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Regulation of a Cyclin-CDK-CDK Inhibitor Complex by Inositol Pyrophosphates

机译:肌醇焦磷酸盐对Cyclin-CDK-CDK抑制剂复合物的调节

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摘要

In budding yeast, phosphate starvation triggers inhibition of the Pho80-Pho85 cyclin-cyclin-dependent kinase (CDK) complex by the CDK inhibitor Pho81, leading to expression of genes involved in nutrient homeostasis. We isolated myo-D-inositol heptakisphosphate (IP_7) as a cellular component that stimulates Pho81-dependent inhibition of Pho80-Pho85. IP_7 is necessary for Pho81-dependent inhibition of Pho80-Pho85 in vitro. Moreover, intracellular concentrations of IP_7 increased upon phosphate starvation, and yeast mutants defective in IP_7 production failed to inhibit Pho80-Pho85 in response to phosphate starvation. These observations reveal regulation of a cyclin-CDK complex by a metabolite and suggest that a complex metabolic network mediates signaling of phosphate availability.
机译:在出芽的酵母中,磷酸饥饿会触发CDK抑制剂Pho81对Pho80-Pho85细胞周期蛋白-细胞周期蛋白依赖性激酶(CDK)复合物的抑制,从而导致营养平衡的基因表达。我们分离了肌D-肌醇七磷酸(IP_7)作为刺激Pho81依赖Pho80-Pho85抑制的细胞成分。 IP_7对于体外依赖Pho81抑制Pho80-Pho85是必需的。此外,细胞内IP_7的浓度在磷酸盐饥饿时增加,并且IP_7产生缺陷的酵母突变体未能响应磷酸盐饥饿而抑制Pho80-Pho85。这些观察揭示了代谢物对细胞周期蛋白-CDK复合物的调节,并表明复合物代谢网络介导了磷酸盐可用性的信号。

著录项

  • 来源
    《Science》 |2007年第5821期|p.109-112|共4页
  • 作者单位

    Howard Hughes Medical Institute, Faculty of Arts and Sciences Center for Systems Biology, Department of Molecular and Cellular Biology, Harvard University, 7 Divinity Avenue, Cambridge, MA 02138, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 自然科学总论;
  • 关键词

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