Yamanaka Yasunari, Faghihi Mohammad Ali, Magistri Marco, Alvarez-Garcia Oscar, Lotz Martin, Wahlestedt Claes
Center for Therapeutic Innovation and Department of Psychiatry and Behavioral Sciences, University of Miami Miller School of Medicine, Miami, FL 33136, USA.
Department of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, CA 92037, USA.
Cell Rep. 2015 May 12;11(6):967-976. doi: 10.1016/j.celrep.2015.04.011. Epub 2015 Apr 30.
Long non-coding RNAs (lncRNAs), including natural antisense transcripts (NATs), are expressed more extensively than previously anticipated and have widespread roles in regulating gene expression. Nevertheless, the molecular mechanisms of action of the majority of NATs remain largely unknown. Here, we identify a NAT of low-density lipoprotein receptor-related protein 1 (Lrp1), referred to as Lrp1-AS, that negatively regulates Lrp1 expression. We show that Lrp1-AS directly binds to high-mobility group box 2 (Hmgb2) and inhibits the activity of Hmgb2 to enhance Srebp1a-dependent transcription of Lrp1. Short oligonucleotides targeting Lrp1-AS inhibit the interaction of antisense transcript and Hmgb2 protein and increase Lrp1 expression by enhancing Hmgb2 activity. Quantitative RT-PCR analysis of brain tissue samples from Alzheimer's disease patients and aged-matched controls revealed upregulation of LRP1-AS and downregulation of LRP1. Our data suggest a regulatory mechanism whereby a NAT interacts with a ubiquitous chromatin-associated protein to modulate its activity in a locus-specific fashion.
长链非编码RNA(lncRNA),包括天然反义转录本(NAT),其表达比之前预期的更为广泛,并且在调节基因表达方面具有广泛作用。然而,大多数NAT的分子作用机制仍基本未知。在此,我们鉴定出一种低密度脂蛋白受体相关蛋白1(Lrp1)的NAT,称为Lrp1-AS,它对Lrp1表达起负调节作用。我们发现Lrp1-AS直接与高迁移率族蛋白盒2(Hmgb2)结合,并抑制Hmgb2增强Lrp1的Srebp1a依赖性转录的活性。靶向Lrp1-AS的短寡核苷酸抑制反义转录本与Hmgb2蛋白的相互作用,并通过增强Hmgb2活性来增加Lrp1表达。对阿尔茨海默病患者和年龄匹配对照的脑组织样本进行定量RT-PCR分析,结果显示LRP1-AS上调而LRP1下调。我们的数据表明了一种调节机制,即一个NAT与一种普遍存在的染色质相关蛋白相互作用,以位点特异性方式调节其活性。