Shen Tian Huai, Lin Hui-Kuan, Scaglioni Pier Paolo, Yung Thomas M, Pandolfi Pier Paolo
Cancer Biology and Genetics Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
Mol Cell. 2006 Nov 3;24(3):331-9. doi: 10.1016/j.molcel.2006.09.013.
PML nuclear bodies (NBs) are nuclear structures that have been implicated in processes such as transcriptional regulation, genome stability, response to viral infection, apoptosis, and tumor suppression. PML has been found to be essential for the formation of the NBs, as these structures do not form in Pml null cells, although PML add back fully rescues their formation. However, the basis for such a structural role of PML is unknown. We demonstrate that PML contains a SUMO binding motif that is independent of its SUMOylation sites and is surprisingly necessary for PML-NB formation. We demonstrate that the PML RING domain is critical for PML SUMOylation and PML-NB formation. We propose a model for PML-NB formation whereby PML SUMOylation and noncovalent binding of PML to SUMOylated PML through the SUMO binding motif constitutes the nucleation event for subsequent recruitment of SUMOylated proteins and/or proteins containing SUMO binding motifs to the PML NBs.
早幼粒细胞白血病(PML)核体(NBs)是一种核结构,参与转录调控、基因组稳定性、病毒感染应答、细胞凋亡和肿瘤抑制等过程。已发现PML对NBs的形成至关重要,因为在Pml基因缺失的细胞中这些结构无法形成,不过重新引入PML可完全恢复其形成。然而,PML发挥这种结构作用的基础尚不清楚。我们证明PML含有一个SUMO结合基序,该基序独立于其SUMO化位点,且令人惊讶的是对PML-NB的形成是必需的。我们证明PML环指结构域对PML的SUMO化和PML-NB的形成至关重要。我们提出了一个PML-NB形成的模型,即PML的SUMO化以及PML通过SUMO结合基序与SUMO化的PML的非共价结合构成了随后将SUMO化蛋白和/或含有SUMO结合基序的蛋白招募到PML核体的成核事件。