Department of Neuroscience and Brain Technologies, Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova, Italy.
Development. 2012 Sep;139(18):3332-42. doi: 10.1242/dev.078063. Epub 2012 Aug 8.
MicroRNAs (miRNAs) are rapidly emerging as a new layer of regulation of mammalian brain development. However, most of the miRNA target genes remain unidentified. Here, we explore gene expression profiling upon miRNA depletion and in vivo target validation as a strategy to identify novel miRNA targets in embryonic mouse neocortex. By this means, we find that Foxp2, a transcription factor associated with speech and language development and evolution, is a novel miRNA target. In particular, we find that miR-9 and miR-132 are able to repress ectopic expression of Foxp2 protein by targeting its 3' untranslated region (3'UTR) in vivo. Interestingly, ectopic expression of Foxp2 in cortical projection neurons (a scenario that mimics the absence of miRNA-mediated silencing of Foxp2 expression) delays neurite outgrowth in vitro and impairs their radial migration in embryonic mouse neocortex in vivo. Our results uncover a new layer of control of Foxp2 expression that may be required for proper neuronal maturation.
MicroRNAs (miRNAs) 迅速成为哺乳动物大脑发育调控的新层次。然而,大多数 miRNA 靶基因仍未被识别。在这里,我们通过 miRNA 耗竭后的基因表达谱分析和体内靶标验证来探索鉴定胚胎小鼠新皮质中新型 miRNA 靶标的策略。通过这种方法,我们发现 Foxp2,一种与言语和语言发展及进化相关的转录因子,是一种新型的 miRNA 靶标。具体来说,我们发现 miR-9 和 miR-132 能够通过靶向其 3'非翻译区(3'UTR)在体内抑制 Foxp2 蛋白的异位表达。有趣的是,在皮质投射神经元中异位表达 Foxp2(模拟 miRNA 介导的 Foxp2 表达沉默缺失的情况)会延迟体外神经突生长,并损害体内胚胎小鼠新皮质中它们的放射状迁移。我们的研究结果揭示了 Foxp2 表达的新调控层,这可能是神经元成熟所必需的。