Genome-wide chromatin contacts of super-enhancer-associated lncRNA identify LINC01013 as a regulator of fibrosis in the aortic valve.
Arnaud ChignonDéborah ArgaudMarie-Chloé BoulangerGhada MkannezValentin Bon-BaretZhonglin LiSébastien ThériaultYohan BossePatrick MathieuPublished in: PLoS genetics (2022)
Calcific aortic valve disease (CAVD) is characterized by a fibrocalcific process. The regulatory mechanisms that drive the fibrotic response in the aortic valve (AV) are poorly understood. Long noncoding RNAs derived from super-enhancers (lncRNA-SE) control gene expression and cell fate. Herein, multidimensional profiling including chromatin immunoprecipitation and sequencing, transposase-accessible chromatin sequencing, genome-wide 3D chromatin contacts of enhancer-promoter identified LINC01013 as an overexpressed lncRNA-SE during CAVD. LINC01013 is within a loop anchor, which has contact with the promoter of CCN2 (CTGF) located at ~180 kb upstream. Investigation showed that LINC01013 acts as a decoy factor for the negative transcription elongation factor E (NELF-E), whereby it controls the expression of CCN2. LINC01013-CCN2 is part of a transforming growth factor beta 1 (TGFB1) network and exerts a control over fibrogenesis. These findings illustrate a novel mechanism whereby a dysregulated lncRNA-SE controls, through a looping process, the expression of CCN2 and fibrogenesis of the AV.
Keyphrases
- aortic valve
- long non coding rna
- transcription factor
- poor prognosis
- genome wide
- long noncoding rna
- dna methylation
- gene expression
- transcatheter aortic valve replacement
- transcatheter aortic valve implantation
- aortic valve replacement
- transforming growth factor
- aortic stenosis
- single cell
- cell fate
- binding protein
- epithelial mesenchymal transition
- dna damage
- copy number
- systemic sclerosis
- signaling pathway
- idiopathic pulmonary fibrosis
- heart failure
- network analysis
- high throughput sequencing