miR-7a regulation of Pax6 controls spatial origin of forebrain dopaminergic neurons

被引:112
作者
de Chevigny, Antoine [1 ,2 ]
Core, Nathalie [1 ,2 ]
Follert, Philipp [1 ,2 ]
Gaudin, Marion [1 ,2 ]
Barbry, Pascal [3 ,4 ]
Beclin, Christophe [1 ,2 ]
Cremer, Harold [1 ,2 ]
机构
[1] Aix Marseille Univ, Inst Biol Dev Marseille Luminy, Marseille, France
[2] CNRS, UMR 7288, Marseille, France
[3] Univ Nice Sophia Antipolis, Inst Pharmacol Mol & Cellulaire, Sophia Antipolis, France
[4] CNRS, Sophia Antipolis, France
关键词
ALPHA-SYNUCLEIN EXPRESSION; NEURAL STEM-CELLS; POSTTRANSCRIPTIONAL REGULATION; MICRORNAS; ELECTROPORATION; DIFFERENTIATION; SPECIFICATION; NEUROGENESIS; PROGENITORS; REPRESSION;
D O I
10.1038/nn.3142
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the postnatal and adult mouse forebrain, a mosaic of spatially separated neural stem cells along the lateral wall of the ventricles generates defined types of olfactory bulb neurons. To understand the mechanisms underlying the regionalization of the stem cell pool, we focused on the transcription factor Pax6, a determinant of the dopaminergic phenotype in this system. We found that, although Pax6 mRNA was transcribed widely along the ventricular walls, Pax6 protein was restricted to the dorsal aspect. This dorsal restriction was a result of inhibition of protein expression by miR-7a, a microRNA (miRNA) that was expressed in a gradient opposing Pax6. In vivo inhibition of miR-7a in Pax6-negative regions of the lateral wall induced Pax6 protein expression and increased dopaminergic neurons in the olfactory bulb. These findings establish miRNA-mediated fine-tuning of protein expression as a mechanism for controlling neuronal stem cell diversity and, consequently, neuronal phenotype.
引用
收藏
页码:1120 / +
页数:8
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