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  Kinase-dependent and kinase-independent functions of EphA4 receptors in major axon tract formation in vivo

Kullander, K., Mather, N. K., Diella, F., Dottori, M., Boyd, A. W., & Klein, R. (2001). Kinase-dependent and kinase-independent functions of EphA4 receptors in major axon tract formation in vivo. Neuron, 29(1), 73-84. doi:10.1016/s0896-6273(01)00181-7.

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Kullander, K., Autor
Mather, N. K., Autor
Diella, F., Autor
Dottori, M., Autor
Boyd, A. W., Autor
Klein, Rüdiger1, Autor           
Affiliations:
1European Molecular Biology Laboratory, Heidelberg, ou_persistent22              

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Schlagwörter: central-nervous-system tyrosine kinase neural development sam domain cardiovascular development transmembrane ligands commissural axons ephrinb ligands cell-contact family Neurosciences & Neurology
 Zusammenfassung: The EphA4 receptor tyrosine kinase regulates the formation of the corticospinal tract (CST), a pathway controlling voluntary movements, and of the anterior commissure (AC), connecting the neocortical temporal robes. To study EphA4 kinase signaling in these processes, we generated mice expressing mutant EphA4 receptors either lacking kinase activity or with severely downregulated kinase activity. We demonstrate that EphA4 is required for CST formation as a receptor for which it requires an active kinase domain. In contrast, the formation of the AC is rescued by kinase-dead EphA4, suggesting that in this structure EphA4 acts as a ligand for which its kinase activity is not required. Unexpectedly, the cytoplasmic sterile-alpha motif (SAM) domain is not required for EphA4 functions. Our findings establish both kinase-dependent and kinase-independent functions of EphA4 in the formation of major axon tracts.

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Sprache(n): eng - English
 Datum: 2001
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: Anderer: WOS:000166702700010
DOI: 10.1016/s0896-6273(01)00181-7
ISSN: 0896-6273
 Art des Abschluß: -

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Titel: Neuron
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Cambridge, Mass. : Cell Press
Seiten: - Band / Heft: 29 (1) Artikelnummer: - Start- / Endseite: 73 - 84 Identifikator: ISSN: 0896-6273
CoNE: https://pure.mpg.de/cone/journals/resource/954925560565