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Cell division, growth and death - Editorial overview

机译:细胞分裂,生长和死亡-编辑概述

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摘要

The size of a cell population -- whether it is the size of a yeast colony on a grape leaf or the size of a cow's liver -- is determined by the rates of three processes in the cells of that population: division, growth, and death. This issue of Current Opinion in Cell Biology focuses on recent advances in our understanding of these processes - with particular emphasis on mechanisms of cell cycle control and programmed cell death (apoptosis). The eukaryotic cell cycle is governed by a complex regulatory system that generates waves of cyclin-dependent kinase (Cdk) activities that trigger cell cycle events. Although we know a great deal about the individual components of this system, we still possess only a limited understanding of how the myriad connections between these components result in the complex behaviours of the system as a whole: how the system generates switch-like Cdk oscillations that are linked together in a properly timed, coordinated and ordered series. Many of the best insights into this problem have come from studies of the transcriptional network that helps drive the cell cycle in the budding yeast Saccharomyces cerevisiae. A handful of transcription factors arc responsible for controlling many of the hundreds of genes that are expressed at specific cell cycle stages. These transcription factors each control genes that stimulate or inhibit the actions of the other factors, resulting in an interwoven regulatory network that has the potential to produce an autonomous cell cycle oscillator. Progress in our understanding of this oscillator has been bolstered recently by the use of powerful new techniques for genome-wide expression analysis and transcription factor target identification. As reviewed by Futcher (pp 676-683), these new techniques are leading to a comprehensive understanding of the regulatory interactions in this system. This allows us not only to refine our models of yeast cell cycle control, but will undoubtedly lead to important insights into the oscillators that control the cell cycle in multicellular eukaryotes.
机译:细胞种群的大小-无论是葡萄叶上的酵母菌落大小还是牛肝的大小-都取决于该种群细胞中三个过程的速率:分裂,生长和死亡。本期《细胞生物学最新观点》着重介绍了我们对这些过程的理解的最新进展,尤其着重于细胞周期控制和程序性细胞死亡(细胞凋亡)的机制。真核细胞周期由复杂的调节系统控制,该系统会产生细胞周期蛋白依赖性激酶(Cdk)活性波,从而触发细胞周期事件。尽管我们对该系统的各个组件了解很多,但对于这些组件之间的无数连接如何导致整个系统的复杂行为,我们仍然只有有限的了解:系统如何生成类似开关的Cdk振荡以适当的时间,协调和有序的序列链接在一​​起。关于此问题的许多最佳见识来自对转录网络的研究,该网络有助于驱动发芽的酵母酿酒酵母中的细胞周期。少数转录因子负责控制在特定细胞周期阶段表达的数百个基因中的许多基因。这些转录因子各自控制刺激或抑制其他因子作用的基因,从而形成交织的调节网络,该网络具有产生自主细胞周期振荡器的潜力。最近,通过使用功能强大的新技术进行全基因组范围内的表达分析和转录因子靶标识别,我们对这种振荡器的理解有了进一步的发展。正如Futcher(pp 676-683)所评论的那样,这些新技术正在导致人们对该系统中监管相互作用的全面理解。这不仅使我们能够完善酵母细胞周期控制模型,而且无疑将对控制多细胞真核生物中细胞周期的振荡器产生重要的见解。

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