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Homer Binds a Novel Proline-Rich Motif and Links Group 1 Metabotropic Glutamate Receptors with IP3 Receptors
Open accessAbstract
Group I metabotropic glutamate receptors (mGluRs) activate PI turnover and thereby trigger intracellular calcium release. Previously, we demonstrated that mGluRs form natural complexes with members of a family of Homer-related synaptic proteins. Here, we present evidence that Homer proteins form a physical tether linking mGluRs with the inositol trisphosphate receptors (IP3R). A novel proline-rich "Homer ligand" (PPXXFr) is identified in group 1 mGluRs and IP3R, and these receptors coimmunoprecipitate as a complex with Homer from brain. Expression of the IEG form of Homer, which lacks the ability to cross-link, modulates mGluR-induced intracellular calcium release. These studies identify a novel mechanism in calcium signaling and provide evidence that an IEG, whose expression is driven by synaptic activity, can directly modify a specific synaptic function.
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“For example, a gene that encodes a synaptic scaffolding protein, HOMER132, was engaged in NeuN+ specific peaks and loops and its expression was significantly higher in NeuN+ cells compared with NeuN− cells (Fig. 2b).”
From Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders (2021) · cites this paper as [32]
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The integrative function of TRPC channels
Kiselyov, K. I. (2009) · Frontiers in bioscience · doi:10.2741/3230 · Cited by 69
In Vivo Regulation of Homer1a Expression in the Striatum by Cocaine
Zhang, G.-C., Mao, L., Liu, X., Parelkar, N. K., Arora, A. K., Yang, L., Hains, M., Fibuch, E. E., & Wang, J. Q. (2007) · Molecular Pharmacology · doi:10.1124/mol.106.028399 · Cited by 69
Kindling‐induced overexpression of Homer 1A and its functional implications for epileptogenesis
Potschka, H., Krupp, E., Ebert, U., Gümbel, C., Leichtlein, C. B., Lorch, B., Pickert, A., Kramps, S., Young, K., Grüne, U., et al. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02265.x · Cited by 68
Self-citationLiu, X., Yang, J., Chen, L., Zhang, Y., Yang, M., Wu, Y., Li, F., Tang, M., Liang, S., & Wei, Y. (2008) · PROTEOMICS · doi:10.1002/pmic.200700514 · Cited by 68
Mutation ofDrosophila homerDisrupts Control of Locomotor Activity and Behavioral Plasticity
Diagana, T. T., Thomas, U., Prokopenko, S. N., Xiao, B., Worley, P. F., & Thomas, J. B. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-02-00428.2002 · Cited by 69
Self-citationGao, L., Blair, L. A. C., Salinas, G. D., Needleman, L. A., & Marshall, J. J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0481-06.2006 · Cited by 67
Select overexpression of homer1a in dorsal hippocampus impairs spatial working memory
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Yiannakas, A., & Rosenblum, K. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00335 · Cited by 72
Homer1 promotes dendritic spine growth through ankyrin-G and its loss reshapes the synaptic proteome
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Luo, P., Fei, F., Zhang, L., Qu, Y., & Fei, Z. (2011) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2011.05.004 · Cited by 69
Metadata
- Authors
- Tu, J. C., Xiao, B., Yuan, J. P., Lanahan, A. A., Leoffert, K., Li, M., Linden, D. J., & Worley, P. F.
- Affiliations
- Johns Hopkins University (US)
- Corresponding author
- Worley, Paul F
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 1998-10
- Volume
- 21
- Issue
- 4
- Pages
- 717-726
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2164762131
- Cited by
- 862
- References
- 68
- Citations by year
- 2026: 14 · 2025: 7 · 2024: 12 · 2023: 6 · 2022: 21 · 2021: 23 · 2020: 12 · 2019: 19 · 2018: 23 · 2017: 32 · 2016: 23 · 2015: 23 · 2014: 27 · 2013: 36 · 2012: 41
- FWCI
- 15.70
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Neuron (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Funders
- Genentech
- National Institute of Mental Health (K02MH001152, KO2 MH01152)
- National Institute on Drug Abuse (DA 10309, DA 11742, R01DA011742)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Keywords
- Homer proteins, group I metabotropic glutamate receptors, IP3 receptor, proline-rich motif, receptor complex formation, intracellular calcium release, calcium signaling, immediate early genes, synaptic proteins
- MeSH terms
- Homer Scaffolding Proteins, Amino Acid Sequence, Animals, Calcium, Carrier Proteins, Intracellular Membranes, Ligands, Molecular Sequence Data, Neuropeptides, Proline, Time Factors, Calcium Channels, Gene Expression, Genes, Immediate-Early, Receptors, Metabotropic Glutamate, Receptors, Cytoplasmic and Nuclear, Glutamic Acid, GTP Phosphohydrolases, Dynamins, Rats, Inositol 1,4,5-Trisphosphate Receptors
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