Germ Line Deletion Reveals a Nonessential Role of Atypical Mitogen-Activated Protein Kinase 6/Extracellular

N Ronkina1, K Schuster-Gossler2, F Hansmann3

  • 1Institute of Cell Biochemistry, Hannover Medical School, Hannover, Germany.

Insights

Mitogen-activated protein kinase 6 (MAPK6/ERK3) is not essential for lung or T-cell development. Previous studies suggesting otherwise were likely due to unrelated effects of genetic modifications.

Area of Science:

  • Molecular Biology
  • Immunology
  • Genetics

Background:

  • Mitogen-activated protein kinase 6/extracellular signal-regulated kinase 3 (MAPK6/ERK3) is an atypical MAPK.
  • Previous studies suggested essential roles for ERK3 in pulmonary and T-cell development, based on knockout mouse phenotypes.

Purpose of the Study:

  • To investigate the in vivo role of ERK3 using a conditional knockout mouse model.
  • To clarify the discrepancies in previously reported ERK3 knockout phenotypes.

Main Methods:

  • Generated conditional Erk3 knockout mice with exon 3 flanked by loxP sites.
  • Utilized Zp3-cre to delete Erk3 in the female germ line.
  • Validated ERK3 protein loss and assessed MK5 protein levels.

Main Results:

  • Conditional knockout mice lacking ERK3 were viable and fertile.
  • These mice did not exhibit pulmonary hypoplasia or T-cell development defects.
  • Evidence for an ERK3/MK5 signaling complex in vivo was observed.
  • The previously reported lethal phenotype was attributed to the lacZ-neomycin cassette.

Conclusions:

  • ERK3 is dispensable for pulmonary and T-cell functions in vivo.
  • The lacZ-neomycin cassette in prior studies caused ERK3-unrelated defects.
  • Atypical MAPKs like ERK3 and ERK4 may have redundant functions.

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