Department of Medicine, University of Chicago, 5841 S. Maryland Avenue, MC6026, Chicago, IL 60637, USA.
Am J Respir Cell Mol Biol. 2011 Sep;45(3):453-8. doi: 10.1165/rcmb.2008-0393OC. Epub 2010 Dec 3.
We have previously shown that the transcription-promoting activity of serum response factor (SRF) is partially regulated by its extranuclear redistribution. In this study, we examined the cellular mechanisms that facilitate SRF nuclear entry in canine tracheal smooth muscle cells. We used in vitro pull-down assays to determine which karyopherin proteins bound SRF and found that SRF binds KPNA1 and KPNB1 through its nuclear localization sequence. Immunoprecipitation studies also demonstrated direct SRF-KPNA1 interaction in HEK293 cells. Import assays demonstrated that KPNA1 and KPNB1 together were sufficient to mediate rapid nuclear import of SRF-GFP. Our studies also suggest that SRF is able to gain nuclear entry through an auxiliary, nuclear localization sequence-independent mechanism.
我们之前已经表明,血清反应因子(SRF)的转录促进活性部分受其核外重新分布调控。在这项研究中,我们研究了促进犬气管平滑肌细胞中 SRF 核内进入的细胞机制。我们使用体外下拉测定法来确定与 SRF 结合的核转运蛋白,发现 SRF 通过其核定位序列与 KPNA1 和 KPNB1 结合。免疫沉淀研究也表明在 HEK293 细胞中存在直接的 SRF-KPNA1 相互作用。导入测定表明,KPNA1 和 KPNB1 共同足以介导 SRF-GFP 的快速核内导入。我们的研究还表明,SRF 能够通过辅助的、不依赖核定位序列的机制获得核内进入。