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来自大肠杆菌 K-12 的硝酸盐响应型 NarX-NarL 和 NarQ-NarP 双组分调控系统之间的非对称交叉调控。

Asymmetric cross-regulation between the nitrate-responsive NarX-NarL and NarQ-NarP two-component regulatory systems from Escherichia coli K-12.

机构信息

Department of Microbiology, University of California, Davis, CA 95616-8665, USA.

出版信息

Mol Microbiol. 2010 Jan;75(2):394-412. doi: 10.1111/j.1365-2958.2009.06987.x. Epub 2009 Dec 4.

Abstract

The NarX-NarL and NarQ-NarP sensor-response regulator pairs control Escherichia coli gene expression in response to nitrate and nitrite. Previous analysis suggests that the Nar two-component systems form a cross-regulation network in vivo. Here we report on the kinetics of phosphoryl transfer between different sensor-regulator combinations in vitro. NarX exhibited a noticeable kinetic preference for NarL over NarP, whereas NarQ exhibited a relatively slight kinetic preference for NarL. These findings were substantiated in reactions containing one sensor and both response regulators, or with two sensors and a single response regulator. We isolated 21 NarX mutants with missense substitutions in the cytoplasmic central and transmitter modules. These confer phenotypes that reflect defects in phospho-NarL dephosphorylation. Five of these mutants, all with substitutions in the transmitter DHp domain, also exhibited NarP-blind phenotypes. Phosphoryl transfer assays in vitro confirmed that these NarX mutants have defects in catalysing NarP phosphorylation. By contrast, the corresponding NarQ mutants conferred phenotypes indicating comparable interactions with both NarP and NarL. Our overall results reveal asymmetry in the Nar cross-regulation network, such that NarQ interacts similarly with both response regulators, whereas NarX interacts preferentially with NarL.

摘要

NarX-NarL 和 NarQ-NarP 传感器-响应调节剂对控制大肠杆菌基因表达硝酸盐和亚硝酸盐作出响应。之前的分析表明,Nar 双组分系统在体内形成交叉调控网络。在此,我们报告了不同传感器-调节剂组合之间体外磷酸转移的动力学。NarX 对 NarL 的磷酸化转移表现出明显的动力学偏好,而 NarQ 对 NarL 的磷酸化转移则表现出相对轻微的动力学偏好。这些发现得到了含有一个传感器和两个响应调节剂,或两个传感器和一个响应调节剂的反应的证实。我们分离了 21 个 NarX 突变体,它们在细胞质中央和传输模块中有错义取代。这些突变体表现出的表型反映了磷酸化 NarL 去磷酸化的缺陷。其中 5 个突变体,均在传输器 DHp 结构域中有取代,也表现出 NarP 盲性表型。体外磷酸转移测定证实这些 NarX 突变体在催化 NarP 磷酸化方面存在缺陷。相比之下,相应的 NarQ 突变体表现出与两个响应调节剂相互作用相似的表型。我们的总体结果揭示了 Nar 交叉调控网络的不对称性,即 NarQ 与两个响应调节剂相互作用相似,而 NarX 则与 NarL 优先相互作用。

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