Spatial, temporal and subcellular localization of islet-brain 1 (IB1), a homologue of JIP-1, in mouse brain
Abstract
Islet-brain 1 (IB1) was recently identified as a DNA-binding protein of the GLUT2 gene promoter. The mouse IB1 is the rat and human homologue of the Jun-interacting protein 1 (JIP-1) which has been recognized as a key player in the regulation of c-Jun amino-terminal kinase (JNK) mitogen-activated protein kinase (MAPK) pathways. JIP-1 is involved in the control of apoptosis and may play a role in brain development and aging. Here, IB1 was studied in adult and developing mouse brain tissue by in situ hybridization, Northern and Western blot analysis at cellular and subcellular levels, as well as by immunocytochemistry in brain sections and cell cultures. IB1 expression was localized in the synaptic regions of the olfactory bulb, retina, cerebral and cerebellar cortex and hippocampus in the adult mouse brain. IB1 was also detected in a restricted number of axons, as in the mossy fibres from dentate gyrus in the hippocampus, and was found in soma, dendrites and axons of cerebellar Purkinje cells. After birth, IB1 expression peaks at postnatal day 15. IB1 was located in axonal and dendritic growth cones in primary telencephalon cells. By biochemical and subcellular fractionation of neuronal cells, IB1 was detected both in the cytosolic and membrane fractions. Taken together with previous data, the restricted neuronal expression of IB1 in developing and adult brain and its prominent localization in synapses suggest that the protein may be critical for cell signalling in developing and mature nerve terminals.
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JIP is localized at post-synaptic densities (PSD) in neurons and is indispensable for normal function of NMDA receptors.
“Recent studies have shown that JIP is localized at post-synaptic densities (PSD) in neurons, and is indispensable for the normal function of NMDA receptors (Kennedy et al., 2007; Pellet et al., 2000).”
From The E3 ubiquitin ligase IDOL regulates synaptic ApoER2 levels and is important for plasticity and learning (2017) · cites this paper as Pellet et al., 2000
JIPs are highly enriched at synaptic junctions in adult and developing brains.
“JIPs are also highly enriched at synaptic junctions in adult and developing brains (Pellet et al. 2000).”
From Cargo of kinesin identified as JIP scaffolding proteins and associated signaling molecules (2001) · cites this paper as Pellet et al. 2000
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References 41 · Cited by 55
- Authors
- Pellet, J., Haefliger, J., Staple, J. K., Widmann, C., Welker, E., Hirling, H., Bonny, C., Nicod, P., Catsicas, S., Waeber, G., & Riederer, B. M.
- Affiliations
- Centre Hospitalier Universitaire Vaudois (CH)
- University of Lausanne (CH)
- Venue
- European Journal of Neuroscience
- Publisher
- Wiley
- Published
- 2000-02
- Volume
- 12
- Issue
- 2
- Pages
- 621-632
- ISSN
- 0953-816X (ISSN-L)
- 1460-9568
- OpenAlex
- W2045214083
- Cited by
- 55
- References
- 41
- Citations by year
- 2026: 1 · 2023: 2 · 2022: 1 · 2020: 3 · 2019: 1 · 2018: 2 · 2017: 2 · 2016: 1 · 2014: 1 · 2013: 1
- FWCI
- 2.82
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- European Journal of Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- IRIS (submittedVersion)
- SERVAL (Université de Lausanne) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Keywords
- JIP1, subcellular localization, brain development, postnatal brain development, synapses, axonal growth cones, Purkinje cells, hippocampus, olfactory bulb, retina, telencephalon, JNK MAPK pathway, neuronal expression
- MeSH terms
- Animals, Brain, Brain Chemistry, Carrier Proteins, Cells, Cultured, Cerebral Cortex, Eye Proteins, Fetal Proteins, Nerve Tissue Proteins, Nuclear Proteins, Organ Specificity, Retina, Species Specificity, Subcellular Fractions, Telencephalon, Trans-Activators, Rats, Wistar, In Situ Hybridization, Gene Expression Regulation, Developmental, Protein Isoforms, Reverse Transcriptase Polymerase Chain Reaction, Mitogen-Activated Protein Kinases, MAP Kinase Signaling System, JNK Mitogen-Activated Protein Kinases, Adaptor Proteins, Signal Transducing, Mice, Rats
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