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. 1968 Sep;47(9):2099–2108. doi: 10.1172/JCI105895

Transsulfuration in mammals: fetal and early development of methionine-activating enzyme and its relation to hormonal influences

H Peter Chase 1, Joseph J Volpe 1, Leonard Laster 1
PMCID: PMC297370  PMID: 5691982

Abstract

The development of activity of methionine-activating enzyme was studied in four organs of the rat. Three different patterns were observed: (a) in the liver, specific activity began to increase in late fetal life and reached a maximum 2 days after birth; (b) in the small intestine, specific activity began to rise in the 2nd wk after birth and reached a maximum at age 18 days; and (c) in the brain and kidney, specific activity did not change markedly from the earliest stage of fetal development studied to adult life. Hydrocortisone increased hepatic methionine-activating enzyme activity as much as 55% in the young rat. However, adrenalectomy in the newborn rat did not prevent the postnatal rise in hepatic methionine-activating enzyme activity, nor did adrenalectomy at age 10 days prevent the developmental rise of intestinal activity at age 18 days. Conjugated estrogens partially inhibited both the neonatal rise in hepatic methionine-activating enzyme activity and the rise in activity after adrenal steroid injection. Injection of L-methionine did not increase hepatic methionine-activating enzyme activity in the developing or adult rat.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BUSH I. E. Species differences in adrenocortical secretion. J Endocrinol. 1953 Jan;9(1):95–100. doi: 10.1677/joe.0.0090095. [DOI] [PubMed] [Google Scholar]
  2. CANTONI G. L., DURELL J. Activation of methionine for transmethylation. II. The methionine-activating enzyme; studies on the mechanism of the reaction. J Biol Chem. 1957 Apr;225(2):1033–1048. [PubMed] [Google Scholar]
  3. DOELL R. G., KRETCHMER N. INTESTINAL INVERTASE: PRECOCIOUS DEVELOPMENT OF ACTIVITY AFTER INJECTION OF HYDROCORTISONE. Science. 1964 Jan 3;143(3601):42–44. doi: 10.1126/science.143.3601.42. [DOI] [PubMed] [Google Scholar]
  4. Etzler M. E., Moog F. Inactive alkaline phosphatase in duodenum of nursling mouse: immunological evidence. Science. 1966 Nov 25;154(3752):1037–1038. doi: 10.1126/science.154.3752.1037. [DOI] [PubMed] [Google Scholar]
  5. Finkelstein J. D., Mudd S. H. Trans-sulfuration in mammals. The methionine-sparing effect of cystine. J Biol Chem. 1967 Mar 10;242(5):873–880. [PubMed] [Google Scholar]
  6. GOSWAMI M. N., KNOX W. E. Developmental changes of p-hydroxyphenylpyruvate-oxidase activity in mammalian liver. Biochim Biophys Acta. 1961 Jun 10;50:35–40. doi: 10.1016/0006-3002(61)91056-3. [DOI] [PubMed] [Google Scholar]
  7. Hancock R. L. S-adenosylmethionine-synthesizing activity of normal and neoplastic mouse tissues. Cancer Res. 1966 Dec;26(12):2425–2430. [PubMed] [Google Scholar]
  8. King E. J., Armstrong A. R. A CONVENIENT METHOD FOR DETERMINING SERUM AND BILE PHOSPHATASE ACTIVITY. Can Med Assoc J. 1934 Oct;31(4):376–381. [PMC free article] [PubMed] [Google Scholar]
  9. LEVITZ M., CONDON G. P., DANCIS J. Sulfurylation of estrogens by the human fetus. Endocrinology. 1961 May;68:825–830. doi: 10.1210/endo-68-5-825. [DOI] [PubMed] [Google Scholar]
  10. LIN E. C., KNOX W. E. Adaptation of the rat liver tyrosine-alpha-ketoglutarate transaminase. Biochim Biophys Acta. 1957 Oct;26(1):85–88. doi: 10.1016/0006-3002(57)90057-4. [DOI] [PubMed] [Google Scholar]
  11. MASON M., GULLEKSON E. H. Estrogen-enzyme interactions: Inhibition and protection of kynurenine transaminase by the sulfate esters of diethylstilbestrol, estradiol, and estrone. J Biol Chem. 1960 May;235:1312–1316. [PubMed] [Google Scholar]
  12. MOOG F., THOMAS E. R. The influence of various adrenal and gonadal steroids on the accumulation of alkaline phosphatase in the duodenum of the suckling mouse. Endocrinology. 1955 Feb;56(2):187–196. doi: 10.1210/endo-56-2-187. [DOI] [PubMed] [Google Scholar]
  13. Mudd S. H., Finkelstein J. D., Irreverre F., Laster L. Transsulfuration in mammals. Microassays and tissue distributions of three enzymes of the pathway. J Biol Chem. 1965 Nov;240(11):4382–4392. [PubMed] [Google Scholar]
  14. NEMETH A. M. Mechanisms controlling changes in tryptophan peroxidase activity in developing mammalian liver. J Biol Chem. 1959 Nov;234:2921–2924. [PubMed] [Google Scholar]
  15. PETERSON R. E., HERTZ R., LUBS H. A. Suppression of biosynthesis of adrenal cortical steroids in man by amphenone. Proc Soc Exp Biol Med. 1957 Mar;94(3):421–425. doi: 10.3181/00379727-94-22964. [DOI] [PubMed] [Google Scholar]
  16. REEM G. H., KRETCHMER N. Development of phenylalanine hydroxylase in liver of the rat. Proc Soc Exp Biol Med. 1957 Nov;96(2):458–460. doi: 10.3181/00379727-96-23506. [DOI] [PubMed] [Google Scholar]
  17. RUBINO A., ZIMBALATTI F., AURICCHIO S. INTESTINAL DISACCHARIDASE ACTIVITIES IN ADULT AND SUCKLING RATS. Biochim Biophys Acta. 1964 Nov 22;92:305–311. doi: 10.1016/0926-6569(64)90187-7. [DOI] [PubMed] [Google Scholar]
  18. SERENI F., KENNEY F. T., KRETCHMER N. Factors influencing the development of tyrosine-alpha-ketoglutarate transaminase activity in rat liver. J Biol Chem. 1959 Mar;234(3):609–612. [PubMed] [Google Scholar]

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