Division of Infectious Diseases and Immunology, Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Science. 2013 Aug 16;341(6147):789-92. doi: 10.1126/science.1240925. Epub 2013 Aug 1.
An inducible program of inflammatory gene expression is central to antimicrobial defenses. This response is controlled by a collaboration involving signal-dependent activation of transcription factors, transcriptional co-regulators, and chromatin-modifying factors. We have identified a long noncoding RNA (lncRNA) that acts as a key regulator of this inflammatory response. Pattern recognition receptors such as the Toll-like receptors induce the expression of numerous lncRNAs. One of these, lincRNA-Cox2, mediates both the activation and repression of distinct classes of immune genes. Transcriptional repression of target genes is dependent on interactions of lincRNA-Cox2 with heterogeneous nuclear ribonucleoprotein A/B and A2/B1. Collectively, these studies unveil a central role of lincRNA-Cox2 as a broad-acting regulatory component of the circuit that controls the inflammatory response.
诱导性炎症基因表达程序是抗菌防御的核心。这种反应受到信号依赖性转录因子激活、转录共调节剂和染色质修饰因子的协同控制。我们已经鉴定出一种长非编码 RNA(lncRNA),它是这种炎症反应的关键调节剂。模式识别受体,如 Toll 样受体,诱导许多 lncRNA 的表达。其中之一,lncRNA-Cox2,介导不同类别的免疫基因的激活和抑制。靶基因的转录抑制依赖于 lincRNA-Cox2 与异质核核糖核蛋白 A/B 和 A2/B1 的相互作用。总之,这些研究揭示了 lincRNA-Cox2 作为控制炎症反应的电路的一个广泛作用的调节成分的核心作用。