Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression - PubMed (original) (raw)
. 2010 Sep 21;5(9):e12862.
doi: 10.1371/journal.pone.0012862.
James A Lautenberger, Leslie Wei Chinn, Michael Malasky, Efe Sezgin, Lawrence A Kingsley, James J Goedert, Gregory D Kirk, Edward D Gomperts, Susan P Buchbinder, Jennifer L Troyer, Stephen J O'Brien
Affiliations
- PMID: 20877624
- PMCID: PMC2943476
- DOI: 10.1371/journal.pone.0012862
Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression
Sher L Hendrickson et al. PLoS One. 2010.
Abstract
Background: 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.
Methodology/principal findings: 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.
Conclusions: 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.
Conflict of interest statement
Competing Interests: The authors have declared that no competing interests exist.
Figures
Figure 1. Association of SNPs within the PECI gene region of chromosome 6 with AIDS 1987.
A Manhattan plot (a.) and corresponding QQ plot (b.) for 10012 SNPs in NEMP genes showing the additive model that implicates SNPs in the PECI gene region exceeding the GT significance threshold (horizontal line, 9.2×10−6). A gene view of PECI showing SNPs tested and corresponding linkage disequilibrium as inferred by D' between SNPs (c.) and a bar-plot of genotypes of PECI versus the AIDS-1987 diagnosis in years past seroconversion (d.) are shown.
Figure 2. Association of SNPs within the ACSM4 gene region of chromosome 12 with AIDS 1987.
Shown as a a) Manhattan plot for time to AIDS-1987 (genetic model-recessive, GT significance threshold is shown as a horizontal line at 9.2×10−6), b) QQ plot, c) gene view of ACSM4 showing SNPs tested and corresponding linkage disequilibrium as inferred by D' between SNPs, and d) Kaplan-Meier plot of time to AIDS-1987 showing the three ACSM4 genotypes and the p-value for the recessive model.
Figure 3. The effect of rs629362 (a) and rs626080 (b) in PECI on progression to AIDS-defining illness (ADI) Kaposi Sarcoma (KS).
Similar articles
- Mitochondrial DNA haplogroups influence AIDS progression.
Hendrickson SL, Hutcheson HB, Ruiz-Pesini E, Poole JC, Lautenberger J, Sezgin E, Kingsley L, Goedert JJ, Vlahov D, Donfield S, Wallace DC, O'Brien SJ. Hendrickson SL, et al. AIDS. 2008 Nov 30;22(18):2429-39. doi: 10.1097/QAD.0b013e32831940bb. AIDS. 2008. PMID: 19005266 Free PMC article. - Mitochondrial haplogroups are associated with clinical pattern of AIDS progression in HIV-infected patients.
Guzmán-Fulgencio M, Jiménez JL, García-Álvarez M, Bellón JM, Fernández-Rodriguez A, Campos Y, Rodríguez C, González-Garcia J, Riera M, Viciana P, Muñoz-Fernández MÁ, Resino S. Guzmán-Fulgencio M, et al. J Acquir Immune Defic Syndr. 2013 Jun 1;63(2):178-83. doi: 10.1097/QAI.0b013e3182893f74. J Acquir Immune Defic Syndr. 2013. PMID: 23666137 - Modulating influence on HIV/AIDS by interacting RANTES gene variants.
An P, Nelson GW, Wang L, Donfield S, Goedert JJ, Phair J, Vlahov D, Buchbinder S, Farrar WL, Modi W, O'Brien SJ, Winkler CA. An P, et al. Proc Natl Acad Sci U S A. 2002 Jul 23;99(15):10002-7. doi: 10.1073/pnas.142313799. Epub 2002 Jul 11. Proc Natl Acad Sci U S A. 2002. PMID: 12114533 Free PMC article. - Mitochondrial determinants of cancer health disparities.
Choudhury AR, Singh KK. Choudhury AR, et al. Semin Cancer Biol. 2017 Dec;47:125-146. doi: 10.1016/j.semcancer.2017.05.001. Epub 2017 May 6. Semin Cancer Biol. 2017. PMID: 28487205 Free PMC article. Review. - The Impact of HIV- and ART-Induced Mitochondrial Dysfunction in Cellular Senescence and Aging.
Schank M, Zhao J, Moorman JP, Yao ZQ. Schank M, et al. Cells. 2021 Jan 16;10(1):174. doi: 10.3390/cells10010174. Cells. 2021. PMID: 33467074 Free PMC article. Review.
Cited by
- Ornithine Aminotransferase, an Important Glutamate-Metabolizing Enzyme at the Crossroads of Multiple Metabolic Pathways.
Ginguay A, Cynober L, Curis E, Nicolis I. Ginguay A, et al. Biology (Basel). 2017 Mar 7;6(1):18. doi: 10.3390/biology6010018. Biology (Basel). 2017. PMID: 28272331 Free PMC article. Review. - Maternal and fetal mitochondrial gene dysregulation in hypertensive disorders of pregnancy.
Ricci CA, Reid DM, Sun J, Santillan DA, Santillan MK, Phillips NR, Goulopoulou S. Ricci CA, et al. Physiol Genomics. 2023 Jul 1;55(7):275-285. doi: 10.1152/physiolgenomics.00005.2023. Epub 2023 May 15. Physiol Genomics. 2023. PMID: 37184228 Free PMC article. - Host genomic influences on HIV/AIDS.
O'Brien SJ, Hendrickson SL. O'Brien SJ, et al. Genome Biol. 2013 Jan 31;14(1):201. doi: 10.1186/gb-2013-14-1-201. Genome Biol. 2013. PMID: 23369251 Free PMC article. Review. - HIV-1 infection is blocked at an early stage in cells devoid of mitochondrial DNA.
Lu G, Matsuura SE, Barrientos A, Scott WA. Lu G, et al. PLoS One. 2013 Oct 21;8(10):e78035. doi: 10.1371/journal.pone.0078035. eCollection 2013. PLoS One. 2013. PMID: 24205077 Free PMC article. - Genome-wide and candidate gene association studies of placental abruption.
Workalemahu T, Enquobahrie DA, Moore A, Sanchez SE, Ananth CV, Pacora PN, Liang L, Salazar M, Williams MA. Workalemahu T, et al. Int J Mol Epidemiol Genet. 2013 Sep 12;4(3):128-39. eCollection 2013. Int J Mol Epidemiol Genet. 2013. PMID: 24046805 Free PMC article.
References
- Wen W, Chen S, Cao Y, Zhu Y, Yamamoto Y. HIV-1 infection initiates changes in the expression of a wide array of genes in U937 promonocytes and HUT78 T cells. Virus Res. 2005;113:26–35. - PubMed
Publication types
MeSH terms
Grants and funding
- R01-DA-12568/DA/NIDA NIH HHS/United States
- 5-M01-RR-00722/RR/NCRR NIH HHS/United States
- U01-AI-37613/AI/NIAID NIH HHS/United States
- R01 DA004334/DA/NIDA NIH HHS/United States
- U1-AI-35041/AI/NIAID NIH HHS/United States
- M01 RR000722/RR/NCRR NIH HHS/United States
- U01 AI035041/AI/NIAID NIH HHS/United States
- HHSN261200800001C/CA/NCI NIH HHS/United States
- N02CP55504/CP/NCI NIH HHS/United States
- R01 HD041224/HD/NICHD NIH HHS/United States
- U01-AI-35040/AI/NIAID NIH HHS/United States
- M01 RR000425/RR/NCRR NIH HHS/United States
- U01-AI-37984/AI/NIAID NIH HHS/United States
- U01 AI035043/AI/NIAID NIH HHS/United States
- U01 AI035040/AI/NIAID NIH HHS/United States
- N01CO12400/CA/NCI NIH HHS/United States
- U01 AI035039/AI/NIAID NIH HHS/United States
- 1 R01 HD41224/HD/NICHD NIH HHS/United States
- R01-DA-04334/DA/NIDA NIH HHS/United States
- U01 AI035042/AI/NIAID NIH HHS/United States
- M01 RR00425/RR/NCRR NIH HHS/United States
- U01 AI037984/AI/NIAID NIH HHS/United States
- U01-AI-35043/AI/NIAID NIH HHS/United States
- U01-AI-35042/AI/NIAID NIH HHS/United States
- R56 DA004334/DA/NIDA NIH HHS/United States
- U01 AI037613/AI/NIAID NIH HHS/United States
- U01-AI-35041/AI/NIAID NIH HHS/United States
- R01 DA012568/DA/NIDA NIH HHS/United States
- U01-AI-35039/AI/NIAID NIH HHS/United States
- N01-CO-12400/CO/NCI NIH HHS/United States
- HHSN261200800001E/CA/NCI NIH HHS/United States
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases