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PMID: 12676536 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Association of the type 1 inositol (1,4,5)-trisphosphate receptor with 4.1N protein in neurons.

Molecular and cellular neurosciences ·Vol. 22 ·No. 2 ·2003-02-00 ·Pages 271-83

Maximov A, Tang TS, Bezprozvanny I

Abstract

The type 1 inositol (1,4,5)-trisphosphate receptor (InsP(3)R1) is an intracellular calcium (Ca(2+)) release channel that plays an important role in neuronal function. In yeast two-hybrid screen of rat brain cDNA library with the InsP(3)R1 carboxy-terminal bait we isolated multiple clones of neuronal cytoskeletal protein 4.1N. We mapped the 4.1N-interaction site to a short fragment (50 amino acids) within the carboxy-terminal tail of the InsP(3)R1 and the InsP(3)R1-interaction site to the carboxy-terminal domain (CTD) of 4.1N. We established that InsP(3)R1 carboxy-terminal binds selectively to the CTDDelta alternatively spliced form of the 4.1N protein. In biochemical experiments we demonstrated that 4.1N and InsP(3)R1 specifically associate in vitro. We showed that both 4.1N and InsP(3)R1 were enriched in synaptic locations and immunoprecipitated the 4.1N-InsP(3)R1 complex from rat brain synaptosomes. In biochemical experiments we demonstrated a possibility of InsP(3)R1-4.1N-CASK-syndecan-2 quaternary complex formation. From our findings we hypothesize that InsP(3)R1-4.1N association may play a role in InsP(3)R1 localization or Ca(2+) signaling in neurons.

MeSH Terms
Alternative Splicing/genetics Amino Acid Sequence/genetics Animals Brain/cytology,metabolism Calcium/metabolism Calcium Channels/metabolism Calcium Signaling/genetics Calcium-Calmodulin-Dependent Protein Kinases Cytoskeletal Proteins/genetics,metabolism Guanylate Kinases Inositol 1,4,5-Trisphosphate Receptors Macromolecular Substances Membrane Glycoproteins/metabolism Membrane Proteins Molecular Sequence Data Neuropeptides/genetics,metabolism Nucleoside-Phosphate Kinase/metabolism Presynaptic Terminals/metabolism Protein Binding/genetics Protein Structure, Tertiary/genetics Proteoglycans/metabolism Rats Receptors, Cytoplasmic and Nuclear/metabolism Synaptosomes/metabolism Syndecan-2 Two-Hybrid System Techniques
Chemicals
Calcium Channels Cytoskeletal Proteins Inositol 1,4,5-Trisphosphate Receptors Macromolecular Substances Membrane Glycoproteins Membrane Proteins Neuropeptides Proteoglycans Receptors, Cytoplasmic and Nuclear Sdc2 protein, rat erythrocyte membrane protein band 4.1-like 1 Syndecan-2 CASK kinases Calcium-Calmodulin-Dependent Protein Kinases Nucleoside-Phosphate Kinase Guanylate Kinases Calcium
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Maximov Anton
Department of Physiology, UT Southwestern Medical Center at Dallas, 75390, Dallas, TX, USA.
Tang Tie Shan
Bezprozvanny Ilya
Article Info
Journal
Molecular and cellular neurosciences
Abbr.
Mol Cell Neurosci
ISSN
1044-7431
Published
2003-02-00
Pages
271-83
Language
English
Region
United States
NLM ID
9100095
Subset
IM
Grants
NINDS NIH HHS · R01 NS38082 · United States
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