Boschelli F
Department of Biochemistry, Wayne State University School of Medicine, Detroit, Michigan 48201.
Mol Cell Biol. 1993 Aug;13(8):5112-21. doi: 10.1128/mcb.13.8.5112-5121.1993.
Expression of the oncogenic protein tyrosine kinase p60v-src in the yeast Saccharomyces cerevisiae has been shown to result in rapid cell death (J. S. Brugge, G. Jarosik, J. Andersen, A. Queral-Lustig, M. Fedor-Chaiken, and J. R. Broach, Mol. Cell. Biol. 7:2180-2187, 1987). Work described here demonstrates that v-Src expression results in accumulation of large-budded cells and a nuclear division block without blocking cytokinesis. Flow-cytometric analysis indicates that the DNA content of these cells is elevated beyond the G2 DNA content, and genetic studies indicate that v-Src expression causes aneuploidy. The activity of Cdc28 kinase, which controls the G1/S and G2/M transitions in S. cerevisiae, increases during galactose induction in a Src+ strain but not in an isogenic Src- strain. These observations indicate that v-Src expression disrupts p34CDC28 kinase regulation, allowing DNA replication to proceed in the absence of a prior mitotic event.
致癌蛋白酪氨酸激酶p60v-src在酿酒酵母中的表达已被证明会导致细胞迅速死亡(J. S. 布鲁格、G. 亚罗西克、J. 安德森、A. 奎拉尔-卢斯蒂格、M. 费多尔-柴肯和J. R. 布罗奇,《分子细胞生物学》7:2180 - 2187,1987年)。本文所述的研究表明,v-Src的表达会导致大芽殖细胞的积累以及核分裂阻滞,但不影响胞质分裂。流式细胞术分析表明,这些细胞的DNA含量升高超过了G2期的DNA含量,遗传学研究表明v-Src的表达会导致非整倍体。控制酿酒酵母中G1/S和G2/M转换的Cdc28激酶的活性,在Src+菌株的半乳糖诱导过程中会增加,但在同基因的Src-菌株中则不会。这些观察结果表明,v-Src的表达会破坏p34CDC28激酶的调节,使得DNA复制在没有先前有丝分裂事件的情况下仍能进行。