Transcriptome-wide Discovery of microRNA Binding Sites in Human Brain

被引:170
作者
Boudreau, Ryan L. [1 ]
Jiang, Peng [1 ]
Gilmore, Brian L. [1 ]
Spengler, Ryan M. [4 ]
Tirabassi, Rebecca [5 ]
Nelson, Jay A. [5 ]
Ross, Christopher A. [6 ,7 ,8 ,9 ,10 ]
Xing, Yi [1 ,11 ]
Davidson, Beverly L. [1 ,2 ,3 ,4 ]
机构
[1] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Neurol, Iowa City, IA 52242 USA
[3] Univ Iowa, Dept Mol Physiol & Biophys, Iowa City, IA 52242 USA
[4] Univ Iowa, Program Mol & Cellular Biol, Iowa City, IA 52242 USA
[5] Oregon Hlth & Sci Univ, Vaccine & Gene Therapy Inst, Beaverton, OR 97006 USA
[6] Johns Hopkins Univ, Sch Med, Div Neurobiol, Baltimore, MD 21287 USA
[7] Johns Hopkins Univ, Sch Med, Dept Psychiat, Baltimore, MD 21287 USA
[8] Johns Hopkins Univ, Sch Med, Dept Neurol Neurosci, Baltimore, MD 21287 USA
[9] Johns Hopkins Univ, Sch Med, Dept Pharmacol, Baltimore, MD 21287 USA
[10] Johns Hopkins Univ, Sch Med, Program Cellular & Mol Med, Baltimore, MD 21287 USA
[11] Univ Calif Los Angeles, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
ALPHA-SYNUCLEIN; TARGET SITES; MAMMALIAN MICRORNAS; HUMAN GENES; DISEASE; IDENTIFICATION; DATABASE; ASSOCIATION; EXPRESSION; DECAY;
D O I
10.1016/j.neuron.2013.10.062
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The orchestration of brain function requires complex gene regulatory networks that are modulated, in part, by microRNAs (miRNAs). These noncoding RNAs associate with argonaute (Ago) proteins in order to direct posttranscriptional gene suppression via base pairing with target transcripts. In order to better understand how miRNAs contribute to human-specialized brain processes and neurological phenotypes, identifying their targets is of paramount importance. Here, we address the latter by profiling Ago2:RNA interactions using HITS-CLIP to generate a transcriptome-wide map of miRNA binding sites in human brain. We uncovered similar to 7,000 stringent Ago2 binding sites that are highly enriched for conserved sequences corresponding to abundant brain miRNAs. This interactome points to functional miRNA:target pairs across > 3,000 genes and represents a valuable resource for accelerating our understanding of miRNA functions in brain. We demonstrate the utility of this map for exploring clinically relevant miRNA binding sites that may facilitate the translation of genetic studies of complex neuropsychiatric diseases into therapeutics.
引用
收藏
页码:294 / 305
页数:12
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