Semin Thromb Hemost 2000; Volume 26(Number 03): 219-226
DOI: 10.1055/s-2000-8466
Copyright © 2000 by Thieme Medical Publishers, Inc., 333 Seventh Avenue, New York, NY 10001, USA. Tel.: +1(212) 584-4662

Pathways and Regulation of Homocysteine Metabolism in Mammals

JAMES. D. FINKELSTEIN
  • Department of Veteran Affairs Medical Center and George Washington University, Washington, D.C
Further Information

Publication History

Publication Date:
31 December 2000 (online)

ABSTRACT

Two intersecting pathways, the methionine cycle and the transsulfuration sequence, compose the mechanisms for homocysteine metabolism in mammals. The methionine cycle occurs in all tissues and provides for the remethylation of homocysteine, which conserves methionine. In addition, the cycle is essential for the recycling of methyltetrahydrofolate. The synthesis of cystathionine is the first reaction in the irreversible pathway for the catabolism of homocysteine by means of the sequential conversion to cysteine and sulfate. This pathway has a limited distribution and is found primarily in the liver, kidney, small intestine and pancreas. Regulation of homocysteine metabolism is achieved by changes in the quantity of homocysteine distributed between the two competing pathways. Two mechanisms are basic to the regulatory process. Changes in tissue content of the relevant enzymes are the response to sustained perturbations. The inherent kinetic properties of the enzymes provide an immediate response to alterations in the tissue concentrations of substrates and other metabolic effectors. S-adenosylmethionine, S-adenosylhomocysteine, and methyltetrahydrofolate are of particular importance in that context.

REFERENCES

  • 1 Finkelstein J D. Concluding remarks: Epilogue or prologue. in: Mato JM, Caballero J, eds Methionine Metabolism: Molecular Mechanisms and Clinical Implications. Madrid: CSIC, 1996: 277-282
  • 2 Finkelstein J D. Methionine metabolism in mammals.  J Nutr Biochem . 1990;  1 228-237
  • 3 Ueland P M, Refsum H, Brattstrom L. Plasma homocysteine and cardiovascular disease. in: Francis RB Jr, ed. Arteriosclerotic Cardiovascular Disease, Hemostasis and Endothelial Function New York: Marcel Dekker, 1992: 183-196
  • 4 Mudd S H, Levy H L, Skovby F. Disorders of transsulfuration. in: Scriver CR, Beaudet AL, Slys WS, Valle D, eds. The Metabolic Basis of Inherited Disease New York: McGraw-Hill, 1995: 1279-1328
  • 5 Surtees R. Demyelination and inborn errors of the single carbon transfer pathway.  Eur J Pediatr . 1998;  S118-S121 (S118-S121)
  • 6 Capdevila A, Wagner C. Measurement of plasma S-adenosylmethionine and S-adenosylhomocysteine as their fluorescent isoindoles.  Anal Biochem . 1998;  264 180-184
  • 7 Mudd S H, Poole J R. Labile methyl balances for normal humans on various dietary regimens.  Metabolism . 1975;  24 721-735
  • 8 Svardal A M, Ueland P M. Compartmentalization of S-adenosylhomocysteine in rat liver. Determination and characterization of the in vivo protein binding.  J Biol Chem . 1987;  262 15413-15417
  • 9 de la Haba G, Cantoni G L. The enzymatic synthesis of S-adenosyl-l-homocysteine from adenosine and homocysteine.  J Biol Chem . 1959;  234 603-608
  • 10 Duerre J A, Miller C H, Reams G G. Metabolism of S-adenosyl-L-homocysteine in vivo by the rat.  J Biol Chem . 1969;  244 107-111
  • 11 Banerjee R V, Matthews R G. Cobalamin-dependent methionine synthase.  FASEB J . 1990;  4 1450-1459
  • 12 Matthews R G, Goulding C W. Enzyme-catalyzed methyl transfers to thiols: The role of zinc.  Curr Opin Chem Biol . 1997;  1 332-339
  • 13 McKeever M P, Weir D G, Molloy A, Scott J M. Betaine-homocysteine methyltransferase: Organ distribution in man, pig and rat and subcellular distribution in the rat.  Clin Sci . 1991;  81 551-556
  • 14 Rao P V, Garrow T A, John F. Betaine-homocysteine methyltransferase is a developmentally regulated enzyme crystallin in rhesus monkey lens.  J Biol Chem . 1998;  273 30669-30674
  • 15 Kery V, Bukovska G, Kraus J P. Transsulfuration depends on heme in addition to pyridoxal 5′-phosphate.  J Biol Chem . 1994;  269 25283-25288
  • 16 Finkelstein J D, Mudd S H. Transsulfuration in mammals. The methionine sparing effect of cystine.  J Biol Chem . 1967;  242 873-880
  • 17 Finkelstein J D. Regulation of methionine metabolism in mammals. In: Usdin E, Borchardt RT, Creveling CR, eds Transmethylation. New York: Elsevier, 1979: 49-58
  • 18 Meister A. Metabolism and transport of glutathione and other γ-glutamyl compounds. in: Larsson A, Orrenius S, Holmgren A, Mannervik B, eds. Functions of Glutathione: Biochemical, Physiological, Toxicological and Clinical Aspects New York: Raven Press, 1983: 1-2
  • 19 Kutzbach C, Stokstad E LR. Mammalian methylenetetrahydrofolate reductase. Partial purification, properties and inhibition by S-adenosylmethionine.  Biochim Biophys Acta . 1971;  250 459-477
  • 20 Jencks D A, Matthews R G. Allosteric inhibition of methylenetetrahydrofolate reductase by adenosylmethionine.  J Biol Chem . 1987;  262 2485-2493
  • 21 Kerr S J. Competing methyltransferase systems.  J Biol Chem . 1972;  247 4248-4252
  • 22 Yeo E-J, Wagner C. Tissue distribution of glycine N-methyltransferase, a major folate-binding protein of liver.  Proc Natl Acad Sci USA . 1994;  91 210-214
  • 23 Wagner C, Briggs W T, Cook R J. Inhibition of glycine N-methyltransferase activity by folate derivatives: Implications for regulation of methyl group metabolism.  Biochem Biophys Res Commun . 1985;  127 746-752
  • 24 Finkelstein J D, Kyle W E, Martin J J, Pick A. Activation of cystathionine synthase by adenosylmethionine and adenosylethionine.  Biochem Biophys Res Commun . 1975;  66 81-87
  • 25 Finkelstein J D, Martin J J. Inactivation of betaine-homocysteine methyltransferase by adenosylmethionine and adenosylethionine.  Biochem Biophys Res Commun . 1984;  118 14-19
  • 26 Finkelstein J D, Kyle W E, Harris B. Methionine metabolism in mammals: Regulatory effects of S-adenosylhomocysteine.  Arch Biochem Biophys . 1974;  165 774-779
  • 27 Finkelstein J D, Martin J J. Methionine metabolism in mammals: Distribution of homocysteine between competing pathways.  J Biol Chem . 1984;  259 9508-9513
  • 28 Watson Brody T., Stokstad ELR. Folate pentaglutamate and folate hexaglutamate mediated one carbon metabolism.  Biochemistry. 1982;  21 276-282
  • 29 Taoka S, Ohja S, Shan X, Kruger W D, Banerjee R. Evidence for heme-mediated redox regulation of human cystathionine β-synthase activity.  J Biol Chem . 1998;  273 25179-25184
  • 30 Chen Z, Banerjee R. Purification of soluble cytochrome b5 as a component of the reductive activation of porcine methionine synthase.  J Biol Chem . 1998;  273 26248-26255
  • 31 Scislowski P WD, Pickard K. Methionine transamination-metabolic function and subcellular compartmentation.  Mol Cell Biochem . 1993;  129 39-45
  • 32 Blom H J, Boers G HJ, van den Elzen J PAM, Gahl W A, Tangerman A. Transamination of methionine in humans.  Clin Sci . 1989;  76 43-49
  • 33 Moskovitz J, Jenkins N A, Gilbert D J. Chromosomal localization of the mammalian peptide-methionine sulfoxide reductase gene and its differential expression in various tissues.  Proc Natl Acad Sci U S A . 1996;  93 3205-3208
  • 34 Jakubowski H. Metabolism of homocysteine thiolactone in human cell cultures.  J Biol Chem . 1997;  272 1935-1942
  • 35 Jakubowski H. Protein homocysteinylation: Possible mechanisms underlying pathological consequences of elevated homocysteine levels.  FASEB J . 1999;  13 2277-2283
    >