Cameroni Elisabetta, Hulo Nicolas, Roosen Johnny, Winderickx Joris, De Virgilio Claudio
Department of Microbiology and Molecular Medicine, Centre Médical Universitaire, Univeristy of Geneva, Switzerland.
Cell Cycle. 2004 Apr;3(4):462-8.
The highly conserved PKA and TOR proteins define key signaling pathways that control cell proliferation in response to growth factors and/or nutrients. In yeast, inactivation of PKA and/or TOR causes cells to arrest growth early G1 and induces a program that is characteristic of G0 cells. We have recently shown that the protein kinase Rim15 integrates both PKA- and TOR-mediated signals. In this work, we demonstrate that the Rim15-activated genomic expression program following glucose limitation at the diauxic shift is mediated by the three transcription factors Gis1, Msn2, and Msn4. The Rim15 regulon comprises several gene clusters implicated in the adaptation to respiratory growth, including classical oxidative stress genes such as SOD1 and SOD2, suggesting that the reduced life span of rim15delta cells may be due to their deficiency in oxidative damage prevention. Interestingly, we found that the primary amino acid sequence of Rim15 includes in its amino-terminal part a conserved PAS domain, known to act as a sensor for a variety of stimuli, We propose that Rim15 has evolved to integrate nutrient signals (transduced via TOR and PKA) and redox and/or oxidative stress signals to appropriately induce a transcriptional program that ensures survival in G0.
高度保守的蛋白激酶A(PKA)和雷帕霉素靶蛋白(TOR)定义了关键的信号通路,这些通路响应生长因子和/或营养物质来控制细胞增殖。在酵母中,PKA和/或TOR的失活会导致细胞在G1早期停止生长,并诱导出一种G0细胞特有的程序。我们最近发现,蛋白激酶Rim15整合了PKA和TOR介导的信号。在这项工作中,我们证明在双相转变时葡萄糖受限后,Rim15激活的基因组表达程序是由三个转录因子Gis1、Msn2和Msn4介导的。Rim15调控子包括几个与适应呼吸生长有关的基因簇,包括经典的氧化应激基因如SOD1和SOD2,这表明rim15delta细胞寿命缩短可能是由于它们在预防氧化损伤方面存在缺陷。有趣的是,我们发现Rim15的一级氨基酸序列在其氨基末端部分包含一个保守的PAS结构域,已知该结构域可作为多种刺激的传感器。我们提出,Rim15已经进化到可以整合营养信号(通过TOR和PKA传导)以及氧化还原和/或氧化应激信号,并适当地诱导一个转录程序,以确保在G0期存活。