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复杂的 Rcs 调控级联反应。

The Complex Rcs Regulatory Cascade.

机构信息

Laboratory of Molecular Biology, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland 20892, USA; emails:

出版信息

Annu Rev Microbiol. 2018 Sep 8;72:111-139. doi: 10.1146/annurev-micro-090817-062640. Epub 2018 Jun 13.

Abstract

RcsB, a response regulator of the FixJ/NarL family, is at the center of a complex network of regulatory inputs and outputs. Cell surface stress is sensed by an outer membrane lipoprotein, RcsF, which regulates interactions of the inner membrane protein IgaA, lifting negative regulation of a phosphorelay. In vivo evidence supports a pathway in which histidine kinase RcsC transfers phosphate to phosphotransfer protein RcsD, resulting in phosphorylation of RcsB. RcsB acts either alone or in combination with RcsA to positively regulate capsule synthesis and synthesis of small RNA (sRNA) RprA as well as other genes, and to negatively regulate motility. RcsB in combination with other FixJ/NarL auxiliary proteins regulates yet other functions, independent of RcsB phosphorylation. Proper expression of Rcs and its targets is critical for success of Escherichia coli commensal strains, for proper development of biofilm, and for virulence in some pathogens. New understanding of how the Rcs phosphorelay works provides insight into the flexibility of the two-component system paradigm.

摘要

RcsB 是 FixJ/NarL 家族的响应调节子,处于复杂的调控输入和输出网络的中心。细胞膜应激由外膜脂蛋白 RcsF 感知,它调节内膜蛋白 IgaA 的相互作用,解除磷酸接力的负调控。体内证据支持一条途径,其中组氨酸激酶 RcsC 将磷酸基转移给磷酸转移蛋白 RcsD,导致 RcsB 的磷酸化。RcsB 单独或与 RcsA 一起正向调节荚膜合成和小 RNA(sRNA)RprA 以及其他基因的合成,并负向调节运动性。RcsB 与其他 FixJ/NarL 辅助蛋白结合,调节其他功能,与 RcsB 磷酸化无关。Rcs 及其靶标的正确表达对大肠杆菌共生菌株的成功、生物膜的正常发育以及某些病原体的毒力至关重要。对 Rcs 磷酸接力如何工作的新理解提供了对双组分系统范例灵活性的深入了解。

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