Boque-Sastre Raquel, Soler Marta, Oliveira-Mateos Cristina, Portela Anna, Moutinho Catia, Sayols Sergi, Villanueva Alberto, Esteller Manel, Guil Sonia
Cancer Epigenetics and Biology Program, and.
Translational Research Laboratory, Catalan Institute of Oncology, Bellvitge Biomedical Research Institute, L'Hospitalet, 08908 Barcelona, Catalonia, Spain;
Proc Natl Acad Sci U S A. 2015 May 5;112(18):5785-90. doi: 10.1073/pnas.1421197112. Epub 2015 Apr 22.
The mechanisms used by antisense transcripts to regulate their corresponding sense mRNAs are not fully understood. Herein, we have addressed this issue for the vimentin (VIM) gene, a member of the intermediate filament family involved in cell and tissue integrity that is deregulated in different types of cancer. VIM mRNA levels are positively correlated with the expression of a previously uncharacterized head-to-head antisense transcript, both transcripts being silenced in colon primary tumors concomitant with promoter hypermethylation. Furthermore, antisense transcription promotes formation of an R-loop structure that can be disfavored in vitro and in vivo by ribonuclease H1 overexpression, resulting in VIM down-regulation. Antisense knockdown and R-loop destabilization both result in chromatin compaction around the VIM promoter and a reduction in the binding of transcriptional activators of the NF-κB pathway. These results are the first examples to our knowledge of R-loop-mediated enhancement of gene expression involving head-to-head antisense transcription at a cancer-related locus.
反义转录本用于调控其相应正义mRNA的机制尚未完全明确。在此,我们针对波形蛋白(VIM)基因解决了这一问题,VIM基因是中间丝家族的成员,参与细胞和组织完整性,在不同类型癌症中其表达失调。VIM mRNA水平与一种先前未被表征的头对头反义转录本的表达呈正相关,在结肠原发性肿瘤中,这两种转录本均因启动子高甲基化而沉默。此外,反义转录促进R环结构的形成,在体外和体内,核糖核酸酶H1的过表达会不利于该结构的形成,从而导致VIM表达下调。反义敲低和R环去稳定化均导致VIM启动子周围的染色质压缩以及NF-κB途径转录激活因子结合减少。据我们所知,这些结果是癌症相关位点上涉及头对头反义转录的R环介导基因表达增强的首个实例。