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The effects of graded levels of calorie restriction: VII. Topological rearrangement of hypothalamic aging networks

机译:卡路里限制等级的影响:VII。下丘脑衰老网络的拓扑重排

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摘要

Connectivity in a gene-gene network declines with age, typically within gene clusters. We explored the effect of short-term (3 months) graded calorie restriction (CR) (up to 40 %) on network structure of aging-associated genes in the murine hypothalamus by using conditional mutual information. The networks showed a topological rearrangement when exposed to graded CR with a higher relative within cluster connectivity at 40CR. We observed changes in gene centrality concordant with changes in CR level, with Ppargc1a, and Ppt1 having increased centrality and Etfdh, Traf3 and Abcc1 decreased centrality as CR increased. This change in gene centrality in a graded manner with CR, occurred in the absence of parallel changes in gene expression levels. This study emphasizes the importance of augmenting traditional differential gene expression analyses to better understand structural changes in the transcriptome. Overall our results suggested that CR induced changes in centrality of biological relevant genes that play an important role in preventing the age-associated loss of network integrity irrespective of their gene expression levels.
机译:基因-基因网络中的连接性会随着年龄的增长而下降,通常是在基因簇中。我们通过使用条件共有信息,探索了短期(3个月)分级卡路里限制(CR)(最高40%)对鼠下丘脑衰老相关基因网络结构的影响。当暴露于40CR的集群连接中具有较高相对值的渐变CR时,网络显示出拓扑重排。我们观察到基因中心性的变化与CR水平的变化一致,其中Ppargc1a和Ppt1具有增加的中心性,而Etfdh,Traf3和Abcc1随着CR的增加而中心性降低。在不伴随基因表达水平平行变化的情况下,以CR的分级方式发生的基因中心性变化。这项研究强调了增强传统差异基因表达分析以更好地了解转录组结构变化的重要性。总的来说,我们的研究结果表明,CR诱导了生物学相关基因中心性的改变,无论其基因表达水平如何,它们都在防止与年龄相关的网络完整性丧失中起着重要作用。

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