Abstract
Smad proteins play key roles in intracellular signaling of the transforming growth factor-β (TGF-β) superfamily. E1A, an adenoviral oncoprotein, is known to inhibit TGF-β-induced transactivation through binding to Smad proteins. Recently, an EID-1 (E1A-like inhibitor of differentiation-1) and EID-2 (EID-1-like inhibitor of differentiation-2) were identified. In this study, we examined the effect of EID-2 on Smad-mediated TGF-β signaling. Here, we show that EID-2 inhibits TGF-β/Smad transcriptional responses. EID-2 interacts constitutively with Smad proteins, and most strongly with Smad3. Stable expression of EID-2 in the TGF-β1-responsive cell line inhibits endogenous Smad3-Smad4 complex formation and TGF-β1-induced expression of p21 and p15. These results suggest that EID-2 may function as an endogenous suppressor of TGF-β signaling.
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CITATION STYLE
Lee, H. J., Lee, J. K., Miyake, S., & Kim, S. J. (2004). A Novel E1A-like Inhibitor of Differentiation (EID) Family Member, EID-2, Suppresses Transforming Growth Factor (TGF)-β Signaling by Blocking TGF-β-induced Formation of Smad3-Smad4 Complexes. Journal of Biological Chemistry, 279(4), 2666–2672. https://doi.org/10.1074/jbc.M310591200
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