首页> 外文期刊>Journal of Cell Science >THE KINETICS OF THE B CYCLIN P56(CDC13) AND THE PHOSPHATASE P80(CDC25) DURING THE CELL CYCLE OF THE FISSION YEAST SCHIZOSACCHAROMYCES POMBE
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THE KINETICS OF THE B CYCLIN P56(CDC13) AND THE PHOSPHATASE P80(CDC25) DURING THE CELL CYCLE OF THE FISSION YEAST SCHIZOSACCHAROMYCES POMBE

机译:裂殖酵母裂殖糖酵母细胞周期中B环蛋白P56(CDC13)和磷酸酶P80(CDC25)的动力学

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The levels of the B cyclin p56(cdc13) and the phosphatase p80(cdc25) have been followed in selection-synchronised cultures of Schizosaccharomyces pombe wild-type and wee1 mutant cells. p56(cdc13) has also been followed in induction-synchronised cells of the mutant cdc2-33. The main conclusions are: (1) cdc13 levels in wild-type cells start to rise from base line at about mid-G(2), reach a peak before mitosis and then fall slowly through G(1). Cells exit mitosis with appreciable levels of cdc13. (2) cdc13 levels in wee1 cells fall to zero in interphase. They also start to rise at the beginning of G(2), which may be related to the absence of a mitotic size control, (3) cdc25 starts to rise later and reaches a peak after mitosis. This is not what would be expected from a simple mitotic inducer and suggests that cdc25 has an important function at the end of mitosis. (4) An upper (heavier) band of cdc25 peaks at the same time as the main band but rises and falls more rapidly. If this is a hyperphosphorylated form, its timing shows that it is most unlikely to function in the ways shown for such a form in eggs and mammalian cells. (5) Experiments with the mutant cdc10-129 and with hydroxyurea show that the initial signal to begin synthesis of cdc13 originates at Start. (6) In induction synchrony, where G(2) spans across cell division, there is evidence that some events in one cycle cannot start in the previous one. (7) Revised timings are given for the times of mitosis in these cultures. [References: 34]
机译:B cyclin p56(cdc13)和磷酸酶p80(cdc25)的水平已在粟酒裂殖酵母野生型和wee1突变细胞的选择同步培养物中进行了跟踪。 p56(cdc13)也已经在突变的cdc2-33的诱导同步细胞中被追踪。主要结论是:(1)野生型细胞中的cdc13水平在G(2)左右从基线开始上升,在有丝分裂之前达到峰值,然后缓慢通过G(1)下降。细胞以一定水平的cdc13退出有丝分裂。 (2)wee1细胞中的cdc13水平在相间降至零。它们也从G(2)的开始开始上升,这可能与缺乏有丝分裂大小控制有关。(3)cdc25开始上升,随后在有丝分裂后达到峰值。这不是简单的有丝分裂诱导剂所预期的结果,并且表明cdc25在有丝分裂结束时具有重要的功能。 (4)cdc25的较高(较重)频带与主频带同时达到峰值,但上升和下降更快。如果这是一种高磷酸化形式,则其时间表明,它极不可能以这种形式在卵和哺乳动物细胞中发挥作用。 (5)使用突变体cdc10-129和羟基脲进行的实验表明,开始合成cdc13的初始信号始于Start。 (6)在感应同步中,G(2)跨细胞分裂,有证据表明一个周期中的某些事件不能在前一个周期中开始。 (7)修改了这些文化中有丝分裂的时间。 [参考:34]

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