| Literature DB >> 2032290 |
T G Boulton1, S H Nye, D J Robbins, N Y Ip, E Radziejewska, S D Morgenbesser, R A DePinho, N Panayotatos, M H Cobb, G D Yancopoulos.
Abstract
We recently described the purification and cloning of extracellular signal-regulated kinase 1 (ERK1), which appears to play a pivotal role in converting tyrosine phosphorylation into the serine/threonine phosphorylations that regulate downstream events. We now describe cloning and characterization of two ERK1-related kinases, ERK2 and ERK3, and provide evidence suggesting that there are additional ERK family members. At least two of the ERKs are activated in response to growth factors; their activations correlate with tyrosine phophorylation, but also depend on additional modifications. Transcripts corresponding to the three cloned ERKs are distinctly regulated both in vivo and in a differentiating cell line. Thus, this family of kinases may serve as intermediates that depend on tyrosine phosphorylation to activate serine/threonine phosphorylation cascades. Individual family members may mediate responses in different developmental stages, in different cell types, or following exposure to different extracellular signals.Entities:
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Year: 1991 PMID: 2032290 DOI: 10.1016/0092-8674(91)90098-j
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582