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 Previous Article

Molecular and Cellular Biology, January 2008, p. 511-527, Vol. 28, No. 1
0270-7306/08/$08.00+0     doi:10.1128/MCB.00800-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Single and Combined Silencing of ERK1 and ERK2 Reveals Their Positive Contribution to Growth Signaling Depending on Their Expression Levels{triangledown}

Renaud Lefloch, Jacques Pouysségur, and Philippe Lenormand*

Institute of Signaling Developmental Biology and Cancer, CNRS UMR 6543, Université de Nice Sophia Antipolis, Centre A. Lacassagne, 33 Avenue de Valombrose, 06189 Nice, France

Received 7 May 2007/ Returned for modification 22 June 2007/ Accepted 11 October 2007

The proteins ERK1 and ERK2 are highly similar, are ubiquitously expressed, and share activators and substrates; however, erk2 gene invalidation is lethal in mice, while erk1 inactivation is not. We ablated ERK1 and/or ERK2 by RNA interference and explored their relative roles in cell proliferation and immediate-early gene (IEG) expression. Reducing expression of either ERK1 or ERK2 lowered IEG induction by serum; however, silencing of only ERK2 slowed down cell proliferation. When both isoforms were silenced simultaneously, compensating activation of the residual pool of ERK1/2 masked a more deleterious effect on cell proliferation. It was only when ERK2 activation was clamped at a limiting level that we demonstrated the positive contribution of ERK1 to cell proliferation. We then established that ERK isoforms are activated indiscriminately and that their expression ratio correlated exactly with their activation ratio. Furthermore, we determined for the first time that ERK1 and ERK2 kinase activities are indistinguishable in vitro and that erk gene dosage is essential for survival of mice. We propose that the expression levels of ERK1 and ERK2 drive their apparent biological differences. Indeed, ERK1 is dispensable in some vertebrates, since it is absent from chicken and frog genomes despite being present in all mammals and fishes sequenced so far.

* Corresponding author. Mailing address. Institute of Signaling Developmental Biology and Cancer, CNRS UMR 6543, Centre A. Lacassagne, 33 Avenue de Valombrose, 06189 Nice, France. Phone: 33 (0) 492031227. Fax: 33 (0) 492031225. E-mail: lenorman{at}unice.fr

{triangledown} Published ahead of print on 29 October 2007.

Molecular and Cellular Biology, January 2008, p. 511-527, Vol. 28, No. 1
0270-7306/08/$08.00+0     doi:10.1128/MCB.00800-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.



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