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.
Abstract:
Mitogen-activated protein kinase 6/extracellular signal-regulated kinase 3 (MAPK6/ERK3) is an atypical member of the MAPKs. An essential role has been suggested by the perinatal lethal phenotype of ERK3 knockout mice carrying a lacZ insertion in exon 2 due to pulmonary dysfunction and by defects in function, activation, and positive selection of T cells. To study the role of ERK3 in vivo, we generated mice carrying a conditional Erk3 allele with exon 3 flanked by loxP sites. Loss of ERK3 protein was validated after deletion of Erk3 in the female germ line using zona pellucida 3 (Zp3)-cre and a clear reduction of the protein kinase MK5 is detected, providing the first evidence for the existence of the ERK3/MK5 signaling complex in vivo In contrast to the previously reported Erk3 knockout phenotype, these mice are viable and fertile and do not display pulmonary hypoplasia, acute respiratory failure, abnormal T-cell development, reduction of thymocyte numbers, or altered T-cell selection. Hence, ERK3 is dispensable for pulmonary and T-cell functions. The perinatal lethality and lung and T-cell defects of the previous ERK3 knockout mice are likely due to ERK3-unrelated effects of the inserted lacZ-neomycin resistance cassette. The knockout mouse of the closely related atypical MAPK ERK4/MAPK4 is also normal, suggesting redundant functions of both protein kinases.
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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