The mouse stargazer gene encodes a neuronal Ca2+-channel γ subunit

被引:454
作者
Letts, VA
Felix, R
Biddlecome, GH
Arikkath, J
Mahaffey, CL
Valenzuela, A
Bartlett, FS
Mori, Y
Campbell, KP
Frankel, WN
机构
[1] Jackson Lab, Bar Harbor, ME 04609 USA
[2] Univ Iowa, Coll Med, Dept Physiol & Biophys, Howard Hughes Med Inst, Iowa City, IA 52242 USA
[3] Univ Iowa, Coll Med, Dept Neurol, Iowa City, IA 52242 USA
[4] Natl Inst Physiol Sci, Dept Informat Physiol, Okazaki, Aichi 444, Japan
关键词
D O I
10.1038/1228
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Stargazer mice have spike-wave seizures characteristic of absence epilepsy, with accompanying defects in the cerebellum and inner ear. We describe here a novel gene, Cacng2, whose expression is disrupted in two stargazer alleles. It encodes a 36-kD protein (stargazin) with structural similarity to the gamma-subunit of skeletal muscle voltage-gated calcium (Ca2+) channels. Stargazin is brain-specific and, like other neuronal Ca2+-channel subunits, is enriched in synaptic plasma membranes. In vitro, stargazin increases steady-state inactivation of alpha(1) class A Ca2+ channels. The anticipated effect in stargazer mutants, inappropriate Ca2+ entry, may contribute to their more pronounced seizure phenotype compared with other mouse absence models with Ca2+-channel defects. The discovery that the stargazer gene encodes a gamma-subunit completes the identification of the major subunit types for neuronal Ca2+ channels, namely alpha(1) alpha(2)delta,beta and gamma, providing a new opportunity to understand how these channels function in the mammalian brain and how they may be targeted in the treatment of neuroexcitability disorders.
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收藏
页码:340 / 347
页数:8
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