Literature DB >> 3566731

Polyamine administration reduces ornithine decarboxylase activity without affecting its mRNA content.

G J Sertich, A E Pegg.   

Abstract

Ornithine decarboxylase, the first enzyme in the polyamine biosynthetic pathway, is induced by androgens in the mouse kidney. Enzyme activity, as well as enzyme protein levels are increased 100-400 fold. Utilizing a specific cDNA probe to ODC, mRNA levels in these cells were found to increase 7-25 fold as measured by densitometric scanning. Treatment of the mice for 5 hours with 2 mmol/kg doses of putrescine or 1,3-diaminopropane after androgen stimulation reduced enzyme activity to control levels, while mRNA levels remained elevated 18-30 fold above control. In a different system, serum starved SV-3T3 cells showed low ODC activity and amounts of ODC mRNA. Serum stimulation increased the 2.2 kilobase mRNA levels 6 fold and enzyme activity 13 fold in a coordinate fashion within 5 hours. While the rise in activity was blocked by the simultaneous addition of serum and 1 mM putrescine, ODC mRNA levels appeared unchanged. The addition of 50 microM spermidine or 100 microM spermine also had no effect on ODC mRNA levels, while at the same time reducing enzyme activity amounts. These results suggest that the mechanism by which polyamines regulate ODC activity in the mouse is primarily translational.

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Year:  1987        PMID: 3566731     DOI: 10.1016/0006-291x(87)91371-4

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  7 in total

1.  Combined regulation of ornithine and S-adenosylmethionine decarboxylases by spermine and the spermine analogue N1 N12-bis(ethyl)spermine.

Authors:  C W Porter; A E Pegg; B Ganis; R Madhabala; R J Bergeron
Journal:  Biochem J       Date:  1990-05-15       Impact factor: 3.857

2.  Polyamine regulation of ornithine decarboxylase synthesis in Neurospora crassa.

Authors:  M A Hoyt; M Broun; R H Davis
Journal:  Mol Cell Biol       Date:  2000-04       Impact factor: 4.272

3.  Modulation of polyamine-biosynthetic activity by S-adenosylmethionine depletion.

Authors:  D L Kramer; J R Sufrin; C W Porter
Journal:  Biochem J       Date:  1988-01-15       Impact factor: 3.857

4.  Selective regulation of S-adenosylmethionine decarboxylase activity by the spermine analogue 6-spermyne.

Authors:  C W Porter; J McManis; D Lee; R J Bergeron
Journal:  Biochem J       Date:  1988-09-01       Impact factor: 3.857

5.  Effect of inhibitors of S-adenosylmethionine decarboxylase on the contents of ornithine decarboxylase and S-adenosylmethionine decarboxylase in L1210 cells.

Authors:  R Madhubala; J A Secrist; A E Pegg
Journal:  Biochem J       Date:  1988-08-15       Impact factor: 3.857

6.  Effects of S-adenosyl-1,8-diamino-3-thio-octane and S-methyl-5'-methylthioadenosine on polyamine synthesis in Ehrlich ascites-tumour cells.

Authors:  I Holm; L Persson; A E Pegg; O Heby
Journal:  Biochem J       Date:  1989-07-01       Impact factor: 3.857

7.  K-FGF mediated transformation and induction of metastatic potential involves altered ornithine decarboxylase and S-adenosylmethionine decarboxylase expression--role in cellular invasion.

Authors:  Marcus S Hardin; Rene Mader; Robert A R Hurta
Journal:  Mol Cell Biochem       Date:  2002-04       Impact factor: 3.396

  7 in total

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