Literature DB >> 6190690

Polyamine-mediated protein phosphorylations: a possible target for intracellular polyamine action.

C Cochet, E M Chambaz.   

Abstract

Polyamines are well-known ubiquitous components of living cells. Although these polycations have been implicated in the regulation of major cellular functions such as DNA, RNA and protein synthesis occurring during cellular proliferation and/or differentiation processes, their mechanism of action at the molecular level has remained obscure. On the other hand, protein phosphorylation has emerged as a regulatory process of prime importance in cellular regulation. Data have recently been presented suggesting that polyamines may express at least part of their biological action through an effect upon selective protein phosphorylation systems. Two types of polyamine-sensitive protein kinases have been characterized in the last few years. The best known in molecular terms is the widespread casein kinase G (also termed casein kinase II), which represents a multifunctional protein kinase, at present classified as a messenger-independent activity. The other is a polyamine-dependent nuclear ornithine decarboxylase kinase characterized in Physarum polycephalum and several mammalian tissues. Both protein kinases are activated by polyamines in vitro at concentrations compatible with a physiological role, by a mechanism which most likely also involves an effect through the protein substrate conformation. Preliminary evidence suggests that both kinases may be implicated in the regulation of DNA-dependent RNA polymerase activities, although several other potential substrates have been suggested for casein kinase G. Another suggestion is that these kinases may also participate in the post-translational regulation of ornithine decarboxylase, the rate-limiting step in the polyamine biosynthetic pathway. A novel class of protein kinase activities may thus be defined as polyamine-mediated phosphorylation systems for which polyamines may function as intracellular messenger. Although their biological significance remains to be fully established, especially with regard to the definition of their specific intracellular target(s) and subsequent biological functions, these systems will be interesting to consider in future studies aimed at understanding the role of polyamines in cell regulation.

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Year:  1983        PMID: 6190690     DOI: 10.1016/0303-7207(83)90062-x

Source DB:  PubMed          Journal:  Mol Cell Endocrinol        ISSN: 0303-7207            Impact factor:   4.102


  13 in total

1.  Dissecting subdomains involved in multiple functions of the CK2beta subunit.

Authors:  D Leroy; O Filhol; N Quintaine; D Sarrouilhe; P Loue-Mackenbach; E M Chambaz; C Cochet
Journal:  Mol Cell Biochem       Date:  1999-01       Impact factor: 3.396

2.  Natural polyamines stimulate G-proteins.

Authors:  J L Bueb; A Da Silva; M Mousli; Y Landry
Journal:  Biochem J       Date:  1992-03-01       Impact factor: 3.857

3.  Catalytic properties of a purified phosphatidylinositol-4-phosphate kinase from rat brain.

Authors:  C Cochet; E M Chambaz
Journal:  Biochem J       Date:  1986-07-01       Impact factor: 3.857

4.  Purification of a 107 kilodalton (kDa) casein kinase G substrate from thyroid cytosol.

Authors:  S Levasseur; T Poleck; Y Friedman; G Burke
Journal:  Mol Cell Biochem       Date:  1988-10       Impact factor: 3.396

5.  Polyamine-enhanced casein kinase II in mouse pancreatic islets.

Authors:  P Thams; K Capito; C J Hedeskov
Journal:  Diabetologia       Date:  1986-12       Impact factor: 10.122

6.  Polyamine-sensitive protein kinase from chick intestinal mucosa.

Authors:  G Mezzetti; M Moruzzi; M G Monti; G Piccinini; B Barbiroli
Journal:  Mol Cell Biochem       Date:  1985-03       Impact factor: 3.396

Review 7.  Protein kinases phosphorylating acidic ribosomal proteins from yeast cells.

Authors:  R Szyszka
Journal:  Folia Microbiol (Praha)       Date:  1999       Impact factor: 2.099

8.  Isolation and sequencing of cDNA clones encoding alpha and beta subunits of Drosophila melanogaster casein kinase II.

Authors:  A Saxena; R Padmanabha; C V Glover
Journal:  Mol Cell Biol       Date:  1987-10       Impact factor: 4.272

9.  Inhibitory action of polyamines on protein kinase C association to membranes.

Authors:  M Moruzzi; B Barbiroli; M G Monti; B Tadolini; G Hakim; G Mezzetti
Journal:  Biochem J       Date:  1987-10-01       Impact factor: 3.857

10.  Localization and biosynthesis of polyamines in insulin-producing cells.

Authors:  D M Hougaard; J H Nielsen; L I Larsson
Journal:  Biochem J       Date:  1986-08-15       Impact factor: 3.857

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