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Music-performance regulates microRNAs in professional musicians

机译:音乐性能调节专业音乐家的MicroRNA

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摘要

Musical training and performance require precise integration of multisensory and motor centres of the human brain and can be regarded as an epigenetic modifier of brain functions. Numerous studies have identified structural and functional differences between the brains of musicians and non-musicians and superior cognitive functions in musicians. Recently, music-listening and performance has also been shown to affect the regulation of several genes, many of which were identified in songbird singing. MicroRNAs affect gene regulation and studying their expression may give new insights into the epigenetic effect of music. Here, we studied the effect of 2 hours of classical music-performance on the peripheral blood microRNA expressions in professional musicians with respect to a control activity without music for the same duration. As detecting transcriptomic changes in the functional human brain remains a challenge for geneticists, we used peripheral blood to study music-performance induced microRNA changes and interpreted the results in terms of potential effects on brain function, based on the current knowledge about the microRNA function in blood and brain. We identified significant (FDR <0.05) up-regulation of five microRNAs; hsa-miR-3909, hsa-miR-30d-5p, hsa-miR-92a-3p, hsa-miR-222-3p and hsa-miR-30a-5p; and down-regulation of two microRNAs; hsa-miR-6803-3p and hsa-miR-1249-3p. hsa-miR-222-3p and hsa-miR-92a-3p putatively target FOXP2, which was found down-regulated by microRNA regulation in songbird singing. miR-30d and miR-222 corroborate microRNA response observed in zebra finch song-listening/learning. miR-222 is induced by ERK cascade, which is important for memory formation, motor neuron functions and neuronal plasticity. miR-222 is also activated by FOSL1, an immediate early gene from the FOS family of transcriptional regulators which are activated by auditory-motor stimuli. miR-222 and miR-92 promote neurite outgrowth by negatively regulating the neuronal growth inhibitor, PTEN, and by activating CREB expression and phosphorylation. The up-regulation of microRNAs previously found to be regulators of auditory and nervous system functions (miR-30d, miR-92a and miR-222) is indicative of the sensory perception processes associated with music-performance. Akt signalling pathway which has roles in cell survival, cell differentiation, activation of CREB signalling and dopamine transmission was one of the functions regulated by the up-regulated microRNAs; in accordance with functions identified from songbird learning. The up-regulated microRNAs were also found to be regulators of apoptosis, suggesting repression of apoptotic mechanisms in connection with music-performance. Furthermore, comparative analyses of the target genes of differentially expressed microRNAs with that of the song-responsive microRNAs in songbirds suggest convergent regulatory mechanisms underlying auditory perception.
机译:音乐训练和性能需要精确地整合人脑的多思科和电机中心,并且可以被视为脑功能的表观遗传改性剂。许多研究确定了音乐家和非音乐家的大脑和音乐家中的高级认知功能之间的结构和功能差异。最近,还显示了音乐聆听和性能来影响几种基因的调节,其中许多是在鸣禽歌唱中确定的。 MicroRNA影响基因调节并研究其表达可能会对音乐的表观效果产生新的见解。在这里,我们研究了2小时的古典音乐性能对专业音乐家的外周血小鼠表达的效果相对于没有音乐的控制活动,在没有音乐的情况下进行相同的持续时间。由于检测功能性人脑中的转录组变化仍然是遗传学家的挑战,我们使用外周血来研究音乐性能诱导的微小RORNA变化,并根据目前关于MicroRNA功能的目前的知识来解释对脑功能的潜在影响的结果血和脑。我们确定了五个microRNA的显着(FDR <0.05)上调; HSA-MIR-3909,HSA-MIR-30D-5P,HSA-MIR-92A-3P,HSA-MIR-222-3P和HSA-MIR-30A-5P;和下调两个microRNA; HSA-MIR-6803-3P和HSA-MIR-1249-3P。 HSA-MIR-222-3P和HSA-MIR-92A-3P提供型FOXP2,由MicroRNA调节在鸣禽歌唱中发现下调。 MiR-30D和MiR-222在Zebra Finch歌曲聆听/学习中观察到MICRORATE MicroRNA反应。 MiR-222由ERK级联诱导,这对于记忆形成,运动神经元功能和神经元塑性非常重要。 MiR-222也由FOSL1激活,来自FOS系列转录调节剂的直接早期基因,通过听觉电动机刺激激活。 MiR-222和MiR-92通过对神经元生长抑制剂,PTEN产生负面调节神经元生长抑制剂,并通过激活CREB表达和磷酸化来促进神经突的过度。以前发现的MicroRNA的上调是对听觉和神经系统功能的监管机构(MIR-30D,MIR-92A和MIR-222)表示与音乐性能相关的感官感知过程。具有细胞存活,细胞分化,CREB信号传导和多巴胺传输激活的作用的AKT信号通路是由上调微大研磨的功能之一;根据歌曲学习中确定的职能。还发现上调的微小RNA是细胞凋亡的调节因子,表明抑制与音乐性能有关的凋亡机制。此外,差异表达微小RNA的靶基因的对比分析与鸣禽歌曲响应微大罗斯的靶基因建议了听觉患者潜视监管机制。

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