首页> 外文期刊>Molecular and Cellular Biology >Expression of p60v-src in Saccharomyces cerevisiae results in elevation of p34CDC28 kinase activity and release of the dependence of DNA replication on mitosis.
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Expression of p60v-src in Saccharomyces cerevisiae results in elevation of p34CDC28 kinase activity and release of the dependence of DNA replication on mitosis.

机译:p60v-src在酿酒酵母中的表达导致p34CDC28激酶活性升高,并释放DNA复制对有丝分裂的依赖性。

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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.
机译:致癌蛋白酪氨酸激酶p60v-src在酿酒酵母中的表达已显示可导致细胞快速死亡(JS Brugge,G。Jarosik,J。Andersen,A。Queral-Lustig,M。Fedor-Chaiken和JR Broach,Mol.Cell.Biol.7:2180-2187,1987)。此处描述的工作证明v-Src表达导致大预算细胞的积累和核分裂阻滞,而不会阻止胞质分裂。流式细胞仪分析表明这些细胞的DNA含量增加到超过G2 DNA含量,遗传研究表明v-Src表达引起非整倍性。控制S.cerevisiae中G1 / S和G2 / M转变的Cdc28激酶的活性在半乳糖诱导过程中在Src +菌株中增加,但在同基因Src-菌株中不增加。这些观察结果表明,v-Src表达破坏了p34CDC28激酶的调控,从而使DNA复制在没有先前有丝分裂事件的情况下得以进行。

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