Moreno S, Nurse P, Russell P
Department of Biochemistry, University of Oxford, UK.
Nature. 1990 Apr 5;344(6266):549-52. doi: 10.1038/344549a0.
The coordination of somatic cell division with cell size must be accomplished by the accumulation of mitotic inducers or the dilution, in the course of cell growth, of mitotic inhibitors. In fission yeast (Schizosaccharomyces pombe), cell size at mitosis is determined by expression of the cdc25+ and nim1+ inducer genes and of the inhibitor gene wee1+, which between them regulate the M-phase protein kinase p34cdc2. We now report that both the phosphoprotein product of cdc25+ (p80cdc25, with apparent relative molecular mass 80,000) and the corresponding messenger RNA increase in concentration as cells proceed through interphase, peaking at mitosis. We propose that the cell-cycle timing of mitosis in somatic cells is regulated by the cyclic accumulation of the cdc25 mitotic inducer, which on reaching a critical level results in activation of p34cdc2 protein kinase. Accumulation of this inducer could play a part in coordinating cell division with growth.
体细胞分裂与细胞大小的协调必须通过有丝分裂诱导物的积累或在细胞生长过程中有丝分裂抑制剂的稀释来实现。在裂殖酵母(粟酒裂殖酵母)中,有丝分裂时的细胞大小由cdc25⁺和nim1⁺诱导基因以及抑制剂基因wee1⁺的表达决定,它们共同调节M期蛋白激酶p34cdc2。我们现在报告,随着细胞进入分裂间期,cdc25⁺的磷蛋白产物(p80cdc25,表观相对分子质量为80,000)和相应的信使核糖核酸浓度都会增加,并在有丝分裂时达到峰值。我们提出,体细胞有丝分裂的细胞周期时间是由cdc25有丝分裂诱导物的周期性积累调节的,当达到临界水平时会导致p34cdc2蛋白激酶的激活。这种诱导物的积累可能在协调细胞分裂与生长方面发挥作用。