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Consensus miRNA expression profiles derived from interplatform normalization of microarray data

机译:从微阵列数据的平台间标准化获得共识的miRNA表达谱

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摘要

Eukaryotic gene expression is controlled at the post-transcriptional level by small noncoding RNAs called microRNAs (miRNA). miRNAs play important roles during early development and participate in gene regulatory circuits in the cell. Different high-throughput expression analysis methods including microarrays, bead-based detection, and small RNA cloning have been applied to quantitatively detect miRNAs in various tissues, cell types, and biological conditions. High-throughput expression data was collected from public repositories and processed to create a database of miRNA expression profiles. Several commonly used normalization methods were compared to identify suitable methods for cross-platform comparison of high-throughput miRNA expression data. The database provides interlaboratory and interplatform validated reference expression levels for miRNAs. The normalized expression profiles were validated by querying for well-established features of miRNA expression. Firstly, expression profiles of several tissue-specific miRNAs showed good agreement between the database and previously reported profiles. We have also identified a set of miRNAs that are constitutively expressed across mammalian tissues. Secondly, we used the database to compare the expression patterns of miRNAs belonging to the let-7 family, where the divergence in expression patterns implies that they may have diversified functionally. Lastly, we compared expression profiles of intronic and clustered miRNAs. Expression profiles of intronic miRNAs and clustered miRNAs showed either very good, or in certain cases, very poor correlation with the host gene. Interplatform comparison of miRNA expression profiles thus provides a resource of consensus expression profiles that can be used in the future for studying miRNA function and regulation.
机译:真核基因的表达在转录后水平受到称为microRNA(miRNA)的小型非编码RNA的控制。 miRNA在早期发育中起重要作用,并参与细胞中的基因调控电路。不同的高通量表达分析方法(包括微阵列,基于珠子的检测和小RNA克隆)已用于定量检测各种组织,细胞类型和生物学状况中的miRNA。从公共存储库收集高通量表达数据,并对其进行处理以创建miRNA表达谱数据库。比较了几种常用的归一化方法,以鉴定适用于高通量miRNA表达数据跨平台比较的方法。该数据库提供了miRNA的实验室间和平台间验证的参考表达水平。通过查询成熟的miRNA表达特征来验证归一化的表达谱。首先,几种组织特异性miRNA的表达谱显示出数据库与先前报道的谱之间的良好一致性。我们还鉴定了在整个哺乳动物组织中组成性表达的一组miRNA。其次,我们使用该数据库比较属于let-7家族的miRNA的表达模式,其中表达模式的差异意味着它们可能在功能上有所差异。最后,我们比较了内含子和簇状miRNA的表达谱。内含子miRNA和簇状miRNA的表达谱显示与宿主基因的相关性非常好,或在某些情况下非常差。因此,miRNA表达谱的平台间比较提供了共识表达谱的资源,可用于将来研究miRNA功能和调控。

著录项

  • 来源
    《RNA》 |2010年第1期|16-25|共10页
  • 作者单位

    Functional Genomics Unit, Institute of Genomics and Integrative Biology, Council of Scientific and Industrial Research (CSIR), Delhi 110 007, India;

    G.N. Ramachandran Knowledge Center for Genome Informatics, Institute of Genomics and Integrative Biology, Council of Scientific and Industrial Research (CSIR), Delhi 110 007, India;

    G.N. Ramachandran Knowledge Center for Genome Informatics, Institute of Genomics and Integrative Biology, Council of Scientific and Industrial Research (CSIR), Delhi 110 007, India;

    Functional Genomics Unit, Institute of Genomics and Integrative Biology, Council of Scientific and Industrial Research (CSIR), Delhi 110 007, India;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    microarray; microRNA; expression; meta-analysis; cluster;

    机译:基因芯片;微RNA;表达;元分析;聚类;

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