Effect of phosphorylation on activities of Rap1A to interact with Raf-1 and to suppress Ras-dependent Raf-1 activation

被引:47
作者
Hu, CD [1 ]
Kariya, K [1 ]
Okada, T [1 ]
Qi, XD [1 ]
Song, CH [1 ]
Kataoka, T [1 ]
机构
[1] Kobe Univ, Sch Med, Dept Physiol 2, Chuo Ku, Kobe, Hyogo 6500017, Japan
关键词
D O I
10.1074/jbc.274.1.48
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
Rap1A is phosphorylated by cAMP-dependent protein kinase (PRA), and this phosphorylation has been shown to modulate its interaction with other proteins. However, it is not known whether Rap1A phosphorylation is involved in regulation of its cellular functions, including suppression of Ras-dependent Raf-l activation. We have previously shown that this suppressive activity of Rap1A is attributable to its greatly enhanced ability to bind to the cysteine-rich region (CRR, residues 152-184) of Raf-l compared with that of Ras, Here, we show that phosphorylation of Rap1A by PKA abolished its binding activity to CRR, Furthermore, a mutant Rap1A(S180E), whose sole PKA phosphorylation residue, Ser-180, was substituted by an acidic residue, Glu, to mimic its phosphorylated form, failed to suppress Ras-dependent Raf-l activation in COS-7 cells. These results indicate that the CRR binding activity and the Ras-suppressive function of Rap1A can be modulated through phosphorylation and suggest that Rap1A may function as a PKA-dependent regulator of Raf-l activation, not merely as a suppressor.
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页码:48 / 51
页数:4
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