Cell cycle arrest and morphological alterations following microinjection of NIH3T3 cells with Puraα

被引:54
作者
Stacey, DW
Hitomi, M
Kanovsky, M
Gan, L
Johnson, EM
机构
[1] Cleveland Clin Fdn, Dept Biol Mol, Lerner Res Inst, Cleveland, OH 44195 USA
[2] CUNY Mt Sinai Sch Med, Dept Pathol, New York, NY 10029 USA
[3] CUNY Mt Sinai Sch Med, Brookdale Ctr Mol Biol, New York, NY 10029 USA
关键词
Pura; cell cycle; checkpoint; microinjection; time lapse quantitative photometry;
D O I
10.1038/sj.onc.1202795
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Levels of Pur alpha, a protein implicated in control of both DNA replication and gene transcription, fluctuate during the cell cycle, being lowest in early S phase and highest just after mitosis. Here we have employed a new video time-lapse technique enabling us to determine the cell cycle position of each cell in an asynchronous culture at a given time and to ask whether introduction of Pur alpha protein at specific times can affect cell cycle progression. Approximately 80% of all NIH3T3 cells injected with Pur alpha were inhibited from passing through mitosis, Cells injected with Puree during S or G2 phases were efficiently blocked with a 4N (G2 phase) DNA level, as determined by quantitative DNA photometry of individual cells. Of the cells injected with Pur alpha. during G1 phase, 40% experienced a rapid cell death characterized by extreme cellular fragmentation. Of those G1 injected cells which remained viable, approximately equal numbers were arrested with either 2N or 4N DNA levels. Cells arrested by Pur alpha in G2 phase grew to cover a large surface area. These results link fluctuations in Pur alpha levels to aspects of cell cycle control.
引用
收藏
页码:4254 / 4261
页数:8
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