Huang Hua-Shan, Pozarowski Piotr, Gao Yan, Darzynkiewicz Zbigniew, Lee Ernest Y C
Department of Biochemistry and Molecular Biology, New York Medical College, Valhalla, NY 10595, USA.
Arch Biochem Biophys. 2005 Nov 15;443(1-2):33-44. doi: 10.1016/j.abb.2005.08.021.
In this study, we show that protein phosphatase-1 (PP1) inhibitor-3 (Inh3) is localized to the nucleoli and centrosomes in interphase HEK 293 cells. Inh3 exhibited a specific co-localization to the nucleoli with PP1gamma1, and to the centrosomes with PP1alpha. These findings indicate that Inh3 may act as a modulator of PP1 functions in the processes of cytokinesis, as well as of nucleolar events. The specificity of the interaction of Inh3 with the PP1 isoforms was also demonstrated in vitro, where Inh3 co-immunoprecipitated with PP1alpha and PP1gamma1, but not with PP1beta. The nuclear localization signal of Inh3 was identified as a N-terminal basic cluster (33RKRK36), while nucleolar localization was shown to be dependent on a C-terminal basic cluster (94HRKGRRR100). The importance of the individual basic residues was quantitatively assessed by site-directed mutagenesis and a novel use of laser scanning cytometry.
在本研究中,我们发现蛋白磷酸酶-1(PP1)抑制剂-3(Inh3)定位于间期人胚肾293细胞的核仁及中心体。Inh3与PP1γ1在核仁处呈现特异性共定位,与PP1α在中心体处呈现特异性共定位。这些发现表明,Inh3可能在胞质分裂以及核仁相关事件过程中作为PP1功能的调节因子发挥作用。Inh3与PP1亚型相互作用的特异性在体外实验中也得到了证实,在体外实验中,Inh3与PP1α和PP1γ1进行了共免疫沉淀,但未与PP1β进行共免疫沉淀。Inh3的核定位信号被确定为N端碱性簇(33RKRK36),而核仁定位则显示依赖于C端碱性簇(94HRKGRRR100)。通过定点诱变和激光扫描细胞术的一种新应用,对各个碱性残基的重要性进行了定量评估。