Literature DB >> 8354283

Feedback regulation of mammalian ornithine decarboxylase. Studies using a transient expression system.

E Lövkvist1, L Stjernborg, L Persson.   

Abstract

Ornithine decarboxylase catalyzes the first step in the biosynthesis of polyamines in mammalian cells. The enzyme is subject to various control mechanisms to maintain adequate intracellular levels of polyamines. Polyamines exert a strong feedback control on ornithine decarboxylase. In a recent study [van Daalen Wetters, T., Macrae, M., Brabant, M., Sittler, A. & Coffino, P. (1989) Mol. Cell. Biol. 9, 5484-5490], it was concluded that feedback control of ornithine decarboxylase is mainly, if not exclusively, a posttranslational phenomenon. The existence of a fast-acting polyamine-stimulated component of ornithine decarboxylase degradation that acts on newly synthesized monomeric forms of the enzyme was postulated. In the present study we have used a transient expression system to test this hypothesis. The expression of ornithine decarboxylase in mock-transfected COS cells varied depending on the cellular supply of polyamines as has been found in other mammalian cells. Thus, supplementing the cells with exogenous spermidine resulted in a marked decrease in ornithine decarboxylase activity, whereas depletion of intracellular polyamines, using an ornithine decarboxylase inhibitor, gave a large increase in the cellular content of the enzyme. COS cells expressing an ornithine decarboxylase mRNA devoid of its 5' non-translated region did not exhibit any feedback control of the enzyme, neither in the presence of exogenous spermidine nor when the intracellular polyamine levels were depleted to the same extent as in the mock-transfected COS cells. The results strongly suggest that the feedback control of ornithine decarboxylase is not merely a posttranslational phenomenon.

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Year:  1993        PMID: 8354283     DOI: 10.1111/j.1432-1033.1993.tb18089.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  7 in total

1.  Co-operation of the 5' and 3' untranslated regions of ornithine decarboxylase mRNA and inhibitory role of its 3' untranslated region in regulating the translational efficiency of hybrid RNA species via cellular factor.

Authors:  E C Lorenzini; I E Scheffler
Journal:  Biochem J       Date:  1997-09-01       Impact factor: 3.857

Review 2.  Rapid and regulated degradation of ornithine decarboxylase.

Authors:  S Hayashi; Y Murakami
Journal:  Biochem J       Date:  1995-02-15       Impact factor: 3.857

3.  Feedback repression of ornithine decarboxylase synthesis mediated by antizyme.

Authors:  J L Mitchell; C Y Choe; G G Judd
Journal:  Biochem J       Date:  1996-12-15       Impact factor: 3.857

4.  No role of the 5' untranslated region of ornithine decarboxylase mRNA in the feedback control of the enzyme.

Authors:  E L Wallström; L Persson
Journal:  Mol Cell Biochem       Date:  1999-07       Impact factor: 3.396

5.  Excess putrescine accumulation inhibits the formation of modified eukaryotic initiation factor 5A (eIF-5A) and induces apoptosis.

Authors:  M E Tome; S M Fiser; C M Payne; E W Gerner
Journal:  Biochem J       Date:  1997-12-15       Impact factor: 3.857

6.  Polyamine metabolism in gliomas.

Authors:  R I Ernestus; G Röhn; R Schröder; T Els; J Y Lee; N Klug; W Paschen
Journal:  J Neurooncol       Date:  1996-08       Impact factor: 4.130

Review 7.  Polyamine Metabolism and Gene Methylation in Conjunction with One-Carbon Metabolism.

Authors:  Kuniyasu Soda
Journal:  Int J Mol Sci       Date:  2018-10-10       Impact factor: 5.923

  7 in total

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