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基于知识的微小RNA种子区域突变功能影响分析

Knowledge-based analysis of functional impacts of mutations in microRNA seed regions.

作者信息

Bhattacharya Anindya, Cui Yan

机构信息

Department of Microbiology, Immunology and Biochemistry and Center for Integrative and Translational Genomics, University of Tennessee Health Science Center, Memphis, TN 38163, USA,

出版信息

J Biosci. 2015 Oct;40(4):791-8. doi: 10.1007/s12038-015-9560-2.

DOI:10.1007/s12038-015-9560-2
PMID:26564979
Abstract

MicroRNAs are a class of important post-transcriptional regulators. Genetic and somatic mutations in miRNAs, especially those in the seed regions, have profound and broad impacts on gene expression and physiological and pathological processes. Over 500 SNPs were mapped to the miRNA seeds, which are located at position 2-8 of the mature miRNA sequences. We found that the central positions of the miRNA seeds contain fewer genetic variants and therefore are more evolutionary conserved than the peripheral positions in the seeds. We developed a knowledgebased method to analyse the functional impacts of mutations in miRNA seed regions. We computed the gene ontology-based similarity score GOSS and the GOSS percentile score for all 517 SNPs in miRNA seeds. In addition to the annotation of SNPs for their functional effects, in the present article we also present a detailed analysis pipeline for finding the key functional changes for seed SNPs. We performed a detailed gene ontology graph-based analysis of enriched functional categories for miRNA target gene sets. In the analysis of a SNP in the seed region of hsa-miR-96 we found that two key biological processes for progressive hearing loss 'Neurotrophin TRK receptor signaling pathway' and 'Epidermal growth factor receptor signaling pathway' were significantly and differentially enriched by the two sets of allele-specific target genes of miRNA hsa-miR-96.

摘要

微小RNA是一类重要的转录后调节因子。微小RNA中的遗传突变和体细胞突变,尤其是种子区域的突变,对基因表达以及生理和病理过程具有深远而广泛的影响。超过500个单核苷酸多态性(SNP)定位于微小RNA种子区域,这些区域位于成熟微小RNA序列的2至8位。我们发现,微小RNA种子区域的中心位置所含遗传变异较少,因此比种子区域的外围位置在进化上更保守。我们开发了一种基于知识的方法来分析微小RNA种子区域突变的功能影响。我们计算了微小RNA种子区域中所有517个SNP基于基因本体论的相似性得分GOSS和GOSS百分位数得分。除了对SNP的功能效应进行注释外,在本文中我们还展示了一个详细的分析流程,用于找出种子SNP的关键功能变化。我们对微小RNA靶基因集的富集功能类别进行了基于基因本体论图的详细分析。在对hsa-miR-96种子区域一个SNP的分析中,我们发现进行性听力损失的两个关键生物学过程“神经营养因子TRK受体信号通路”和“表皮生长因子受体信号通路”在hsa-miR-96两组等位基因特异性靶基因中显著且差异富集。

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本文引用的文献

1
Functional and evolutionary significance of human microRNA seed region mutations.人类微小RNA种子区域突变的功能及进化意义
PLoS One. 2014 Dec 12;9(12):e115241. doi: 10.1371/journal.pone.0115241. eCollection 2014.
2
Common features of microRNA target prediction tools.微小RNA靶标预测工具的共同特征。
Front Genet. 2014 Feb 18;5:23. doi: 10.3389/fgene.2014.00023. eCollection 2014.
3
miRBase: annotating high confidence microRNAs using deep sequencing data.miRBase:利用深度测序数据注释高可信度 microRNAs。
微小RNA:耳部相关疾病和听力损失中的有效元件
Eur Arch Otorhinolaryngol. 2017 Jun;274(6):2373-2380. doi: 10.1007/s00405-017-4470-6. Epub 2017 Feb 21.
4
SomamiR 2.0: a database of cancer somatic mutations altering microRNA-ceRNA interactions.SomamiR 2.0:一个改变微小RNA-竞争性内源RNA相互作用的癌症体细胞突变数据库。
Nucleic Acids Res. 2016 Jan 4;44(D1):D1005-10. doi: 10.1093/nar/gkv1220. Epub 2015 Nov 17.
Nucleic Acids Res. 2014 Jan;42(Database issue):D68-73. doi: 10.1093/nar/gkt1181. Epub 2013 Nov 25.
4
PolymiRTS Database 3.0: linking polymorphisms in microRNAs and their target sites with human diseases and biological pathways.PolymiRTS 数据库 3.0:将 microRNAs 中的多态性及其靶位点与人类疾病和生物途径联系起来。
Nucleic Acids Res. 2014 Jan;42(Database issue):D86-91. doi: 10.1093/nar/gkt1028. Epub 2013 Oct 24.
5
Progressive hearing loss and gradual deterioration of sensory hair bundles in the ears of mice lacking the actin-binding protein Eps8L2.缺乏肌动蛋白结合蛋白 Eps8L2 的小鼠的渐进性听力损失和内耳感觉毛束的逐渐恶化。
Proc Natl Acad Sci U S A. 2013 Aug 20;110(34):13898-903. doi: 10.1073/pnas.1304644110. Epub 2013 Aug 5.
6
Genome-wide in silico screening for microRNA genetic variability in livestock species.全基因组计算机筛选家畜物种中的 microRNA 遗传变异。
Anim Genet. 2013 Dec;44(6):669-77. doi: 10.1111/age.12072. Epub 2013 Jul 19.
7
RamiGO: an R/Bioconductor package providing an AmiGO visualize interface.RamiGO:一个提供 AmiGO 可视化界面的 R/Bioconductor 包。
Bioinformatics. 2013 Mar 1;29(5):666-8. doi: 10.1093/bioinformatics/bts708. Epub 2013 Jan 6.
8
SomamiR: a database for somatic mutations impacting microRNA function in cancer.索玛米 R:一个数据库,用于癌症中影响 microRNA 功能的体细胞突变。
Nucleic Acids Res. 2013 Jan;41(Database issue):D977-82. doi: 10.1093/nar/gks1138. Epub 2012 Nov 24.
9
A single-base substitution in the seed region of miR-184 causes EDICT syndrome.一个碱基在 miR-184 的种子区发生单点突变会导致 EDICT 综合征。
Invest Ophthalmol Vis Sci. 2012 Jan 25;53(1):348-53. doi: 10.1167/iovs.11-8783.
10
PolymiRTS Database 2.0: linking polymorphisms in microRNA target sites with human diseases and complex traits.PolymiRTS 数据库 2.0:将 miRNA 靶位的多态性与人类疾病和复杂特征联系起来。
Nucleic Acids Res. 2012 Jan;40(Database issue):D216-21. doi: 10.1093/nar/gkr1026. Epub 2011 Nov 10.