A POTASSIUM CHANNEL MUTATION IN WEAVER MICE IMPLICATES MEMBRANE EXCITABILITY IN GRANULE CELL-DIFFERENTIATION

被引:464
作者
PATIL, N
COX, DR
BHAT, D
FAHAM, M
MYERS, RM
PETERSON, AS
机构
[1] DUKE UNIV,MED CTR,DEPT GENET,DURHAM,NC 27710
[2] DUKE UNIV,MED CTR,DEPT NEUROBIOL,DURHAM,NC 27710
[3] UNIV CALIF SAN FRANCISCO,DEPT BIOCHEM & BIOPHYS,SAN FRANCISCO,CA 94305
关键词
D O I
10.1038/ng1095-126
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Early events in neuronal differentiation are generally considered to be regulated by factors independent of alterations in membrane permeability. Weaver mice harbour a mutation that blocks neuronal differentiation just after cessation of cell division, prior to cell migration and synaptogenesis. Cerebellar granule cells in homozygous weaver mice fail to differentiate, either because intrinsic cues are absent or because the granule cells are unable to respond to those cues. We now report that weaver mice have a missense mutation in a gene encoding a G-protein coupled inward rectifier potassium channel. The mutation alters the putative ion-permeable, pore-forming domain of the protein, suggesting that granule cell differentiation is regulated by changes in membrane permeability.
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收藏
页码:126 / 129
页数:4
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