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No Need to Stick Together to Be Connected: Multiple Types of Enhancers’ Networking

SIMPLE SUMMARY: Transcription regulation programs require the functional interaction of distal and proximal regulatory regions, interacting by specific 3D chromatin configurations. Enhancers are cis-acting regulatory elements able to promote gene expression regardless their orientation and distance...

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Autores principales: Vitale, Emanuele, Gugnoni, Mila, Ciarrocchi, Alessia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533737/
https://www.ncbi.nlm.nih.gov/pubmed/34680347
http://dx.doi.org/10.3390/cancers13205201
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author Vitale, Emanuele
Gugnoni, Mila
Ciarrocchi, Alessia
author_facet Vitale, Emanuele
Gugnoni, Mila
Ciarrocchi, Alessia
author_sort Vitale, Emanuele
collection PubMed
description SIMPLE SUMMARY: Transcription regulation programs require the functional interaction of distal and proximal regulatory regions, interacting by specific 3D chromatin configurations. Enhancers are cis-acting regulatory elements able to promote gene expression regardless their orientation and distance from the transcription starting site. Their systematic mapping by genome-wide chromatin profiling and chromosome conformation analysis, combined with the development of gene-editing approaches to modulate their function, revealed that many enhancers work together to fine-tune the expression of their target genes. This review aim to describe the functions of different types of enhancers and the modalities of enhancers’ interaction, focusing on their role in the regulation of complex biological processes like cancer development. ABSTRACT: The control of gene expression at a transcriptional level requires a widespread landscape of regulatory elements. Central to these regulatory circuits are enhancers (ENHs), which are defined as cis-acting DNA elements able to increase the transcription of a target gene in a distance- and orientation-independent manner. ENHs are not independent functional elements but work in a complex and dynamic cooperative network, constituting the building blocks of multimodular domains of gene expression regulation. The information from each of these elements converges on the target promoter, contributing to improving the precision and sharpness of gene modulation. ENHs’ interplay varies in its nature and extent, ranging from an additive to redundant effect depending on contexts. Moving from super-enhancers that drive the high expression levels of identity genes, to shadow-enhancers, whose redundant functions contribute to buffering the variation in gene expression, this review aims to describe the different modalities of ENHs’ interaction and their role in the regulation of complex biological processes like cancer development.
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spelling pubmed-85337372021-10-23 No Need to Stick Together to Be Connected: Multiple Types of Enhancers’ Networking Vitale, Emanuele Gugnoni, Mila Ciarrocchi, Alessia Cancers (Basel) Review SIMPLE SUMMARY: Transcription regulation programs require the functional interaction of distal and proximal regulatory regions, interacting by specific 3D chromatin configurations. Enhancers are cis-acting regulatory elements able to promote gene expression regardless their orientation and distance from the transcription starting site. Their systematic mapping by genome-wide chromatin profiling and chromosome conformation analysis, combined with the development of gene-editing approaches to modulate their function, revealed that many enhancers work together to fine-tune the expression of their target genes. This review aim to describe the functions of different types of enhancers and the modalities of enhancers’ interaction, focusing on their role in the regulation of complex biological processes like cancer development. ABSTRACT: The control of gene expression at a transcriptional level requires a widespread landscape of regulatory elements. Central to these regulatory circuits are enhancers (ENHs), which are defined as cis-acting DNA elements able to increase the transcription of a target gene in a distance- and orientation-independent manner. ENHs are not independent functional elements but work in a complex and dynamic cooperative network, constituting the building blocks of multimodular domains of gene expression regulation. The information from each of these elements converges on the target promoter, contributing to improving the precision and sharpness of gene modulation. ENHs’ interplay varies in its nature and extent, ranging from an additive to redundant effect depending on contexts. Moving from super-enhancers that drive the high expression levels of identity genes, to shadow-enhancers, whose redundant functions contribute to buffering the variation in gene expression, this review aims to describe the different modalities of ENHs’ interaction and their role in the regulation of complex biological processes like cancer development. MDPI 2021-10-16 /pmc/articles/PMC8533737/ /pubmed/34680347 http://dx.doi.org/10.3390/cancers13205201 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Vitale, Emanuele
Gugnoni, Mila
Ciarrocchi, Alessia
No Need to Stick Together to Be Connected: Multiple Types of Enhancers’ Networking
title No Need to Stick Together to Be Connected: Multiple Types of Enhancers’ Networking
title_full No Need to Stick Together to Be Connected: Multiple Types of Enhancers’ Networking
title_fullStr No Need to Stick Together to Be Connected: Multiple Types of Enhancers’ Networking
title_full_unstemmed No Need to Stick Together to Be Connected: Multiple Types of Enhancers’ Networking
title_short No Need to Stick Together to Be Connected: Multiple Types of Enhancers’ Networking
title_sort no need to stick together to be connected: multiple types of enhancers’ networking
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533737/
https://www.ncbi.nlm.nih.gov/pubmed/34680347
http://dx.doi.org/10.3390/cancers13205201
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