Molecular traffic cop directs cellul...( Scientists report that a recently ident...)

Scientists report that a recently identified molecule functions as a molecular switch that influences the activity of key signaling molecules by restricting the location of the activated molecules within the cell. The research, published in the July issue of Developmental Cell, provides new insight into how a widely used signaling cascade can be spatially regulated to enhance the specificity of cellular responses.

The Ras/ERK MAP kinase signaling cascade is activated by many extracellular stimuli and is critical to a variety of cellular processes. The molecules that make up this cascade are present in different subcellular compartments and exactly where the cascade is activated depends on the extracellular stimulus. ERK activity can influence molecules in the cell cytoplasm or it can influence whether target genes in the nucleus are turned on or off. It is not known exactly how a particular stimulus can confine Ras/ERK MAP activity to a specific region of the cell.

A molecule called hSef was recently identified as an inhibitor of this cascade but the molecular mechanisms of inhibition are unclear. Dr. Eisuke Nishida from The Department of Cell and Developmental Biology at Kyoto University in Japan examined exactly how hSef influences Ras/ERK MAP kinase signaling in the cytoplasm and nucleus. When cells were stimulated with a common growth factor, hSef interacted with activated ERK in the cytoplasm. The inhibitor was only switched on when the Ras/ERK MAP kinase pathway was activated. Interestingly, activated hSef works not by directly inhibiting the activity of ERK, but by preventing activated ERK from entering the nucleus. When hSef levels were experimentally reduced, stimulus-dependant ERK activation in the nucleus increased dramatically.

These results demonstrate that the newly discovered inhibitor hSef is a signaling-dependent regulator of the Ras/ERK MAP kinase cascade that blocks MAP kinase influence on target genes by res
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Contact: Heidi Hardman
hhardman@cell.com
617-397-2879
Cell Press
12-Jul-2004

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