CeMM, Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
IMP/IMBA Transgenic Service, Institute of Molecular Pathology (IMP), Vienna, Austria.
PLoS Genet. 2019 Jul 22;15(7):e1008268. doi: 10.1371/journal.pgen.1008268. eCollection 2019 Jul.
Long non-coding (lnc) RNAs are numerous and found throughout the mammalian genome, and many are thought to be involved in the regulation of gene expression. However, the majority remain relatively uncharacterised and of uncertain function making the use of model systems to uncover their mode of action valuable. Imprinted lncRNAs target and recruit epigenetic silencing factors to a cluster of imprinted genes on the same chromosome, making them one of the best characterized lncRNAs for silencing distant genes in cis. In this study we examined silencing of the distant imprinted gene Slc22a3 by the lncRNA Airn in the Igf2r imprinted cluster in mouse. Previously we proposed that imprinted lncRNAs may silence distant imprinted genes by disrupting promoter-enhancer interactions by being transcribed through the enhancer, which we called the enhancer interference hypothesis. Here we tested this hypothesis by first using allele-specific chromosome conformation capture (3C) to detect interactions between the Slc22a3 promoter and the locus of the Airn lncRNA that silences it on the paternal chromosome. In agreement with the model, we found interactions enriched on the maternal allele across the entire Airn gene consistent with multiple enhancer-promoter interactions. Therefore, to test the enhancer interference hypothesis we devised an approach to delete the entire Airn gene. However, the deletion showed that there are no essential enhancers for Slc22a2, Pde10a and Slc22a3 within the Airn gene, strongly indicating that the Airn RNA rather than its transcription is responsible for silencing distant imprinted genes. Furthermore, we found that silent imprinted genes were covered with large blocks of H3K27me3 on the repressed paternal allele. Therefore we propose an alternative hypothesis whereby the chromosome interactions may initially guide the lncRNA to target imprinted promoters and recruit repressive chromatin, and that these interactions are lost once silencing is established.
长非编码 (lnc) RNA 数量众多,遍布哺乳动物基因组,许多被认为参与基因表达的调控。然而,大多数 lncRNA 相对没有特征,功能也不确定,因此利用模型系统来揭示其作用模式是有价值的。印迹 lncRNA 靶向并募集表观遗传沉默因子到同一染色体上的一组印迹基因,使它们成为沉默顺式 distant genes 中最具特征的 lncRNA 之一。在这项研究中,我们研究了 lncRNA Airn 在 Igf2r 印迹簇中对 distant 印迹基因 Slc22a3 的沉默作用。之前我们提出,印迹 lncRNA 可能通过转录穿过增强子来破坏启动子-增强子相互作用,从而沉默 distant 印迹基因,我们称之为增强子干扰假说。在这里,我们首先使用等位基因特异性染色体构象捕获(3C)来检测 Slc22a3 启动子与沉默它的 Airn lncRNA 基因座之间的相互作用,以验证该假说。与模型一致,我们发现跨越整个 Airn 基因的母本等位基因上富集了相互作用,这与多个增强子-启动子相互作用一致。因此,为了验证增强子干扰假说,我们设计了一种方法来删除整个 Airn 基因。然而,该删除表明在 Airn 基因内没有 Slc22a2、Pde10a 和 Slc22a3 的必需增强子,这强烈表明 Airn RNA 而不是其转录负责沉默 distant 印迹基因。此外,我们发现沉默的印迹基因在受抑制的父本等位基因上被大的 H3K27me3 块覆盖。因此,我们提出了一个替代假说,即染色体相互作用可能最初指导 lncRNA 靶向印迹启动子并募集抑制性染色质,并且一旦沉默建立,这些相互作用就会丢失。