biol. Chem., October 22, 2004; 279(43): 44303 - 44310. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. F. Struyk and S. C. Cannon Slow Inactivation Does Not Block the Aqueous Accessibility to the Outer Pore of Voltage-gated Na Channels J. Gen. Physiol., September 30, 2002; 120(4): 509 - 516. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. P Takahashi and S. C Cannon Mexiletine block of disease-associated mutations in S6 segments of the human skeletal muscle Na+ channel J. Physiol., December 15, 2001; 537(3): 701 - 714. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Vijayaragavan, M. E. O'Leary, and M. Chahine Gating Properties of Nav1.7 and Nav1.8 Peripheral Nerve Sodium Channels J. Neurosci., October 15, 2001; 21(20): 7909 - 7918. [Abstract] [Full Text] [PDF] |
||||
![]() |
F.-F. Wu, M.P. Takahashi, E. Pegoraro, C. Angelini, P. Colleselli, S.C. Cannon, and E.P. Hoffman A new mutation in a family with cold-aggravated myotonia disrupts Na+ channel inactivation Neurology, April 10, 2001; 56(7): 878 - 884. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. R Bezzina, M. B Rook, and A. A.M Wilde Cardiac sodium channel and inherited arrhythmia syndromes Cardiovasc Res, February 1, 2001; 49(2): 257 - 271. [Full Text] [PDF] |
||||
![]() |
A. F. Struyk, K. A. Scoggan, D. E. Bulman, and S. C. Cannon The Human Skeletal Muscle Na Channel Mutation R669H Associated with Hypokalemic Periodic Paralysis Enhances Slow Inactivation J. Neurosci., December 1, 2000; 20(23): 8610 - 8617. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Lehmann-Horn and K. Jurkat-Rott Voltage-Gated Ion Channels and Hereditary Disease Physiol Rev, October 1, 1999; 79(4): 1317 - 1372. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. J. Hayward, G. M. Sandoval, and S. C. Cannon Defective slow inactivation of sodium channels contributes to familial periodic paralysis Neurology, April 1, 1999; 52(7): 1447 - 1447. [Abstract] [Full Text] |
||||
![]() |
C. V. Rojas, A. Neely, G. Velasco-Loyden, V. Palma, and M. Kukuljan Hyperkalemic periodic paralysis M1592V mutation modifies activation in human skeletal muscle Na+ channel Am J Physiol Cell Physiol, January 1, 1999; 276(1): C259 - C266. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. S Green, A. L George Jr, and S. C Cannon Human sodium channel gating defects caused by missense mutations in S6 segments associated with myotonia: S804F and V1293I J. Physiol., August 1, 1998; 510(3): 685 - 694. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Vedantham and S. C. Cannon Slow Inactivation Does Not Affect Movement of the Fast Inactivation Gate in Voltage-gated Na+ Channels J. Gen. Physiol., January 1, 1998; 111(1): 83 - 93. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. Q. Gu, S. Dib-Hajj, M. A. Rizzo, and S. G. Waxman TTX-Sensitive and -Resistant Na+ Currents, and mRNA for the TTX-Resistant rH1 Channel, Are Expressed in B104 Neuroblastoma Cells J Neurophysiol, January 1, 1997; 77(1): 236 - 246. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. A. Gurnett and K. P. Campbell Transmembrane Auxiliary Subunits of Voltage-dependent Ion Channels J. Biol. Chem., November 8, 1996; 271(45): 27975 - 27978. [Full Text] [PDF] |
||||
![]() |
L. Sangameswaran, S. G. Delgado, L. M. Fish, B. D. Koch, L. B. Jakeman, G. R. Stewart, P. Sze, J. C. Hunter, R. M. Eglen, and R. C. Herman Structure and Function of a Novel Voltage-gated, Tetrodotoxin-resistant Sodium Channel Specific to Sensory Neurons J. Biol. Chem., March 15, 1996; 271(11): 5953 - 5956. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Qu, L. L. Isom, R. E. Westenbroek, J. C. Rogers, T. N. Tanada, K. A. McCormick, T. Scheuer, and W. A. Catterall Modulation of Cardiac Na[IMAGE] Channel Expression in Xenopus Oocytes by beta1 Subunits J. Biol. Chem., October 27, 1995; 270(43): 25696 - 25701. [Abstract] [Full Text] [PDF] |
||||










