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Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression
The human mitochondrial genome includes only 13 coding genes while nuclear-encoded genes account for 99% of proteins responsible for mitochondrial morphology, redox regulation, and energetics. Mitochondrial pathogenesis occurs in HIV patients and genetically, mitochondrial DNA haplogroups with presu...
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Published in: | PloS one 2010-09, Vol.5 (9), p.e12862 |
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creator | Hendrickson, Sher L Lautenberger, James A Chinn, Leslie Wei Malasky, Michael Sezgin, Efe Kingsley, Lawrence A Goedert, James J Kirk, Gregory D Gomperts, Edward D Buchbinder, Susan P Troyer, Jennifer L O'Brien, Stephen J |
description | The human mitochondrial genome includes only 13 coding genes while nuclear-encoded genes account for 99% of proteins responsible for mitochondrial morphology, redox regulation, and energetics. Mitochondrial pathogenesis occurs in HIV patients and genetically, mitochondrial DNA haplogroups with presumed functional differences have been associated with differential AIDS progression.
Here we explore whether single nucleotide polymorphisms (SNPs) within 904 of the estimated 1,500 genes that specify nuclear-encoded mitochondrial proteins (NEMPs) influence AIDS progression among HIV-1 infected patients. We examined NEMPs for association with the rate of AIDS progression using genotypes generated by an Affymetrix 6.0 genotyping array of 1,455 European American patients from five US AIDS cohorts. Successfully genotyped SNPs gave 50% or better haplotype coverage for 679 of known NEMP genes. With a Bonferroni adjustment for the number of genes and tests examined, multiple SNPs within two NEMP genes showed significant association with AIDS progression: acyl-CoA synthetase medium-chain family member 4 (ACSM4) on chromosome 12 and peroxisomal D3,D2-enoyl-CoA isomerase (PECI) on chromosome 6.
Our previous studies on mitochondrial DNA showed that European haplogroups with presumed functional differences were associated with AIDS progression and HAART mediated adverse events. The modest influences of nuclear-encoded mitochondrial genes found in the current study add support to the idea that mitochondrial function plays a role in AIDS pathogenesis. |
doi_str_mv | 10.1371/journal.pone.0012862 |
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Here we explore whether single nucleotide polymorphisms (SNPs) within 904 of the estimated 1,500 genes that specify nuclear-encoded mitochondrial proteins (NEMPs) influence AIDS progression among HIV-1 infected patients. We examined NEMPs for association with the rate of AIDS progression using genotypes generated by an Affymetrix 6.0 genotyping array of 1,455 European American patients from five US AIDS cohorts. Successfully genotyped SNPs gave 50% or better haplotype coverage for 679 of known NEMP genes. With a Bonferroni adjustment for the number of genes and tests examined, multiple SNPs within two NEMP genes showed significant association with AIDS progression: acyl-CoA synthetase medium-chain family member 4 (ACSM4) on chromosome 12 and peroxisomal D3,D2-enoyl-CoA isomerase (PECI) on chromosome 6.
Our previous studies on mitochondrial DNA showed that European haplogroups with presumed functional differences were associated with AIDS progression and HAART mediated adverse events. The modest influences of nuclear-encoded mitochondrial genes found in the current study add support to the idea that mitochondrial function plays a role in AIDS pathogenesis.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0012862</identifier><identifier>PMID: 20877624</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acquired immune deficiency syndrome ; Acquired Immunodeficiency Syndrome - genetics ; Acquired Immunodeficiency Syndrome - metabolism ; Acquired Immunodeficiency Syndrome - pathology ; AIDS ; AIDS (Disease) ; Antigens ; Apoptosis ; Biosynthesis ; Breast cancer ; Cell Nucleus - genetics ; Cell Nucleus - metabolism ; Chromosome 12 ; Chromosome 6 ; Cloning ; Cohort Studies ; Deoxyribonucleic acid ; Development and progression ; Disease Progression ; DNA ; Epidemiology ; Fatty acids ; Female ; Gene expression ; Genes ; Genetic aspects ; Genetic diversity ; Genetic variance ; Genetic Variation ; Genetics and Genomics/Genetics of Disease ; Genetics and Genomics/Genome Projects ; Genomes ; Genomics ; Genotype ; Genotypes ; Genotyping ; Haplotypes ; Hemophilia ; Highly active antiretroviral therapy ; HIV ; HIV patients ; Human immunodeficiency virus ; Humans ; Infections ; Infectious Diseases/HIV Infection and AIDS ; Laboratories ; Liver cancer ; Male ; Mitochondria - genetics ; Mitochondria - metabolism ; Mitochondrial DNA ; Multiculturalism & pluralism ; Pathogenesis ; Patients ; Polymorphism, Single Nucleotide ; Principal components analysis ; Protein Transport ; Proteins ; Public health ; Quantitative analysis ; Single nucleotide polymorphisms ; Single-nucleotide polymorphism ; Studies ; White People - genetics</subject><ispartof>PloS one, 2010-09, Vol.5 (9), p.e12862</ispartof><rights>COPYRIGHT 2010 Public Library of Science</rights><rights>2010. This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c691t-e7c6b5d0b1dc66bfe338353c1914e8becca404c3dbb9e1bd0d7ac5e330fa98ba3</citedby><cites>FETCH-LOGICAL-c691t-e7c6b5d0b1dc66bfe338353c1914e8becca404c3dbb9e1bd0d7ac5e330fa98ba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1292468267/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1292468267?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20877624$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Badger, Jonathan H.</contributor><creatorcontrib>Hendrickson, Sher L</creatorcontrib><creatorcontrib>Lautenberger, James A</creatorcontrib><creatorcontrib>Chinn, Leslie Wei</creatorcontrib><creatorcontrib>Malasky, Michael</creatorcontrib><creatorcontrib>Sezgin, Efe</creatorcontrib><creatorcontrib>Kingsley, Lawrence A</creatorcontrib><creatorcontrib>Goedert, James J</creatorcontrib><creatorcontrib>Kirk, Gregory D</creatorcontrib><creatorcontrib>Gomperts, Edward D</creatorcontrib><creatorcontrib>Buchbinder, Susan P</creatorcontrib><creatorcontrib>Troyer, Jennifer L</creatorcontrib><creatorcontrib>O'Brien, Stephen J</creatorcontrib><title>Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The human mitochondrial genome includes only 13 coding genes while nuclear-encoded genes account for 99% of proteins responsible for mitochondrial morphology, redox regulation, and energetics. Mitochondrial pathogenesis occurs in HIV patients and genetically, mitochondrial DNA haplogroups with presumed functional differences have been associated with differential AIDS progression.
Here we explore whether single nucleotide polymorphisms (SNPs) within 904 of the estimated 1,500 genes that specify nuclear-encoded mitochondrial proteins (NEMPs) influence AIDS progression among HIV-1 infected patients. We examined NEMPs for association with the rate of AIDS progression using genotypes generated by an Affymetrix 6.0 genotyping array of 1,455 European American patients from five US AIDS cohorts. Successfully genotyped SNPs gave 50% or better haplotype coverage for 679 of known NEMP genes. With a Bonferroni adjustment for the number of genes and tests examined, multiple SNPs within two NEMP genes showed significant association with AIDS progression: acyl-CoA synthetase medium-chain family member 4 (ACSM4) on chromosome 12 and peroxisomal D3,D2-enoyl-CoA isomerase (PECI) on chromosome 6.
Our previous studies on mitochondrial DNA showed that European haplogroups with presumed functional differences were associated with AIDS progression and HAART mediated adverse events. The modest influences of nuclear-encoded mitochondrial genes found in the current study add support to the idea that mitochondrial function plays a role in AIDS pathogenesis.</description><subject>Acquired immune deficiency syndrome</subject><subject>Acquired Immunodeficiency Syndrome - genetics</subject><subject>Acquired Immunodeficiency Syndrome - metabolism</subject><subject>Acquired Immunodeficiency Syndrome - pathology</subject><subject>AIDS</subject><subject>AIDS (Disease)</subject><subject>Antigens</subject><subject>Apoptosis</subject><subject>Biosynthesis</subject><subject>Breast cancer</subject><subject>Cell Nucleus - genetics</subject><subject>Cell Nucleus - metabolism</subject><subject>Chromosome 12</subject><subject>Chromosome 6</subject><subject>Cloning</subject><subject>Cohort Studies</subject><subject>Deoxyribonucleic acid</subject><subject>Development and progression</subject><subject>Disease Progression</subject><subject>DNA</subject><subject>Epidemiology</subject><subject>Fatty acids</subject><subject>Female</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genetic diversity</subject><subject>Genetic variance</subject><subject>Genetic Variation</subject><subject>Genetics and Genomics/Genetics of Disease</subject><subject>Genetics and Genomics/Genome Projects</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Genotype</subject><subject>Genotypes</subject><subject>Genotyping</subject><subject>Haplotypes</subject><subject>Hemophilia</subject><subject>Highly active antiretroviral therapy</subject><subject>HIV</subject><subject>HIV patients</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Infections</subject><subject>Infectious Diseases/HIV Infection and AIDS</subject><subject>Laboratories</subject><subject>Liver cancer</subject><subject>Male</subject><subject>Mitochondria - genetics</subject><subject>Mitochondria - metabolism</subject><subject>Mitochondrial DNA</subject><subject>Multiculturalism & pluralism</subject><subject>Pathogenesis</subject><subject>Patients</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Principal components analysis</subject><subject>Protein Transport</subject><subject>Proteins</subject><subject>Public health</subject><subject>Quantitative analysis</subject><subject>Single nucleotide polymorphisms</subject><subject>Single-nucleotide polymorphism</subject><subject>Studies</subject><subject>White People - genetics</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNkl-L1DAUxYso7rr6DUQLguJDx_xr2rwIw6rrwMLCrvoa0uS20yGTjEm76Lc343SXqeyD5CEh-Z2Tm5uTZS8xWmBa4Q8bPwan7GLnHSwQwqTm5FF2igUlBSeIPj5an2TPYtwgVNKa86fZCUF1VXHCTrPrC3Aw9Dq_VaFXboh573I3agsqFOC0N2DybT94vfbOJMTmXVLssdaOCYB8ufp0k--C7wLE2Hv3PHvSKhvhxTSfZd-_fP52_rW4vLpYnS8vC80FHgqoNG9KgxpsNOdNC5TWtKQaC8ygbkBrxRDT1DSNANwYZCqly0ShVom6UfQse33w3Vkf5dSOKDERhPGa8CoRqwNhvNrIXei3KvyWXvXy74YPnVQhPd6CTAUYUzOjhBKsQUhookrKFCEV54y3yevjdNvYbMFocENQdmY6P3H9Wnb-VhLBKKt4Mng3GQT_c4Q4yG0fNVirHPgxyqosBRekLBP55h_y4cdNVKdS_ek7fLpW7z3lklW0LkWqPVGLB6g0DGx7naLT9ml_Jng_EyRmgF9Dp8YY5erm-v_Zqx9z9u0RuwZlh3X0dhxSYuIcZAdQBx9jgPa-xxjJffLvuiH3yZdT8pPs1fH_3Ivuok7_AAwx_18</recordid><startdate>20100921</startdate><enddate>20100921</enddate><creator>Hendrickson, Sher L</creator><creator>Lautenberger, James A</creator><creator>Chinn, Leslie Wei</creator><creator>Malasky, Michael</creator><creator>Sezgin, Efe</creator><creator>Kingsley, Lawrence A</creator><creator>Goedert, James J</creator><creator>Kirk, Gregory D</creator><creator>Gomperts, Edward D</creator><creator>Buchbinder, Susan P</creator><creator>Troyer, Jennifer L</creator><creator>O'Brien, Stephen J</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>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>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20100921</creationdate><title>Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression</title><author>Hendrickson, Sher L ; Lautenberger, James A ; Chinn, Leslie Wei ; Malasky, Michael ; Sezgin, Efe ; Kingsley, Lawrence A ; Goedert, James J ; Kirk, Gregory D ; Gomperts, Edward D ; Buchbinder, Susan P ; Troyer, Jennifer L ; O'Brien, Stephen J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c691t-e7c6b5d0b1dc66bfe338353c1914e8becca404c3dbb9e1bd0d7ac5e330fa98ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Acquired immune deficiency syndrome</topic><topic>Acquired Immunodeficiency Syndrome - 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Mitochondrial pathogenesis occurs in HIV patients and genetically, mitochondrial DNA haplogroups with presumed functional differences have been associated with differential AIDS progression.
Here we explore whether single nucleotide polymorphisms (SNPs) within 904 of the estimated 1,500 genes that specify nuclear-encoded mitochondrial proteins (NEMPs) influence AIDS progression among HIV-1 infected patients. We examined NEMPs for association with the rate of AIDS progression using genotypes generated by an Affymetrix 6.0 genotyping array of 1,455 European American patients from five US AIDS cohorts. Successfully genotyped SNPs gave 50% or better haplotype coverage for 679 of known NEMP genes. With a Bonferroni adjustment for the number of genes and tests examined, multiple SNPs within two NEMP genes showed significant association with AIDS progression: acyl-CoA synthetase medium-chain family member 4 (ACSM4) on chromosome 12 and peroxisomal D3,D2-enoyl-CoA isomerase (PECI) on chromosome 6.
Our previous studies on mitochondrial DNA showed that European haplogroups with presumed functional differences were associated with AIDS progression and HAART mediated adverse events. The modest influences of nuclear-encoded mitochondrial genes found in the current study add support to the idea that mitochondrial function plays a role in AIDS pathogenesis.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>20877624</pmid><doi>10.1371/journal.pone.0012862</doi><tpages>e12862</tpages><oa>free_for_read</oa></addata></record> |
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language | eng |
recordid | cdi_plos_journals_1292468267 |
source | Open Access: PubMed Central; Publicly Available Content Database (Proquest) (PQ_SDU_P3) |
subjects | Acquired immune deficiency syndrome Acquired Immunodeficiency Syndrome - genetics Acquired Immunodeficiency Syndrome - metabolism Acquired Immunodeficiency Syndrome - pathology AIDS AIDS (Disease) Antigens Apoptosis Biosynthesis Breast cancer Cell Nucleus - genetics Cell Nucleus - metabolism Chromosome 12 Chromosome 6 Cloning Cohort Studies Deoxyribonucleic acid Development and progression Disease Progression DNA Epidemiology Fatty acids Female Gene expression Genes Genetic aspects Genetic diversity Genetic variance Genetic Variation Genetics and Genomics/Genetics of Disease Genetics and Genomics/Genome Projects Genomes Genomics Genotype Genotypes Genotyping Haplotypes Hemophilia Highly active antiretroviral therapy HIV HIV patients Human immunodeficiency virus Humans Infections Infectious Diseases/HIV Infection and AIDS Laboratories Liver cancer Male Mitochondria - genetics Mitochondria - metabolism Mitochondrial DNA Multiculturalism & pluralism Pathogenesis Patients Polymorphism, Single Nucleotide Principal components analysis Protein Transport Proteins Public health Quantitative analysis Single nucleotide polymorphisms Single-nucleotide polymorphism Studies White People - genetics |
title | Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression |
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