Differences in AMPA and Kainate Receptor Interactomes Facilitate Identification of AMPA Receptor Auxiliary Subunit GSG1L

Cell Reports

Volumn 1, Issue 6, 2012, Pages 590-598

  Shanks, Natalie F ^a   Savas, Jeffrey N ^b   Maruo, Tomohiko ^a   Cais, Ondrej ^d   Hirao, Atsushi ^c   Oe, Souichi ^c   Ghosh, Anirvan ^a   Noda, Yasuko ^c   Greger, Ingo H ^d   Yates, John R ^b   Nakagawa, Terunaga ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b SCRIPPS RESEARCH INSTITUTE   (United States)

^c JICHI MEDICAL UNIVERSITY   (Japan)

^d MRC LABORATORY OF MOLECULAR BIOLOGY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AMPA RECEPTOR; BINDING PROTEIN; CLAUDIN; GSG1L PROTEIN; KAINIC ACID RECEPTOR; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BIOCHEMISTRY; BRAIN REGION; CHANNEL GATING; CONTROLLED STUDY; ELECTROPHYSIOLOGY; HUMAN; HUMAN CELL; LIQUID CHROMATOGRAPHY; NERVE CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; PROTEIN ANALYSIS; PROTEIN FUNCTION; PROTEIN INTERACTION; PROTEIN LOCALIZATION; PROTEIN PURIFICATION; RAT; SEQUENCE HOMOLOGY; TANDEM MASS SPECTROMETRY;

AMINO ACID SEQUENCE; ANIMALS; BRAIN; CLAUDINS; HEK293 CELLS; HUMANS; MALE; MASS SPECTROMETRY; MOLECULAR SEQUENCE DATA; NEURONS; PROTEIN BINDING; PROTEIN INTERACTION MAPS; PROTEIN SUBUNITS; PROTEIN TRANSPORT; PROTEINS; RATS; RECEPTORS, AMPA; RECEPTORS, KAINIC ACID; SEQUENCE HOMOLOGY, AMINO ACID;

RATTUS;

EID: 84863100938     PISSN: None     EISSN: 22111247     Source Type: Journal    
DOI: 10.1016/j.celrep.2012.05.004     Document Type: Article

References (35)

1. Arai A., Lynch G. AMPA receptor desensitization modulates synaptic responses induced by repetitive afferent stimulation in hippocampal slices. Brain Res. 1998, 799:235-242.
2. Becanovic K., Pouladi M.A., Lim R.S., Kuhn A., Pavlidis P., Luthi-Carter R., Hayden M.R., Leavitt B.R. Transcriptional changes in Huntington disease identified using genome-wide expression profiling and cross-platform analysis. Hum. Mol. Genet. 2010, 19:1438-1452.
3. Brusés J.L. Identification of gene transcripts expressed by postsynaptic neurons during synapse formation encoding cell surface proteins with presumptive synaptogenic activity. Synapse 2010, 64:47-60.
4. Chen L., Chetkovich D.M., Petralia R.S., Sweeney N.T., Kawasaki Y., Wenthold R.J., Bredt D.S., Nicoll R.A. Stargazin regulates synaptic targeting of AMPA receptors by two distinct mechanisms. Nature 2000, 408:936-943.
5. Collingridge G.L., Olsen R.W., Peters J., Spedding M. A nomenclature for ligand-gated ion channels. Neuropharmacology 2009, 56:2-5.
6. de Wit J., Sylwestrak E., O'Sullivan M.L., Otto S., Tiglio K., Savas J.N., Yates J.R., Comoletti D., Taylor P., Ghosh A. LRRTM2 interacts with Neurexin1 and regulates excitatory synapse formation. Neuron 2009, 64:799-806.
7. Farina A.N., Blain K.Y., Maruo T., Kwiatkowski W., Choe S., Nakagawa T. Separation of domain contacts is required for heterotetrameric assembly of functional NMDA receptors. J. Neurosci. 2011, 31:3565-3579.
8. Farrant M., Cull-Candy S.G. Neuroscience. AMPA receptors-another twist?. Science 2010, 327:1463-1465.
9. Jackson A.C., Nicoll R.A. The expanding social network of ionotropic glutamate receptors: TARPs and other transmembrane auxiliary subunits. Neuron 2011, 70:178-199.
10. Kalashnikova E., Lorca R.A., Kaur I., Barisone G.A., Li B., Ishimaru T., Trimmer J.S., Mohapatra D.P., Díaz E. SynDIG1: an activity-regulated, AMPA- receptor-interacting transmembrane protein that regulates excitatory synapse development. Neuron 2010, 65:80-93.
11. Kato A.S., Gill M.B., Ho M.T., Yu H., Tu Y., Siuda E.R., Wang H., Qian Y.W., Nisenbaum E.S., Tomita S., Bredt D.S. Hippocampal AMPA receptor gating controlled by both TARP and cornichon proteins. Neuron 2010, 68:1082-1096.
12. Kessels H.W., Kopec C.D., Klein M.E., Malinow R. Roles of stargazin and phosphorylation in the control of AMPA receptor subcellular distribution. Nat. Neurosci. 2009, 12:888-896.
13. Kim E., Sheng M. PDZ domain proteins of synapses. Nat. Rev. Neurosci. 2004, 5:771-781.
14. Lai H.C., Klisch T.J., Roberts R., Zoghbi H.Y., Johnson J.E. In vivo neuronal subtype-specific targets of Atoh1 (Math1) in dorsal spinal cord. J. Neurosci. 2011, 31:10859-10871.
15. Lein E.S., Hawrylycz M.J., Ao N., Ayres M., Bensinger A., Bernard A., Boe A.F., Boguski M.S., Brockway K.S., Byrnes E.J., et al. Genome-wide atlas of gene expression in the adult mouse brain. Nature 2007, 445:168-176.
16. Menuz K., O'Brien J.L., Karmizadegan S., Bredt D.S., Nicoll R.A. TARP redundancy is critical for maintaining AMPA receptor function. J. Neurosci. 2008, 28:8740-8746.
17. Nakagawa T., Cheng Y., Ramm E., Sheng M., Walz T. Structure and different conformational states of native AMPA receptor complexes. Nature 2005, 433:545-549.
18. Pei J., Grishin N.V. Unexpected diversity in Shisa-like proteins suggests the importance of their roles as transmembrane adaptors. Cell. Signal. 2012, 24:758-769.
19. Priel A., Kolleker A., Ayalon G., Gillor M., Osten P., Stern-Bach Y. Stargazin reduces desensitization and slows deactivation of the AMPA-type glutamate receptors. J. Neurosci. 2005, 25:2682-2686.
20. Rossmann M., Sukumaran M., Penn A.C., Veprintsev D.B., Babu M.M., Greger I.H. Subunit-selective N-terminal domain associations organize the formation of AMPA receptor heteromers. EMBO J. 2011, 30:959-971.
21. Sala C., Futai K., Yamamoto K., Worley P.F., Hayashi Y., Sheng M. Inhibition of dendritic spine morphogenesis and synaptic transmission by activity-inducible protein Homer1a. J. Neurosci. 2003, 23:6327-6337.
22. Sans N., Prybylowski K., Petralia R.S., Chang K., Wang Y.X., Racca C., Vicini S., Wenthold R.J. NMDA receptor trafficking through an interaction between PDZ proteins and the exocyst complex. Nat. Cell Biol. 2003, 5:520-530.
23. Savas J.N., Stein B.D., Wu C.C., Yates J.R. Mass spectrometry accelerates membrane protein analysis. Trends Biochem. Sci. 2011, 36:388-396.
24. Schwenk J., Harmel N., Zolles G., Bildl W., Kulik A., Heimrich B., Chisaka O., Jonas P., Schulte U., Fakler B., Klöcker N. Functional proteomics identify cornichon proteins as auxiliary subunits of AMPA receptors. Science 2009, 323:1313-1319.
25. Shanks N.F., Maruo T., Farina A.N., Ellisman M.H., Nakagawa T. Contribution of the global subunit structure and stargazin on the maturation of AMPA receptors. J. Neurosci. 2010, 30:2728-2740.
26. Shepherd J.D., Huganir R.L. The cell biology of synaptic plasticity: AMPA receptor trafficking. Annu. Rev. Cell Dev. Biol. 2007, 23:613-643.
27. Tanaka H., Yoshimura Y., Nishina Y., Nozaki M., Nojima H., Nishimune Y. Isolation and characterization of cDNA clones specifically expressed in testicular germ cells. FEBS Lett. 1994, 355:4-10.
28. Tomita S., Chen L., Kawasaki Y., Petralia R.S., Wenthold R.J., Nicoll R.A., Bredt D.S. Functional studies and distribution define a family of transmembrane AMPA receptor regulatory proteins. J. Cell Biol. 2003, 161:805-816.
29. Tomita S., Adesnik H., Sekiguchi M., Zhang W., Wada K., Howe J.R., Nicoll R.A., Bredt D.S. Stargazin modulates AMPA receptor gating and trafficking by distinct domains. Nature 2005, 435:1052-1058.
30. Traynelis S.F., Wollmuth L.P., McBain C.J., Menniti F.S., Vance K.M., Ogden K.K., Hansen K.B., Yuan H., Myers S.J., Dingledine R., Sibley D. Glutamate receptor ion channels: structure, regulation, and function. Pharmacol. Rev. 2010, 62:405-496.
31. von Engelhardt J., Mack V., Sprengel R., Kavenstock N., Li K.W., Stern-Bach Y., Smit A.B., Seeburg P.H., Monyer H. CKAMP44: a brain-specific protein attenuating short-term synaptic plasticity in the dentate gyrus. Science 2010, 327:1518-1522.
32. Wang R., Walker C.S., Brockie P.J., Francis M.M., Mellem J.E., Madsen D.M., Maricq A.V. Evolutionary conserved role for TARPs in the gating of glutamate receptors and tuning of synaptic function. Neuron 2008, 59:997-1008.
33. Washburn M.P., Wolters D., Yates J.R. Large-scale analysis of the yeast proteome by multidimensional protein identification technology. Nat. Biotechnol. 2001, 19:242-247.
34. Zhang W., St-Gelais F., Grabner C.P., Trinidad J.C., Sumioka A., Morimoto-Tomita M., Kim K.S., Straub C., Burlingame A.L., Howe J.R., Tomita S. A transmembrane accessory subunit that modulates kainate-type glutamate receptors. Neuron 2009, 61:385-396.
35. Zheng Y., Mellem J.E., Brockie P.J., Madsen D.M., Maricq A.V. SOL-1 is a CUB-domain protein required for GLR-1 glutamate receptor function in C. elegans. Nature 2004, 427:451-457.