Literature DB >> 1918176

A new perspective on ornithine decarboxylase regulation: prevention of polyamine toxicity is the overriding theme.

D R Morris1.   

Abstract

The polyamines are essential cellular components for growth. Control of a key regulated enzyme of polyamine biosynthesis, ornithine decarboxylase (ODC), as a function of growth, is an area of intense interest. A unique regulatory property of ODC is the short half-life of the protein, which has been suggested to be an important factor in rapid activation of polyamine biosynthesis after cells are mitogenically stimulated. In this paper, it is argued that the biological significance of the short half-life of ODC is unrelated to the rate of its induction to a new steady state by growth factors, which is in fact limited by the relatively long half-life of the ODC mRNA. Instead, I suggest that the rapid turnover of ODC protein becomes of significance when cells cease growth and expeditious downregulation of the enzyme is important in preventing polyamine overproduction, which would result in cytotoxicity in the arrested cells. Although mitogenic activation of ODC expression has been studied extensively, there is very little known about the mechanisms controlling downregulation of polyamine biosynthesis during the arrest of animal cell growth. These considerations suggest that this would be a fertile area of future inquiry.

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Year:  1991        PMID: 1918176     DOI: 10.1002/jcb.240460203

Source DB:  PubMed          Journal:  J Cell Biochem        ISSN: 0730-2312            Impact factor:   4.429


  12 in total

1.  Polyamines mediate glutamine-dependent induction of the intestinal epithelial heat shock response.

Authors:  Yuji Iwashita; Toshio Sakiyama; Mark W Musch; Mark J Ropeleski; Hirohito Tsubouchi; Eugene B Chang
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2011-04-21       Impact factor: 4.052

Review 2.  A free-radical hypothesis for the instability and evolution of genotype and phenotype in vitro.

Authors:  R E Parchment; K Natarajan
Journal:  Cytotechnology       Date:  1992       Impact factor: 2.058

3.  Leishmania donovani polyamine biosynthetic enzyme overproducers as tools to investigate the mode of action of cytotoxic polyamine analogs.

Authors:  Sigrid C Roberts; Yuqui Jiang; Judith Gasteier; Benjamin Frydman; Laurence J Marton; Olle Heby; Buddy Ullman
Journal:  Antimicrob Agents Chemother       Date:  2006-11-20       Impact factor: 5.191

4.  Feedback repression of polyamine transport is mediated by antizyme in mammalian tissue-culture cells.

Authors:  J L Mitchell; G G Judd; A Bareyal-Leyser; S Y Ling
Journal:  Biochem J       Date:  1994-04-01       Impact factor: 3.857

Review 5.  Rapid and regulated degradation of ornithine decarboxylase.

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

6.  Spermidine acetyltransferase is required to prevent spermidine toxicity at low temperatures in Escherichia coli.

Authors:  K Limsuwun; P G Jones
Journal:  J Bacteriol       Date:  2000-10       Impact factor: 3.490

7.  Rapid induction of apoptosis by deregulated uptake of polyamine analogues.

Authors:  R H Hu; A E Pegg
Journal:  Biochem J       Date:  1997-11-15       Impact factor: 3.857

8.  A mammalian sequence-dependent upstream open reading frame mediates polyamine-regulated translation in yeast.

Authors:  G J Mize; D R Morris
Journal:  RNA       Date:  2001-03       Impact factor: 4.942

9.  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

10.  Cytosolic and nuclear spermidine acetyltransferases in growing NIH 3T3 fibroblasts stimulated with serum or polyamines: relationship to polyamine-biosynthetic decarboxylases and histone acetyltransferase.

Authors:  M A Desiderio; S Mattei; G Biondi; M P Colombo
Journal:  Biochem J       Date:  1993-07-15       Impact factor: 3.857

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