A10 Accurate data-driven approaches for modeling MIRNA regulation in the brain of huntington’s disease mice

L. Mégret, S. Nair, J. Aaronson, J. Rosinski, C. Néri
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Abstract

MicroRNA regulation could play important roles in modulating the dynamics of the Huntington’s disease (HD) process. The problems in question include those about the role of specific miRNAs in significantly modulating selective target genes and about the relations between these effects and the cellular context in which they operate. To address this question, we developed a data-driven approach based on network- and tree-based concepts for the unbiased and accurate characterization of miRNA regulation in the brain of HD knock-in mice (allelic series). This approach does not make use of prior knowledge on the relationships between miRNAs and their targets. Rather, it aims at predicting the miRNA-target pairs that are most strongly associated with the temporal dynamics of the HD process based on the in-depth analysis of age- and CAG repeat-dependent profiles of miRNA expression and target gene expression. Our results suggest that on a global level miRNA regulation may poorly explain gene deregulation in the cortex and striatum of HD knock-in mice. Nonetheless, our model retained a small number of miRNA-target pairs that in the striatum of HD knock-in mice are well anti-correlated in terms of change of expression level across age points and CAG-repeat lengths and that may be relevant to the modulation of neuronal activity in these HD mice.
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在亨廷顿氏病小鼠大脑中建立MIRNA调控模型的精确数据驱动方法
MicroRNA调控可能在调节亨廷顿氏病(HD)过程的动力学中发挥重要作用。所讨论的问题包括特异性mirna在显著调节选择性靶基因中的作用,以及这些作用与它们所处的细胞环境之间的关系。为了解决这个问题,我们开发了一种基于网络和树的概念的数据驱动方法,用于无偏和准确地表征HD敲入小鼠大脑中的miRNA调控(等位基因系列)。这种方法没有利用mirna与其靶标之间关系的先验知识。相反,它的目的是基于对miRNA表达和靶基因表达的年龄和CAG重复依赖性谱的深入分析,预测与HD过程的时间动态最密切相关的miRNA-靶对。我们的研究结果表明,在全球水平上,miRNA调控可能很难解释HD敲入小鼠皮层和纹状体的基因失调。尽管如此,我们的模型保留了少量的mirna靶对,这些mirna靶对在HD敲入小鼠的纹状体中,在不同年龄点和cag重复长度的表达水平变化方面具有很好的抗相关性,这可能与这些HD小鼠的神经元活动调节有关。
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A10 Accurate data-driven approaches for modeling MIRNA regulation in the brain of huntington’s disease mice A08 Early transcriptional changes in human HD-IPS cell lines revealed by RNASEQ A35 An altered metabolism of nucleotides leads to huntington’s disease related cardiomyopathy A42 Reactive astrocytes promote proteostasis in huntington’s disease
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