Local hypomethylation in atherosclerosis found in rabbit ec-sod gene

Arteriosclerosis, Thrombosis, and Vascular Biology

Volumn 19, Issue 9, 1999, Pages 2171-2178

  Laukkanen, Mikko O ^a   Mannermaa, Sanna ^a   Hiltunen, Mikko O ^a   Aittomäki, Saara ^b   Airenne, Kari ^a   Jänne, Juhani ^a   Ylä Herttuala, Seppo ^a  

^a UNIVERSITY OF EASTERN FINLAND   (Finland)

^b UNIVERSITY OF TAMPERE   (Finland)

Author keywords

Atherosclerosis; CpG island; DNA methylation; EC SOD; Mutations

Indexed keywords

5 METHYLCYTOSINE; DNA; SUPEROXIDE DISMUTASE;

ANIMAL TISSUE; AORTA INTIMA; AORTA MEDIA; ARTICLE; ATHEROGENESIS; ATHEROSCLEROSIS; CELL PROLIFERATION; CONTROLLED STUDY; DNA METHYLATION; GENE EXPRESSION; GENE SEQUENCE; MOLECULAR CLONING; NONHUMAN; PRIORITY JOURNAL;

EID: 0032846947     PISSN: 10795642     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.ATV.19.9.2171     Document Type: Article

References (47)

1. Abrahamsson T, Brandt U, Marklund SL, Sjöqvist P-O. Vascular bound recombinant extracellular superoxide dismutase type C protects against the detrimental effects of superoxide radicals on endothelium-dependent arterial relaxation. Circ Res. 1992;70:264-271.
2. Strålin P, Karlsson K, Johansson BO, Marklund SL. Interstitium of the human arterial wall contains very large amounts of extracellular superoxide dismutase. Arterioscler Thromb Vasc Biol. 1995;15: 2032-2036.
3. Luoma JS, Strålin P, Marklund SL, Hiltunen TP, Särkioja T, Ylä-Herttuala S. Expression of extracellular SOD and iNOS in macrophages and smooth muscle cells in human and rabbit atherosclerotic lesions. Arterioscler Thromb Vasc Biol. 1998;18:157-167.
4. Hiramatsu K, Rosen H, Heinecke JW, Wolfbauer G, Chait A. Superoxide initiates oxidation of low density lipoprotcin by human monocytes. Arteriosclerosis. 1987;7:55-60.
5. Rubanyi GM, Ho EH, Cantor EH, Lumma WC, Botelho LH. Cytoprotective function of nitric oxide: Inactivation of superoxide radicals produced by human leukocytes. Biochem Biophys Res Commun. 1991; 181:1392-1397.
6. Li E, Bestor TH, Jaenich R. Targeted mutation of DNA methyltransferase gene results in embryonic lethality. Cell. 1992;69:915-926.
7. Bird AP. CpG rich islands and the function of DNA methylation. Nature. 1986;321:209-213.
8. Bird AP. The essentials of DNA methylation. Cell. 1992;70:5-8.
9. Gama-Sosa MA, Slagel VA. Trevyn RW. Oxenhandler R, Kuo KC, Gehrke CW, Ehrlich M. The 5-methylcytosine content of DNA from human tumors. Nucleic Acids Res. 1983;11:6883-6894.
10. Barbieri R, Mischiati C, Piva R, Nastruzzi C, Giacomini P, Natali PG, Gambari R. DNA methylation of the Ha-ras-1 oncogene in neoplastic cells. Anticancer Res. 1989;9:1787-1791.
11. Cheah MSC, Wallace CD, Hoffman RM. Hypomethylation of DNA in human cancer cells: A site-specific change in the c-myc oncogene. J Natl Cancer Inst. 1984;73:1057-1065.
12. Lipsanen V, Leinonen P, Alhonen L, Jänne J. Hypomethylation of ornithine decarboxylase gene and erb-A1 oncogene in human chronic lymphatic leukemia. Blood. 1988;72:2042-2044.
13. Weitzman SA, Lee RM, Oulette AJ. Alterations in c-abl gene methylation in cells transformed by phagocyte-generated oxidants. Biochem Bioph Res Commun. 1989;158:24-30.
14. Feinberg AP, Gehrke CW, Kuo KC, Ehrlich M. Reduced genomic 5-methylcytosine content in human colonie neoplasia. Cancer Res. 1988; 48:1159-1161.
15. Mohandas T, Sparkes RS, Shapiro LJ. Reactivation of an inactive X chromosome evidence for x inactivation by DNA methylation. Science. 1981;211:393-396.
16. Feinberg AP. Genomic imprinting and gene activation in cancer. Nat Genet. 1993;4:110-113.
17. Ausubel FM, Brent R, Kingston RE, Moore DD, Seidman JG, Smith JA, Struhl K, eds. Current Protocols in Molecular Biology. John Wiley & Sons, Inc; 1995.
18. Jurka J, Klonowski P, Dagman V, Pelton P. Censor: A program for identification and elimination of repetitive elements from DNA sequence. Comput Chem. 1996;20:119-122.
19. Watanabe Y. Serial inbreeding of rabbits with hereditary hyperlipidemia (WHHL-rabbit). Atherosclerosis. 1980;36:261-268.
20. Rosenfeld ME, Tsukada T, Chait A, Bierman EL, Gown AM, Ross R. Fatty streak expansion and maturation in Watanabe Heritable Hyperlipemic and comparably hypercholesterolemic fat-fed rabbits. Arteriosclerosis. 1987;7:24-34.
21. Raizis AM, Schmitt F, Jost J-P. A bisulfite method of 5-methylcytosine mapping that minimizes template degradation. Anal Biochem. 1995;226: 161-166.
22. Herman JG, Graff JR, Myöhänen S, Nelkin BR, Baylin SB. Methylation specific PCR: A novel PCR assay for methylation status of CpG islands. Proc Natl Acad Sci U S A. 1996;93:9821-9826.
23. Myöhänen S, Wahlfors J, Jänne J. Automated fluorescent genomic sequencing as applied to the methylation analysis of the human ornithine decarboxylase gene. DNA Seq. 1994;5:1-8.
24. Wise CK, Hass BS. HPLC analysis for 5-methylcylidine in cellular DNA obtained directly from the culture flask. BioTechniques. 1994;16: 218-222.
25. Haaf T. The effect of 5-azacytidine on chromosome structure and function: implications for methylation-associated cellular process. Pharmac Ther. 1995;65:19-46.
26. Folz RJ, Crapo JD. Extracellular superoxide dismutase (SOD3): Tissue-specific expression, genomic characterization, and computer-assisted sequence analysis of the human EC SOD gene. Genomics. 1994;22: 162-171.
27. Nepliouev IV, Folz RJ. Mus musculus extracellular superoxide dismutase (SOD3) gene. Direct submission, genbank accession No. AF039602.
28. Schmid CW, Shen C-KJ. The evolution of interspersed repetitive DNA sequences in mammals and other vertebrates. In: MacIntyre RJ, ed. Molecular Evolutionary Genetics. New York: Plenum; 1985:323-358.
29. Daniels GR, Deiniger PL. Repeat sequence families derived from mammalian tRNA genes. Nature. 1985;317:819-822.
30. Weiner AM, Deininger PL, Efstratiadis A. Nonviral retroposons: Genes, pseudogenes and transposable elements generated by the reverse flow of genetic information. Annu Rev Biochem. 1986;55:631-661.
31. Singer MF. SINEs, and LINEs. Highly repeated short and long interspersed sequences in mammalian genomes. Cell. 1982;28:433-434.
32. Gardiner-Garden M, Frommer M. CpG islands in vertebrate genomes. J Mol Biol. 1987;196:261-282.
33. Sandstrom J, Nilsson P, Karlsson K, Marklund S L. 10-fold increase in human plasma extracellular superoxide dismutase content caused by a mutation in heparin-binding domain. J Biol Chem. 1994;269: 19163-19166.
34. Folz RJ, Peno-Green L, Crapo JD. Identification of a homozygous missense mutation (Arg to Gly) in the critical binding region of the human EC-SOD gene (SOD3) and its association with dramatically increased serum enzyme levels. Hum Mol Genet. 1994;12:2251-2254.
35. Fukai T, Galis ZS, Meng XP, Parthasarathy S, Harrison DG. Vascular expression of extracellular superoxide dismutase in atherosclerosis. J Clin Invest. 1998;101:2101-2111.
36. Antequera F, Boyes J, Bird A. High levels of de novo methylation and altered chromatin structure at CpG islands in cell lines. Cell. 1990;62: 503-514.
37. Marklund SL. Extracellular superoxide dismutase in human tissues and human cell lines. J Clin Invest. 1984;74:1398-1403.
38. Kazuichi S, Okada N. Rodent type 2 Alu family, rat identifier sequence, rabbit C family and bovine or goat 73-bp repeat may have evolved from tRNA genes. J Mol Evol. 1985;22:134-140.
39. Bird AP. DNA methylation and frequency of CpG in animal DNA. Nucleic Acids Res. 1980;8:1499-1504.
40. Cooper D, Youssoufian H. The CpG dinucleotide and human genetic disease. Hum Genet. 1988;78:151-155.
41. Ross R. The pathogenesis of atherosclerosis: A perspective for the 1990s. Nature. 1993;362:801-809.
42. Benditt EP, Benditt JM. Evidence for a monoclonal origin of human atherosclerotic plaques. Proc Natl Acad Sci U S A. 1973;70:1753-1756.
43. Campbell GR, Chamley-Camphell JH. Invited review: The cellular pathobiology of atherosclerosis. Pathology. 1981;13:423-440.
44. Schwartz SM, deBlois D, O'Brien ERM. The intima. Soil for atherosclerosis and restenosis. Circ Res. 1995;77:445-465.
45. Willems J, Zwijsen A, Siegers H, Nicolai S, Bettadapura J, Raymackers J, Scarcez T. Purification and sequence of rat extracellular superoxide dismutase B secreted by C6 glioma. J Biol Chem. 1993;268: 24614-24621.
46. Folz RJ, Guan J, Seldin MF, Oury TD, Enghild JJ, Crapo JD. Mouse extracellular superoxide dismutase: Primary structure, tissue-specific gene expression, chromosomal localization, and lung in situ hybridization. Am J Respir Cell Mol Biol. 1997;17:393-403.
47. Carlsson LM, Marklund SL, Edlund T. The rat extracellular superoxide dismutase dimer is converted to a tetramer by the change of a single amino acid. Proc Natl Acad Sci U S A. 1996;93:5219-5222.