Kim Myoung-Dong, Hong Seung-Pyo, Carlson Marian
Department of Genetics and Development and Microbiology, Columbia University, HSC922, New York, NY 10032, USA.
Eukaryot Cell. 2005 May;4(5):861-6. doi: 10.1128/EC.4.5.861-866.2005.
In Saccharomyces cerevisiae, Snf1 protein kinase of the Snf1/AMP-activated protein kinase family is required for growth on nonfermentable carbon sources and nonpreferred sugars. Three kinases, Pak1, Elm1, and Tos3, activate Snf1 by phosphorylation of its activation-loop threonine, and the absence of all three causes the Snf(-) phenotype. No phenotype has previously been reported for the tos3Delta single mutation. We show here that, when cells are grown on glycerol-ethanol, tos3Delta reduces growth rate, Snf1 catalytic activity, and activation of the Snf1-dependent carbon source-responsive element (CSRE) in the promoters of gluconeogenic genes. In contrast, tos3Delta did not significantly affect Snf1 catalytic activity or CSRE function during abrupt glucose depletion, indicating that Tos3 has a more substantial role in activating Snf1 protein kinase during growth on a nonfermentable carbon source than during acute carbon stress. We also report that Tos3 is localized in the cytosol during growth in either glucose or glycerol-ethanol. These findings lend support to the idea that the Snf1 protein kinase kinases make different contributions to cellular regulation under different growth conditions.
在酿酒酵母中,Snf1/AMP激活蛋白激酶家族的Snf1蛋白激酶是在非发酵性碳源和非首选糖类上生长所必需的。三种激酶,即Pak1、Elm1和Tos3,通过磷酸化Snf1的激活环苏氨酸来激活Snf1,而这三种激酶全部缺失会导致Snf(-)表型。此前尚未有关于tos3Δ单突变表型的报道。我们在此表明,当细胞在甘油 - 乙醇上生长时,tos3Δ会降低生长速率、Snf1催化活性以及糖异生基因启动子中Snf1依赖性碳源响应元件(CSRE)的激活。相比之下,在突然葡萄糖耗尽期间,tos3Δ对Snf1催化活性或CSRE功能没有显著影响,这表明Tos3在非发酵性碳源上生长期间激活Snf1蛋白激酶方面比在急性碳胁迫期间发挥着更重要的作用。我们还报道,在葡萄糖或甘油 - 乙醇中生长时,Tos3定位于细胞质中。这些发现支持了Snf1蛋白激酶激酶在不同生长条件下对细胞调节做出不同贡献的观点。