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Enhancer RNA: What we know and what we can achieve

Enhancers are important cis‐acting elements that can regulate gene transcription and cell fate alongside promoters. In fact, many human cancers and diseases are associated with the malfunction of enhancers. Recent studies have shown that enhancers can produce enhancer RNAs (eRNAs) by RNA polymerase...

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Detalles Bibliográficos
Autores principales: Han, Zhenzhen, Li, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055912/
https://www.ncbi.nlm.nih.gov/pubmed/35170113
http://dx.doi.org/10.1111/cpr.13202
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author Han, Zhenzhen
Li, Wei
author_facet Han, Zhenzhen
Li, Wei
author_sort Han, Zhenzhen
collection PubMed
description Enhancers are important cis‐acting elements that can regulate gene transcription and cell fate alongside promoters. In fact, many human cancers and diseases are associated with the malfunction of enhancers. Recent studies have shown that enhancers can produce enhancer RNAs (eRNAs) by RNA polymerase II. In this review, we discuss eRNA production, characteristics, functions and mechanics. eRNAs can determine chromatin accessibility, histone modification and gene expression by constructing a ‘chromatin loop’, thereby bringing enhancers to their target gene. eRNA can also be involved in the phase separation with enhancers and other proteins. eRNAs are abundant, and importantly, tissue‐specific in tumours, various diseases and stem cells; thus, eRNAs can be a potential target for disease diagnosis and treatment. As eRNA is produced from the active transcription of enhancers and is involved in the regulation of cell fate, its manipulation will influence cell function, and therefore, it can be a new target for biological therapy.
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spelling pubmed-90559122022-05-03 Enhancer RNA: What we know and what we can achieve Han, Zhenzhen Li, Wei Cell Prolif Review Enhancers are important cis‐acting elements that can regulate gene transcription and cell fate alongside promoters. In fact, many human cancers and diseases are associated with the malfunction of enhancers. Recent studies have shown that enhancers can produce enhancer RNAs (eRNAs) by RNA polymerase II. In this review, we discuss eRNA production, characteristics, functions and mechanics. eRNAs can determine chromatin accessibility, histone modification and gene expression by constructing a ‘chromatin loop’, thereby bringing enhancers to their target gene. eRNA can also be involved in the phase separation with enhancers and other proteins. eRNAs are abundant, and importantly, tissue‐specific in tumours, various diseases and stem cells; thus, eRNAs can be a potential target for disease diagnosis and treatment. As eRNA is produced from the active transcription of enhancers and is involved in the regulation of cell fate, its manipulation will influence cell function, and therefore, it can be a new target for biological therapy. John Wiley and Sons Inc. 2022-02-16 /pmc/articles/PMC9055912/ /pubmed/35170113 http://dx.doi.org/10.1111/cpr.13202 Text en © 2022 The Authors. Cell Proliferation Published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Han, Zhenzhen
Li, Wei
Enhancer RNA: What we know and what we can achieve
title Enhancer RNA: What we know and what we can achieve
title_full Enhancer RNA: What we know and what we can achieve
title_fullStr Enhancer RNA: What we know and what we can achieve
title_full_unstemmed Enhancer RNA: What we know and what we can achieve
title_short Enhancer RNA: What we know and what we can achieve
title_sort enhancer rna: what we know and what we can achieve
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055912/
https://www.ncbi.nlm.nih.gov/pubmed/35170113
http://dx.doi.org/10.1111/cpr.13202
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