Borden Katherine L B
Institute for Research in Immunology and Cancer and Department of Pathology and Cell Biology, Université de Montréal, Montréal, Québec, Canada H4M 1J6.
Biochim Biophys Acta. 2008 Nov;1783(11):2145-54. doi: 10.1016/j.bbamcr.2008.06.005. Epub 2008 Jun 18.
The promyelocytic leukemia protein PML and its associated nuclear bodies are hot topics of investigation. This interest arises for multiple reasons including the tight link between the integrity of PML nuclear bodies and several disease states and the impact of the PML protein and PML nuclear bodies on proliferation, apoptosis and viral infection. Unfortunately, an understanding of the molecular underpinnings of PML nuclear body function remains elusive. Here, a general overview of the PML field is provided and is extended to discuss whether some of the basic tenets of "PML-ology" are still valid. For instance, recent findings suggest that some components of PML nuclear bodies form bodies in the absence of the PML protein. Also, a new model for PML nuclear body function is proposed which provides a unifying framework for its effects on diverse biochemical pathways such as Akt signaling and the p53-Mdm2 axis. In this model, the PML protein acts as an inhibitor of gene expression post-transcriptionally via inhibiting a network node in the eIF4E RNA regulon. An example is given for how the PML RNA regulon model provided the basis for the development of a new anti-cancer strategy being tested in the clinic.
早幼粒细胞白血病蛋白PML及其相关的核体是研究的热点。人们对其产生兴趣有多种原因,包括PML核体的完整性与多种疾病状态之间的紧密联系,以及PML蛋白和PML核体对增殖、凋亡和病毒感染的影响。不幸的是,对PML核体功能的分子基础的理解仍然难以捉摸。本文提供了PML领域的总体概述,并进一步讨论了“PML学”的一些基本原理是否仍然有效。例如,最近的研究结果表明,PML核体的一些成分在没有PML蛋白的情况下也能形成核体。此外,还提出了一种PML核体功能的新模型,该模型为其对多种生化途径(如Akt信号传导和p53-Mdm2轴)的影响提供了一个统一的框架。在这个模型中,PML蛋白通过抑制eIF4E RNA调节子中的一个网络节点,在转录后作为基因表达的抑制剂。文中给出了一个例子,说明PML RNA调节子模型如何为一种正在临床测试的新抗癌策略的开发提供了基础。