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Rho鸟苷酸解离抑制剂(RhoGDIs)通过与GAPs直接相互作用对Rho GTPase活性进行正向调节。

Positive regulation of Rho GTPase activity by RhoGDIs as a result of their direct interaction with GAPs.

作者信息

Ota Takahide, Maeda Masayo, Okamoto Mayumi, Tatsuka Masaaki

机构信息

Division of Tumor Biology, Department of Life Science, Medical Research Institute, Kanazawa Medical University, Uchinada 920-0293, Ishikawa, Japan.

出版信息

BMC Syst Biol. 2015 Jan 28;9:3. doi: 10.1186/s12918-015-0143-5.

Abstract

BACKGROUND

Rho GTPases function as molecular switches in many different signaling pathways and control a wide range of cellular processes. Rho GDP-dissociation inhibitors (RhoGDIs) regulate Rho GTPase signaling and can function as both negative and positive regulators. The role of RhoGDIs as negative regulators of Rho GTPase signaling has been extensively investigated; however, little is known about how RhoGDIs act as positive regulators. Furthermore, it is unclear how this opposing role of GDIs influences the Rho GTPase cycle. We constructed ordinary differential equation models of the Rho GTPase cycle in which RhoGDIs inhibit the regulatory activities of guanine nucleotide exchange factors (GEFs) and GTPase-activating proteins (GAPs) by interacting with them directly as well as by sequestering the Rho GTPases. Using this model, we analyzed the role of RhoGDIs in Rho GTPase signaling.

RESULTS

The model constructed in this study showed that the functions of GEFs and GAPs are integrated into Rho GTPase signaling through the interactions of these regulators with GDIs, and that the negative role of GDIs is to suppress the overall Rho activity by inhibiting GEFs. Furthermore, the positive role of GDIs is to sustain Rho activation by inhibiting GAPs under certain conditions. The interconversion between transient and sustained Rho activation occurs mainly through changes in the affinities of GDIs to GAPs and the concentrations of GAPs.

CONCLUSIONS

RhoGDIs positively regulate Rho GTPase signaling primarily by interacting with GAPs and may participate in the switching between transient and sustained signals of the Rho GTPases. These findings enhance our understanding of the physiological roles of RhoGDIs and Rho GTPase signaling.

摘要

背景

Rho GTP酶在许多不同的信号通路中起分子开关的作用,并控制广泛的细胞过程。Rho GDP解离抑制剂(RhoGDI)调节Rho GTP酶信号传导,并且可以作为负调节因子和正调节因子发挥作用。RhoGDI作为Rho GTP酶信号传导的负调节因子的作用已得到广泛研究;然而,关于RhoGDI如何作为正调节因子发挥作用却知之甚少。此外,尚不清楚GDI的这种相反作用如何影响Rho GTP酶循环。我们构建了Rho GTP酶循环的常微分方程模型,其中RhoGDI通过直接与鸟嘌呤核苷酸交换因子(GEF)和GTP酶激活蛋白(GAP)相互作用以及通过隔离Rho GTP酶来抑制它们的调节活性。使用该模型,我们分析了RhoGDI在Rho GTP酶信号传导中的作用。

结果

本研究构建的模型表明,GEF和GAP的功能通过这些调节因子与GDI的相互作用整合到Rho GTP酶信号传导中,并且GDI的负作用是通过抑制GEF来抑制整体Rho活性。此外,GDI的正作用是在某些条件下通过抑制GAP来维持Rho激活。短暂和持续的Rho激活之间的相互转换主要通过GDI对GAP的亲和力变化和GAP的浓度变化来发生。

结论

RhoGDI主要通过与GAP相互作用来正向调节Rho GTP酶信号传导,并可能参与Rho GTP酶短暂和持续信号之间的转换。这些发现增强了我们对RhoGDI和Rho GTP酶信号传导生理作用的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a189/4312443/364078f5d228/12918_2015_143_Fig1_HTML.jpg

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