Improved motor performance in Dyt1 ¦¤GAG heterozygous knock-in mice by cerebellar Purkinje-cell specific Dyt1 conditional knocking-out

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• 作者：Fumiaki Yokoi^a ; Mai Tu Dang^b ; Yuqing Li^a ; ^{yuqing.li@neurology.ufl.edu}
• 关键词：CT mouse ; control littermate mouse ; DYT1 (TOR1A) ; torsinA gene in human ; Dyt1 (Tor1a) ; torsinA gene in mouse ; Dyt1 cKO mouse ; cerebral cortex-specific Dyt1 conditional knockout mouse ; Dyt1 pKO mouse ; cerebellar Purkinje cell-specific Dyt1 conditional knoc
• 刊名：Behavioural Brain Research
• 出版年：2012
• 出版时间：1 May, 2012
• 年：2012
• 卷：230
• 期：2
• 页码：389-398
• 全文大小：1530 K

文摘

Early-onset generalized torsion dystonia (dystonia 1) is an inherited movement disorder caused by mutations in DYT1 (TOR1A), which codes for torsinA. Most patients have a 3-base pair deletion (¦¤GAG) in one allele of DYT1, corresponding to a loss of a glutamic acid residue (¦¤E) in the C-terminal region of the protein. Functional alterations in basal ganglia circuits and the cerebellum have been reported in dystonia. Pharmacological manipulations or mutations in genes that result in functional alterations of the cerebellum have been reported to have dystonic symptoms and have been used as phenotypic rodent models. Additionally, structural lesions in the abnormal cerebellar circuits, such as cerebellectomy, have therapeutic effects in these models. A previous study has shown that the Dyt1 ¦¤GAG heterozygous knock-in (KI) mice exhibit motor deficits in the beam-walking test. Both Dyt1 ¦¤GAG heterozygous knock-in (KI) and Dyt1 Purkinje cell-specific knockout (Dyt1 pKO) mice exhibit dendritic alterations of cerebellar Purkinje cells. Here, Dyt1 pKO mice exhibited significantly less slip numbers in the beam-walking test, suggesting better motor performance than control littermates, and normal gait. Furthermore, Dyt1 ¦¤GAG KI/Dyt1 pKO double mutant mice exhibited significantly lower numbers of slips than Dyt1 ¦¤GAG heterozygous KI mice, suggesting Purkinje-cell specific knockout of Dyt1 wild-type (WT) allele in Dyt1 ¦¤GAG heterozygous KI mice rescued the motor deficits. The results suggest that molecular lesions of torsinA in Purkinje cells by gene therapy or intervening in the signaling pathway downstream of the cerebellar Purkinje cells may rescue motor symptoms in dystonia 1.