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Diacylglycerol Kinase η Augments C-Raf Activity and B-Raf/C-Raf Heterodimerization

机译:二酰基甘油激酶η增强C-Raf活性和B-Raf / C-Raf异二聚

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摘要

The Ras/B-Raf/C-Raf/MEK/ERK signaling cascade is critical for the control of many fundamental cellular processes, including proliferation, survival, and differentiation. This study demonstrated that small interfering RNA-dependent knockdown of diacylglycerol kinase η (DGKη) impaired the Ras/B-Raf/C-Raf/MEK/ERK pathway activated by epidermal growth factor (EGF) in HeLa cells. Conversely, the overexpression of DGKη1 could activate the Ras/B-Raf/C-Raf/MEK/ERK pathway in a DGK activity-independent manner, suggesting that DGKη serves as a scaffold/adaptor protein. By determining the activity of all the components of the pathway in DGKη-silenced HeLa cells, this study revealed that DGKη activated C-Raf but not B-Raf. Moreover, this study demonstrated that DGKη enhanced EGF-induced heterodimerization of C-Raf with B-Raf, which transmits the signal to C-Raf. DGKη physically interacted with B-Raf and C-Raf, regulating EGF-induced recruitment of B-Raf and C-Raf from the cytosol to membranes. The DGKη-dependent activation of C-Raf occurred downstream or independently of the already known C-Raf modifications, such as dephosphorylation at Ser-259, phosphorylation at Ser-338, and interaction with 14-3-3 protein. Taken together, the results obtained strongly support that DGKη acts as a novel critical regulatory component of the Ras/B-Raf/C-Raf/MEK/ERK signaling cascade via a previously unidentified mechanism.
机译:Ras / B-Raf / C-Raf / MEK / ERK信号级联对于控制许多基本细胞过程(包括增殖,存活和分化)至关重要。这项研究表明,小分子干扰RNA依赖性的二酰基甘油激酶η(DGKη)抑制了HeLa细胞中被表皮生长因子(EGF)激活的Ras / B-Raf / C-Raf / MEK / ERK途径。相反,DGKη1的过度表达可以以不依赖DGK活性的方式激活Ras / B-Raf / C-Raf / MEK / ERK途径,这表明DGKη可以作为支架/适配器蛋白。通过确定沉默DGKη的HeLa细胞中该途径所有成分的活性,这项研究表明DGKη激活了C-Raf,但未激活B-Raf。此外,这项研究表明DGKη增强了EGF诱导的C-Raf与B-Raf的异二聚化,从而将信号传递给C-Raf。 DGKη与B-Raf和C-Raf发生物理相互作用,调节EGF诱导的B-Raf和C-Raf从细胞质到细胞膜的募集。 C-Raf的DGKη依赖性活化发生在下游或独立于已知的C-Raf修饰,例如Ser-259处的去磷酸化,Ser-338处的磷酸化以及与14-3-3蛋白的相互作用。综上所述,获得的结果有力地支持了DGKη通过先前未知的机制作为Ras / B-Raf / C-Raf / MEK / ERK信号级联的新型关键调控成分。

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