Sekimoto T, Nakajima K, Tachibana T, Hirano T, Yoneda Y
Department of Anatomy and Cell Biology, Biomedical Research Center, Osaka University Medical School, 2-2 Yamada-oka, Suita, Osaka 565, Japan.
J Biol Chem. 1996 Dec 6;271(49):31017-20. doi: 10.1074/jbc.271.49.31017.
In response to interferon-gamma (IFN-gamma), Stat1 enters the nucleus, where it activates transcription. In order to better understand the mechanism of the extracellular signal-induced protein import into the nucleus, we have established an in vivo assay system that uses recombinant Stat1 protein as a model transport substrate. Using this system, we found that Stat1 is actively transported through the nuclear pores in an IFN-gamma-dependent manner and tyrosine (Tyr701) phosphorylation of Stat1 is actually required for its nuclear import. When the antibody against Ran, which was identified as an essential factor for active nuclear protein transport, was injected, the IFN-gamma-dependent nuclear transport of Stat1 was completely inhibited. Furthermore, nuclear import of Stat1 was suppressed by microinjection of two mutant Ran proteins, one defective in GTP hydrolysis (G19V) and the other with little or no binding to GTP (T24N), both of which are known to act as dominant negative inhibitors of nuclear import. These results indicate that the conditional nuclear import of Stat1 requires GTP hydrolysis by Ran.
在干扰素-γ(IFN-γ)的作用下,信号转导子和转录激活子1(Stat1)进入细胞核并在其中激活转录。为了更好地理解细胞外信号诱导的蛋白质进入细胞核的机制,我们建立了一种体内检测系统,该系统使用重组Stat1蛋白作为模型转运底物。利用这个系统,我们发现Stat1以IFN-γ依赖的方式通过核孔进行主动转运,并且Stat1的酪氨酸(Tyr701)磷酸化实际上是其核输入所必需的。当注射针对Ran的抗体时,Stat1的IFN-γ依赖的核转运被完全抑制,Ran被确定为主动核蛋白转运的必需因子。此外,通过显微注射两种突变的Ran蛋白抑制了Stat1的核输入,一种在GTP水解方面有缺陷(G19V),另一种与GTP的结合很少或没有结合(T24N),这两种蛋白都已知作为核输入的显性负性抑制剂起作用。这些结果表明,Stat1的条件性核输入需要Ran进行GTP水解。