Voltage-dependent block by MgZ+ of NMDA responses in spinal cord neurones. Nature 309, 261-263. 4.2 MULLER, D. & LYNCH, G. (1989). Does increased transmitter release sustain long-term potentiation. Europ J Neurosci. (Suppl.) (In the press.) 43 NELSON, R. B., ROUTENBERG, A,, HYMAN, H. & F%m"Ncm, K. H
“JIP”ing along the axon: the complex roles of JIPs in axonal transport
✍ Scribed by Sandhya P. Koushika
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 100 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0265-9247
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
JIPs are JNK interacting proteins and bind to JNK cascade kinases. JIP1 and JIP3 were known to be adaptors linking cargo to Kinesin‐I, a major molecular motor for axonal transport. Recent research sheds further light on JIPs' complex roles in axonal transport, namely in activation of Kinesin‐I and in cargo release. In Drosophila, APLIP1/JIP1 allows the Kinesin‐I complex to enable cargo release through activation of JNK signaling.1 In mammalian cell culture, JIP1 is necessary and, together with UNC‐76/FEZ1, sufficient for activating Kinesin‐I.2 I discuss and compare the many roles played by JIP1 and JIP3 through interactions with several distinct players, in retrograde as well as anterograde transport. BioEssays 30:10–14, 2008. © 2007 Wiley Periodicals, Inc.
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