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J Neurophysiol (April 1, 2003). 10.1152/jn.00837.2002
Submitted on Submitted 20 September 2002; accepted in final form 19 December
2002
1Department of Neurobiology and Behavior, Cornell University, Ithaca, New York 14853; and 2Millennium Pharmaceuticals, Cambridge, Massachusetts 02139
Zhang, Y.,
J. N. MacLean,
W. F. An,
C. C. Lanning, and
R. M. Harris-Warrick.
KChIP1 and Frequenin Modify shal-Evoked Potassium
Currents in Pyloric Neurons in the Lobster Stomatogastric
Ganglion. J. Neurophysiol. 89: 1902-1909, 2003. The
transient potassium current (IA) plays
an important role in shaping the firing properties of pyloric neurons
in the stomatogastric ganglion (STG) of the spiny lobster,
Panulirus interruptus. The shal gene encodes
IA in pyloric neurons. However, when
we over-expressed the lobster Shal protein by shal RNA
injection into the pyloric dilator (PD) neuron, the increased
IA had somewhat different properties from the endogenous IA. The recently
cloned K-channel interacting proteins (KChIPs) can modify vertebrate
Kv4 channels in cloned cell lines. When we co-expressed
hKChIP1 with lobster shal in Xenopus
oocytes or lobster PD neurons, they produced A-currents resembling the
endogenous IA in PD neurons; compared
with currents evoked by shal alone, their voltage for half
inactivation was depolarized, their kinetics of inactivation were
slowed, and their recovery from inactivation was accelerated. We also
co-expressed shal in PD neurons with lobster
frequenin, which encodes a protein belonging to the same
EF-hand family of Ca2+ sensing proteins as
hKChIP. Frequenin also restored most of properties of the
shal-evoked currents to those of the endogenous A-currents, but the time course of recovery from inactivation was not corrected. These results suggest that lobster shal proteins normally interact with
proteins in the KChIP/frequenin family to produce the transient potassium current in pyloric neurons.
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