Creanor J, Mitchison J M
Institute of Cell, Animal and Population Biology, University of Edinburgh, Ashworth Laboratories, Scotland, UK.
J Cell Sci. 1994 May;107 ( Pt 5):1197-204. doi: 10.1242/jcs.107.5.1197.
H1 histone kinase activity has been followed in selection-synchronised cultures of fission yeast wild-type and wee1 mutant cells, and in induction-synchronised cells of the mutant cdc2-33. The main conclusions are: (1) in all three cases, the peak of activity is near mitosis. (2) The rise in activity is relatively slow starting in wild type at 0.4 of the cycle before mitosis. It is proposed that the beginning of the rise is the first identified event in the mitotic control. (3) The rise is twice as fast in wee and starts nearer to mitosis. (4) In all cases the beginning of the rise is in G2. (5) The fall in activity is also slow, lasting for 0.25 of the cycle, in wild type. Exit from mitosis happens well before activity has fallen to baseline. (6) In a range of size mutants, activity is roughly proportional to cell size. It is suggested that the kinase may have a cytoplasmic function. (7) Estimates have been made of the timing of mitosis in the mutants. In wee, mitosis is 0.14 of the cycle earlier than in wild type because the cells have a longer septated period at the end of the cycle. (8) A novel method has been developed for eliminating the effects of the partial asynchrony in synchronous cultures, without which the kinetic analysis would have been inaccurate.
在裂殖酵母野生型和wee1突变体细胞的选择同步培养物中,以及在突变体cdc2 - 33的诱导同步细胞中,对H1组蛋白激酶活性进行了跟踪研究。主要结论如下:(1) 在所有这三种情况下,活性峰值都接近有丝分裂期。(2) 活性上升相对缓慢,在野生型中从有丝分裂前0.4个细胞周期开始。有人提出,活性上升的开始是有丝分裂调控中第一个被确定的事件。(3) 在wee1突变体中,活性上升速度快两倍,且开始时间更接近有丝分裂期。(4) 在所有情况下,活性上升均始于G2期;(5) 在野生型中,活性下降也很缓慢,持续0.25个细胞周期,细胞退出有丝分裂期远在活性降至基线之前。(6) 在一系列大小突变体中,活性大致与细胞大小成正比,提示该激酶可能具有细胞质功能。(7) 已对突变体中有丝分裂的时间进行估计。在wee1突变体中,有丝分裂比野生型早0.14个细胞周期出现,因为细胞在周期末期具有更长的分隔期。(8) 已开发出一种新方法,用于消除同步培养物中部分异步性的影响,否则动力学分析将不准确。