Xu Yu-Xin, Manley James L
Department of Biological Sciences, Sherman Fairchild Building, Columbia University, New York, NY 10027, USA.
Mol Cell. 2007 Apr 27;26(2):287-300. doi: 10.1016/j.molcel.2007.03.020.
The prolyl isomerase Pin1 plays important roles in numerous cellular processes. Here we provide evidence that Pin1 has an important function in chromosome condensation during mitosis. We first demonstrate that the interaction of Pin1 with chromatin is greatly elevated in G2/M phase and that this correlates with the presence on chromosomes of several mitotic phosphoproteins, especially topoisomerase (Topo) IIalpha. Inducible overexpression of Pin1 was shown to result in higher M phase-specific phosphorylation, while downregulation of Pin1 by siRNA treatment reduced phosphorylation of TopoIIalpha and other mitotic proteins. Furthermore, immunodepletion of Pin1 from mitotic cell extracts prevented such extracts from inducing chromosome condensation when added to S phase nuclei. Indeed, purified Pin1 and cdc2/cyclin B kinase were by themselves sufficient to induce condensation. This reflects the ability of Pin1 to increase TopoIIalpha phosphorylation by cdc2/cyclin B in vitro, which in turn dramatically increased formation of a TopoIIalpha/Pin1/DNA complex.
脯氨酰异构酶Pin1在众多细胞过程中发挥着重要作用。在此,我们提供证据表明Pin1在有丝分裂期间的染色体浓缩过程中具有重要功能。我们首先证明,Pin1与染色质的相互作用在G2/M期显著增强,且这与几种有丝分裂磷酸化蛋白,特别是拓扑异构酶(Topo)IIα在染色体上的存在相关。Pin1的诱导性过表达导致更高的M期特异性磷酸化,而通过siRNA处理下调Pin1则降低了TopoIIα和其他有丝分裂蛋白的磷酸化。此外,从有丝分裂细胞提取物中免疫去除Pin1后,当将此类提取物添加到S期细胞核时,会阻止其诱导染色体浓缩。实际上,纯化的Pin1和cdc2/细胞周期蛋白B激酶自身就足以诱导染色体浓缩。这反映出Pin1在体外能够通过cdc2/细胞周期蛋白B增加TopoIIα的磷酸化,进而显著增加TopoIIα/Pin1/DNA复合物的形成。