Sequence-Based Polymorphisms in the Mitochondrial D-Loop and Potential SNP Predictors for Chronic Dialysis

Background The mitochondrial (mt) displacement loop (D-loop) is known to accumulate structural alterations and mutations. The aim of this study was to investigate the prevalence of single nucleotide polymorphisms (SNPs) within the D-loop among chronic dialysis patients and healthy controls. Methodology and Principal Findings We enrolled 193 chronic dialysis patients and 704 healthy controls. SNPs were identified by large scale D-loop sequencing and bioinformatic analysis. Chronic dialysis patients had lower body mass index, blood thiols, and cholesterol levels than controls. A total of 77 SNPs matched with the positions in reference of the Revised Cambridge Reference Sequence (CRS) were found in the study population. Chronic dialysis patients had a significantly higher incidence of 9 SNPs compared to controls. These include SNP5 (16108Y), SNP17 (16172Y), SNP21 (16223Y), SNP34 (16274R), SNP35 (16278Y), SNP55 (16463R), SNP56 (16519Y), SNP64 (185R), and SNP65 (189R) in D-loop of CRS. Among these SNPs with genotypes, SNP55-G, SNP56-C, and SNP64-A were 4.78, 1.47, and 5.15 times more frequent in dialysis patients compared to controls (P<0.05), respectively. When adjusting the covariates of demographics and comorbidities, SNP64-A was 5.13 times more frequent in dialysis patients compared to controls (P<0.01). Furthermore, SNP64-A was found to be 35.80, 3.48, 4.69, 5,55, and 4.67 times higher in female patients and in patients without diabetes, coronary artery disease, smoking, and hypertension in an independent significance manner (P<0.05), respectively. In patients older than 50 years or with hypertension, SNP34-A and SNP17-C were found to be 7.97 and 3.71 times more frequent (P<0.05) compared to patients younger than 50 years or those without hypertension, respectively. Conclusions and Significance The results of large-scale sequencing suggest that specific SNPs in the mtDNA D-loop are significantly associated with chronic dialysis. These SNPs can be considered as potential predictors for chronic dialysis.

[1]  K. Yagi,et al.  Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. , 1979, Analytical biochemistry.

[2]  N. Bresolin,et al.  Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication. , 1999, Science.

[3]  D. Turnbull,et al.  Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA , 1999, Nature Genetics.

[4]  D. Clayton Transcription and replication of mitochondrial DNA. , 2000, Human reproduction.

[5]  D. Sidransky,et al.  High frequency of mitochondrial DNA mutations in breast cancer: potential application for cancer detection , 2001 .

[6]  K. Yarasheski,et al.  Muscle-specific mutations accumulate with aging in critical human mtDNA control sites for replication , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[7]  J. T. Wachsman,et al.  Mitochondrial DNA in human malignancy. , 2001, Mutation research.

[8]  E Gabrielson,et al.  Detection of mitochondrial DNA mutations in primary breast cancer and fine-needle aspirates. , 2001, Cancer research.

[9]  Peter Stenvinkel,et al.  The elephant in uremia: oxidant stress as a unifying concept of cardiovascular disease in uremia. , 2002, Kidney international.

[10]  J. Califano,et al.  Mitochondrial C-tract alteration in premalignant lesions of the head and neck: a marker for progression and clonal proliferation. , 2002, Clinical cancer research : an official journal of the American Association for Cancer Research.

[11]  Katsuya Yamashita,et al.  Mitochondrial D-loop mutations as clonal markers in multicentric hepatocellular carcinoma and plasma. , 2002, Clinical cancer research : an official journal of the American Association for Cancer Research.

[12]  C. Franceschi,et al.  The variability of the mitochondrial genome in human aging: a key for life and death? , 2002, The international journal of biochemistry & cell biology.

[13]  A. Nagy,et al.  Mutations of mtDNA in renal cell tumours arising in end‐stage renal disease , 2003, The Journal of pathology.

[14]  S. Toyooka,et al.  Alterations in the mitochondrial displacement loop in lung cancers. , 2003, Clinical cancer research : an official journal of the American Association for Cancer Research.

[15]  K. Yeh,et al.  Novel heteroplasmic frameshift and missense somatic mitochondrial DNA mutations in oral cancer of betel quid chewers , 2003, Genes, chromosomes & cancer.

[16]  D. Wallace,et al.  Control region mtDNA variants: Longevity, climatic adaptation, and a forensic conundrum , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[17]  J. Fish,et al.  Strikingly higher frequency in centenarians and twins of mtDNA mutation causing remodeling of replication origin in leukocytes , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[18]  M. Manjanatha,et al.  Accumulation of point mutations in mitochondrial DNA of aging mice. , 2003, Mutation research.

[19]  C. Chi,et al.  Mitochondrial DNA mutations and mitochondrial DNA depletion in gastric cancer , 2005, Genes, chromosomes & cancer.

[20]  P. Beaune,et al.  Clinical value of mitochondrial mutations in colorectal cancer. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[21]  A. Hung,et al.  An angiotensin converting enzyme haplotype predicts survival in patients with end stage renal disease , 2006, Human Genetics.

[22]  C. Chi,et al.  Mitochondrial DNA mutations and mitochondrial DNA depletion in breast cancer , 2005, Genes, chromosomes & cancer.

[23]  R. Boles,et al.  Individual human hair mitochondrial DNA control region heteroplasmy proportions in mothers and children. , 2006, Mitochondrion.

[24]  Jianbo Wang,et al.  Mitochondrial DNA mutations and 8-hydroxy-2'-deoxyguanosine Content in Japanese patients with urinary bladder and renal cancers. , 2006, Anticancer research.

[25]  Oliver Lenz,et al.  Chronic kidney disease care delivered by US family medicine and internal medicine trainees: results from an online survey , 2006, BMC medicine.

[26]  Pierre Baldi,et al.  An enhanced MITOMAP with a global mtDNA mutational phylogeny , 2006, Nucleic Acids Res..

[27]  Laurent Briollais,et al.  Methodological issues in detecting gene-gene interactions in breast cancer susceptibility: a population-based study in Ontario , 2007, BMC medicine.

[28]  P. Dorman,et al.  Homoplasmy, heteroplasmy, and mitochondrial dystonia , 2007, Neurology.

[29]  T. Zima,et al.  A419C (E111A) Polymorphism of the Glyoxalase I Gene and Vascular Complications in Chronic Hemodialysis Patients , 2008, Annals of the New York Academy of Sciences.

[30]  Shyun-Yeu Liu,et al.  Combinational polymorphisms of four DNA repair genes XRCC1, XRCC2, XRCC3, and XRCC4 and their association with oral cancer in Taiwan. , 2007, Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology.

[31]  Pär Stattin,et al.  Cumulative association of five genetic variants with prostate cancer. , 2008, The New England journal of medicine.

[32]  Li-Yeh Chuang,et al.  SNP combinations in chromosome-wide genes are associated with bone mineral density in Taiwanese women. , 2008, The Chinese journal of physiology.

[33]  Dong-jik Shin,et al.  Mitochondrial DNA Haplogroup Analysis Reveals no Association between the Common Genetic Lineages and Prostate Cancer in the Korean Population , 2008, PloS one.

[34]  C. McIntyre,et al.  Vascular Calcification Is Associated with Impaired Microcirculatory Function in Chronic Haemodialysis Patients , 2008, Nephron Clinical Practice.

[35]  Tsu-Kung Lin,et al.  Correlation of Oxidative Stress Biomarkers and Peritoneal Urea Clearance with Mitochondrial DNA Copy Number in Continuous Ambulatory Peritoneal Dialysis Patients , 2008, American Journal of Nephrology.

[36]  B. Jaber,et al.  Mitochondrial DNA injury and mortality in hemodialysis patients. , 2009, Journal of the American Society of Nephrology : JASN.

[37]  Hyun Hee Lee,et al.  Genetic Polymorphisms of Hypoxia-Inducible Factor-1 Alpha and Cardiovascular Disease in Hemodialysis Patients , 2009, Nephron Clinical Practice.

[38]  Lack of association between mutations of gene-encoding mitochondrial D310 (displacement loop) mononucleotide repeat and oxidative stress in chronic dialysis patients in Taiwan , 2009, Journal of Negative Results in BioMedicine.

[39]  M. Dichgans,et al.  Two Common Mitochondrial DNA Polymorphisms are Highly Associated with Migraine Headache and Cyclic Vomiting Syndrome , 2009, Cephalalgia : an international journal of headache.

[40]  R. Boles,et al.  Are pediatric and adult‐onset cyclic vomiting syndrome (CVS) biologically different conditions? Relationship of adult‐onset CVS with the migraine and pediatric CVS‐associated common mtDNA polymorphisms 16519T and 3010A , 2009, Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society.

[41]  N. Powe,et al.  Association of single-nucleotide polymorphisms in JAK3, STAT4, and STAT6 with new cardiovascular events in incident dialysis patients. , 2009, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[42]  Chih-Jen Huang,et al.  Combinational polymorphisms of seven CXCL12-related genes are protective against breast cancer in Taiwan. , 2009, Omics : a journal of integrative biology.

[43]  H. Klocker,et al.  Mitochondrial Haplogroups and Control Region Polymorphisms Are Not Associated with Prostate Cancer in Middle European Caucasians , 2009, PloS one.

[44]  Wenjun Zhong,et al.  Classification tree for detection of single-nucleotide polymorphism (SNP)-by-SNP interactions related to heart disease: Framingham Heart Study , 2009, BMC proceedings.

[45]  Barbara C. Levin,et al.  Detection of Heteroplasmic Mitochondrial DNA in Single Mitochondria , 2010, PloS one.

[46]  D. Dressman,et al.  Heteroplasmic mitochondrial DNA mutations in normal and tumor cells , 2010, Nature.

[47]  C. Liou,et al.  Association between a common mitochondrial DNA D-loop polycytosine variant and alteration of mitochondrial copy number in human peripheral blood cells , 2010, Journal of Medical Genetics.

[48]  N. Kashihara,et al.  Oxidative stress in diabetic nephropathy. , 2010, Current medicinal chemistry.

[49]  F. Sotgia,et al.  Mitochondrial oxidative stress drives tumor progression and metastasis: should we use antioxidants as a key component of cancer treatment and prevention? , 2011, BMC medicine.

[50]  S. Santos,et al.  Human aging and somatic point mutations in mtDNA: A comparative study of generational differences (grandparents and grandchildren) , 2010, Genetics and molecular biology.

[51]  B. Paulweber,et al.  Mitochondrial Haplogroups, Control Region Polymorphisms and Malignant Melanoma: A Study in Middle European Caucasians , 2011, PloS one.

[52]  Jin-Ching Lin,et al.  Somatic mutations in the D-loop of mitochondrial DNA in oral squamous cell carcinoma , 2012, European Archives of Oto-Rhino-Laryngology.

[53]  A. Botezatu,et al.  Mitochondrial DNA mutations in patients with HRHPV-related cervical lesions. , 2011, Roumanian archives of microbiology and immunology.

[54]  Chien-Te Lee,et al.  Mitochondrial DNA copy number correlates with oxidative stress and predicts mortality in nondiabetic hemodialysis patients. , 2011, Journal of nephrology.

[55]  Hsueh-Wei Chang,et al.  Computational analysis of simulated SNP interactions between 26 growth factor-related genes in a breast cancer association study. , 2011, Omics : a journal of integrative biology.

[56]  P. Reddy,et al.  Aging and amyloid beta-induced oxidative DNA damage and mitochondrial dysfunction in Alzheimer's disease: implications for early intervention and therapeutics. , 2011, Biochimica et biophysica acta.

[57]  Zhanjun Guo,et al.  Sequence polymorphisms of mitochondrial D-loop and hepatocellular carcinoma outcome. , 2011, Biochemical and biophysical research communications.

[58]  B. Paulweber,et al.  The Mitochondrial T16189C Polymorphism Is Associated with Coronary Artery Disease in Middle European Populations , 2011, PloS one.

[59]  Gail P. Clement,et al.  A Twin Study of Mitochondrial DNA Polymorphisms Shows that Heteroplasmy at Multiple Sites Is Associated with mtDNA Variant 16093 but Not with Zygosity , 2011, PloS one.

[60]  M. Karbowski,et al.  Neurodegeneration as a consequence of failed mitochondrial maintenance , 2012, Acta Neuropathologica.

[61]  P. Kimmel,et al.  Genetic association and gene-gene interaction analyses in African American dialysis patients with nondiabetic nephropathy. , 2012, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[62]  Li-Yeh Chuang,et al.  An Improved PSO Algorithm for Generating Protective SNP Barcodes in Breast Cancer , 2012, PloS one.

[63]  Li-Yeh Chuang,et al.  Chaotic particle swarm optimization for detecting SNP–SNP interactions for CXCL12-related genes in breast cancer prevention , 2012, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

[64]  Li-Yeh Chuang,et al.  Single nucleotide polymorphism barcoding to evaluate oral cancer risk using odds ratio‐based genetic algorithms , 2012, The Kaohsiung journal of medical sciences.