Human REV3 DNA Polymerase Zeta Localizes to Mitochondria and Protects the Mitochondrial Genome
To date, mitochondrial DNA polymerase γ (POLG) is the only polymerase known to be present in mammalian mitochondria. A dogma in the mitochondria field is that there is no other polymerase present in the mitochondria of mammalian cells. Here we demonstrate localization of REV3 DNA polymerase in the m...
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description | To date, mitochondrial DNA polymerase γ (POLG) is the only polymerase known to be present in mammalian mitochondria. A dogma in the mitochondria field is that there is no other polymerase present in the mitochondria of mammalian cells. Here we demonstrate localization of REV3 DNA polymerase in the mammalian mitochondria. We demonstrate localization of REV3 in the mitochondria of mammalian tissue as well as cell lines. REV3 associates with POLG and mitochondrial DNA and protects the mitochondrial genome from DNA damage. Inactivation of Rev3 leads to reduced mitochondrial membrane potential, reduced OXPHOS activity, and increased glucose consumption. Conversely, inhibition of the OXPHOS increases expression of Rev3. Rev3 expression is increased in human primary breast tumors and breast cancer cell lines. Inactivation of Rev3 decreases cell migration and invasion, and localization of Rev3 in mitochondria increases survival and the invasive potential of cancer cells. Taken together, we demonstrate that REV3 functions in mammalian mitochondria and that mitochondrial REV3 is associated with the tumorigenic potential of cells. |
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A dogma in the mitochondria field is that there is no other polymerase present in the mitochondria of mammalian cells. Here we demonstrate localization of REV3 DNA polymerase in the mammalian mitochondria. We demonstrate localization of REV3 in the mitochondria of mammalian tissue as well as cell lines. REV3 associates with POLG and mitochondrial DNA and protects the mitochondrial genome from DNA damage. Inactivation of Rev3 leads to reduced mitochondrial membrane potential, reduced OXPHOS activity, and increased glucose consumption. Conversely, inhibition of the OXPHOS increases expression of Rev3. Rev3 expression is increased in human primary breast tumors and breast cancer cell lines. Inactivation of Rev3 decreases cell migration and invasion, and localization of Rev3 in mitochondria increases survival and the invasive potential of cancer cells. Taken together, we demonstrate that REV3 functions in mammalian mitochondria and that mitochondrial REV3 is associated with the tumorigenic potential of cells.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0140409</identifier><identifier>PMID: 26462070</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Aging ; Amino Acid Sequence ; Analysis ; Animals ; Biotechnology ; Breast cancer ; Breast Neoplasms - pathology ; Cancer ; Carcinogenesis - pathology ; Cell growth ; Cell Line, Tumor ; Cell migration ; Cell proliferation ; Cell survival ; Cytoprotection ; Deactivation ; Deoxyribonucleic acid ; DNA ; DNA Damage ; DNA polymerase ; DNA Polymerase gamma ; DNA polymerases ; DNA repair ; DNA, Mitochondrial - genetics ; DNA-Binding Proteins - chemistry ; DNA-Binding Proteins - metabolism ; DNA-directed DNA polymerase ; DNA-Directed DNA Polymerase - chemistry ; DNA-Directed DNA Polymerase - metabolism ; Female ; Fibroblasts ; Genetics ; Genome, Mitochondrial ; Genomes ; HEK293 Cells ; HeLa Cells ; Humans ; Inactivation ; Invasiveness ; Localization ; Mammalian cells ; Mammals ; Membrane potential ; Mice ; Mitochondria ; Mitochondria - enzymology ; Mitochondrial DNA ; Molecular Sequence Data ; Mutagenesis ; Mutation ; NIH 3T3 Cells ; Oxidative Phosphorylation ; Protein Binding ; Protein Transport ; Proteins ; Saccharomyces cerevisiae ; Tumor cell lines ; Tumors</subject><ispartof>PloS one, 2015-10, Vol.10 (10), p.e0140409</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Singh et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Singh et al 2015 Singh et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c758t-88e75da96fcf4f9b675cf2cb4cce37c2ed00acd685700138f15b929df4b9722b3</citedby><cites>FETCH-LOGICAL-c758t-88e75da96fcf4f9b675cf2cb4cce37c2ed00acd685700138f15b929df4b9722b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604079/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604079/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2100,2926,23864,27922,27923,53789,53791,79370,79371</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26462070$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Santos, Janine</contributor><creatorcontrib>Singh, Bhupendra</creatorcontrib><creatorcontrib>Li, Xiurong</creatorcontrib><creatorcontrib>Owens, Kjerstin M</creatorcontrib><creatorcontrib>Vanniarajan, Ayyasamy</creatorcontrib><creatorcontrib>Liang, Ping</creatorcontrib><creatorcontrib>Singh, Keshav K</creatorcontrib><title>Human REV3 DNA Polymerase Zeta Localizes to Mitochondria and Protects the Mitochondrial Genome</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>To date, mitochondrial DNA polymerase γ (POLG) is the only polymerase known to be present in mammalian mitochondria. A dogma in the mitochondria field is that there is no other polymerase present in the mitochondria of mammalian cells. Here we demonstrate localization of REV3 DNA polymerase in the mammalian mitochondria. We demonstrate localization of REV3 in the mitochondria of mammalian tissue as well as cell lines. REV3 associates with POLG and mitochondrial DNA and protects the mitochondrial genome from DNA damage. Inactivation of Rev3 leads to reduced mitochondrial membrane potential, reduced OXPHOS activity, and increased glucose consumption. Conversely, inhibition of the OXPHOS increases expression of Rev3. Rev3 expression is increased in human primary breast tumors and breast cancer cell lines. Inactivation of Rev3 decreases cell migration and invasion, and localization of Rev3 in mitochondria increases survival and the invasive potential of cancer cells. Taken together, we demonstrate that REV3 functions in mammalian mitochondria and that mitochondrial REV3 is associated with the tumorigenic potential of cells.</description><subject>Aging</subject><subject>Amino Acid Sequence</subject><subject>Analysis</subject><subject>Animals</subject><subject>Biotechnology</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - pathology</subject><subject>Cancer</subject><subject>Carcinogenesis - pathology</subject><subject>Cell growth</subject><subject>Cell Line, Tumor</subject><subject>Cell migration</subject><subject>Cell proliferation</subject><subject>Cell survival</subject><subject>Cytoprotection</subject><subject>Deactivation</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA Damage</subject><subject>DNA polymerase</subject><subject>DNA Polymerase gamma</subject><subject>DNA polymerases</subject><subject>DNA repair</subject><subject>DNA, Mitochondrial - genetics</subject><subject>DNA-Binding Proteins - chemistry</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>DNA-directed DNA polymerase</subject><subject>DNA-Directed DNA Polymerase - chemistry</subject><subject>DNA-Directed DNA Polymerase - metabolism</subject><subject>Female</subject><subject>Fibroblasts</subject><subject>Genetics</subject><subject>Genome, Mitochondrial</subject><subject>Genomes</subject><subject>HEK293 Cells</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Inactivation</subject><subject>Invasiveness</subject><subject>Localization</subject><subject>Mammalian cells</subject><subject>Mammals</subject><subject>Membrane potential</subject><subject>Mice</subject><subject>Mitochondria</subject><subject>Mitochondria - enzymology</subject><subject>Mitochondrial DNA</subject><subject>Molecular Sequence Data</subject><subject>Mutagenesis</subject><subject>Mutation</subject><subject>NIH 3T3 Cells</subject><subject>Oxidative Phosphorylation</subject><subject>Protein Binding</subject><subject>Protein Transport</subject><subject>Proteins</subject><subject>Saccharomyces cerevisiae</subject><subject>Tumor cell lines</subject><subject>Tumors</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNklFrFDEUhQdRbK3-A9EBQfBh1ySTmUxeCkut7cJqS9U--GDIZG52ssxM1iQj1l9v6k7LDihIHhLu_e5JODlJ8hyjOc4Yfruxg-tlO9_aHuYIU0QRf5AcYp6RWUFQ9nDvfJA88X6DUJ6VRfE4OSAFjWWGDpNv50Mn-_Tq9DpL331cpJe2venASQ_pVwgyXVklW_MLfBps-sEEqxrb187IVPZ1eulsABVis4FJt03PoLcdPE0eadl6eDbuR8mX96efT85nq4uz5cliNVMsL8OsLIHlteSFVppqXhUsV5qoiioFGVMEaoSkqosyZwjhrNQ4rzjhtaYVZ4RU2VHycqe7ba0XozVeYEYwxySnZSSWO6K2ciO2znTS3QgrjfhTsG4tpAtGtSCKquQZ15ozVVMCZaUZI5wUqsaoolBErePxtqHqoFbQByfbiei005tGrO0PQYv4S4xHgVejgLPfB_DhH08eqbWMrzK9tlFMdcYrsaAZphErWaTmf6HiqqEzKoZDm1ifDLyZDEQmwM-wloP3Yvnp6v_Zi-sp-3qPbUC2ofG2HYKxvZ-CdAcqZ713oO-dw0jcZvvODXGbbTFmO4692Hf9fuguzNlvMTTz3g</recordid><startdate>20151013</startdate><enddate>20151013</enddate><creator>Singh, Bhupendra</creator><creator>Li, Xiurong</creator><creator>Owens, Kjerstin M</creator><creator>Vanniarajan, Ayyasamy</creator><creator>Liang, Ping</creator><creator>Singh, Keshav K</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20151013</creationdate><title>Human REV3 DNA Polymerase Zeta Localizes to Mitochondria and Protects the Mitochondrial Genome</title><author>Singh, Bhupendra ; Li, Xiurong ; Owens, Kjerstin M ; Vanniarajan, Ayyasamy ; Liang, Ping ; Singh, Keshav K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c758t-88e75da96fcf4f9b675cf2cb4cce37c2ed00acd685700138f15b929df4b9722b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Aging</topic><topic>Amino Acid Sequence</topic><topic>Analysis</topic><topic>Animals</topic><topic>Biotechnology</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - pathology</topic><topic>Cancer</topic><topic>Carcinogenesis - pathology</topic><topic>Cell growth</topic><topic>Cell Line, Tumor</topic><topic>Cell migration</topic><topic>Cell proliferation</topic><topic>Cell survival</topic><topic>Cytoprotection</topic><topic>Deactivation</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA Damage</topic><topic>DNA polymerase</topic><topic>DNA Polymerase gamma</topic><topic>DNA polymerases</topic><topic>DNA repair</topic><topic>DNA, Mitochondrial - genetics</topic><topic>DNA-Binding Proteins - chemistry</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>DNA-directed DNA polymerase</topic><topic>DNA-Directed DNA Polymerase - chemistry</topic><topic>DNA-Directed DNA Polymerase - metabolism</topic><topic>Female</topic><topic>Fibroblasts</topic><topic>Genetics</topic><topic>Genome, Mitochondrial</topic><topic>Genomes</topic><topic>HEK293 Cells</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Inactivation</topic><topic>Invasiveness</topic><topic>Localization</topic><topic>Mammalian cells</topic><topic>Mammals</topic><topic>Membrane potential</topic><topic>Mice</topic><topic>Mitochondria</topic><topic>Mitochondria - enzymology</topic><topic>Mitochondrial DNA</topic><topic>Molecular Sequence Data</topic><topic>Mutagenesis</topic><topic>Mutation</topic><topic>NIH 3T3 Cells</topic><topic>Oxidative Phosphorylation</topic><topic>Protein Binding</topic><topic>Protein Transport</topic><topic>Proteins</topic><topic>Saccharomyces cerevisiae</topic><topic>Tumor cell lines</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Singh, Bhupendra</creatorcontrib><creatorcontrib>Li, Xiurong</creatorcontrib><creatorcontrib>Owens, Kjerstin M</creatorcontrib><creatorcontrib>Vanniarajan, Ayyasamy</creatorcontrib><creatorcontrib>Liang, Ping</creatorcontrib><creatorcontrib>Singh, Keshav K</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection (ProQuest)</collection><collection>Natural Science Collection (ProQuest)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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A dogma in the mitochondria field is that there is no other polymerase present in the mitochondria of mammalian cells. Here we demonstrate localization of REV3 DNA polymerase in the mammalian mitochondria. We demonstrate localization of REV3 in the mitochondria of mammalian tissue as well as cell lines. REV3 associates with POLG and mitochondrial DNA and protects the mitochondrial genome from DNA damage. Inactivation of Rev3 leads to reduced mitochondrial membrane potential, reduced OXPHOS activity, and increased glucose consumption. Conversely, inhibition of the OXPHOS increases expression of Rev3. Rev3 expression is increased in human primary breast tumors and breast cancer cell lines. Inactivation of Rev3 decreases cell migration and invasion, and localization of Rev3 in mitochondria increases survival and the invasive potential of cancer cells. Taken together, we demonstrate that REV3 functions in mammalian mitochondria and that mitochondrial REV3 is associated with the tumorigenic potential of cells.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26462070</pmid><doi>10.1371/journal.pone.0140409</doi><oa>free_for_read</oa></addata></record> |
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subjects | Aging Amino Acid Sequence Analysis Animals Biotechnology Breast cancer Breast Neoplasms - pathology Cancer Carcinogenesis - pathology Cell growth Cell Line, Tumor Cell migration Cell proliferation Cell survival Cytoprotection Deactivation Deoxyribonucleic acid DNA DNA Damage DNA polymerase DNA Polymerase gamma DNA polymerases DNA repair DNA, Mitochondrial - genetics DNA-Binding Proteins - chemistry DNA-Binding Proteins - metabolism DNA-directed DNA polymerase DNA-Directed DNA Polymerase - chemistry DNA-Directed DNA Polymerase - metabolism Female Fibroblasts Genetics Genome, Mitochondrial Genomes HEK293 Cells HeLa Cells Humans Inactivation Invasiveness Localization Mammalian cells Mammals Membrane potential Mice Mitochondria Mitochondria - enzymology Mitochondrial DNA Molecular Sequence Data Mutagenesis Mutation NIH 3T3 Cells Oxidative Phosphorylation Protein Binding Protein Transport Proteins Saccharomyces cerevisiae Tumor cell lines Tumors |
title | Human REV3 DNA Polymerase Zeta Localizes to Mitochondria and Protects the Mitochondrial Genome |
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