New and Improved Tools for In Utero Electroporation Studies of Developing Cerebral Cortex

被引:93
作者
LoTurco, Joseph [1 ]
Manent, Jean-Bernard [1 ]
Sidiqi, Faez [1 ]
机构
[1] Univ Connecticut, Dept Physiol & Neurobiol, Storrs, CT 06269 USA
关键词
migration; neocortex; transgenesis; stem cell; DEVELOPING MOUSE-BRAIN; NEURONAL MIGRATION; GENE-TRANSFER; VIVO ELECTROPORATION; RNA INTERFERENCE; NEOCORTEX; DCX; TELENCEPHALON; DOUBLECORTIN; HETEROTOPIA;
D O I
10.1093/cercor/bhp033
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In utero electroporation (IUE) has become a method of choice for rapid gain and loss of function studies in embryonic cerebral cortex. In this review we highlight some of the proven and recent advances in ME technology that make it applicable to an increasingly wide array of experiments requiring spatial and temporal control of gene expression. Recently, cell-type-specific promoters and tarnoxifen-gated cre-recombinase have been shown to work effectively with IUE. Experiments can now be designed and carried out to test whether and which cell-type-specific mechanisms operate within defined periods of neuronal migration and maturation. We have recently adapted this conditional expression approach to implement conditional rescue experiments. In conditional rescue, expression of an RNA interference (RNAi) target is restored by tamoxifen-induced cre-mediated recombination. An initial disruption in migration, and resultant malformation, caused by DCX RNAi was reversed by delayed re-expression of Dcx. In the future, combinations of spatially directed, cell-type-specific, and tamoxifen-gated transgene expression can be used to address the complex mechanisms likely to operate during development of cerebral cortex.
引用
收藏
页码:I120 / I125
页数:6
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