Nature Communications (Mar 2020)

Paradoxical activation of the protein kinase-transcription factor ERK5 by ERK5 kinase inhibitors

  • Pamela A. Lochhead,
  • Julie A. Tucker,
  • Natalie J. Tatum,
  • Jinhua Wang,
  • David Oxley,
  • Andrew M. Kidger,
  • Victoria P. Johnson,
  • Megan A. Cassidy,
  • Nathanael S. Gray,
  • Martin E. M. Noble,
  • Simon J. Cook

DOI
https://doi.org/10.1038/s41467-020-15031-3
Journal volume & issue
Vol. 11, no. 1
pp. 1 – 16

Abstract

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Selective ERK5 inhibitors target ERK5 kinase activity, but they do not phenocopy the effects of ERK5 genetic depletion. Here, the authors demonstrate that the direct interaction of these inhibitors to ERK5 kinase domain induces conformational changes that promote ERK5 nuclear translocation and transcriptional activities.