Department of Chemistry and Molecular Biology, University of Gothenburg, Box 462, 40530 Gothenburg, Sweden.
Mol Microbiol. 2013 Apr;88(1):5-19. doi: 10.1111/mmi.12174. Epub 2013 Mar 6.
All living cells respond to external stimuli and execute specific physiological responses through signal transduction pathways. Understanding the mechanisms controlling signalling pathways is important for diagnosing and treating diseases and for reprogramming cells with desired functions. Although many of the signalling components in the budding yeast Saccharomyces cerevisiae have been identified by genetic studies, many features concerning the dynamic control of pathway activity, cross-talk, cell-to-cell variability or robustness against perturbation are still incompletely understood. Comparing the behaviour of engineered and natural signalling pathways offers insight complementary to that achievable with standard genetic and molecular studies. Here, we review studies that aim at a deeper understanding of signalling design principles and generation of novel signalling properties by engineering the yeast mitogen-activated protein kinase (MAPK) pathways. The underlying approaches can be applied to other organisms including mammalian cells and offer opportunities for building synthetic pathways and functionalities useful in medicine and biotechnology.
所有活细胞都对外界刺激做出响应,并通过信号转导通路执行特定的生理反应。了解控制信号通路的机制对于诊断和治疗疾病以及对具有所需功能的细胞进行重编程非常重要。尽管通过遗传研究已经鉴定出了酿酒酵母(Saccharomyces cerevisiae)中许多信号成分,但关于通路活性的动态控制、串扰、细胞间变异性或对扰动的鲁棒性等许多特征仍然了解得不够完整。比较工程化和天然信号通路的行为提供了与标准遗传和分子研究可获得的互补见解。在这里,我们综述了旨在通过工程化酵母丝裂原活化蛋白激酶(MAPK)通路来更深入地了解信号设计原则和产生新型信号特性的研究。这些基础方法可应用于包括哺乳动物细胞在内的其他生物体,并为构建在医学和生物技术中有用的合成通路和功能提供了机会。