Identification of the site of inhibition of mitogenic signaling by oncogenic ras-p21 by a ras effector peptide

被引:8
作者
Chie, L
Friedman, FK
Kung, HF
Lin, MCM
Chung, D
Pincus, MR
机构
[1] Vet Adm Med Ctr, Dept Pathol & Lab Med, Brooklyn, NY 11209 USA
[2] Long Isl Univ, Dept Biol, Brooklyn, NY 11201 USA
[3] Long Isl Univ, Dept Chem, Brooklyn, NY 11201 USA
[4] NCI, Lab Metab, Bethesda, MD 20892 USA
[5] Univ Hong Kong, Inst Mol Technol Drug Design & Synth, Biol Chem Lab, Inst Mol Biol, Hong Kong, Hong Kong, Peoples R China
[6] SUNY Hlth Sci Ctr, Dept Pathol, Brooklyn, NY 11203 USA
来源
JOURNAL OF PROTEIN CHEMISTRY | 2002年 / 21卷 / 05期
关键词
oncogenic ras-p21; switch; 1; domain; 35-47; peptide; constitutively activated raf;
D O I
10.1023/A:1019998403181
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
We have previously found that a ras switch 1 domain peptide (PNC-7, residues 35-47) selectively blocks oocyte maturation induced by oncogenic (Val 12-containing) ras-p21 protein and also blocks c-raf-induced oocyte maturation. We now find that oncogenic ras-p21 does not inhibit oocyte maturation of a constitutively activated raf protein (raf BXB) that is lacking most of the first 301 amino terminal amino acids, including the major ras binding domain and accessory ras-binding regions. We also find that a dominant negative raf that completely blocks c-raf-induced maturation likewise does not block raf-BXB-induced maturation. We conclude that PNC-7 blocks ras by binding to the amino-terminal domain of raf and that raf BXB must initiate signal transduction in the cytosol.
引用
收藏
页码:367 / 370
页数:4
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