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National Academy of Sciences, Proceedings of the National Academy of Sciences, 13(97), p. 7272-7277, 2000

DOI: 10.1073/pnas.130176697

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MEK kinase 1 gene disruption alters cell migration and c-Jun NH <sub>2</sub> -terminal kinase regulation but does not cause a measurable defect in NF-κB activation

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

MEK kinase 1 (MEKK1) is a 196-kDa mitogen-activated protein kinase (MAPK) kinase kinase that, in addition to regulating the c-Jun NH 2 -terminal kinase (JNK) pathway, is involved in the control of cell motility. MEKK1 −/− mice are defective in eyelid closure, a TGFα-directed process involving the migration of epithelial cells. MEKK1 expression in epithelial cells stimulates lamellipodia formation, a process required for cell movement. In addition, mouse embryo fibroblasts derived from MEKK1 −/− mice are inhibited in their migration relative to MEKK1 +/+ fibroblasts. MEKK1 is required for JNK but not NF-κB activation in response to virus infection, microtubule disruption, and stimulation of embryonic stem cells with lysophosphatidic acid. MEKK1 is not required for TNFα or IL-1 regulation of JNK or NF-κB activation in macrophages or fibroblasts. Thus, MEKK1 senses microtubule integrity, contributes to the regulation of fibroblast and epithelial cell migration, and is required for activation of JNK but not NF-κB in response to selected stress stimuli.