Research Articles
Single nucleotide and copy number polymorphisms of the SULT1A1 gene in a South African Tswana population group
Submitted: 07 August 2010 | Published: 21 October 2011
About the author(s)
Hlengiwe P. Mbongwa, Centre for Human Metabonomics, North-West University, South AfricaPetrus J. Pretorius, Centre for Human Metabonomics, North-West University, South Africa
Annemarie Kruger, Africa Unit for Transdisciplinary Health Research, North-West University, South Africa
Gerhard Koekemoer, Statistical Consultation Service, North-West University, South Africa
Carolus J. Reinecke, Centre for Human Metabonomics, North-West University, South Africa
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References
Visser TJ, Kaptein E, Glatt H, Bartsch I, Hagen M, Coughtrie MWH.Characterization of thyroid hormone sulfotransferases. Chem-Biol Interact. 1998;109:279–291. http://dx.doi.org/10.1016/S0009-2797(97)00139-7
Hempel N, Gamage N, Martin JL, McManus ME. Human cytosolic sulfotransferase SULT1A1. Int J Biochem Cell Biol. 2007;39:685–689. http://dx.doi.org/10.1016/j.biocel.2006.10.002
Negishi M, Pedersen LG, Petrotchenko E, et al. Structure and function of sulfotransferases. Arch Biochem Biophys. 2001;390:149–157. http://dx.doi.org/10.1006/abbi.2001.2368, PMid:11396917
Rath VL, Verdugo D, Hemmerich S. Sulfotransferase structural biology and inhibitor discovery. Drug Discov Today. 2004;9:1003–1011. http://dx.doi.org/10.1016/S1359-6446(04)03273-8
Taskinen J, Ethell B, Lautala P, Hood AM, Burchell B, Coughtrie MWH. Conjugation of catechols by recombinant human sulfotransferases, UDP glucuronosyltransferases, and soluble catechol O-methyltransferase: Structure-conjugation relationships and predictive models. Drug Met Dispos. 2003;31:1187–1197. http://dx.doi.org/10.1124/dmd.31.9.1187, PMid:12920175
Coughtrie MWH. Sulfation through the looking glass – recent advances in sulfotransferase research for the curious. Pharmacogenomics. 2002;2:297–308. http://dx.doi.org/10.1038/sj.tpj.6500117, PMid:12439736
Coughtrie WHC, Gilissen RAHJ, Shek B, et al. Phenol sulphotransferase SULT1A1 polymorphism: Molecular diagnosis and allele frequencies in Caucasian and African populations. Biochem J. 1999;337:45–49. http://dx.doi.org/10.1042/0264-6021:3370045, PMid:9854023, PMCid:1219934
Weinshilboum R. Phenol sulfotransferase inheritance. Cell Mol Neurobiol. 1988;8(1):27–34. http://dx.doi.org/10.1007/BF00712908, PMid:3042142
Ozawa S, Shimizu M, Katoh T, et al. Sulfating-activity and stability of cDNA expressed allozymes of human phenol sulfotransferase, ST1A3*1 ((213)Arg) and ST1A3*2 ((213)His), both of which exist in Japanese as well as Caucasians. Biochemistry. 1999;126:271–277.
Sun XF, Ahmadi A, Arbman G, Wallin A, Asklid D, Zhang H. Polymorphisms in sulfotransferase 1A1 and glutathione S-transferase P1 genes in relation tocolorectal cancer risk and patients’ survival. World J Gastroenterol. 2005;11:6875–6879. PMid:16425401
Nowell S, Ratnasinghe DL, Ambrosone CB, et al. Association of SULT1A1 phenotype and genotype with prostate cancer risk in African–Americans and Caucasians. Cancer Epidem Biomar. 2004:13:270–276. http://dx.doi.org/10.1158/1055-9965.EPI-03-0047
Glatt HR. Bioactivation of mutagens via sulfation. FASEB J. 1997;11:314–321. PMid:9141497
Nowell S, Sweeney C, Winters M, et al. Association between sulfotransferase 1A1 genotype and survival of breast cancer patients receiving tamoxifen therapy. Nat Cancer Instit. 2002;94:1635–1640.
Buckley PG, Mantripragada KK, Piotrowski A, De Stahl TD, Dumanski JP. Copy-number polymorphisms: Mining the tip of an iceberg. Trends Genet. 2005;21:315–317. http://dx.doi.org/10.1016/j.tig.2005.04.007, PMid:15922827
McCarroll SA, Hadnott TN, Perry GH, et al. Common deletion polymorphism in human genome. Nature Genet. 2006;38:86–92. http://dx.doi.org/10.1038/ng1696
Redon R, Ishikawa S, Fitch KR, et al. Global variation in copy number in the human genome. Nature. 2006;444:444–454. http://dx.doi.org/10.1038/nature05329, PMid:17122850, PMCid:2669898
Fredman D, White SJ, Potter S, Eichler EE, Den Dunnen JT, Brookes AJ. Complex SNP-related sequence variation in segmental genome duplications. Nature Genet. 2004;36(8):861–866. http://dx.doi.org/10.1038/ng1401, PMid:15247918
Feuk L, Marshall CR, Wintle RF, Scherer SW. Structural variants: changing the landscape of chromosomes and design of disease studies. Hum Mol Gen. 2006;15(1):R57–R66. http://dx.doi.org/10.1093/hmg/ddl057, PMid:16651370
Sebat J, Lakshmi B, Troge J, et al. Large-scale copy number polymorphism in the human genome. Science. 2004;305:525–527. http://dx.doi.org/10.1126/science.1098918, PMid:15273396
Hebbring SJ, Adjei AA, Baer JL, et al. Human SULT1A1 gene: Copy number differences and functional implications. Hum Mol Gen. 2007;16:463–470. http://dx.doi.org/10.1093/hmg/ddl468, PMid:17189289
Dandara C, Li DP, Walther G, Parker MI. Gene-environment interaction: The role of SULT1A1 and CYP3A5 polymorphisms as risk modifiers for squamous cell carcinoma of the oesophagus. Carcinogenesis. 2006;27(4):791–797. http://dx.doi.org/10.1093/carcin/bgi257, PMid:16272171
Schuster SC, Miller W, Ratan A, et al. Complete Khoisan and Bantu genomes from southern Africa. Nature Lett. 2010;463:943–947. http://dx.doi.org/10.1038/nature08795, PMid:20164927
Teo K, Chow CK, Vaz M, Rangarajan S, Yusuf S. The Prospective Urban Rural Epidemiology (PURE) study: Examining the impact of societal influences on chronic noncommunicable diseases in low-, middle-, and high-income countries. Am Heart J. 2009;158:1–8. http://dx.doi.org/10.1016/j.ahj.2009.04.019, PMid:19540385
Population genetics. In: Snyder LA, Freifelder D, Hartl DL, editors. General genetics. Boston, MA: Jones and Bartlett, 1985; 494–528.
Goodman LA. On simultaneous confidence intervals for multinomial proportions. Technometrics. 1965;7:247–254. http://dx.doi org/10.2307/ 1266673
Statistical Package for the Social Sciences (SPSS). Version 18. Armonk, NY: IBM; 2009.
Statistica. Version 9. Tulsa, OK: StatSoft; 2009.
R. Version 2.12.0. Vienna: R Development Core Team; 2010.
Windows Excel 7. Redmond, WA: Microsoft Corporation; 2009.
Hempel N, Masahiko N, McManus ME. Human SULT1A genes: Cloning and activity assays of the SULT1A promoters. Methods Enzymol. 2005;400:147–165. http://dx.doi.org/10.1016/S0076-6879(05)00009-1
Gjerde J, Hauglid M, Breilid H, et al. Effects of CYP2D6 and SULT1A1 genotypes including SULT1A1 gene copy number on tamoxifen metabolism. Ann Oncol. 2007;19(1):56-61. http://dx.doi.org/10.1093/annonc/mdm434, PMid:17947222
Han DF, Zhou X, Hu MB, et al. Sulfotransferase 1A1 (SULT1A1) polymorphism and breast cancer risk in Chinese women. Toxicol Lett. 2004;150:167–177. http://dx.doi.org/10.1016/j.toxlet.2004.01.012, PMid:15093672
Ohtake E, Kakihara F, Matsumoto N, et al. Frequency distribution of phenol sulfotransferase 1A1 activity in platelet cells from healthy Japanese subjects. Eur J Pharm Sci. 2006;28:272–277. http://dx.doi.org/10.1016/j.ejps.2006.02.008, PMid:16621480
Cann RL, Stoneking M, Wilson AC. Mitochondrial DNA and human evolution. Nature. 1987;325:31–36. http://dx.doi.org/10.1038/325031a0, PMid:3025745
Korbel JO, Kim PM, Chen X, et al. The current excitement about copy-number variation: How it relates to gene duplications and protein families. Curr Opin Struct Biol. 2008;18:1–9. http://dx.doi.org/10.1016/j.sbi.2008.02.005, PMid:18511261, PMCid:2577873
McCarroll SA, Altshuler DM. Copy-number variation and association studies of human disease. Nat Genet Suppl. 2007;39:S37-S42.
Freeman JL, Perry GH, Feuk L, et al. Copy number variation: New insights in genome diversity. Genome Res. 2006;16:949-961.
Desta Z, Zhao X, Shin JG, Flockhart DA. Clinical significance of the cytochrome P450 2C19 genetic polymorphism. Clin Pharmacokinet. 2002;41:913-958.
Devi SS, Vinayagamoorthy N, Agrawal M, et al. Distribution of detoxifying genes polymorphism in Maharastrian population of central India.Chemosphere. 2008;70:1835-1839.
Dalhoff K, Buus JK, Enghusen PH. Cancer and molecular biomarkers of phase 2. Methods Enzymol. 2005;400:618–627. http://dx.doi.org/10.1016/S00766879(05)00035-2
Raftogianis RB, Wood TC, Otterness DM, et al. Phenol sulfotransferase pharmacogenetics in humans: Association of common SULT1A1 alleles with TS PST phenotype. Biochem Biophys Res Commun. 1997;239:298–304. http://dx.doi.org/10.1006/bbrc.1997.7466, PMid:9345314
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