Activation of stress-activated protein kinase by MEKK1 phosphorylation of its activator SEK1 View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1994-12-29

AUTHORS

Mlnhong Yan, Tianang Dai, Joseph C. Deak, John M. Kyriakis, Leonard I. Zon, James R. Woodgett, Dennis J. Templeton

ABSTRACT

A KINASE distinct from the MEK activator Raf1–3, termed MEK kinase-1 (MEKK), was originally identified by virtue of its homo-logy to kinases involved in yeast mating signal cascades4. Like Raf, MEKK is capable of activating MEK in vitro4,5. High-level expression of MEKK in COS-7 cells4 or using vaccinia virus vectors5 also activates MEK and MAPK, indicating that MEKK and Raf provide alternative means of activating the MAPK signal-ling pathway. We have derived NIH3T3 cell sublines that can be induced to express active MEKK. Here we show that induction of MEKK does not result in the activation of MAPK, but instead stimulates the stress-activated protein kinases (SAPKs)6–8 which are identical to a Jun amino-terminal kinase9,10. We find that MEKK regulates a new signalling cascade by phosphorylating an SAPK activator, SEK1 which in turn phosphorylates and activates SAPK. More... »

PAGES

798-800

Journal

TITLE

Nature

ISSUE

6508

VOLUME

372

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  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1038/372798a0

    DOI

    http://dx.doi.org/10.1038/372798a0

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1022511929

    PUBMED

    https://www.ncbi.nlm.nih.gov/pubmed/7997270


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