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Integromics network meta-analysis on cardiac aging offers robust multi-layer modular signatures and reveals micronome synergism

机译:关于心脏衰老的Integromics网络荟萃分析提供了强大的多层模块化特征并揭示了微米组的协同作用

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摘要

BackgroundThe avalanche of integromics and panomics approaches shifted the deciphering of aging mechanisms from single molecular entities to communities of them. In this orientation, we explore the cardiac aging mechanisms – risk factor for multiple cardiovascular diseases - by capturing the micronome synergism and detecting longevity signatures in the form of communities (modules).For this, we developed a meta-analysis scheme that integrates transcriptome expression data from multiple cardiac-specific independent studies in mouse and human along with proteome and micronome interaction data in the form of multiple independent weighted networks. Modularization of each weighted network produced modules, which in turn were further analyzed so as to define consensus modules across datasets that change substantially during lifespan. Also, we established a metric that determines - from the modular perspective - the synergism of microRNA-microRNA interactions as defined by significantly functionally associated targets.
机译:背景技术人体工程学和人体工程学方法的大量涌现,将衰老机制的解读从单分子实体转变为它们的群落。在这种情况下,我们通过捕获微米组的协同作用并检测以社区(模块)形式的长寿标志来探索心脏衰老的机制(多种心血管疾病的危险因素)。为此,我们开发了一个整合转录组表达的荟萃分析方案。来自小鼠和人类的多项心脏特异性独立研究的数据,以及蛋白质组和微米组相互作用数据(以多个独立加权网络的形式)。每个加权网络产生的模块的模块化,然后对模块进行进一步分析,以定义在整个生命周期中发生很大变化的数据集中的共识模块。此外,我们建立了一个指标,从模块化的角度出发,该指标确定了功能密切相关的靶标所定义的microRNA与microRNA相互作用的协同作用。

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