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dc.contributor.authorKelkar, Nyaya
dc.contributor.authorStanden, Claire L.
dc.contributor.authorDavis, Roger J.
dc.date2022-08-11T08:09:33.000
dc.date.accessioned2022-08-23T16:35:23Z
dc.date.available2022-08-23T16:35:23Z
dc.date.issued2005-03-16
dc.date.submitted2009-03-24
dc.identifier.citationMol Cell Biol. 2005 Apr;25(7):2733-43. <a href="http://dx.doi.org/10.1128/MCB.25.7.2733-2743.2005">Link to article on publisher's site</a>
dc.identifier.issn0270-7306 (Print)
dc.identifier.doi10.1128/MCB.25.7.2733-2743.2005
dc.identifier.pmid15767678
dc.identifier.urihttp://hdl.handle.net/20.500.14038/38545
dc.description.abstractThe c-Jun NH2-terminal kinase (JNK)-interacting protein (JIP) group of scaffold proteins (JIP1, JIP2, and JIP3) can interact with components of the JNK signaling pathway and potently activate JNK. Here we describe the identification of a fourth member of the JIP family. The primary sequence of JIP4 is most closely related to that of JIP3. Like other members of the JIP family of scaffold proteins, JIP4 binds JNK and also the light chain of the microtubule motor protein kinesin-1. However, the function of JIP4 appears to be markedly different from other JIP proteins. Specifically, JIP4 does not activate JNK signaling. In contrast, JIP4 serves as an activator of the p38 mitogen-activated protein (MAP) kinase pathway by a mechanism that requires the MAP kinase kinases MKK3 and MKK6. The JIP4 scaffold protein therefore appears to be a new component of the p38 MAP kinase signaling pathway.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=15767678&dopt=Abstract">Link to Article in PubMed</a>
dc.subjectAdaptor Proteins, Signal Transducing
dc.subjectAnimals
dc.subjectCells, Cultured
dc.subjectCercopithecus aethiops
dc.subjectCloning, Molecular
dc.subjectCytoplasm
dc.subjectEnzyme Activation
dc.subjectJNK Mitogen-Activated Protein Kinases
dc.subjectMAP Kinase Kinase 3
dc.subjectMAP Kinase Kinase 6
dc.subjectMAP Kinase Kinase 7
dc.subjectMAP Kinase Kinase Kinases
dc.subject*MAP Kinase Signaling System
dc.subjectMice
dc.subjectMice, Knockout
dc.subjectMicrotubule-Associated Proteins
dc.subjectNerve Tissue Proteins
dc.subjectPhosphorylation
dc.subjectProtein Binding
dc.subjectp38 Mitogen-Activated Protein Kinases
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleRole of the JIP4 scaffold protein in the regulation of mitogen-activated protein kinase signaling pathways
dc.typeJournal Article
dc.source.journaltitleMolecular and cellular biology
dc.source.volume25
dc.source.issue7
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2413&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/1414
dc.identifier.contextkey794911
refterms.dateFOA2022-08-23T16:35:23Z
html.description.abstract<p>The c-Jun NH2-terminal kinase (JNK)-interacting protein (JIP) group of scaffold proteins (JIP1, JIP2, and JIP3) can interact with components of the JNK signaling pathway and potently activate JNK. Here we describe the identification of a fourth member of the JIP family. The primary sequence of JIP4 is most closely related to that of JIP3. Like other members of the JIP family of scaffold proteins, JIP4 binds JNK and also the light chain of the microtubule motor protein kinesin-1. However, the function of JIP4 appears to be markedly different from other JIP proteins. Specifically, JIP4 does not activate JNK signaling. In contrast, JIP4 serves as an activator of the p38 mitogen-activated protein (MAP) kinase pathway by a mechanism that requires the MAP kinase kinases MKK3 and MKK6. The JIP4 scaffold protein therefore appears to be a new component of the p38 MAP kinase signaling pathway.</p>
dc.identifier.submissionpathoapubs/1414
dc.contributor.departmentHoward Hughes Medical Institute, Program in Molecular Medicine
dc.source.pages2733-43


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