首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Antagonistic Interactions Between the cAMP-Dependent Protein Kinase and Tor Signaling Pathways Modulate Cell Growth in Saccharomyces cerevisiae
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Antagonistic Interactions Between the cAMP-Dependent Protein Kinase and Tor Signaling Pathways Modulate Cell Growth in Saccharomyces cerevisiae

机译:cAMP依赖性蛋白激酶和Tor信号通路之间的拮抗相互作用调节酿酒酵母中的细胞生长。

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摘要

Eukaryotic cells integrate information from multiple sources to respond appropriately to changes in the environment. Here, we examined the relationship between two signaling pathways in Saccharomyces cerevisiae that are essential for the coordination of cell growth with nutrient availability. These pathways involve the cAMP-dependent protein kinase (PKA) and Tor proteins, respectively. Although these pathways control a similar set of processes important for growth, it was not clear how their activities were integrated in vivo. The experiments here examined this coordination and, in particular, tested whether the PKA pathway was primarily a downstream effector of the TORC1 signaling complex. Using a number of reporters for the PKA pathway, we found that the inhibition of TORC1 did not result in diminished PKA signaling activity. To the contrary, decreased TORC1 signaling was generally associated with elevated levels of PKA activity. Similarly, TORC1 activity appeared to increase in response to lower levels of PKA signaling. Consistent with these observations, we found that diminished PKA signaling partially suppressed the growth defects associated with decreased TORC1 activity. In all, these data suggested that the PKA and TORC1 pathways were functioning in parallel to promote cell growth and that each pathway might restrain, either directly or indirectly, the activity of the other. The potential significance of this antagonism for the regulation of cell growth and overall fitness is discussed.
机译:真核细胞整合了来自多种来源的信息,以对环境的变化做出适当的反应。在这里,我们检查了酿酒酵母中两个信号通路之间的关系,这对于协调细胞生长与养分利用率至关重要。这些途径分别涉及cAMP依赖性蛋白激酶(PKA)和Tor蛋白。尽管这些途径控制着一系列对生长至关重要的过程,但尚不清楚它们的活性如何在体内整合。此处的实验检查了这种协调,尤其是测试了PKA途径是否主要是TORC1信号复合物的下游效应子。使用许多PKA通路的报告基因,我们发现抑制TORC1不会导致PKA信号传导活性降低。相反,降低的TORC1信号传导通常与PKA活性水平升高有关。同样,TORC1活性似乎响应于较低水平的PKA信号传导而增加。与这些观察结果一致,我们发现减弱的PKA信号传导部分抑制了与TORC1活性降低相关的生长缺陷。总之,这些数据表明,PKA和TORC1途径并行发挥作用,以促进细胞生长,并且每种途径都可能直接或间接抑制另一种途径的活性。讨论了这种拮抗作用对细胞生长和整体适应性调节的潜在意义。

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