Membrane currents of pawn mutants of the pwA group in Paramecium tetraurelia.

Membrane currents were recorded from the wild type and two pawn mutants of the pwA complementation group in Paramecium tetraurelia under a voltage clamp. Most currents are not changed by the mutations. Transient inward currents of a leaky mutant, pwA132, upon step depolarizations are less than those in the wild type. The inward transient is completely lacking in a non-leaky mutant, pwA500. The time course of the residual inward currents in the leaky mutant is not significantly different from that of wild type. The voltage sensitivity of the Ca channels in the leaky mutant is also similar to that of wild type. The inward currents upon membrane hyperpolarizations in the mutants show normal characteristics in the presence or absence of external K+. With sufficiently large, prolonged depolarization, outward currents progressively develop in the wild type but decay in the mutants. The simplest conclusion we can draw is that the pwA mutations reduce the number of functional Ca channels but do not change the channel characteristics. From the conductance measurements, 45% of the Ca channels remain in the leaky mutant pwA132, and none remain in the non-leaky mutant pwA500. By subtracting the outward currents of pwA500 from the slow and prolonged outward currents of the wild type, we have tentatively separated a Ca-induced K+ current from the voltage-dependent K+ current. The time courses of these two currents differ by two orders of magnitude.

[1]  C. Kung,et al.  Voltage Sensitive Ca-Channels and the Transient Inward Current in Paramecium Tetraurelia , 1979 .

[2]  R. Eckert,et al.  Calcium entry leads to inactivation of calcium channel in Paramecium. , 1978, Science.

[3]  C. Kung,et al.  K-resistant mutants and "adaptation" in Paramecium. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[4]  S. Schein,et al.  Separation of membrane currents using a Paramecium mutant , 1977, Nature.

[5]  S. Schein,et al.  Altered calcium conductance in pawns, behavioural mutants of Paramecium aurelia. , 1976, Journal of Experimental Biology.

[6]  C. Kung,et al.  A 'TEA+-insensitive' mutant with increased potassium conductance in Paramecium aurelia. , 1976, The Journal of experimental biology.

[7]  J. Berger Gene expression and phenotypic change in Paramecium tetraurelia exconjugants. , 1976, Genetical research.

[8]  G. Vassort,et al.  Initial and delayed membrane currents in crab muscle fibre under voltage‐clamp conditions. , 1975, The Journal of physiology.

[9]  C. Kung,et al.  Membrane excitability: made temperature-dependent by mutations. , 1974, Proceedings of the National Academy of Sciences of the United States of America.

[10]  C. Kung,et al.  An extensive behavioural and genetic analysis of the pawn mutants in Paramecium aurelia. , 1974, Genetical research.

[11]  C. Kung,et al.  Genetic Dissection of Active Electrogenesis in Paramecium aurelia , 1974, Nature.

[12]  R. Eckert,et al.  Electrical properties of Paramecium caudatum: all-or-none electrogenesis , 1968, Zeitschrift für vergleichende Physiologie.

[13]  B. Katz,et al.  The electrical properties of crustacean muscle fibres , 1953, The Journal of physiology.

[14]  C. Kung,et al.  A regenerative hyperpolarization inParamecium , 2004, Journal of Comparative Physiology.

[15]  P Brehm,et al.  Ionic mechanisms of excitation in Paramecium. , 1979, Annual review of biophysics and bioengineering.

[16]  Y. Satow Internal calcium concentration and potassium permeability in Paramecium. , 1978, Journal of neurobiology.

[17]  R. Eckert,et al.  Calcium‐dependent repolarization in Paramecium , 1978, The Journal of physiology.

[18]  S. Hagiwara Ca spike. , 1973, Advances in biophysics.

[19]  S. Dryl Chemotaxis in Ciliate Protozoa , 1973 .

[20]  T. M. Sonneborn Chapter 12 Methods in Paramecium Research , 1970 .

[21]  H. Jennings Behavior of the Lower Organisms , 1907 .