International School for Advanced Studies SISSA/ISAS, Trieste, Italy.
Curr Gene Ther. 2013 Apr;13(2):152-61. doi: 10.2174/1566523211313020009.
Emx2 encodes for a transcription factor controlling several aspects of cerebral cortex development. Its overexpression promotes self-renewal of young cortico-cerebral precursors, it promotes neuronal rather than gliogenic fates and it protects neuronal progenitors from cell death. These are all key activities for purposes of gene-promoted brain repair. Artificial pri-miRNAs targeting non-coding cis-active modules and/or conserved sequences of the Emx2 locus were delivered to embryonic cortico-cerebral precursors, by lentiviral vectors. A subset of these pri-miRNAs upregulated Emx2, possibly stimulating its transcription. That led to enhanced self-renewal, delayed differentiation and reduced death of neuronally committed precursors, resulting in an appreciable expansion of the neuronogenic precursors pool. This method makes Emx2 overexpression for purposes of brain repair a more feasible goal, avoiding the drawbacks of exogenous gene copies introduction. Interestingly, the two genomic enhancers targeted by these pri-miRNAs were discovered to be naturally transcribed. Their expression profile suggests their possible involvement in regulation of Emx2 transcription.
Emx2 编码一种转录因子,可控制大脑皮层发育的几个方面。其过表达促进年轻的皮质-大脑前体细胞的自我更新,促进神经元而不是神经胶质命运,并保护神经元祖细胞免于细胞死亡。这些都是基因促进脑修复的关键活动。通过慢病毒载体将靶向 Emx2 基因座的非编码顺式活性模块和/或保守序列的人工 pri-miRNA 递送到胚胎皮质-大脑前体细胞中。这些 pri-miRNA 中的一部分上调了 Emx2,可能刺激其转录。这导致自我更新增强、分化延迟和神经元定向前体细胞死亡减少,从而使神经元发生前体细胞池明显扩大。这种方法使 Emx2 的过表达成为脑修复的一个更可行的目标,避免了外源基因拷贝引入的缺点。有趣的是,这些 pri-miRNA 靶向的两个基因组增强子被发现是自然转录的。它们的表达谱表明它们可能参与调节 Emx2 转录。