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© The Rockefeller University Press, 0022-1295/1997//165/ $5.00
Journal of General Physiology, Volume 110, Number 2, 1997


Article

Inward Rectification in ClC-0 Chloride Channels Caused by Mutations in Several Protein Regions

Uwe Ludewig, Thomas J. Jentsch, and Michael Pusch

From the Center for Molecular Neurobiology (ZMNH), Hamburg University, D-20246 Hamburg, Germany

Several cloned ClC-type Cl channels open and close in a voltage-dependent manner. The Torpedo electric organ Cl channel, ClC-0, is the best studied member of this gene family. ClC-0 is gated by a fast and a slow gating mechanism of opposite voltage direction. Fast gating is dependent on voltage and on the external and internal Cl concentration, and it has been proposed that the permeant anion serves as the gating charge in ClC-0 (Pusch, M., U. Ludewig, A. Rehfeldt, and T.J. Jentsch. 1995. Nature (Lond.). 373:527–531). The deactivation at negative voltages of the muscular ClC-1 channel is similar but not identical to ClC-0. Different from the extrinsic voltage dependence suggested for ClC-0, an intrinsic voltage sensor had been proposed to underlie the voltage dependence in ClC-1 (Fahlke, C., R. Rüdel, N. Mitrovic, M. Zhou, and A.L. George. 1995. Neuron. 15:463–472; Fahlke, C., A. Rosenbohm, N. Mitrovic, A.L. George, and R. Rüdel. 1996. Biophys. J. 71:695–706). The gating model for ClC-1 was partially based on the properties of a point-mutation found in recessice myotonia (D136G). Here we investigate the functional effects of mutating the corresponding residue in ClC-0 (D70). Both the corresponding charge neutralization (D70G) and a charge conserving mutation (D70E) led to an inwardly rectifying phenotype resembling that of ClC-1 (D136G). Several other mutations at very different positions in ClC-0 (K165R, H472K, S475T, E482D, T484S, T484Q), however, also led to a similar phenotype. In one of these mutants (T484S) the typical wild-type gating, characterized by a deactivation at negative voltages, can be partially restored by using external perchlorate (ClO4) solutions. We conclude that gating in ClC-0 and ClC-1 is due to similar mechanisms. The negative charge at position 70 in ClC-0 does not specifically confer the voltage sensitivity in ClC-channels, and there is no need to postulate an intrinsic voltage sensor in ClC-channels.

Key Words: gating • myotonia • voltage dependence • anion


Address correspondence to Thomas J. Jentsch, Center for Molecular Neurobiology (ZMNH), Hamburg University, Martinistr. 52, D-20246 Hamburg, Germany. Fax: 49-40-4717-4839; E-mail: jentsch{at}plexus.uke.uni-hamburg.de

Abbreviations: WT, wild-type


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