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Tunable signal processing in synthetic mitogen-activated protein kinase cascades.

机译:合成的有丝分裂原激活的蛋白激酶级联反应中的可调信号处理。

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摘要

Mitogen-activated protein kinase (MAPK) cascades regulate a vast array of cell-fate decisions. The ability of this module to control diverse processes stems, in part, from its capacity for flexible activation responses. The mechanisms underlying the plasticity of this response have not been fully elucidated and are difficult to parse out given the multifaceted regulation found in signaling networks. We have constructed a synthetic mammalian MAPK cascade in yeast to explore the effects of intrinsic perturbations (concentration variation) and extrinsic perturbations (scaffolding and negative regulation) on the flexibility of this isolated signaling module. Experimentally, increasing the concentration of sequential kinases augmented ultrasensitivity and lowered the threshold of activation. Computational analyses of these intrinsic perturbations indicate that two, well characterized, natural cascades in X. laevis and S. cerevisiae with distinct activation profiles are innately biased toward their respective behaviors by kinase concentration. We also showed that signal propagation through this catalytically efficient cascade is unaltered by moderate scaffold co-expression yet it is greatly attenuated at high scaffold levels. Further, over-expression of the scaffold resulted in a biphasic Hill response. We hypothesized that this complex activation profile arises from sequestration and we tested this computationally with a compartmental model. We showed that negative regulation by both enzymatic phosphatase expression and small-molecule inhibitor binding attenuated the ultrasensitivity and increased the threshold of activation over the range of experimental parameters. Interestingly, a computational model integrating negative regulation and concentration variation revealed parameter regimes in which these different modes of regulation enable distinct activation responses. This integrated computational model also predicted parameters for which specific signal characteristics can be decoupled and we demonstrated this effect experimentally by tuning the ultrasensitivity and threshold independently from the strength of the response. This work demonstrates that tunable signal processing is an inherent feature of minimal MAPK modules and elucidates principles for rational design of more complex synthetic signaling systems.
机译:丝裂原激活的蛋白激酶(MAPK)级联调节多种细胞命运决定。该模块控制各种过程的能力部分源于其灵活的激活响应能力。鉴于在信号网络中发现的多方面的规定,尚未完全阐明这种反应可塑性的基础机制,并且难以解析。我们已经在酵母中构建了一个合成的哺乳动物MAPK级联反应,以探索内源性扰动(浓度变化)和外源性扰动(脚手架和负调控)对该隔离信号模块的灵活性的影响。实验上,增加顺序激酶的浓度可增强超敏性并降低激活阈值。这些内在扰动的计算分析表明,在X. laevis和S. cerevisiae中,两个具有良好活化特性的,特征充分的自然级联通过激酶浓度先天偏向于它们各自的行为。我们还表明,通过这种催化有效级联的信号传播不会受到中等支架共表达的影响,但在高支架水平下会大大衰减。此外,支架的过表达导致双相希尔反应。我们假设这种复杂的激活模式是由螯合引起的,并且我们使用隔室模型对此进行了计算测试。我们表明酶磷酸酶表达和小分子抑制剂结合的负调控减弱了超敏性,并在整个实验参数范围内增加了激活阈值。有趣的是,整合了负调节和浓度变化的计算模型揭示了参数机制,其中这些不同的调节模式能够实现不同的激活响应。这种集成的计算模型还预测了可以解耦特定信号特性的参数,并且我们通过独立于响应强度来调节超灵敏度和阈值,从而通过实验证明了这种效果。这项工作表明,可调信号处理是最小的MAPK模块的固有功能,并阐明了合理设计更复杂的合成信号系统的原理。

著录项

  • 作者单位

    Boston University.;

  • 授予单位 Boston University.;
  • 学科 Engineering Biomedical.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 103 p.
  • 总页数 103
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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