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The regulatory epicenter of miRNAs

机译:miRNA的调控中心

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摘要

miRNAs are small non-coding RNAs with average length of ~21 bp. miRNA formation seems to be dependent upon multiple factors besides Drosha and Dicer, in a tissue/stage-specific manner, with interplay of several specific binding factors. In the present study, we have investigated transcription factor binding sites in and around the genomic sequences of precursor miRNAs and RNA-binding protein (RBP) sites in miRNA precursor sequences, analysed and tested in comprehensive manner. Here, we report that miRNA precursor regions are positionally enriched for binding of transcription factors as well as RBPs around the 3′ end of mature miRNA region in 5′ arm. The pattern and distribution of such regulatory sites appears to be a characteristic of precursor miRNA sequences when compared with non-miRNA sequences as negative dataset and tested statistically. When compared with 1 kb upstream regions, a sudden sharp peak for binding sites arises in the enriched zone near the mature miRNA region. An expression-data-based correlation analysis was performed between such miRNAs and their corresponding transcription factors and RBPs for this region. Some specific groups of binding factors and associated miRNAs were identified. We also identified some of the over-represented transcription factors and associated miRNAs with high expression correlation values which could be useful in cancer-related studies. The highly correlated groups were found to host experimentally validated composite regulatory modules, in which Lmo2-GATA1 appeared as the predominant one. For many of RBP–miRNAs associations, co-expression similarity was also evident among the associated miRNA common to given RBPs, supporting the Regulon model, suggesting a common role and common control of these miRNAs by the associated RBPs. Based on our findings, we propose that the observed characteristic distribution of regulatory sites in precursor miRNA sequence regions could be critical in miRNA transcription, processing, stability and formation and are important for therapeutic studies. Our findings also support the recently proposed theory of self-sufficient mode of transcription by miRNAs, which states that miRNA transcription can be carried out in host-independent mode too.
机译:miRNA是小的非编码RNA,平均长度约为21 bp。 miRNA的形成似乎以组织/阶段特异性方式依赖于Drosha和Dicer之外的多种因素,并且具有多种特异性结合因子的相互作用。在本研究中,我们研究了前体miRNA的基因组序列中和周围的转录因子结合位点以及miRNA前体序列中的RNA结合蛋白(RBP)位点,并进行了全面分析和测试。在这里,我们报告说,miRNA前体区域在位置上富集,可结合转录因子以及5'臂中成熟miRNA区域3'端附近的RBP。与作为阴性数据集的非miRNA序列进行比较并进行统计测试时,此类调控位点的模式和分布似乎是前体miRNA序列的特征。当与1 kb上游区域相比时,在成熟miRNA区域附近的富集区域中出现了一个结合位点的突然尖峰。在此类miRNA及其对应的转录因子和该区域的RBP之间进行了基于表达数据的相关性分析。鉴定了结合因子和相关miRNA的一些特定组。我们还鉴定了一些过表达的转录因子和具有高表达相关值的相关miRNA,可用于癌症相关研究。发现高度相关的群体拥有经过实验验证的复合调节模块,其中Lmo2-GATA1占主导地位。对于许多RBP-miRNA关联,在给定RBP共有的相关miRNA之间共表达相似性也很明显,这支持Regulon模型,表明相关RBP对这些miRNA具有共同的作用和共同的控制。根据我们的发现,我们建议观察到的前体miRNA序列区域中调控位点的特征分布对于miRNA转录,加工,稳定性和形成可能至关重要,并且对治疗研究也很重要。我们的发现还支持最近提出的miRNA转录自足模式的理论,该理论指出miRNA转录也可以独立于宿主的模式进行。

著录项

  • 来源
    《Journal of Biosciences》 |2011年第4期|p.621-638|共18页
  • 作者单位

    Studio of Computational Biology &amp Bioinformatics, Biotechnology Division, CSIR-Institute of Himalayan Bioresource Technology, Council of Scientific &amp Industrial Research, Palampur, 176 061, HP, India;

    Studio of Computational Biology &amp Bioinformatics, Biotechnology Division, CSIR-Institute of Himalayan Bioresource Technology, Council of Scientific &amp Industrial Research, Palampur, 176 061, HP, India;

    Studio of Computational Biology &amp Bioinformatics, Biotechnology Division, CSIR-Institute of Himalayan Bioresource Technology, Council of Scientific &amp Industrial Research, Palampur, 176 061, HP, India;

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

    Biogenesis; miRNA; precursor; RBP; TFBS; transcription;

    机译:生物发生;miRNA;前体;RBP;TFBS;转录;

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