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λ噬菌体阻遏物基因调控的定量模型。

Quantitative model for gene regulation by lambda phage repressor.

作者信息

Ackers G K, Johnson A D, Shea M A

出版信息

Proc Natl Acad Sci U S A. 1982 Feb;79(4):1129-33. doi: 10.1073/pnas.79.4.1129.

Abstract

A statistical thermodynamic model has been developed to account for the cooperative interactions of the bacteriophage lambda repressor with the lambda right operator. The model incorporates a general theory for quantitatively interpreting cooperative site-specific equilibrium binding data. Values for all interaction parameters of the model have been evaluated at 37 degrees C, 0.2 M KCl, from results of DNase protection experiments in vitro [A. D. Johnson, B. J. Meyer, & M. Ptashne, Proc. Natl. Acad. Sci. USA (1979) 76, 5061-5065]. With these values, the model predicts repression curves at the divergent promoters PR and PRM that control transcription of genes coding for the regulatory proteins cro and repressor, respectively. At physiological repressor concentrations, repression at PR is predicted to be nearly complete whereas PRM is predicted to remain highly active. The results demonstrate the importance of cooperative interactions between repressor dimers bound to the adjacent operator sites OR1 and OR2 in maintaining a stable lysogenic state and in allowing efficient switchover to the lytic state during induction.

摘要

已开发出一种统计热力学模型,用于解释噬菌体λ阻遏物与λ右操纵基因的协同相互作用。该模型纳入了一种通用理论,用于定量解释位点特异性平衡结合数据。根据体外DNase保护实验的结果 [A. D. 约翰逊、B. J. 迈耶及M. 普塔什内,《美国国家科学院院刊》(1979年) 76, 5061 - 5065],已在37摄氏度、0.2 M KCl条件下评估了该模型所有相互作用参数的值。利用这些值,该模型预测了分别控制编码调节蛋白cro和阻遏物的基因转录的分歧启动子PR和PRM处的阻遏曲线。在生理阻遏物浓度下,预计PR处的阻遏几乎是完全的,而PRM预计仍保持高活性。结果表明,结合在相邻操纵基因位点OR1和OR2上的阻遏物二聚体之间的协同相互作用对于维持稳定的溶原状态以及在诱导过程中允许有效转换到裂解状态具有重要意义。

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Quantitative model for gene regulation by lambda phage repressor.λ噬菌体阻遏物基因调控的定量模型。
Proc Natl Acad Sci U S A. 1982 Feb;79(4):1129-33. doi: 10.1073/pnas.79.4.1129.

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The lexA gene product represses its own promoter.lexA基因产物可抑制其自身的启动子。
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