Krishnan Remya, Nair Achuthsankar S, Dhar Pawan K
Department of Computational Biology and Bioinformatics, University of Kerala, Thiruvananthapuram, Kerala - 695 581.
School of Biotechnology, Jawaharlal Nehru University, New Delhi 110067.
Bioinformation. 2017 Jan 24;13(1):17-20. doi: 10.6026/97320630013017. eCollection 2017.
MicroRNAs (miRNAs) are small non-coding RNAs ~22 nucleotides long that do not encode for proteins but have been reported to influence gene expression in normal and abnormal health conditions. Though a large body of scientific literature on miRNAs exists, their network level profile linking molecules with their corresponding phenotypes, is less explored. Here, we studied a network of 191 human miRNAs reported to play a role in 30 human cardiac diseases. Our aim was to study miRNA network properties like hubness and preferred associations, using data mining, network graph theory and statistical analysis. A total of 16 miRNAs were found to have a disease node connectivity of >5 edges (i.e., they were linked to more than 5 diseases) and were considered hubs in the miRNAcardiac disease network. Alternatively, when diseases were considered as hubs, >10 of miRNAs showed up on each 'disease hub node'. Of all the miRNAs associated with diseases, 19 miRNAs (19/24= 79.1% of upregulated events) were found to be upregulated in atherosclerosis. The data suggest micro RNAs as early stage biological markers in cardiac conditions with potential towards microRNA based therapeutics.
微小RNA(miRNA)是长度约为22个核苷酸的小型非编码RNA,它们不编码蛋白质,但据报道在正常和异常健康状况下会影响基因表达。尽管存在大量关于miRNA的科学文献,但它们将分子与其相应表型联系起来的网络水平概况却较少被探索。在此,我们研究了一个由191种人类miRNA组成的网络,这些miRNA据报道在30种人类心脏疾病中发挥作用。我们的目的是利用数据挖掘、网络图论和统计分析来研究miRNA网络的特性,如中心性和偏好性关联。总共发现16种miRNA的疾病节点连接性大于5条边(即它们与5种以上疾病相关联),并被认为是miRNA - 心脏疾病网络中的中心节点。另外,当将疾病视为中心节点时,每个“疾病中心节点”上出现了超过10种miRNA。在所有与疾病相关的miRNA中,发现19种miRNA(19/24 = 79.1%的上调事件)在动脉粥样硬化中上调。这些数据表明,微小RNA作为心脏疾病的早期生物学标志物,具有基于微小RNA的治疗潜力。