The cyclopentenone 15-deoxy-Δ12,14-prostagland in J2 binds to and activates H-Ras

被引:116
作者
Oliva, JL
Pérez-Sala, D
Castrillo, A
Martínez, N
Cañada, FJ
Boscá, L
Rojas, JM [1 ]
机构
[1] CSIC, Ctr Invest Biol, Dept Estructura & Funcion Prot, Madrid 28006, Spain
[2] Inst Salud Carlos III, Ctr Nacl Microbiol, Unidad Biol Celular, Madrid 28220, Spain
[3] Univ Complutense, Fac Farm, Inst Bioquim, Ctr Mixto Consejo Super Invest Cient, Madrid 28040, Spain
[4] Univ Complutense, Fac Farm, Ctr Nacl Invest Cardiovasc, Ctr Mixto Consejo Super Invest Cient, Madrid 28040, Spain
关键词
mitogen-activated protein kinase; cell proliferation; posttranslational modification;
D O I
10.1073/pnas.0735842100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The cyclopentenone 15-deoxy-Delta(12,14)-prostaglandin J(2) (15d-PGJ(2)) induces cell proliferation and mitogen-activated protein kinase activation. Here, we describe that these effects are mediated by 15d-PGJ(2)-elicited H-Ras activation. We demonstrate that this pathway is specific for H-Ras through the formation of a covalent adduct of 15d-PGJ(2) with Cys-184 of H-Ras, but not with N-Ras or K-Ras. Mutation of C184 inhibited H-Ras modification and activation by 15d-PGJ(2), whereas serum-elicited stimulation was not affected. These results describe a mechanism for the activation of the Ras signaling pathway, which results from the chemical modification of H-Ras by formation of a covalent adduct with cyclopentenone prostaglandins.
引用
收藏
页码:4772 / 4777
页数:6
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