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First published online 14 November 2006
doi: 10.1242/jcs.03272


Journal of Cell Science 119, 4952-4963 (2006)
Published by The Company of Biologists 2006
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Research Article

Dynamic regulation of ERK2 nuclear translocation and mobility in living cells

Mario Costa1, Matilde Marchi2,3, Francesco Cardarelli2,3, Anusrhee Roy4, Fabio Beltram2, Lamberto Maffei1,5 and Gian Michele Ratto1,*

1 Institute of Neuroscience CNR, Via Moruzzi 1, 56100 Pisa, Italy
2 NEST, Scuola Normale Superiore, Pisa, Italy
3 Italian Institute of Technology, Italy
4 Department of Physics and Meteorology, Indian Institute of Technology, Kharagpur, India
5 Laboratory of Neurobiology, Scuola Normale Superiore, Pisa, Italy

* Author for correspondence (e-mail: gimmi{at}in.cnr.it)

Accepted 20 September 2006

The extracellular signal-regulated protein kinase ERK1/2 is a crucial effector linking extracellular stimuli to cellular responses: upon phosphorylation ERK [also known as mitogen-activated protein kinase P42/P44 (MAPK)] concentrates in the nucleus where it activates specific programs of gene expression. Notwithstanding the importance of this process, little is known about the modalities, time course and regulation of ERK exchange between nucleus and cytoplasm in living cells. We visualized the dynamic of nuclear translocation by expressing low levels (<150 nM) of fluorescently tagged ERK2 in living fibroblasts. Time-lapse imaging demonstrated that nuclear concentration can change bidirectionally with a time constant of a few minutes. The increase of nuclear concentration requires continuous MEK (also known as MAPK kinase) activity upstream of ERK and is rapidly reduced by the operation of phosphatases. We measured quantitatively the speed of ERK2 shuttling between nucleus and cytoplasm and determined that shuttling accelerated after ERK activation, becoming fast enough not to be rate-limiting for translocation. Finally, we demonstrated that ERK2 did not diffuse freely in the nucleus and that diffusion was further impeded after phosphorylation, suggesting the formation of complexes of low mobility. These results show that nucleocytoplasmic trafficking of ERK2 and its mobility are dynamically regulated in living cells.

Key words: Phosphorylation, Signal transduction, Nuclear transport, Kinase, Phosphatase, MAP kinase


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