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DNA Demethylation in the Processes of Repair and Epigenetic Regulation Performed by 2-Ketoglutarate-Dependent DNA Dioxygenases
Site-specific DNA methylation plays an important role in epigenetic regulation of gene expression. Chemical methylation of DNA, including the formation of various methylated nitrogenous bases, leads to the formation of genotoxic modifications that impair DNA functions. Despite the fact that differen...
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Published in: | International journal of molecular sciences 2021-10, Vol.22 (19), p.10540 |
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description | Site-specific DNA methylation plays an important role in epigenetic regulation of gene expression. Chemical methylation of DNA, including the formation of various methylated nitrogenous bases, leads to the formation of genotoxic modifications that impair DNA functions. Despite the fact that different pathways give rise to methyl groups in DNA, the main pathway for their removal is oxidative demethylation, which is catalyzed by nonheme Fe(II)/α-ketoglutarate–dependent DNA dioxygenases. DNA dioxygenases share a common catalytic mechanism of the oxidation of the alkyl groups on nitrogenous bases in nucleic acids. This review presents generalized data on the catalytic mechanism of action of DNA dioxygenases and on the participation of typical representatives of this superfamily, such as prokaryotic enzyme AlkB and eukaryotic enzymes ALKBH1–8 and TET1–3, in both processes of direct repair of alkylated DNA adducts and in the removal of an epigenetic mark (5-methylcytosine). |
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Chemical methylation of DNA, including the formation of various methylated nitrogenous bases, leads to the formation of genotoxic modifications that impair DNA functions. Despite the fact that different pathways give rise to methyl groups in DNA, the main pathway for their removal is oxidative demethylation, which is catalyzed by nonheme Fe(II)/α-ketoglutarate–dependent DNA dioxygenases. DNA dioxygenases share a common catalytic mechanism of the oxidation of the alkyl groups on nitrogenous bases in nucleic acids. This review presents generalized data on the catalytic mechanism of action of DNA dioxygenases and on the participation of typical representatives of this superfamily, such as prokaryotic enzyme AlkB and eukaryotic enzymes ALKBH1–8 and TET1–3, in both processes of direct repair of alkylated DNA adducts and in the removal of an epigenetic mark (5-methylcytosine).</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms221910540</identifier><identifier>PMID: 34638881</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Adducts ; Alkylation ; Bases (nucleic acids) ; catalytic mechanism ; Decomposition ; Demethylation ; Deoxyribonucleic acid ; direct repair ; DNA ; DNA adducts ; DNA damage ; DNA demethylation ; DNA dioxygenase ; DNA methylation ; DNA repair ; Enzymes ; Epigenetics ; Gene expression ; Genotoxicity ; Iron ; Ketoglutaric acid ; Mammals ; Nucleic acids ; Oxidation ; oxygen activation ; Proteins ; Repair ; Review ; Stem cells</subject><ispartof>International journal of molecular sciences, 2021-10, Vol.22 (19), p.10540</ispartof><rights>2021 by the authors. 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/). 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Chemical methylation of DNA, including the formation of various methylated nitrogenous bases, leads to the formation of genotoxic modifications that impair DNA functions. Despite the fact that different pathways give rise to methyl groups in DNA, the main pathway for their removal is oxidative demethylation, which is catalyzed by nonheme Fe(II)/α-ketoglutarate–dependent DNA dioxygenases. DNA dioxygenases share a common catalytic mechanism of the oxidation of the alkyl groups on nitrogenous bases in nucleic acids. 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Kanazhevskaya, Lyubov Yu ; Fedorova, Olga S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c458t-8da1ba5ba10082460019123babcedbe9e1e60d6dc3630ebe413e68f31af15c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adducts</topic><topic>Alkylation</topic><topic>Bases (nucleic acids)</topic><topic>catalytic mechanism</topic><topic>Decomposition</topic><topic>Demethylation</topic><topic>Deoxyribonucleic acid</topic><topic>direct repair</topic><topic>DNA</topic><topic>DNA adducts</topic><topic>DNA damage</topic><topic>DNA demethylation</topic><topic>DNA dioxygenase</topic><topic>DNA methylation</topic><topic>DNA repair</topic><topic>Enzymes</topic><topic>Epigenetics</topic><topic>Gene expression</topic><topic>Genotoxicity</topic><topic>Iron</topic><topic>Ketoglutaric acid</topic><topic>Mammals</topic><topic>Nucleic acids</topic><topic>Oxidation</topic><topic>oxygen activation</topic><topic>Proteins</topic><topic>Repair</topic><topic>Review</topic><topic>Stem cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kuznetsov, Nikita A.</creatorcontrib><creatorcontrib>Kanazhevskaya, Lyubov Yu</creatorcontrib><creatorcontrib>Fedorova, Olga S.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Databases</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kuznetsov, Nikita A.</au><au>Kanazhevskaya, Lyubov Yu</au><au>Fedorova, Olga S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DNA Demethylation in the Processes of Repair and Epigenetic Regulation Performed by 2-Ketoglutarate-Dependent DNA Dioxygenases</atitle><jtitle>International journal of molecular sciences</jtitle><date>2021-10-01</date><risdate>2021</risdate><volume>22</volume><issue>19</issue><spage>10540</spage><pages>10540-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><notes>ObjectType-Article-2</notes><notes>SourceType-Scholarly Journals-1</notes><notes>ObjectType-Feature-3</notes><notes>content type line 23</notes><notes>ObjectType-Review-1</notes><abstract>Site-specific DNA methylation plays an important role in epigenetic regulation of gene expression. Chemical methylation of DNA, including the formation of various methylated nitrogenous bases, leads to the formation of genotoxic modifications that impair DNA functions. Despite the fact that different pathways give rise to methyl groups in DNA, the main pathway for their removal is oxidative demethylation, which is catalyzed by nonheme Fe(II)/α-ketoglutarate–dependent DNA dioxygenases. DNA dioxygenases share a common catalytic mechanism of the oxidation of the alkyl groups on nitrogenous bases in nucleic acids. This review presents generalized data on the catalytic mechanism of action of DNA dioxygenases and on the participation of typical representatives of this superfamily, such as prokaryotic enzyme AlkB and eukaryotic enzymes ALKBH1–8 and TET1–3, in both processes of direct repair of alkylated DNA adducts and in the removal of an epigenetic mark (5-methylcytosine).</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>34638881</pmid><doi>10.3390/ijms221910540</doi><orcidid>https://orcid.org/0000-0002-4016-198X</orcidid><orcidid>https://orcid.org/0000-0002-4001-7187</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adducts Alkylation Bases (nucleic acids) catalytic mechanism Decomposition Demethylation Deoxyribonucleic acid direct repair DNA DNA adducts DNA damage DNA demethylation DNA dioxygenase DNA methylation DNA repair Enzymes Epigenetics Gene expression Genotoxicity Iron Ketoglutaric acid Mammals Nucleic acids Oxidation oxygen activation Proteins Repair Review Stem cells |
title | DNA Demethylation in the Processes of Repair and Epigenetic Regulation Performed by 2-Ketoglutarate-Dependent DNA Dioxygenases |
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