| Literature DB >> 29979962 |
Pei-Fang Tsai1, Stefania Dell'Orso2, Joseph Rodriguez3, Karinna O Vivanco1, Kyung-Dae Ko1, Kan Jiang4, Aster H Juan1, Aishe A Sarshad1, Laura Vian5, Michelle Tran6, Darawalee Wangsa7, A Hongjun Wang1, Jelena Perovanovic1, Dimitrios Anastasakis1, Evelyn Ralston6, Thomas Ried7, Hong-Wei Sun4, Markus Hafner1, Daniel R Larson3, Vittorio Sartorelli8.
Abstract
The enhancer regions of the myogenic master regulator MyoD give rise to at least two enhancer RNAs. Core enhancer eRNA (CEeRNA) regulates transcription of the adjacent MyoD gene, whereas DRReRNA affects expression of Myogenin in trans. We found that DRReRNA is recruited at the Myogenin locus, where it colocalizes with Myogenin nascent transcripts. DRReRNA associates with the cohesin complex, and this association correlates with its transactivating properties. Despite being expressed in undifferentiated cells, cohesin is not loaded on Myogenin until the cells start expressing DRReRNA, which is then required for cohesin chromatin recruitment and maintenance. Functionally, depletion of either cohesin or DRReRNA reduces chromatin accessibility, prevents Myogenin activation, and hinders muscle cell differentiation. Thus, DRReRNA ensures spatially appropriate cohesin loading in trans to regulate gene expression. Published by Elsevier Inc.Entities:
Keywords: Myogenin; cohesin; enhancer RNA; muscle gene transcription; non-coding RNA
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Year: 2018 PMID: 29979962 PMCID: PMC6082425 DOI: 10.1016/j.molcel.2018.06.008
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970