Role of sex and time of blood sampling in SOD1 and SOD2 expression variability

Clinical Biochemistry

Volumn 41, Issue 16-17, 2008, Pages 1348-1354

  Khymenets, Olha ^a,e   Covas, Maria Isabel ^a,e   Farré, Magi ^a,b   Langohr, Klaus ^a,c   Fitó, Montserrat ^a,e   de la Torre, Rafael ^a,d,e  

^a INST MUNIC D INVESTIGACIO MEDICA   (Spain)

^b UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^c UNIVERSITAT POLITÈCNICA DE CATALUNYA   (Spain)

^d UNIVERSITAT POMPEU FABRA   (Spain)

^e Instituto de Salud Carlos III   (Spain)

Author keywords

Daytime; Gene expression variation; qPCR; Sex; SOD1 and SOD2

Indexed keywords

BETA ACTIN; COPPER ZINC SUPEROXIDE DISMUTASE; MANGANESE SUPEROXIDE DISMUTASE;

ADULT; ARTICLE; BLOOD SAMPLING; CONTROLLED STUDY; FEMALE; GENE EXPRESSION; HUMAN; LEUKOCYTE; MALE; NORMAL HUMAN; OVULATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEX DIFFERENCE;

ADULT; BLOOD SPECIMEN COLLECTION; FEMALE; GENE EXPRESSION REGULATION, ENZYMOLOGIC; HUMANS; MALE; SEX CHARACTERISTICS; SUPEROXIDE DISMUTASE; TIME FACTORS;

EID: 55049096678     PISSN: 00099120     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.clinbiochem.2008.08.064     Document Type: Article

References (42)

1. Burczynski ME, Rockett JC, editors. Surrogate tissue analysis: genomics, proteomics, and metabolomic approaches. FL: Taylor and Francis Group, 2006.
2. Zelko I.N., Mariani T.J., and Folz R.J. Superoxide dismutase multigen family: a comparison of the CuZn-SOD (SOD1), Mn-SOD (SOD2), and Ec-SOD (SOD3) gene structures, evolution, and expression. Free Rad Bio. Med. 33 (2002) 337-349
3. Matés J.M., Segura J.M., Pérez-Gómez C., et al. Antioxidant enzymatic activities in human blood cells after an allergic reaction to pollen or house dust mite. Blood Cells, Mol. Disease 25 (1999) 103-109
4. Agilent Technologies, 2100 Expert Software:http://www.chem.agilent.com/scripts/generic.asp?lPage=2721andindcol=Nandprodcol=Y [accessed May 2006].
5. -ΔΔCt method. Methods 25 (2001) 402-408
6. ABI Prism 7900HT Sequence Detection System User Guide, Applied Biosystems, Copyright 2002.
7. Bland J.M., and Altman D.G. Calculating correlation coefficients with repeated observations: Part 2 - correlation within subjects. BMJ (1995) 310:446
8. Bland J.M., and Altman D.G. Calculating correlation coefficients with repeated observations: Part 1-correlation between subjects. BMJ 310 (1995) 633
9. Watson R.W. Redox regulation of neutrophil apoptosis. Antioxid. Redox. Sign. 4 1 (2002) 97-104
10. Sen C.K., and Roy S. Antioxidant regulation of cell adhesion. Med. Sci. Sports Exerc. 33 3 (2001) 377-381
11. Williams M.S., and Kwon J. T cell receptor stimulation, reactive oxygen species, and cell signaling. Free Rad Bio. Med. 37 8 (2004) 1144-1151
12. Nakai H., Tada K., and Abe Y. Erythrocyte superoxide dismutase-1 and 21 monosomy. Cytogenet. Cell Genet. 37 (1984) 547
13. Sichitiu S., Sinet P.M., Lejeune J., and Frezal J. Surdosage de la forme dimerique de l'indophenoloxydase dans la trisomie 21, secondaire au surdosage genique. Humangenetik 23 (1974) 65-72
14. Xu Y., Krishnan A., Wan X.S., et al. Mutations in the promoter reveal a cause for the reduced expression of the human manganese superoxide dismutase gene in cancer cells. Oncogene 18 (1999) 93-102
15. St Clair D. Manganese superoxide dismutase: genetic variation and regulation. J. Nutr. 134 (2004) 3190S-3191S
16. Sharma A., Sharma V.K., Horn-Saban S., Lancet D., Ramachandran S., and Ramachandran S.K. Assessing natural variation in gene expression in humans comparing with monozygotic twins using microarrays. Physiol. Genomics 21 (2005) 117-123
17. Radich J.P., Mao M., Stepaniants S., et al. Individual-specific variation of gene expression in peripheral blood leukocytes. Genomics 83 (2004) 980-988
18. Eady J.J., Wortley G.M., Wormstone Y.M., et al. Variation in gene expression profiles of peripheral blood mononuclear cells from healthy volunteers. Physiol. Genomics 22 (2005) 402-411
19. Debey S., Schoenbeck U., Hellmich M., et al. Comparison of different isolation techniques prior gene expression profiling of blood derived cells: impact on physiological responses, on overall expression and the role of different cell types. Pharmacogenomics J. 4 (2004) 193-207
20. Freezor R.J., Baker H.V., Mindrinos M., et al. Inflammation and host response to injury, large-scale collaborative research program. Whole blood and leukocyte RNA isolation for gene expression analysis. Physiol. Genomics 19 (2004) 247-254
21. Tanner M.A., Berk L.S., Berk D.L., Blidy A.D., Bit S.L., and Ruff D.W. Substantial changes in gene expression level due to the storage temperature and storage duration of human blood. Clin. Lab. Haem. 24 (2002) 337-341
22. Ruff A., Thriery J.P., Magdelénat H., and Radvanyi F. Gene expression analysis by real-time reverse transcription polymerase chain reaction: influence of tissue handling. Anal. Biochem. 328 (2004) 101-108
23. Khymenets O., Ortuño J., Fito M., Covas M.I., Farre M., and de la Torre R. Evaluation of RNA isolation procedures from human blood and its application or gene expression studies (Sod-1, Sod-2). Anal. Biochem. 347 (2005) 156-158
24. Lampe J.W., Stepaniants S.B., Mao M., et al. Signature of environmental exposures using peripheral leukocyte gene expression: tobacco smoke. Cancer Epidem. Biomar. Prev. 13 (2004) 445-453
25. Achiron A., and Gurevich M. Peripheral blood gene expression signature mirrors central nervous system disease: the model of multiple sclerosis. Autoimmun Rev. 5 (2006) 517-522
26. Nannil L., Pomualdi C., Masevi A., and Lanfranchi G. Differential gene expression profiling in genetic and multifactorial cardiovascular diseases. J. Mol. Cell. Cardiol. 41 (2006) 934-948
27. Merrick B.A., and Bruno M.E. Genomic and proteomic profiling for biomarkers and signature profiles of toxicity. Curr. Opin. Mol. Ther. 6 (2004) 600-607
28. Nicholson A.C., Unger E.R., Mangalathu R., Ojaniemi H., and Vernon S.D. Exploration of neuroendocrine and immune gene expression in peripheral blood mononuclear cells. Mol. Brain Res. 129 (2004) 193-197
29. Whitney A.R., Doehn M., Popper S.J., et al. Individuality and variation in gene expression patterns in human blood. PNAS 100 (2003) 1896-1901
30. Kawate T., Abo T., Hinuma S., and Kumagai K. Studies of the bioperiodicity of the immune response. II. Co-variations of murine T and B cells and a role of corticosteroid. J. Immunol. 126 (1981) 1364-1367
31. Rinn J.L., Rozowsky J.S., Laurenzi I.J., et al. Major molecular differences between mammalian sexes are involved in drug metabolism and renal function. Dev. Cell 6 (2004) 791-800
32. Rinn J.L., and Shyder M. Sexual dimorphism in mammalian gene expression. Trends Genet 21 (2005) 298-305
33. Shull S., Shull N.H., Periasame M., et al. Differential regulation of antioxidant enzymes in response to oxidants. J. Biol. Chem. 266 (1991) 24398-24403
34. Strehlow K., et al. Modulation of antioxidant enzyme expression and function by estrogen. Circ. Res. 93 (2003) 170-176
35. Dosiou C., Lathi R.B., Tulac S., Huang S.T.J., and Giudice L.C. Interferon-related and other immune genes are downregulated in peripheral blood leukocytes in the luteal phase of the menstrual cycle. J. Clin. Endocr. Metab. 89 (2004) 2501-2504
36. Boivin D.B., Janes F.O., Wu A., Cho-Park P.F., Xiong H., and Sun Z.S. Circadian clock genes oscillate in human peripheral blood mononuclear cells. Blood 102 (2003) 4143-4145
37. Abo T., Kawate T., Itoh K., and Kumagai K. Studies on the bioperiodicity of the immune response. I. Circadian rhythms of human T, B, and K cell traffic in the peripheral blood. J. Immunol. 126 (1981) 1360-1363
38. Arjona A., and Sarkar D.K. Evidence supporting a circadian control of natural killer cell function. Brain Behav. Immun. 20 (2006) 469-476
39. Oishi K., Ohkura N., Kadota K., et al. Clock mutation affects circadian regulation of circulating blood cells. J. Circadian Rhythms 2 (2006) 4-13
40. Bridges A.B., Fisher T.C., Scott N., McLaren M., and Belch J.J. Circadian rhythm of white blood cells aggregation and free radical status in healthy volunteers. Free Rad. Res. Commun. 16 (1992) 89-97
41. Cardona F. Periodic dip of lipidperoxidation in humans: a redox signal to synchronized peripheral circadian clock?. Med. Hypotheses 63 (2004) 841-846
42. Storch K.F., Lipan O., Leykin I., et al. Extensive and divergent circadian gene expression in liver and heart. Nature 417 (2002) 78-83