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与Ras相关的GTP酶Rhob抑制核因子κB信号传导。

Ras-related GTPase Rhob represses NF-kappaB signaling.

作者信息

Fritz G, Kaina B

机构信息

Division of Applied Toxicology, Institute of Toxicology, University of Mainz, D-55131 Mainz, Germany.

出版信息

J Biol Chem. 2001 Feb 2;276(5):3115-22. doi: 10.1074/jbc.M005058200. Epub 2000 Nov 2.

Abstract

rhoB encoding a Ras-related GTPase is immediate-early inducible by genotoxic treatments, indicating that it is part of the cellular stress response. Here, we investigated the influence of RhoB on signal pathways that are rapidly evoked by genotoxic compounds. The data obtained show that wild-type RhoB neither affects activation of mitogen-activated protein kinases nor AP-1-dependent gene expression. However, RhoB inhibited both basal and genotoxic agent-stimulated activity of the transcription factor nuclear factor kappaB (NF-kappaB). Thus, RhoB attenuated alkylation-induced increase in the DNA binding activity of NF-kappaB and abrogated NF-kappaB-driven gene expression. Furthermore, RhoB inhibited decrease in the cellular amount of IkappaBalpha after genotoxic stress as well as after tumor necrosis factor alpha and 12-O-tetradecanoylphorbol acetate treatment. This indicates that RhoB represses NF-kappaB activation by inhibiting dissociation and subsequent degradation of IkappaBalpha. On the basis of the data, we suggest that RhoB is a novel negative regulator of NF-kappaB signaling.

摘要

编码一种与Ras相关的GTP酶的rhoB可被基因毒性处理快速早期诱导,这表明它是细胞应激反应的一部分。在此,我们研究了RhoB对基因毒性化合物快速引发的信号通路的影响。所获得的数据表明,野生型RhoB既不影响丝裂原活化蛋白激酶的激活,也不影响AP-1依赖的基因表达。然而,RhoB抑制转录因子核因子κB(NF-κB)的基础活性和基因毒性剂刺激的活性。因此,RhoB减弱了烷基化诱导的NF-κB DNA结合活性的增加,并消除了NF-κB驱动的基因表达。此外,RhoB抑制了基因毒性应激后以及肿瘤坏死因子α和12-O-十四烷酰佛波醇-13-乙酸酯处理后IκBα细胞量的减少。这表明RhoB通过抑制IκBα的解离和随后的降解来抑制NF-κB的激活。基于这些数据,我们认为RhoB是NF-κB信号传导的一种新型负调节因子。

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