Wu L, Shiozaki K, Aligue R, Russell P
Department of Molecular Biology, Scripps Research Institute, La Jolla, California 92037, USA.
Mol Biol Cell. 1996 Nov;7(11):1749-58. doi: 10.1091/mbc.7.11.1749.
In Schizosaccharomyces pombe the onset of mitosis is regulated by a network of protein kinases and phosphatases. The M-phase inducing Cdc2-Cdc13 cyclin-dependent kinase is inhibited by Wee1 tyrosine kinase and activated by Cdc25 phosphatase. Wee1 is negatively regulated by Nim1 protein kinase. Here, we describe investigations aimed at better understanding the role of Nim1 in the mitotic control. The most important finding to emerge from these studies is that Wee1 and Nim1 have different patterns of intracellular localization. Immunofluorescence confocal microscopy has revealed that Nim1 is localized in the cytoplasm, whereas it substrate Wee1 is predominantly localized in the nucleus. Previous studies showed that the Cdc2-Cdc13 complex is located in the nucleus. Diversion of Nim1 to the nucleus, accomplished by addition of the SV40 nuclear localization signal, caused the advancement of M, confirming that Nim1 has restricted access to Wee1 in vivo. We propose that the intracellular distribution of Nim1 and Wee1 may serve to coordinate the regulation of nuclear Cdc2-Cdc13 with cytoplasmic growth.
在粟酒裂殖酵母中,有丝分裂的起始由蛋白激酶和磷酸酶网络调控。诱导M期的Cdc2-Cdc13细胞周期蛋白依赖性激酶受Wee1酪氨酸激酶抑制,并被Cdc25磷酸酶激活。Wee1受Nim1蛋白激酶的负调控。在此,我们描述了旨在更好地理解Nim1在有丝分裂控制中作用的研究。这些研究中最重要的发现是,Wee1和Nim1具有不同的细胞内定位模式。免疫荧光共聚焦显微镜显示,Nim1定位于细胞质,而其底物Wee1主要定位于细胞核。先前的研究表明,Cdc2-Cdc13复合物位于细胞核中。通过添加SV40核定位信号将Nim1转移至细胞核,导致M期提前,证实Nim1在体内对Wee1的作用受限。我们认为,Nim1和Wee1的细胞内分布可能有助于协调细胞核Cdc2-Cdc13与细胞质生长的调控。