Kobiler Oren, Rokney Assaf, Friedman Nir, Court Donald L, Stavans Joel, Oppenheim Amos B
Department of Molecular Genetics and Biotechnology, Hebrew University-Hadassah Medical School, Jerusalem 91120, Israel.
Proc Natl Acad Sci U S A. 2005 Mar 22;102(12):4470-5. doi: 10.1073/pnas.0500670102. Epub 2005 Feb 22.
The lysis-lysogeny decision of bacteriophage lambda has been a paradigm for a developmental genetic network, which is composed of interlocked positive and negative feedback loops. This genetic network is capable of responding to environmental signals and to the number of infecting phages. An interplay between CI and Cro functions suggested a bistable switch model for the lysis-lysogeny decision. Here, we present a real-time picture of the execution of lytic and lysogenic pathways with unprecedented temporal resolution. We monitor, in vivo, both the level and function of the CII and Q gene regulators. These activators are cotranscribed yet control opposite developmental pathways. Conditions that favor the lysogenic response show severe delay and down-regulation of Q activity, in both CII-dependent and CII-independent ways. Whereas CII activity correlates with its protein level, Q shows a pronounced threshold before its function is observed. Our quantitative analyses suggest that by regulating CII and CIII, Cro plays a key role in the ability of the lambda genetic network to sense the difference between one and more than one phage particles infecting a cell. Thus, our results provide an improved framework to explain the longstanding puzzle of the decision process.
噬菌体λ的裂解-溶原化决定一直是发育遗传网络的范例,该网络由相互连锁的正反馈和负反馈回路组成。这个遗传网络能够响应环境信号和感染噬菌体的数量。CI和Cro功能之间的相互作用为裂解-溶原化决定提出了一个双稳态开关模型。在这里,我们以前所未有的时间分辨率呈现了裂解和溶原途径执行的实时情况。我们在体内监测CII和Q基因调节因子的水平和功能。这些激活因子是共转录的,但控制相反的发育途径。有利于溶原反应的条件以依赖CII和不依赖CII的方式显示出Q活性的严重延迟和下调。虽然CII活性与其蛋白质水平相关,但Q在其功能被观察到之前显示出明显的阈值。我们的定量分析表明,通过调节CII和CIII,Cro在λ遗传网络感知感染细胞的一个和多个以上噬菌体颗粒之间差异的能力中起关键作用。因此,我们的结果提供了一个改进的框架来解释决策过程中长期存在的谜题。