Effects of carbonic anhydrase VIII deficiency on cerebellar gene expression profiles in the wdl mouse

被引:11
|
作者
Yan, Jian
Jiao, Yan
Jiao, Feng
Stuart, John
Donahue, Leah Rae
Beamer, Wesley G.
Li, Xinmin
Roe, Bruce A.
LeDoux, Mark S.
Gu, Weikuan
机构
[1] Univ Tennessee, Ctr Hlth Sci, Dept Med, Memphis, TN 38163 USA
[2] Univ Tennessee, Ctr Hlth Sci, Campbell Clin & Pathol, Dept Orthoped Surg, Memphis, TN 38163 USA
[3] Jackson Lab, Bar Harbor, ME 04609 USA
[4] Univ Chicago, Funct Genom Facil, Chicago, IL 60637 USA
[5] Univ Oklahoma, Dept Chem & Biochem, Norman, OK 73019 USA
[6] Univ Tennessee, Hlth Sci Ctr, Dept Neurol, Memphis, TN USA
[7] Univ Tennessee, Hlth Sci Ctr, Dept Anat & Neurobiol, Memphis, TN USA
关键词
carbonic anhydrase VIII; dystonia; ataxia; cerebellum; calcium signaling; inositol triphosphate; GABA(A) RECEPTOR ALPHA-6; GOLGI-APPARATUS; RHO-GTPASES; PROTEIN; CALCIUM; NEURONS; BINDING; CELLS; BRAIN; MICE;
D O I
10.1016/j.neulet.2006.11.046
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recently, the waddles (wdl) mouse was identified as a carbonic anhydrase VIII (Car8) mutant. The mutation is associated with marked deficiency of Car8, an inositol triphosphate receptor 1-binding protein expressed at high levels in cerebellar Purkinje cells. To help unravel the molecular aberrations contributing to motor dysfunction in wdl mice, cerebellar gene expression profiles were examined in the mutants and their wild-type littermates. Genes involved in signaling, cell division, zinc ion-binding, synapse integrity and plasticity were downregulated in wdl mice. Several of the upregulated genes encode proteins that function in the Golgi apparatus which suggests that Car8 deficiency has important effects on synaptic vesicle formation and transport. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:196 / 201
页数:6
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