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在微小RNA高通量实验中,靶基因表达水平以及转染的和内源性微小RNA之间的竞争是很强的混杂因素。

Target gene expression levels and competition between transfected and endogenous microRNAs are strong confounding factors in microRNA high-throughput experiments.

作者信息

Saito Takaya, Sætrom Pål

机构信息

Department of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology, Prinsesse Kristinsgt, 1, NO-7491 Trondheim, Norway.

出版信息

Silence. 2012 Feb 10;3:3. doi: 10.1186/1758-907X-3-3.

Abstract

BACKGROUND

MicroRNA (miRNA) target genes tend to have relatively long and conserved 3' untranslated regions (UTRs), but to what degree these characteristics contribute to miRNA targeting is poorly understood. Different high-throughput experiments have, for example, shown that miRNAs preferentially regulate genes with both short and long 3' UTRs and that target site conservation is both important and irrelevant for miRNA targeting.

RESULTS

We have analyzed several gene context-dependent features, including 3' UTR length, 3' UTR conservation, and messenger RNA (mRNA) expression levels, reported to have conflicting influence on miRNA regulation. By taking into account confounding factors such as technology-dependent experimental bias and competition between transfected and endogenous miRNAs, we show that two factors - target gene expression and competition - could explain most of the previously reported experimental differences. Moreover, we find that these and other target site-independent features explain about the same amount of variation in target gene expression as the target site-dependent features included in the TargetScan model.

CONCLUSIONS

Our results show that it is important to consider confounding factors when interpreting miRNA high throughput experiments and urge special caution when using microarray data to compare average regulatory effects between groups of genes that have different average gene expression levels.

摘要

背景

微小RNA(miRNA)的靶基因往往具有相对较长且保守的3'非翻译区(UTR),但这些特征在多大程度上有助于miRNA靶向作用尚不清楚。例如,不同的高通量实验表明,miRNA既优先调控具有短3'UTR的基因,也优先调控具有长3'UTR的基因,并且靶位点保守性对于miRNA靶向作用既重要又无关紧要。

结果

我们分析了几个基因背景相关特征,包括3'UTR长度、3'UTR保守性以及信使核糖核酸(mRNA)表达水平,据报道这些特征对miRNA调控有相互矛盾的影响。通过考虑诸如技术依赖性实验偏差以及转染的miRNA与内源性miRNA之间的竞争等混杂因素,我们发现两个因素——靶基因表达和竞争——可以解释大多数先前报道的实验差异。此外,我们发现这些以及其他与靶位点无关的特征所解释的靶基因表达变异量与TargetScan模型中包含的与靶位点有关的特征所解释的变异量大致相同。

结论

我们的结果表明,在解释miRNA高通量实验时考虑混杂因素很重要,并且在使用微阵列数据比较具有不同平均基因表达水平的基因组之间的平均调控效应时要特别谨慎。

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