Mitochondrial-nuclear DNA interactions contribute to the regulation of nuclear transcript levels as part of the inter-organelle communication system
Nuclear and mitochondrial organelles must maintain a communication system. Loci on the mitochondrial genome were recently reported to interact with nuclear loci. To determine whether this is part of a DNA based communication system we used genome conformation capture to map the global network of DNA...
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description | Nuclear and mitochondrial organelles must maintain a communication system. Loci on the mitochondrial genome were recently reported to interact with nuclear loci. To determine whether this is part of a DNA based communication system we used genome conformation capture to map the global network of DNA-DNA interactions between the mitochondrial and nuclear genomes (Mito-nDNA) in Saccharomyces cerevisiae cells grown under three different metabolic conditions. The interactions that form between mitochondrial and nuclear loci are dependent on the metabolic state of the yeast. Moreover, the frequency of specific mitochondrial-nuclear interactions (i.e. COX1-MSY1 and Q0182-RSM7) showed significant reductions in the absence of mitochondrial encoded reverse transcriptase machinery. Furthermore, these reductions correlated with increases in the transcript levels of the nuclear loci (MSY1 and RSM7). We propose that these interactions represent an inter-organelle DNA mediated communication system and that reverse transcription of mitochondrial RNA plays a role in this process. |
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Loci on the mitochondrial genome were recently reported to interact with nuclear loci. To determine whether this is part of a DNA based communication system we used genome conformation capture to map the global network of DNA-DNA interactions between the mitochondrial and nuclear genomes (Mito-nDNA) in Saccharomyces cerevisiae cells grown under three different metabolic conditions. The interactions that form between mitochondrial and nuclear loci are dependent on the metabolic state of the yeast. Moreover, the frequency of specific mitochondrial-nuclear interactions (i.e. COX1-MSY1 and Q0182-RSM7) showed significant reductions in the absence of mitochondrial encoded reverse transcriptase machinery. Furthermore, these reductions correlated with increases in the transcript levels of the nuclear loci (MSY1 and RSM7). We propose that these interactions represent an inter-organelle DNA mediated communication system and that reverse transcription of mitochondrial RNA plays a role in this process.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0030943</identifier><identifier>PMID: 22292080</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Arabidopsis ; Arabidopsis thaliana ; Baking yeast ; Biological Transport - drug effects ; Biological Transport - genetics ; Biological Transport - physiology ; Biology ; Carbon ; Cell Nucleus - drug effects ; Cell Nucleus - genetics ; Chromosomes ; Chromosomes, Fungal - drug effects ; Chromosomes, Fungal - genetics ; Chromosomes, Fungal - metabolism ; Communications systems ; Conformation ; Cyclooxygenase 1 - genetics ; Cyclooxygenase 1 - metabolism ; Deoxyribonucleic acid ; DNA ; DNA polymerases ; DNA, Mitochondrial - drug effects ; DNA, Mitochondrial - genetics ; DNA-Binding Proteins - genetics ; DNA-Binding Proteins - metabolism ; Epistasis, Genetic - drug effects ; Epistasis, Genetic - physiology ; Galactose - pharmacology ; Gene expression ; Gene Expression Regulation, Fungal - drug effects ; Genetic Loci - physiology ; Genomes ; Genomics ; Glucose ; Glucose - pharmacology ; Glycerol ; Laboratories ; Loci ; Metabolism ; Mitochondria ; Mitochondrial DNA ; Noise ; Nuclear interactions ; Organelles ; Organelles - drug effects ; Organelles - genetics ; Organelles - metabolism ; Organelles - physiology ; Reverse transcription ; Ribonucleic acid ; RNA ; RNA, Fungal - drug effects ; RNA, Fungal - genetics ; RNA, Fungal - metabolism ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; RNA-directed DNA polymerase ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae - genetics ; Saccharomyces cerevisiae - metabolism ; Saccharomyces cerevisiae - physiology ; Saccharomyces cerevisiae - ultrastructure ; Science education ; Synthetic biology ; Time Factors ; Transcription (Genetics) ; Transcription, Genetic - drug effects ; Trends ; Yeast</subject><ispartof>PloS one, 2012-01, Vol.7 (1), p.e30943</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>2012 Rodley et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://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. 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Loci on the mitochondrial genome were recently reported to interact with nuclear loci. To determine whether this is part of a DNA based communication system we used genome conformation capture to map the global network of DNA-DNA interactions between the mitochondrial and nuclear genomes (Mito-nDNA) in Saccharomyces cerevisiae cells grown under three different metabolic conditions. The interactions that form between mitochondrial and nuclear loci are dependent on the metabolic state of the yeast. Moreover, the frequency of specific mitochondrial-nuclear interactions (i.e. COX1-MSY1 and Q0182-RSM7) showed significant reductions in the absence of mitochondrial encoded reverse transcriptase machinery. Furthermore, these reductions correlated with increases in the transcript levels of the nuclear loci (MSY1 and RSM7). We propose that these interactions represent an inter-organelle DNA mediated communication system and that reverse transcription of mitochondrial RNA plays a role in this process.</description><subject>Arabidopsis</subject><subject>Arabidopsis thaliana</subject><subject>Baking yeast</subject><subject>Biological Transport - drug effects</subject><subject>Biological Transport - genetics</subject><subject>Biological Transport - physiology</subject><subject>Biology</subject><subject>Carbon</subject><subject>Cell Nucleus - drug effects</subject><subject>Cell Nucleus - genetics</subject><subject>Chromosomes</subject><subject>Chromosomes, Fungal - drug effects</subject><subject>Chromosomes, Fungal - genetics</subject><subject>Chromosomes, Fungal - metabolism</subject><subject>Communications systems</subject><subject>Conformation</subject><subject>Cyclooxygenase 1 - genetics</subject><subject>Cyclooxygenase 1 - metabolism</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA polymerases</subject><subject>DNA, Mitochondrial - drug effects</subject><subject>DNA, Mitochondrial - genetics</subject><subject>DNA-Binding Proteins - genetics</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Epistasis, Genetic - drug effects</subject><subject>Epistasis, Genetic - physiology</subject><subject>Galactose - pharmacology</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Fungal - drug effects</subject><subject>Genetic Loci - physiology</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Glucose</subject><subject>Glucose - pharmacology</subject><subject>Glycerol</subject><subject>Laboratories</subject><subject>Loci</subject><subject>Metabolism</subject><subject>Mitochondria</subject><subject>Mitochondrial DNA</subject><subject>Noise</subject><subject>Nuclear interactions</subject><subject>Organelles</subject><subject>Organelles - drug effects</subject><subject>Organelles - genetics</subject><subject>Organelles - metabolism</subject><subject>Organelles - physiology</subject><subject>Reverse transcription</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA, Fungal - drug effects</subject><subject>RNA, Fungal - genetics</subject><subject>RNA, Fungal - metabolism</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>RNA-directed DNA polymerase</subject><subject>Saccharomyces cerevisiae</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Saccharomyces cerevisiae - metabolism</subject><subject>Saccharomyces cerevisiae - physiology</subject><subject>Saccharomyces cerevisiae - ultrastructure</subject><subject>Science education</subject><subject>Synthetic biology</subject><subject>Time Factors</subject><subject>Transcription (Genetics)</subject><subject>Transcription, Genetic - drug effects</subject><subject>Trends</subject><subject>Yeast</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNqNk12L1DAUhoso7rr6D0QLguBFx3w1bW-EYf0aWF3w6zZkktOZDGkzJuni_g9_sOlMZ5kBBelFy8nzvsl5m5NlTzGaYVrh1xs3-F7a2db1MEOIoobRe9k5bigpOEH0_tH3WfYohA1CJa05f5idEUIagmp0nv3-ZKJTa9drb6Qt-kFZkD5_-3memz6Clyoa14dcuT56sxwi5NHlcQ25h9Vg5biauzY_CKOXfVDebGNu4QZsyGXIt9LHERplO9fC-ZXswVpIxl039EbtncJtiNA9zh600gZ4Mr0vsu_v3327_FhcXX9YXM6vCsUbHAvCW8RrrbjUdaVxW3KukW6YBM50swTMJCEUNLSqZqjBuIWaqabmFVKaEUovsud73611QUyBBoEpoQxThMtELPaEdnIjtt500t8KJ43YFVIbIvVmUu9C0oZWS4xrvpSMqrIhrJRYU6VpqtQ6eb2ZdhuWHWgFKVFpT0xPV3qzFit3IyjhjJc8GbyYDLz7OUCI_zjyRK1kOpXpW5fMVGeCEnNWVajErKwSNfsLlR4NnUk_G1qT6ieCVyeC8ULAr7iSQwhi8fXL_7PXP07Zl0fsGqSN6-DssLt2pyDbg8q7EDy0d8lhJMaJOKQhxokQ00Qk2bPj1O9EhxGgfwCBFAnd</recordid><startdate>20120123</startdate><enddate>20120123</enddate><creator>Rodley, Chris D M</creator><creator>Grand, Ralph S</creator><creator>Gehlen, Lutz R</creator><creator>Greyling, Gary</creator><creator>Jones, M Beatrix</creator><creator>O'Sullivan, Justin M</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>20120123</creationdate><title>Mitochondrial-nuclear DNA interactions contribute to the regulation of nuclear transcript levels as part of the inter-organelle communication system</title><author>Rodley, Chris D M ; Grand, Ralph S ; Gehlen, Lutz R ; Greyling, Gary ; Jones, M Beatrix ; O'Sullivan, Justin M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c691t-26f068dc6ad87d1f566d0d94ae64d9be14a223edefc840911fe84c98670cd4233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Arabidopsis</topic><topic>Arabidopsis thaliana</topic><topic>Baking yeast</topic><topic>Biological Transport - drug effects</topic><topic>Biological Transport - genetics</topic><topic>Biological Transport - physiology</topic><topic>Biology</topic><topic>Carbon</topic><topic>Cell Nucleus - drug effects</topic><topic>Cell Nucleus - genetics</topic><topic>Chromosomes</topic><topic>Chromosomes, Fungal - drug effects</topic><topic>Chromosomes, Fungal - genetics</topic><topic>Chromosomes, Fungal - metabolism</topic><topic>Communications systems</topic><topic>Conformation</topic><topic>Cyclooxygenase 1 - genetics</topic><topic>Cyclooxygenase 1 - metabolism</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA polymerases</topic><topic>DNA, Mitochondrial - drug effects</topic><topic>DNA, Mitochondrial - genetics</topic><topic>DNA-Binding Proteins - genetics</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Epistasis, Genetic - drug effects</topic><topic>Epistasis, Genetic - physiology</topic><topic>Galactose - pharmacology</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Fungal - drug effects</topic><topic>Genetic Loci - physiology</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Glucose</topic><topic>Glucose - pharmacology</topic><topic>Glycerol</topic><topic>Laboratories</topic><topic>Loci</topic><topic>Metabolism</topic><topic>Mitochondria</topic><topic>Mitochondrial DNA</topic><topic>Noise</topic><topic>Nuclear interactions</topic><topic>Organelles</topic><topic>Organelles - drug effects</topic><topic>Organelles - genetics</topic><topic>Organelles - metabolism</topic><topic>Organelles - physiology</topic><topic>Reverse transcription</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>RNA, Fungal - drug effects</topic><topic>RNA, Fungal - genetics</topic><topic>RNA, Fungal - metabolism</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>RNA-directed DNA polymerase</topic><topic>Saccharomyces cerevisiae</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Saccharomyces cerevisiae - metabolism</topic><topic>Saccharomyces cerevisiae - 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Loci on the mitochondrial genome were recently reported to interact with nuclear loci. To determine whether this is part of a DNA based communication system we used genome conformation capture to map the global network of DNA-DNA interactions between the mitochondrial and nuclear genomes (Mito-nDNA) in Saccharomyces cerevisiae cells grown under three different metabolic conditions. The interactions that form between mitochondrial and nuclear loci are dependent on the metabolic state of the yeast. Moreover, the frequency of specific mitochondrial-nuclear interactions (i.e. COX1-MSY1 and Q0182-RSM7) showed significant reductions in the absence of mitochondrial encoded reverse transcriptase machinery. Furthermore, these reductions correlated with increases in the transcript levels of the nuclear loci (MSY1 and RSM7). We propose that these interactions represent an inter-organelle DNA mediated communication system and that reverse transcription of mitochondrial RNA plays a role in this process.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22292080</pmid><doi>10.1371/journal.pone.0030943</doi><tpages>e30943</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Arabidopsis Arabidopsis thaliana Baking yeast Biological Transport - drug effects Biological Transport - genetics Biological Transport - physiology Biology Carbon Cell Nucleus - drug effects Cell Nucleus - genetics Chromosomes Chromosomes, Fungal - drug effects Chromosomes, Fungal - genetics Chromosomes, Fungal - metabolism Communications systems Conformation Cyclooxygenase 1 - genetics Cyclooxygenase 1 - metabolism Deoxyribonucleic acid DNA DNA polymerases DNA, Mitochondrial - drug effects DNA, Mitochondrial - genetics DNA-Binding Proteins - genetics DNA-Binding Proteins - metabolism Epistasis, Genetic - drug effects Epistasis, Genetic - physiology Galactose - pharmacology Gene expression Gene Expression Regulation, Fungal - drug effects Genetic Loci - physiology Genomes Genomics Glucose Glucose - pharmacology Glycerol Laboratories Loci Metabolism Mitochondria Mitochondrial DNA Noise Nuclear interactions Organelles Organelles - drug effects Organelles - genetics Organelles - metabolism Organelles - physiology Reverse transcription Ribonucleic acid RNA RNA, Fungal - drug effects RNA, Fungal - genetics RNA, Fungal - metabolism RNA, Messenger - genetics RNA, Messenger - metabolism RNA-directed DNA polymerase Saccharomyces cerevisiae Saccharomyces cerevisiae - genetics Saccharomyces cerevisiae - metabolism Saccharomyces cerevisiae - physiology Saccharomyces cerevisiae - ultrastructure Science education Synthetic biology Time Factors Transcription (Genetics) Transcription, Genetic - drug effects Trends Yeast |
title | Mitochondrial-nuclear DNA interactions contribute to the regulation of nuclear transcript levels as part of the inter-organelle communication system |
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