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Integrated analysis of microRNA and mRNA expression: adding biological significance to microRNA target predictions

机译:整合的microRNA和mRNA表达分析:为microRNA靶标预测增加生物学意义

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摘要

Current microRNA target predictions are based on sequence information and empirically derived rules but do not make use of the expression of microRNAs and their targets. This study aimed to improve microRNA target predictions in a given biological context, using in silico predictions, microRNA and mRNA expression. We used target prediction tools to produce lists of predicted targets and used a gene set test designed to detect consistent effects of microRNAs on the joint expression of multiple targets. In a single test, association between microRNA expression and target gene set expression as well as the contribution of the individual target genes on the association are determined. The strongest negatively associated mRNAs as measured by the test were prioritized. We applied our integration method to a well-defined muscle differentiation model. Validation of our predictions in C2C12 cells confirmed predicted targets of known as well as novel muscle-related microRNAs. We further studied associations between microRNA–mRNA pairs in human prostate cancer, finding some pairs that have been recently experimentally validated by others. Using the same study, we showed the advantages of the global test over Pearson correlation and lasso. We conclude that our integrated approach successfully identifies regulated microRNAs and their targets.
机译:当前的microRNA靶标预测是基于序列信息和根据经验得出的规则,但并未利用microRNA及其靶标的表达。这项研究旨在利用计算机模拟,microRNA和mRNA表达,在给定的生物学背景下改善microRNA靶标预测。我们使用靶标预测工具生成了预测靶标列表,并使用了基因组测试,旨在检测microRNA对多个靶标联合表达的一致作用。在单个测试中,确定了microRNA表达与靶基因组表达之间的关联以及各个靶基因对关联的贡献。优先确定由测试测得的最强的负相关mRNA。我们将整合方法应用于定义明确的肌肉分化模型。我们对C2C12细胞中预测的验证证实了已知以及与肌肉相关的新型microRNA的预测靶标。我们进一步研究了人类前列腺癌中microRNA-mRNA对之间的关​​联,发现一些最近已通过其他实验验证的对。使用同一项研究,我们展示了全局测试优于Pearson相关和套索的优势。我们得出的结论是,我们的整合方法成功地确定了受调控的microRNA及其靶标。

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