Friedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, CH-4058 Basel, Switzerland.
Cell Res. 2011 Mar;21(3):474-85. doi: 10.1038/cr.2011.31. Epub 2011 Feb 15.
Recent findings show that chromatin dynamics and nuclear organization are not only important for gene regulation and DNA replication, but also for the maintenance of genome stability. In yeast, nuclear pores play a role in the maintenance of genome stability by means of the evolutionarily conserved family of SUMO-targeted Ubiquitin ligases (STUbLs). The yeast Slx5/Slx8 STUbL associates with a class of DNA breaks that are shifted to nuclear pores. Functionally Slx5/Slx8 are needed for telomere maintenance by an unusual recombination-mediated pathway. The mammalian STUbL RNF4 associates with Promyelocytic leukaemia (PML) nuclear bodies and regulates PML/PML-fusion protein stability in response to arsenic-induced stress. A subclass of PML bodies support telomere maintenance by the ALT pathway in telomerase-deficient tumors. Perturbation of nuclear organization through either loss of pore subunits in yeast, or PML body perturbation in man, can lead to gene amplifications, deletions, translocations or end-to-end telomere fusion events, thus implicating SUMO and STUbLs in the subnuclear organization of select repair events.
最近的研究结果表明,染色质动力学和核组织不仅对基因调控和 DNA 复制很重要,而且对维持基因组稳定性也很重要。在酵母中,核孔通过进化上保守的 SUMO 靶向泛素连接酶(STUbL)家族在维持基因组稳定性方面发挥作用。酵母 Slx5/Slx8 STUbL 与一类转移到核孔的 DNA 断裂有关。功能上 Slx5/Slx8 通过一种不寻常的重组介导途径对于端粒维持是必需的。哺乳动物的 STUbL RNF4 与早幼粒细胞白血病(PML)核体结合,并调节砷诱导应激下 PML/PML 融合蛋白的稳定性。一类 PML 体通过在端粒酶缺陷肿瘤中 ALT 途径支持端粒维持。通过酵母中核孔亚基的缺失或人类中 PML 体的扰动破坏核组织,可导致基因扩增、缺失、易位或端到端端粒融合事件,从而表明 SUMO 和 STUbL 参与了特定修复事件的亚核组织。