| Literature DB >> 35390275 |
Evgeny Deforzh1, Erik J Uhlmann1, Eashita Das1, Aleksandra Galitsyna2, Ramil Arora1, Harini Saravanan1, Rosalia Rabinovsky1, Aditya D Wirawan1, Nadiya M Teplyuk1, Rachid El Fatimy1, Sucika Perumalla1, Anirudh Jairam1, Zhiyun Wei1, Leonid Mirny3, Anna M Krichevsky4.
Abstract
miR-10b is silenced in normal neuroglial cells of the brain but commonly activated in glioma, where it assumes an essential tumor-promoting role. We demonstrate that the entire miR-10b-hosting HOXD locus is activated in glioma via the cis-acting mechanism involving 3D chromatin reorganization and CTCF-cohesin-mediated looping. This mechanism requires two interacting lncRNAs, HOXD-AS2 and LINC01116, one associated with HOXD3/HOXD4/miR-10b promoter and another with the remote enhancer. Knockdown of either lncRNA in glioma cells alters CTCF and cohesin binding, abolishes chromatin looping, inhibits the expression of all genes within HOXD locus, and leads to glioma cell death. Conversely, in cortical astrocytes, enhancer activation is sufficient for HOXD/miR-10b locus reorganization, gene derepression, and neoplastic cell transformation. LINC01116 RNA is essential for this process. Our results demonstrate the interplay of two lncRNAs in the chromatin folding and concordant regulation of miR-10b and multiple HOXD genes normally silenced in astrocytes and triggering the neoplastic glial transformation.Entities:
Keywords: CTCF; HOXD locus; chromatin loops; enhancer-promoter communication; glioblastoma; lncRNAs; low-grade glioma; miR-10b
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Year: 2022 PMID: 35390275 PMCID: PMC9271318 DOI: 10.1016/j.molcel.2022.03.018
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 19.328