Burton Adam, Hu Xiaowen, Saiardi Adolfo
Medical Research Council, Cell Biology Unit, Laboratory for Molecular Cell Biology, Department of Cell and Developmental Biology, University College London, London, UK.
J Cell Physiol. 2009 Jul;220(1):8-15. doi: 10.1002/jcp.21763.
The inositol polyphosphate family of small, cytosolic molecules has a prominent place in the field of cell signalling, and inositol pyrophosphates are the most recent addition to this large family. First identified in 1993, they have since been found in all eukaryotic organisms studied. The defining feature of inositol pyrophosphates is the presence of the characteristic 'high energy' pyrophosphate group, which immediately attracted interest in them as possible signalling molecules. In addition to their unique 'high energy' pyrophosphate bond, their concentration in the cell is tightly regulated with an extremely rapid turnover. This, together with the history of other inositol polyphosphates, makes it likely that they have an important role in intracellular signalling involving some basic cellular processes. This hypothesis is supported by the surprisingly wide range of cellular functions where inositol pyrophosphates seem to be involved. A seminal finding was that inositol pyrophosphates are able to directly phosphorylate pre-phosphorylated proteins, thereby identifying an entirely new post-translational protein modification, namely serine-pyrophosphorylation. Rapid progress has been made in characterising the metabolism of these molecules in the 15 years since their first identification. However, their detailed signalling role in specific cellular processes and in the context of relevant physiological cues has developed more slowly, particularly in mammalian system. We will discuss inositol pyrophosphates from the cell signalling perspective, analysing how their intracellular concentration is modulated, what their possible molecular mechanisms of action are, together with the physiological consequences of this novel form of signalling.
小分子胞质肌醇多磷酸家族在细胞信号传导领域占据显著地位,而肌醇焦磷酸是这个大家族中最新成员。它们于1993年首次被鉴定出来,此后在所有研究过的真核生物中都有发现。肌醇焦磷酸的决定性特征是存在特征性的“高能”焦磷酸基团,这立刻引起了人们对它们作为可能信号分子的兴趣。除了其独特的“高能”焦磷酸键外,它们在细胞内的浓度受到严格调控,周转极快。这一点,连同其他肌醇多磷酸的情况,使得它们很可能在涉及一些基本细胞过程的细胞内信号传导中发挥重要作用。这一假说得到了肌醇焦磷酸似乎参与的广泛细胞功能的支持。一个开创性的发现是,肌醇焦磷酸能够直接磷酸化预磷酸化的蛋白质,从而确定了一种全新的翻译后蛋白质修饰,即丝氨酸焦磷酸化。自首次鉴定以来的15年里,在表征这些分子的代谢方面取得了快速进展。然而,它们在特定细胞过程以及相关生理线索背景下的详细信号传导作用发展得较为缓慢,尤其是在哺乳动物系统中。我们将从细胞信号传导的角度讨论肌醇焦磷酸,分析其细胞内浓度是如何调节的,其可能的分子作用机制是什么,以及这种新型信号传导形式的生理后果。