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DIANA-mirExTra 网络服务器:从基因表达数据到 microRNA 功能。

The DIANA-mirExTra web server: from gene expression data to microRNA function.

机构信息

Biomedical Sciences Research Center "Alexander Fleming", Institute of Molecular Oncology, Varkiza, Greece.

出版信息

PLoS One. 2010 Feb 11;5(2):e9171. doi: 10.1371/journal.pone.0009171.

Abstract

BACKGROUND

High-throughput gene expression experiments are widely used to identify the role of genes involved in biological conditions of interest. MicroRNAs (miRNA) are regulatory molecules that have been functionally associated with several developmental programs and their deregulation with diverse diseases including cancer.

METHODOLOGY/PRINCIPAL FINDINGS: Although miRNA expression levels may not be routinely measured in high-throughput experiments, a possible involvement of miRNAs in the deregulation of gene expression can be computationally predicted and quantified through analysis of overrepresented motifs in the deregulated genes 3' untranslated region (3'UTR) sequences. Here, we introduce a user-friendly web-server, DIANA-mirExTra (www.microrna.gr/mirextra) that allows the comparison of frequencies of miRNA associated motifs between sets of genes that can lead to the identification of miRNAs responsible for the deregulation of large numbers of genes. To this end, we have investigated different approaches and measures, and have practically implemented them on experimental data.

CONCLUSIONS/SIGNIFICANCE: On several datasets of miRNA overexpression and repression experiments, our proposed approaches have successfully identified the deregulated miRNA. Beyond the prediction of miRNAs responsible for the deregulation of transcripts, the web-server provides extensive links to DIANA-mirPath, a functional analysis tool incorporating miRNA targets in biological pathways. Additionally, in case information about miRNA expression changes is provided, the results can be filtered to display the analysis for miRNAs of interest only.

摘要

背景

高通量基因表达实验被广泛用于识别与感兴趣的生物条件相关的基因的作用。MicroRNAs (miRNA) 是调节分子,与几种发育程序及其与多种疾病(包括癌症)的失调有关。

方法/主要发现:尽管 miRNA 表达水平可能不会在高通量实验中常规测量,但可以通过分析失调基因 3'非翻译区 (3'UTR) 序列中重复出现的基序来计算预测和量化 miRNA 对基因表达失调的可能参与。在这里,我们引入了一个用户友好的网络服务器 DIANA-mirExTra(www.microrna.gr/mirextra),它允许在可能导致鉴定大量基因失调的 miRNA 的基因集之间比较与 miRNA 相关的基序的频率。为此,我们研究了不同的方法和措施,并在实验数据上进行了实际实施。

结论/意义:在 miRNA 过表达和抑制实验的几个数据集上,我们提出的方法成功地鉴定了失调的 miRNA。除了预测导致转录物失调的 miRNA 之外,该网络服务器还提供了与 DIANA-mirPath 的广泛链接,DIANA-mirPath 是一个功能分析工具,将 miRNA 靶标纳入生物途径。此外,如果提供了 miRNA 表达变化的信息,则可以过滤结果以仅显示感兴趣的 miRNA 的分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4045/2820085/49cabbc728c7/pone.0009171.g001.jpg

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