Cloning of the human phenol sulfotransferase gene family: Three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs

Chemico-Biological Interactions

Volumn 109, Issue 1-3, 1998, Pages 29-41

  Dooley, Thomas P ^a  

^a SOUTHERN RESEARCH INSTITUTE   (United States)

Author keywords

Gene family; Human chromosome 16; Minoxidil; Pharmacogenetics; Phenol sulfotransferase genes; STM; STP1; STP2; Xenobiotic metabolism

Indexed keywords

4 NITROPHENOL; ARYL SULFOTRANSFERASE; CATECHOLAMINE; COMPLEMENTARY DNA; DOPAMINE; DRUG; PHENOL DERIVATIVE; THYROID HORMONE; XENOBIOTIC AGENT;

AMINO ACID SEQUENCE; CATECHOLAMINE METABOLISM; CONFERENCE PAPER; DNA POLYMORPHISM; DRUG METABOLISM; GENE CONVERSION; GENE DUPLICATION; GENE MAPPING; HUMAN; MOLECULAR CLONING; MOUSE; MULTIGENE FAMILY; NONHUMAN; THYROID HORMONE METABOLISM; XENOBIOTIC METABOLISM;

ANIMALS; ARYLSULFOTRANSFERASE; CATECHOLAMINES; CLONING, MOLECULAR; DNA, COMPLEMENTARY; HUMANS; MICE; THYROID HORMONES;

EID: 0032549066     PISSN: 00092797     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0009-2797(97)00118-X     Document Type: Conference Paper

References (37)

1. Falany C.N. Molecular enzymology of human liver cytosolic sulfotransferases. Trends Pharmacol. Sci. 2:1991;255-259.
2. Yamazoe Y., Nagata K., Ozawa S., Kato R. Structural similarity and diversity of sulfotransferases. Chem.-Biol. Interact. 92:1994;107-117.
3. Coughtrie M.W.H., Bamforth K.J., Sharp S., Jones A.L., Borthwick E.B., Barker E.V., Roberts R.C., Hume R., Burchell A. Sulfation of endogenous compounds and xenobiotics-interactions and function in health and disease. Chem.-Biol. Interact. 92:1994;247-256.
4. Coughtrie M.W.H. Sulphation catalysed by the human cytosolic sulphotransferases-chemical defence or molecular terrorism? Hum. Exp. Toxicol. 15:1996;547-555.
5. Rikke B.A., Roy A.K. Structural relationships among members of the mammalian sulfotransferase gene family. Biochim. Biophys. Acta. 1307:1996;331-338.
6. Falany C.N., Vasquez M.E., Heroux J.A., Roth J.A. Purification and characterization of human liver phenol-sulfating PST. Arch. Biochem. Biophys. 278:1990;312-318.
7. Campbell N.R.C., Van Loon J.A., Weinshilboum R.M. Human liver PST: assay conditions, biochemical properties and partial purification of isozymes of the thermostable form. Biochem. Pharmacol. 36:1987;1435-1446.
8. Zou J., Pentney R., Roth J.A. Immunohistochemical detection of PST-containing neurons in human brain. J. Neurochem. 55:1990;1154-1158.
9. Visser T.J. Role of sulfate in thyroid hormone sulfation. Eur. J. Endocrinol. 134:1996;12-14.
10. Visser T.J. Role of sulfation in thyroid hormone metabolism. Chem.-Biol. Interact. 92:1994;293-303.
11. Price R.A., Spielman R.S., Lucena A.L., Van Loon J.A., Maidak B.L., Weinshilboum R.M. Genetic polymorphism for human platelet thermostable PST (TS PST) activity. Genetics. 122:1989;905-914.
12. Buhl A.E., Waldon D.J., Baker C.A., Johnson G.A. Minoxidil sulfate is the active metabolite that stimulates hair follicles. J. Invest. Dermatol. 95:1990;553-557.
13. Dooley T.P., Walker C.J., Hirshey S.J., Falany C.N., Diani A.R. Localization of minoxidil sulfotransferase in rat liver and the ORS of anagen pelage and vibrissa follicles. J. Invest. Dermatol. 96:1991;65-70.
14. Hirshey S.J., Dooley T.P., Reardon I.M., Heinrikson R.L., Falany C.N. Sequence analysis, in vitro translation and expression of the cDNA for rat liver minoxidil sulfotransferase. Mol. Pharmacol. 42:1992;257-264.
15. Wilborn T.W., Comer K.A., Dooley T.P., Reardon I.M., Heinrikson R.L., Falany C.N. Sequence analysis and expression of the cDNA for the phenol-sulfating form of human liver PST. Mol. Pharmacol. 43:1993;70-77.
16. Hume R., Coughtrie M.W.H. PST: localization in kidney during human embryonic and fetal development. Histochem. J. 26:1994;850-855.
17. Zhu X., Veronese M.E., Bernard C.C.A., Sansom L.N., McManus M.E. Molecular characterization of a human aryl sulfotransferase cDNA. Biochem. Biophys. Res. Comm. 192:1993;671-676.
18. Zhu X., Veronese M.E., Bernard C.C.A., Sansom L.N., McManus M.E. Identification of two human brain aryl sulfotransferase cDNAs. Biochem. Biophys. Res. Comm. 195:1993;120-127.
19. Zhu X., Veronese M.E., Iocco P., McManus M.E. cDNA cloning and expression of a new form of human aryl sulfotransferase. Int. J. Biochem. Cell Biol. 28:1996;565-571.
20. Jones A.L., Hagen M., Coughtrie M.W.H., Roberts R.C., Glatt H. Human platelet PSTs: cDNA cloning, stable expression in V79 cells and identification of a novel allelic variant of the phenol-sulfating form. Biochem. Biophys. Res. Commun. 208:1995;855-862.
21. Bernier F., Lopez-Solache I., Labrie F., Luu-The V. Cloning and expression of cDNA encoding human placental estrogen sulfotransferase. Mol. Cell Endocrinol. 99:1994;R11-R15.
22. Ozawa S., Nagata K., Shimada M., Ueda M., Tsuzuki T., Yamazoe Y., Kato R. Primary structures and properties of two related forms of aryl sulfotransferases in human liver. Pharmacogenetics. 5:1995;s135-s140.
23. Hwang S.-R., Kohn A.B., Hook V.Y.H. Molecular cloning of an isoform of PST from human brain hippocampus. Biochem. Biophys. Res. Commun. 207:1995;701-707.
24. Wood T.C., Aksoy I.A., Aksoy S., Weinshilboum R.M. Human liver thermolabile PST: cDNA cloning, expression and characterization. Biochem. Biophys. Res. Commun. 198:1994;1119-1127.
25. Dooley T.P., Obermoeller R.D., Leiter E.H., Chapman H.D., Falany C.N., Deng Z., Siciliano M.J. Mapping of the PST gene (STP) to human chromosome 16p12.1-p11.2 and to mouse chromosome 7. Genomics. 18:1993;440-443.
26. Dooley T.P., Mitchison H.M., Munroe P.B., Probst P., Neal M., Siciliano M.J., Deng Z., Doggett N.A., Callen D.F., Gardiner R.M., Mole S.E. Mapping of two PST genes, STP and STM, to 16p: candidate genes for Batten disease. Biochem. Biophys. Res. Commun. 205:1994;482-489.
27. Dooley T.P., Huang Z. Genomic organization and DNA sequences of two human PST genes (STP1 and STP2) on the short arm of chromosome 16. Biochem. Biophys. Res. Commun. 228:1996;134-140.
28. Aksoy I.A., Callen D.F., Apostolou S., Her C., Weinshilboum R.M. Thermolabile PST gene (STM): localization to human chromosome 16p11.2. Genomics. 23:1994;275-277.
29. Taschner P.E.M., de Vos N., Thompson A.D., Callen D.F., Doggett N., Mole S., Dooley T.P., Barth P.G., Breuning M.H. Chromosome 16 microdeletion in a patient with juvenile neuronal ceroid lipofuscinosis (Batten disease). Am. J. Hum. Genet. 56:1995;663-668.
30. Mitchison H.M., Thompson A.D., Mulley J.C., Kozman H.M., Richards R.I., Callen D.F., Stallings R.L., Doggett N.A., Attwood J., McKay T.R., Sutherland G.R., Gardiner R.M. Fine genetic mapping of the Batten disease locus (CLN3) by haplotype analysis and demonstration of allelic association with chromosome 16p microsatellite loci. Genomics. 16:1993;455-460.
31. p1) for mouse liver. Biochem. Biophys. Acta. 1171:1993;315-318.
32. Dooley T.P., Probst P., Munroe P.B., Mole S.E., Liu Z., Doggett N.A. Genomic organization and DNA sequence of the human catecholamine-sulfating PST gene (STM). Biochem. Biophys. Res. Commun. 205:1994;1325-1332.
33. Her C., Raftogianis R., Weinshilboum R.M. Human PST STP2 gene: molecular cloning, structural characterization and chromosomal localization. Genomics. 33:1996;409-420.
34. Bernier F., Soucy P., Luu-The V. Human PST gene contains two alternative promoters: structure and expression of the gene. DNA Cell Biol. 15:1996;367-375.
35. Jones A.L., Roberts R.C., Coughtrie M.W.H. The human PST polymorphism is determined by the level of expression of the enzyme protein. Biochem. J. 296:1993;287-290.
36. Henkel R.D., Galindo L.V., Dooley T.P. Detection of a HindIII restriction fragment length polymorphism in the human PST (STP) locus. Hum. Genet. 95:1995;245-246.
37. Henkel R.D., Galindo L.V., Dooley T.P. An EcoRI RFLP in human PST genes. Hum. Mol. Genet. 3:1994;2264.