Yotiao, a Novel Protein of Neuromuscular Junction and Brain That Interacts with Specific Splice Variants of NMDA Receptor Subunit NR1
Open Access
- 15 March 1998
- journal article
- Published by Society for Neuroscience in Journal of Neuroscience
- Vol. 18 (6) , 2017-2027
- https://doi.org/10.1523/jneurosci.18-06-02017.1998
Abstract
The molecular machinery underlying neurotransmitter receptor immobilization at postsynaptic sites is poorly understood. The NMDA receptor subunit NR1 can form clusters in heterologous cells via a mechanism dependent on the alternatively spliced C1 exon cassette in its intracellular C-terminal tail, suggesting a functional interaction between NR1 and the cytoskeleton. The yeast two-hybrid screen was used here to identify yotiao, a novel coiled coil protein that interacts with NR1 in a C1 exon-dependent manner. Yotiao mRNA (11 kb) is present modestly in brain and abundantly in skeletal muscle and pancreas. On Western blots, yotiao appears as an ∼230 kDa band that is present in cerebral cortex, hippocampus, and cerebellum. Biochemical studies reveal that yotiao fractionates with cytoskeleton-associated proteins and with the postsynaptic density. With regard to immunohistochemistry, two anti-yotiao antibodies display a somatodendritic staining pattern similar to each other and to the staining pattern of NR1. Yotiao was colocalized by double-label immunocytochemistry with NR1 in rat brain and could be coimmunoprecipitated with NR1 from heterologous cells. Thus yotiao is an NR1-binding protein potentially involved in cytoskeletal attachment of NMDA receptors. Consistent with a general involvement in postsynaptic structure, yotiao was also found to be specifically concentrated at the neuromuscular junction in skeletal muscle.Keywords
This publication has 52 references indexed in Scilit:
- Ion channel associated proteinsCurrent Opinion in Neurobiology, 1996
- Inactivation of NMDA Receptors by Direct Interaction of Calmodulin with the NR1 SubunitCell, 1996
- Dystrophin and utrophin: the missing links!FEBS Letters, 1995
- Calcium-induced actin depolymerization reduces NMDA channel activityPublished by Elsevier ,1993
- Quantal analysis and synaptic anatomy — integrating two views of hippocampal plasticityTrends in Neurosciences, 1993
- Regulation of Ion Channel Distribution at SynapsesAnnual Review of Neuroscience, 1993
- Synaptic structure and development: The neuromuscular junctionCell, 1993
- Structures and properties of seven isoforms of the NMDA receptor generated by alternative splicingBiochemical and Biophysical Research Communications, 1992
- Predicting Coiled Coils from Protein SequencesScience, 1991
- Immunochemical identification of desmin in Torpedo postsynaptic membranes and at the rat neuromuscular junctionSynapse, 1988