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Functional expression of the Ile693Thr Na + channel mutation associated with paramyotonia congenita in a human cell line
Author(s) -
PlassartSchiess Emmanuelle,
Lhuillier Loïc,
George Alfred L.,
Fontaine Bertrand,
Tabti Nacira
Publication year - 1998
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1111/j.1469-7793.1998.721bs.x
Subject(s) - mutation , skeletal muscle , chemistry , hek 293 cells , mutant , myotonia congenita , microbiology and biotechnology , biology , endocrinology , genetics , gene , biochemistry , myotonia , myotonic dystrophy
1 The Ile693Thr mutation of the skeletal muscle Na + channel α‐subunit is associated with an unusual phenotype of paramyotonia congenita characterized by cold‐induced muscle weakness but no stiffness. This mutation occurs in the S4‐S5 linker of domain II, a region that has not been previously implicated in paramyotonia congenita. 2 The Ile693Thr mutation was introduced into the human skeletal muscle Na + gene for functional expression in human embryonic kidney (HEK) cells. The currents expressed were recorded with the whole‐cell voltage‐clamp technique. 3 In comparison with wild‐type currents, Ile693Thr mutant currents showed a clear shift of about −9 mV in the voltage dependence of activation. 4 In contrast to other mutations of the Na + channel known to cause paramyotonia congenita, the Ile693Thr mutation did not induce any significant change in the kinetics, nor in the voltage dependence, of fast inactivation. 5 In conclusion, this study provides further evidence of the involvement of the S4‐S5 linker in the voltage dependence of Na + channel activation. The negative shift in the voltage dependence found in this mutation must be associated to other defects, plausibly an impairment of the slow inactivation, to account for the long periods of muscle weakness experienced by the patients.