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Transcriptome Analysis Identifies Multifaceted Regulatory Mechanisms Dictating a Genetic Switch from Neuronal Network Establishment to Maintenance During Postnatal Prefrontal Cortex Development

机译:转录组分析识别多方面的调节机制,在后期前期皮质开发期间对神经元网络建立到维持的遗传开关

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摘要

The prefrontal cortex (PFC) is one of the latest brain regions to mature, which allows the acquisition of complex cognitive abilities through experience. To unravel the underlying gene expression changes during postnatal development, we performed RNA-sequencing (RNA-seq) in the rat medial PFC (mPFC) at five developmental time points from infancy to adulthood, and analyzed the differential expression of protein-coding genes, long intergenic noncoding RNAs (lincRNAs), and alternative exons. We showed that most expression changes occur in infancy, and that the number of differentially expressed genes reduces toward adulthood. We observed 137 differentially expressed lincRNAs and 796 genes showing alternative exon usage during postnatal development. Importantly, we detected a genetic switch from neuronal network establishment in infancy to maintenance of neural networks in adulthood based on gene expression dynamics, involving changes in protein-coding and lincRNA gene expression as well as alternative exon usage. Our gene expression datasets provide insights into the multifaceted transcriptional regulation of the developing PFC. They can be used to study the basic developmental processes of the mPFC and to understand the mechanisms of neurodevelopmental and neuropsychiatric disorders. Our study provides an important contribution to the ongoing efforts to complete the “brain map”, and to the understanding of PFC development.
机译:前额叶皮质(PFC)是成熟的最新大脑区域之一,允许通过经验获取复杂的认知能力。为了在产后开发期间解开潜在的基因表达变化,我们在从婴儿期至成年期的五个发育时间点,在从婴儿到成年期的5个发育时间点进行RNA测序(RNA-SEQ),并分析了蛋白质编码基因的差异表达,长期性非致rnas(Lincrnas)和替代外显子。我们表明,大多数表达发生变化发生在初期,并且差异表达基因的数量降低到成年期。我们观察到137个差异表达的Lincrnas和796个基因,显示出产后开发期间的替代外显子使用。重要的是,我们根据基因表达动态检测了初学者中神经元网络建立的遗传切换,涉及蛋白质编码和LincrNA基因表达的变化以及替代外显子的改变。我们的基因表达数据集提供了进入显影PFC的多方面转录调节的见解。它们可用于研究MPFC的基本发展过程,并了解神经发育和神经精神病学障碍的机制。我们的研究为完成“脑地图”的持续努力提供了重要贡献,并对PFC开发的理解提供了重要贡献。

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