Please use this identifier to cite or link to this item: https://doi.org/10.1074/jbc.M201385200
DC FieldValue
dc.titleIdentification of a JAK2-independent pathway regulating growth hormone (GH)-stimulated p44/42 mitogen-activated protein kinase activity: GH activation of Ral and phospholipase D is Src-dependent
dc.contributor.authorZhu, T.
dc.contributor.authorLing, L.
dc.contributor.authorLobie, P.E.
dc.date.accessioned2014-12-01T06:55:18Z
dc.date.available2014-12-01T06:55:18Z
dc.date.issued2002-11-22
dc.identifier.citationZhu, T., Ling, L., Lobie, P.E. (2002-11-22). Identification of a JAK2-independent pathway regulating growth hormone (GH)-stimulated p44/42 mitogen-activated protein kinase activity: GH activation of Ral and phospholipase D is Src-dependent. Journal of Biological Chemistry 277 (47) : 45592-45603. ScholarBank@NUS Repository. https://doi.org/10.1074/jbc.M201385200
dc.identifier.issn00219258
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/113510
dc.description.abstractWe have demonstrated here that growth hormone (GH) stimulates the formation of the active GTP-bound form of both RalA and RalB in NIH-3T3 cells. Full activation of RalA and RalB by GH required the combined activity of c-Src and JAK2, both kinases activated by GH independent of the other. Activation of RalA and RalB by growth hormone did not require the activity of JAK2 per se. Ras was also activated by GH and was required for the GH-stimulated formation of GTP-bound RalA and RalB. Activation of RalA by GH subsequently resulted in increased phospholipase D activity and the formation of its metabolite, phosphatidic acid. GH-stimulated RalA-phospholipase D-dependent formation of phosphatidic acid was required for activation of p44/42 MAPK and subsequent Elk-1-mediated transcription stimulated by GH. Thus we report the identification of a JAK2-independent pathway regulating GH-stimulated p44/42 MAPK activity.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1074/jbc.M201385200
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentMEDICINE
dc.description.doi10.1074/jbc.M201385200
dc.description.sourcetitleJournal of Biological Chemistry
dc.description.volume277
dc.description.issue47
dc.description.page45592-45603
dc.description.codenJBCHA
dc.identifier.isiut000179404800125
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