Beveridge Natalie J, Santarelli Danielle M, Wang Xi, Tooney Paul A, Webster Maree J, Weickert Cynthia S, Cairns Murray J
To whom correspondence should be addressed; School of Biomedical Sciences & Pharmacy, The University of Newcastle, University Drive, Callaghan, NSW 2308, Australia; tel: +61-2-4921-8670, fax: +61-2-4921-7903, e-mail:
Schizophr Bull. 2014 Mar;40(2):399-409. doi: 10.1093/schbul/sbs198. Epub 2013 Jan 31.
MicroRNA are small RNAs that provide specificity for the RNA induced silencing complex, which forms the basis of an exquisite combinatorial system for posttranscriptional regulation. This system, essential for complex metazoans, is exemplified in the development of the cerebral cortex. To explore the complexity of human cortical miRNA expression in detail, we analyzed RNA from postmortem prefrontal cortex from 97 subjects aged 2 months to 78 years using miRNA microarray. Global miRNA expression was highest in the early years before declining significantly after adolescence (n = 140 decreased, n = 32 increased). Late adolescence was also marked by an inflection point between miRNA on an upward trajectory vs the majority going down. Functional annotation of target genes displaying inverse mRNA expression patterns in the same tissue were overrepresented in neurodevelopmentally significant pathways including neurological disease (most significantly schizophrenia), nervous system development, and cell-to-cell signaling. As mature miRNA expression is largely posttranscriptionally regulated, miRNA biogenesis gene expression was also examined. Dicer and Exportin-5 displayed significant associations with age; however, neither correlated with global miRNA expression across the lifespan. This investigation of cortical miRNA expression provides a framework for understanding the complex posttranscriptional regulatory environment during development and aging that may form a substrate for changes observed in neurodevelopmental disorders.
微小RNA是一类小RNA,它们为RNA诱导沉默复合体提供特异性,该复合体构成了一种用于转录后调控的精妙组合系统的基础。这个对复杂后生动物至关重要的系统,在大脑皮层的发育中得到了体现。为了详细探究人类皮质微小RNA表达的复杂性,我们使用微小RNA微阵列分析了97名年龄从2个月到78岁的受试者死后前额叶皮层的RNA。整体微小RNA表达在早年最高,在青春期后显著下降(n = 140下降,n = 32上升)。青春期后期的特征还在于微小RNA表达呈上升轨迹与大多数呈下降趋势之间的一个转折点。在同一组织中显示出相反mRNA表达模式的靶基因的功能注释在包括神经疾病(最显著的是精神分裂症)、神经系统发育和细胞间信号传导等神经发育相关的重要途径中过度富集。由于成熟微小RNA的表达在很大程度上受到转录后调控,因此也对微小RNA生物合成基因的表达进行了检测。Dicer和Exportin-5与年龄存在显著关联;然而,两者均与整个生命周期的整体微小RNA表达无关。这项对皮质微小RNA表达的研究为理解发育和衰老过程中复杂的转录后调控环境提供了一个框架,这种环境可能构成了在神经发育障碍中观察到的变化的基础。