Functional Redundancy of ERK1 and ERK2 MAP Kinases during Development

• Genetic inactivation of Erk2 in the embryo leads to severe developmental defects
• Developmental outcome dose-dependently correlates with global ERK1/2 activity
• Transgenic ERK1 rescues all developmental defects resulting from the loss of ERK2
• ERK1-only mice are viable, morphologically normal, and fertile

SummaryERK1 and ERK2 are the effector kinases of the ERK1/2 MAP-kinase signaling pathway, which plays a central role in transducing signals controlling cell proliferation, differentiation, and survival. Deregulated activity of the ERK1/2 pathway is linked to a group of developmental syndromes and contributes to the pathogenesis of various human diseases. One fundamental question that remains unaddressed is whether ERK1 and ERK2 have evolved unique physiological functions or whether they are used redundantly to reach a threshold of global ERK activity. Here, we show that the extent of development of the mouse placenta and embryo bearing different combinations of Erk1 and Erk2 alleles is strictly correlated with total ERK1/2 activity. We further demonstrate that transgenic expression of ERK1 fully rescues the embryonic and placental developmental defects associated with the loss of ERK2. We conclude that ERK1 and ERK2 exert redundant functions in mouse development.

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