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首页> 外文期刊>Cell cycle >The association of Tap42 phosphatase complexes with TORC1: another level of regulation in Tor signaling.
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The association of Tap42 phosphatase complexes with TORC1: another level of regulation in Tor signaling.

机译:Tap42磷酸酶复合物与TORC1的关联:Tor信号传导的另一个调控水平。

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摘要

In the budding yeast Saccharomyces cerevisiae, rapamycin has been known to induce a rapid dephosphorylation of many downstream targets of Tor. The key components mediating this dephosphorylation process are the Tap42-associated phosphatases, which become active upon rapamycin treatment. However, the mechanism by which rapamycin rapidly activates phosphatases is unclear. A recent report has provided evidence demonstrating a physical association of the Tap42-phosphatase complexes with TORC1, which is sensitive to rapamycin treatment or nutrient starvation. This association adds another level of regulation in Tor signaling, and explains why rapamycin or nutrient availability is able to initiate a rapid and robust response in the cell.
机译:在出芽的酿酒酵母中,已知雷帕霉素可诱导Tor的许多下游靶标快速脱磷酸。介导该去磷酸化过程的关键成分是Tap42相关的磷酸酶,该酶在雷帕霉素治疗后变得活跃。但是,雷帕霉素快速激活磷酸酶的机制尚不清楚。最近的一份报告提供了证据,证明Tap42磷酸酶复合物与TORC1的物理联系,TORC1对雷帕霉素治疗或营养缺乏很敏感。这种联系增加了Tor信号转导的另一个调控水平,并解释了雷帕霉素或营养素利用为何能够在细胞中引发快速而稳定的反应的原因。

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