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The Muscle Chloride Channel ClC-1 Has a Double-Barreled Appearance that Is Differentially Affected in Dominant and Recessive Myotonia
Open accessAbstract
Single-channel recordings of the currents mediated by the muscle Cl− channel, ClC-1, expressed in Xenopus oocytes, provide the first direct evidence that this channel has two equidistant open conductance levels like the Torpedo ClC-0 prototype. As for the case of ClC-0, the probabilities and dwell times of the closed and conducting states are consistent with the presence of two independently gated pathways with ≈ 1.2 pS conductance enabled in parallel via a common gate. However, the voltage dependence of the common gate is different and the kinetics are much faster than for ClC-0. Estimates of single-channel parameters from the analysis of macroscopic current fluctuations agree with those from single-channel recordings. Fluctuation analysis was used to characterize changes in the apparent double-gate behavior of the ClC-1 mutations I290M and I556N causing, respectively, a dominant and a recessive form of myotonia. We find that both mutations reduce about equally the open probability of single protopores and that mutation I290M yields a stronger reduction of the common gate open probability than mutation I556N. Our results suggest that the mammalian ClC-homologues have the same structure and mechanism proposed for the Torpedo channel ClC-0. Differential effects on the two gates that appear to modulate the activation of ClC-1 channels may be important determinants for the different patterns of inheritance of dominant and recessive ClC-1 mutations.
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Cited by
Molecular Structure and Physiological Function of Chloride Channels
Jentsch, T. J., Stein, V., Weinreich, F., & Zdebik, A. A. (2002) · Physiological Reviews · doi:10.1152/physrev.00029.2001 · Cited by 1,256
Pores Formed by Single Subunits in Mixed Dimers of Different CLC Chloride Channels
Weinreich, F., & Jentsch, T. J. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m005733200 · Cited by 131
Structure of the CLC-1 chloride channel from Homo sapiens
Park, E., & MacKinnon, R. (2018) · eLife · doi:10.7554/elife.36629 · Cited by 109
Ion permeation through a Cl − -selective channel designed from a CLC Cl − /H + exchanger
Jayaram, H., Accardi, A., Wu, F., Williams, C., & Miller, C. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804503105 · Cited by 101
The ClC-0 chloride channel is a 'broken' Cl−/H+ antiporter
Lísal, J., & Maduke, M. (2008) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1466 · Cited by 100
Metadata
- Authors
- Saviane, C., Conti, F., & Pusch, M.
- Venue
- The Journal of General Physiology
- Publisher
- Rockefeller University Press
- Published
- 1999-03-01
- Volume
- 113
- Issue
- 3
- Pages
- 457-468
- ISSN
- 0022-1295 (ISSN-L)
- 1540-7748
- OpenAlex
- W2104177088
- Cited by
- 189
- References
- 0
- FWCI
- 3.91
- Type
- journal article
- Language
- en
- Open access
- green
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- CoChat. (2026). Citation check: The Muscle Chloride Channel ClC-1 Has a Double-Barreled Appearance that Is Differentially Affected in Dominant and Recessive Myotonia. https://app.cochat.ai/papers/10.1085/jgp.113.3.457
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- Saviane, C., Conti, F., & Pusch, M. (1999). The Muscle Chloride Channel ClC-1 Has a Double-Barreled Appearance that Is Differentially Affected in Dominant and Recessive Myotonia. The Journal of General Physiology. https://doi.org/10.1085/jgp.113.3.457
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