Rho small G-protein-dependent binding of mDia to an Src homology 3 domain-containing IRSp53/BAIAP2

被引:67
作者
Fujiwara, T [1 ]
Mammoto, A [1 ]
Kim, Y [1 ]
Takai, Y [1 ]
机构
[1] Osaka Univ, Grad Sch Med, Fac Med, Dept Mol Biol & Biochem, Suita, Osaka 5650871, Japan
关键词
D O I
10.1006/bbrc.2000.2671
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
mDial is a downstream effector of Rho small G: protein that is implicated in stress fiber formation and cytokinesis. We isolated an mDial-binding protein and identified it to be IRSp53/BAIAP2. IRSp53 and BAIAP2 have independently been isolated as a 58/53-kDa protein tyrosine phosphorylated in response to insulin and a BAI1-binding protein, respectively. BAI1 is a brain-specific seven-span transmembrane protein capable of inhibiting angiogenesis. The proline-rich formin homology 1 domain of mDial bound the Src homology 3 domain of IRSp53/BAIAP2 in a GTP-Rho-dependent manner. The results suggest that IRSp53/BAIAP2 is a downstream effector of mDial. (C) 2000 Academic Press.
引用
收藏
页码:626 / 629
页数:4
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