Cochet C, Chambaz E M
Mol Cell Endocrinol. 1983 Jun;30(3):247-66. doi: 10.1016/0303-7207(83)90062-x.
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.
多胺是活细胞中普遍存在的成分,广为人知。尽管这些聚阳离子参与了细胞增殖和/或分化过程中发生的主要细胞功能(如DNA、RNA和蛋白质合成)的调节,但其在分子水平上的作用机制仍不清楚。另一方面,蛋白质磷酸化已成为细胞调节中至关重要的调节过程。最近有数据表明,多胺可能至少部分通过对选择性蛋白质磷酸化系统的影响来发挥其生物学作用。在过去几年中,已鉴定出两种对多胺敏感的蛋白激酶。从分子角度最广为人知的是广泛存在的酪蛋白激酶G(也称为酪蛋白激酶II),它是一种多功能蛋白激酶,目前被归类为不依赖信使的活性。另一种是在多头绒泡菌和几种哺乳动物组织中鉴定出的多胺依赖性核鸟氨酸脱羧酶激酶。两种蛋白激酶在体外均能被与生理作用相适应浓度的多胺激活,其机制很可能也涉及对蛋白质底物构象的影响。初步证据表明,尽管有人提出酪蛋白激酶G还有其他几种潜在底物,但这两种激酶可能都参与了DNA依赖性RNA聚合酶活性的调节。另一种观点认为,这些激酶也可能参与鸟氨酸脱羧酶的翻译后调节,鸟氨酸脱羧酶是多胺生物合成途径中的限速步骤。因此,一类新的蛋白激酶活性可被定义为多胺介导的磷酸化系统,多胺可能作为细胞内信使发挥作用。尽管它们的生物学意义仍有待充分确定,特别是关于其特定细胞内靶点的定义及其后续生物学功能,但在未来旨在理解多胺在细胞调节中作用的研究中,考虑这些系统将很有意义。