Saiwaki Takuya, Kotera Ippei, Sasaki Mitsuho, Takagi Masatoshi, Yoneda Yoshihiro
Department of Cell Biology and Neuroscience, Graduate School of Medicine, Osaka University, 2-2 Yamada-oka, Suita, Osaka 565-0871, Japan.
Exp Cell Res. 2005 Aug 1;308(1):123-34. doi: 10.1016/j.yexcr.2005.04.010.
A cell proliferation marker protein, pKi-67, distributes to the chromosome periphery during mitosis and nucleolar heterochromatin in the interphase. We report here on the structural domains of pKi-67 that are required for its correct distribution. While both the LR domain and the conserved domain were involved in localization to the nucleolar heterochromatin, both the LR domain and the Ki-67 repeat domain were required for its distribution to the mitotic chromosome periphery. Using in vivo time-lapse microscopy, GFP-pKi-67 was dynamically tracked from the mitotic chromosome periphery to reforming nucleoli via prenucleolar bodies (PNBs). The signals in PNBs then moved towards and fused into the reforming nucleoli with a thin string-like fluorescence during early G1 phase. An analysis of the in vivo kinetics of pKi-67 using photobleaching indicated that the association of pKi-67 with chromatin was progressively altered from "loose" to "tight" after the onset of anaphase. These findings indicate that pKi-67 dynamically alters the nature of the interaction with chromatin structure during the cell cycle, which is closely related to the reformation process of the interphase nucleolar chromatin.
一种细胞增殖标记蛋白pKi - 67,在有丝分裂期间分布于染色体周边,在间期分布于核仁异染色质。我们在此报告pKi - 67正确分布所需的结构域。虽然LR结构域和保守结构域都参与了定位于核仁异染色质,但LR结构域和Ki - 67重复结构域都是其分布到有丝分裂染色体周边所必需的。使用体内延时显微镜,GFP - pKi - 67从有丝分裂染色体周边通过前核仁体(PNB)动态追踪到重新形成的核仁。然后在G1早期阶段,PNB中的信号朝着重新形成的核仁移动,并以细的线状荧光融合到核仁中。使用光漂白对pKi - 67的体内动力学分析表明,后期开始后,pKi - 67与染色质的结合逐渐从“松散”变为“紧密”。这些发现表明,pKi - 67在细胞周期中动态改变与染色质结构相互作用的性质,这与间期核仁染色质的重新形成过程密切相关。