| Literature DB >> 33568070 |
Emmanuel Odame1, Yuan Chen1, Shuailong Zheng1, Dinghui Dai1, Bismark Kyei1, Siyuan Zhan1, Jiaxue Cao1, Jiazhong Guo1, Tao Zhong1, Linjie Wang1, Li Li2, Hongping Zhang3.
Abstract
miRNAs are well known to be gene repressors. A newly identified class of miRNAs termed nuclear activating miRNAs (NamiRNAs), transcribed from miRNA loci that exhibit enhancer features, promote gene expression via binding to the promoter and enhancer marker regions of the target genes. Meanwhile, activated enhancers produce endogenous non-coding RNAs (named enhancer RNAs, eRNAs) to activate gene expression. During chromatin looping, transcribed eRNAs interact with NamiRNAs through enhancer-promoter interaction to perform similar functions. Here, we review the functional differences and similarities between eRNAs and NamiRNAs in myogenesis and disease. We also propose models demonstrating their mutual mechanism and function. We conclude that eRNAs are active molecules, transcriptional regulators, and partners of NamiRNAs, rather than mere RNAs produced during enhancer activation.Entities:
Keywords: Enhancer RNA; MicroRNA; Myogenesis; NamiRNAs; Transcriptional regulator
Year: 2021 PMID: 33568070 PMCID: PMC7877072 DOI: 10.1186/s11658-021-00248-x
Source DB: PubMed Journal: Cell Mol Biol Lett ISSN: 1425-8153 Impact factor: 5.787