The adaptor molecule Disabled-2 links the transforming growth factor β receptors to the Smad pathway

被引:192
作者
Hocevar, BA
Smine, A
Xu, XX
Howe, PH
机构
[1] Cleveland Clin Fdn, Lerner Res Inst, Dept Cell Biol, Cleveland, OH 44195 USA
[2] Emory Univ, Sch Med, Dept Biochem, Atlanta, GA 30322 USA
[3] Emory Univ, Sch Med, Winship Canc Ctr, Atlanta, GA 30322 USA
关键词
Dab2; Smad; TGF beta;
D O I
10.1093/emboj/20.11.2789
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Using a genetic complementation approach we have identified disabled-2 (Dab2), a structural homolog of the Dab1 adaptor molecule, as a critical link between the transforming growth factor beta (TGF beta) receptors and the Smad family of proteins, Expression of wildtype Dab2 in a TGF beta -signaling mutant restores TGF beta -mediated Smad2 phosphorylation, Smad translocation to the nucleus and Smad-dependent transcriptional responses. TGF beta stimulation triggers a transient increase in association of Dab2 with Smad2 and Smad3, which is mediated by a direct interaction between the N-terminal phosphotyrosine binding domain of Dab2 and the MH2 domain of Smad2, Dab2 associates with both the type I and type II TGF beta receptors in vive, suggesting that Dab2 is part of a multiprotein signaling complex. Together, these data indicate that Dab2 is an essential component of the TGF beta signaling pathway, aiding in transmission of TGF beta signaling from the TGF beta receptors to the Smad family of transcriptional activators.
引用
收藏
页码:2789 / 2801
页数:13
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