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Role of the JIP4 Scaffold Protein in the Regulation of Mitogen-Activated Protein Kinase Signaling Pathways
Abstract
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.
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JIP4 is a scaffold protein that interacts with c-Jun NH2-terminal kinase (JNK) and functions as an activator of the p38 mitogen-activated protein (MAP) kinase pathway.
“JIP4 is a scaffold protein that interacts with c-Jun NH2-terminal kinase (JNK) and functions as an activator of the p38 mitogen-activated protein (MAP) kinase pathway56, suggesting that JIP4 might link transport of lysosomes to signaling.”
From TFEB regulates lysosomal positioning by modulating TMEM55B expression and JIP4 recruitment to lysosomes (2017) · cites this paper as [56]
Citations
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“JIP3, and KLC were described previously (13, 34).”
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Cited by
Sorted by citations
Differential regulation and properties of MAPKs
Raman, M., Chen, W., & Cobb, M. H. (2007) · Oncogene · doi:10.1038/sj.onc.1210392 · Cited by 1,430
The JNK signal transduction pathway
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Metadata
- Authors
- Kelkar, N., Standen, C. L., & Davis, R. J.
- Venue
- Molecular and Cellular Biology
- Publisher
- Informa UK Limited
- Published
- 2005-04-01
- Volume
- 25
- Issue
- 7
- Pages
- 2733-2743
- ISSN
- 1098-5549
- Cited by
- 157
- References
- 4
- Language
- en
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