Walter Joachim, Schermelleh Lothar, Cremer Marion, Tashiro Satoshi, Cremer Thomas
Dept. Biologie II, Lehrstuhl für Anthropologie und Humangenetik, LMU, Richard-Wagner-Strasse 10/I, 80333 München, Germany.
J Cell Biol. 2003 Mar 3;160(5):685-97. doi: 10.1083/jcb.200211103. Epub 2003 Feb 25.
Whether chromosomes maintain their nuclear positions during interphase and from one cell cycle to the next has been controversially discussed. To address this question, we performed long-term live-cell studies using a HeLa cell line with GFP-tagged chromatin. Positional changes of the intensity gravity centers of fluorescently labeled chromosome territories (CTs) on the order of several microm were observed in early G1, suggesting a role of CT mobility in establishing interphase nuclear architecture. Thereafter, the positions were highly constrained within a range of approximately 1 microm until the end of G2. To analyze possible changes of chromosome arrangements from one cell cycle to the next, nuclei were photobleached in G2 maintaining a contiguous zone of unbleached chromatin at one nuclear pole. This zone was stably preserved until the onset of prophase, whereas the contiguity of unbleached chromosome segments was lost to a variable extent, when the metaphase plate was formed. Accordingly, chromatin patterns observed in daughter nuclei differed significantly from the mother cell nucleus. We conclude that CT arrangements were stably maintained from mid G1 to late G2/early prophase, whereas major changes of CT neighborhoods occurred from one cell cycle to the next. The variability of CT neighborhoods during clonal growth was further confirmed by chromosome painting experiments.
染色体在间期以及从一个细胞周期到下一个细胞周期过程中是否维持其在细胞核内的位置一直存在争议。为了解决这个问题,我们使用带有绿色荧光蛋白标记染色质的HeLa细胞系进行了长期活细胞研究。在G1早期观察到荧光标记的染色体区域(CTs)强度重心发生了几微米量级的位置变化,这表明CT移动性在建立间期核结构中发挥了作用。此后,直到G2期末,这些位置都被高度限制在大约1微米的范围内。为了分析从一个细胞周期到下一个细胞周期染色体排列可能发生的变化,在G2期对细胞核进行光漂白,在一个核极保留一个未漂白染色质的连续区域。这个区域一直稳定保存到前期开始,而当形成中期板时,未漂白染色体片段的连续性在不同程度上丧失了。因此,在子细胞核中观察到的染色质模式与母细胞核有显著差异。我们得出结论,CT排列从G1中期到G2晚期/前期早期是稳定维持的,而CT邻域从一个细胞周期到下一个细胞周期发生了重大变化。染色体涂染实验进一步证实了克隆生长过程中CT邻域的变异性。