Friends-Enemies: Endogenous Retroviruses Are Major Transcriptional Regulators of Human DNA

Endogenous retroviruses are mobile genetic elements hardly distinguishable from infectious, or “exogenous,” retroviruses at the time of insertion in the host DNA. Human endogenous retroviruses (HERVs) are not rare. They gave rise to multiple families of closely related mobile elements that occupy ~8...

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Main Authors: Anton A. Buzdin, Vladimir Prassolov, Andrew V. Garazha
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-06-01
Series:Frontiers in Chemistry
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fchem.2017.00035/full
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spelling doaj-e0e94b6d20b44dcbbabda2790faeafa02020-11-24T23:37:27ZengFrontiers Media S.A.Frontiers in Chemistry2296-26462017-06-01510.3389/fchem.2017.00035249301Friends-Enemies: Endogenous Retroviruses Are Major Transcriptional Regulators of Human DNAAnton A. Buzdin0Anton A. Buzdin1Vladimir Prassolov2Andrew V. Garazha3Andrew V. Garazha4Department of Cell Biology, Engelhardt Institute of Molecular Biology, Russian Academy of SciencesMoscow, RussiaCentre for Convergence of Nano-, Bio-, Information and Cognitive Sciences and Technologies, National Research Centre “Kurchatov Institute,”Moscow, RussiaDepartment of Cell Biology, Engelhardt Institute of Molecular Biology, Russian Academy of SciencesMoscow, RussiaGroup for Genomic Regulation of Cell Signaling Systems, Shemyakin-Ovchinnikov Institute of Bioorganic ChemistryMoscow, RussiaDepartment of Biomedicine, Moscow Institute of Physics and TechnologyMoscow, RussiaEndogenous retroviruses are mobile genetic elements hardly distinguishable from infectious, or “exogenous,” retroviruses at the time of insertion in the host DNA. Human endogenous retroviruses (HERVs) are not rare. They gave rise to multiple families of closely related mobile elements that occupy ~8% of the human genome. Together, they shape genomic regulatory landscape by providing at least ~320,000 human transcription factor binding sites (TFBS) located on ~110,000 individual HERV elements. The HERVs host as many as 155,000 mapped DNaseI hypersensitivity sites, which denote loci active in the regulation of gene expression or chromatin structure. The contemporary view of the HERVs evolutionary dynamics suggests that at the early stages after insertion, the HERV is treated by the host cells as a foreign genetic element, and is likely to be suppressed by the targeted methylation and mutations. However, at the later stages, when significant number of mutations has been already accumulated and when the retroviral genes are broken, the regulatory potential of a HERV may be released and recruited to modify the genomic balance of transcription factor binding sites. This process goes together with further accumulation and selection of mutations, which reshape the regulatory landscape of the human DNA. However, developmental reprogramming, stress or pathological conditions like cancer, inflammation and infectious diseases, can remove the blocks limiting expression and HERV-mediated host gene regulation. This, in turn, can dramatically alter the gene expression equilibrium and shift it to a newer state, thus further amplifying instability and exacerbating the stressful situation.http://journal.frontiersin.org/article/10.3389/fchem.2017.00035/fullretrovirusgene expression regulationpathologycancerinflammationstress
collection DOAJ
language English
format Article
sources DOAJ
author Anton A. Buzdin
Anton A. Buzdin
Vladimir Prassolov
Andrew V. Garazha
Andrew V. Garazha
spellingShingle Anton A. Buzdin
Anton A. Buzdin
Vladimir Prassolov
Andrew V. Garazha
Andrew V. Garazha
Friends-Enemies: Endogenous Retroviruses Are Major Transcriptional Regulators of Human DNA
Frontiers in Chemistry
retrovirus
gene expression regulation
pathology
cancer
inflammation
stress
author_facet Anton A. Buzdin
Anton A. Buzdin
Vladimir Prassolov
Andrew V. Garazha
Andrew V. Garazha
author_sort Anton A. Buzdin
title Friends-Enemies: Endogenous Retroviruses Are Major Transcriptional Regulators of Human DNA
title_short Friends-Enemies: Endogenous Retroviruses Are Major Transcriptional Regulators of Human DNA
title_full Friends-Enemies: Endogenous Retroviruses Are Major Transcriptional Regulators of Human DNA
title_fullStr Friends-Enemies: Endogenous Retroviruses Are Major Transcriptional Regulators of Human DNA
title_full_unstemmed Friends-Enemies: Endogenous Retroviruses Are Major Transcriptional Regulators of Human DNA
title_sort friends-enemies: endogenous retroviruses are major transcriptional regulators of human dna
publisher Frontiers Media S.A.
series Frontiers in Chemistry
issn 2296-2646
publishDate 2017-06-01
description Endogenous retroviruses are mobile genetic elements hardly distinguishable from infectious, or “exogenous,” retroviruses at the time of insertion in the host DNA. Human endogenous retroviruses (HERVs) are not rare. They gave rise to multiple families of closely related mobile elements that occupy ~8% of the human genome. Together, they shape genomic regulatory landscape by providing at least ~320,000 human transcription factor binding sites (TFBS) located on ~110,000 individual HERV elements. The HERVs host as many as 155,000 mapped DNaseI hypersensitivity sites, which denote loci active in the regulation of gene expression or chromatin structure. The contemporary view of the HERVs evolutionary dynamics suggests that at the early stages after insertion, the HERV is treated by the host cells as a foreign genetic element, and is likely to be suppressed by the targeted methylation and mutations. However, at the later stages, when significant number of mutations has been already accumulated and when the retroviral genes are broken, the regulatory potential of a HERV may be released and recruited to modify the genomic balance of transcription factor binding sites. This process goes together with further accumulation and selection of mutations, which reshape the regulatory landscape of the human DNA. However, developmental reprogramming, stress or pathological conditions like cancer, inflammation and infectious diseases, can remove the blocks limiting expression and HERV-mediated host gene regulation. This, in turn, can dramatically alter the gene expression equilibrium and shift it to a newer state, thus further amplifying instability and exacerbating the stressful situation.
topic retrovirus
gene expression regulation
pathology
cancer
inflammation
stress
url http://journal.frontiersin.org/article/10.3389/fchem.2017.00035/full
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