Computational Biology Unit, Bergen Center for Computational Science, and Sars International Centre for Marine Molecular Biology, University of Bergen, Bergen, 5008, Norway.
BMC Genomics. 2011 May 27;12:270. doi: 10.1186/1471-2164-12-270.
Recent functional studies have demonstrated that many microRNAs (miRNAs) are expressed by RNA polymerase II in a specific spatiotemporal manner during the development of organisms and play a key role in cell-lineage decisions and morphogenesis. They are therefore functionally related to a number of key protein coding developmental genes, that form genomic regulatory blocks (GRBs) with arrays of highly conserved non-coding elements (HCNEs) functioning as long-range enhancers that collaboratively regulate the expression of their target genes. Given this functional similarity as well as recent zebrafish transgenesis assays showing that the miR-9 family is indeed regulated by HCNEs with enhancer activity, we hypothesized that this type of miRNA regulation is prevalent. In this paper, we therefore systematically investigate the regulatory landscape around conserved self-transcribed miRNAs (ST miRNAs), with their own known or computationally inferred promoters, by analyzing the hallmarks of GRB target genes. These include not only the density of HCNEs in their vicinity but also the presence of large CpG islands (CGIs) and distinct patterns of histone modification marks associated with developmental genes.
Our results show that a subset of the conserved ST miRNAs we studied shares properties similar to those of protein-coding GRB target genes: they are located in regions of significantly higher HCNE/enhancer binding density and are more likely to be associated with CGIs. Furthermore, their putative promoters have both activating as well as silencing histone modification marks during development and differentiation. Based on these results we used both an elevated HCNE density in the genomic vicinity as well as the presence of a bivalent promoter to identify 29 putative GRB target miRNAs/miRNA clusters, over two-thirds of which are known to play a role during development and differentiation. Furthermore these predictions include miRNAs of the miR-9 family, which are the only experimentally verified GRB target miRNAs.
A subset of the conserved miRNA loci we investigated exhibits typical characteristics of GRB target genes, which may partially explain their complex expression profiles during development.
最近的功能研究表明,许多 microRNAs(miRNAs)在生物体发育过程中由 RNA 聚合酶 II 以特定的时空方式表达,并在细胞谱系决定和形态发生中发挥关键作用。因此,它们在功能上与许多关键的蛋白质编码发育基因相关,这些基因与高度保守的非编码元件(HCNEs)的阵列形成基因组调控块(GRBs),作为长距离增强子协同调节其靶基因的表达。鉴于这种功能相似性,以及最近的斑马鱼转基因实验表明 miR-9 家族确实受到具有增强子活性的 HCNEs 的调节,我们假设这种 miRNA 调节方式很普遍。在本文中,我们通过分析 GRB 靶基因的特征,系统地研究了具有自身已知或计算推断启动子的保守自我转录 miRNA(ST miRNAs)的调控景观。这些特征不仅包括其附近 HCNE 的密度,还包括大的 CpG 岛(CGIs)的存在以及与发育基因相关的独特组蛋白修饰标记模式。
我们的研究结果表明,我们研究的保守 ST miRNAs 中有一部分具有与蛋白质编码 GRB 靶基因相似的性质:它们位于 HCNE/增强子结合密度显著较高的区域,并且更可能与 CGIs 相关。此外,它们的假定启动子在发育和分化过程中既有激活也有沉默的组蛋白修饰标记。基于这些结果,我们使用基因组附近的 HCNE 密度升高和双价启动子来识别 29 个可能的 GRB 靶 miRNA/miRNA 簇,其中超过三分之二已知在发育和分化过程中发挥作用。此外,这些预测包括 miR-9 家族的 miRNA,这是唯一经过实验验证的 GRB 靶 miRNA。
我们研究的保守 miRNA 基因座的一部分表现出 GRB 靶基因的典型特征,这可能部分解释了它们在发育过程中复杂的表达谱。