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ERK5 and ERK2 cooperate to regulate NF-κB and cell transformation
被引:114
作者:

Pearson, G
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h-index: 0
机构: Univ Texas, SW Med Ctr, Dept Pharmacol, Dallas, TX 75390 USA

English, JM
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h-index: 0
机构: Univ Texas, SW Med Ctr, Dept Pharmacol, Dallas, TX 75390 USA

White, MA
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h-index: 0
机构: Univ Texas, SW Med Ctr, Dept Pharmacol, Dallas, TX 75390 USA

Cobb, MH
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, SW Med Ctr, Dept Pharmacol, Dallas, TX 75390 USA
机构:
[1] Univ Texas, SW Med Ctr, Dept Pharmacol, Dallas, TX 75390 USA
[2] Univ Texas, SW Med Ctr, Dept Cell Biol & Neurosci, Dallas, TX 75390 USA
[3] Schering Plough Corp, Res Inst, Dept Biol Res Oncol, Kenilworth, NJ 07033 USA
关键词:
D O I:
10.1074/jbc.M009764200
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 [生物化学与分子生物学];
081704 [应用化学];
摘要:
We have previously demonstrated an involvement of MEK5 and ERK5 in RafBXB-stimulated focus formation in NIH3T3 cells. We find here that MEK5 and ERK5 cooperate with the RafBXB effecters MEK1/2 and ERK1/2 to induce foci. To further understand MEK5-ERK5-dependent signaling, we examined potential MEK5-ERK5 effecters that might influence focus-forming activity. Consistent with results from our focus-formation assays, constitutively active variants of MEK5 and MEK1 synergize to activate NF-kappaB, and MEK5 and ERK5 are required for activation of NP-kappaB by RafBXB. The MEK5-ERK5 pathway is also sufficient to activate both NF-kappaB and p90 ribosomal S6 kinase, Our results support the hypothesis that NF-kappaB and p90 ribosomal S6 kinase are involved in MEK5-ERK5-dependent focus formation and may serve as integration points for ERK5 and ERK1/2 signaling.
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页码:7927 / 7931
页数:5
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