Cloning by functional expression of a member of the glutamate receptor family

We have isolated a complementary DNA clone by screening a rat brain cDNA library for expression of kainate-gated ion channels in Xenopus oocytes. The cDNA encodes a single protein of relative molecular mass (Mr) 99,800 which on expression in oocytes forms a functional ion channel possessing the electrophysiological and pharmacological properties of the kainate subtype of the glutamate receptor family in the mammalian central nervous system.

[1]  P. Leder,et al.  Purification of biologically active globin messenger RNA by chromatography on oligothymidylic acid-cellulose. , 1972, Proceedings of the National Academy of Sciences of the United States of America.

[2]  B. Müller-Hill,et al.  Filamentous coliphage M13 as a cloning vehicle: insertion of a HindII fragment of the lac regulatory region in M13 replicative form in vitro. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[3]  F. Sanger,et al.  DNA sequencing with chain-terminating inhibitors. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[4]  W. Rutter,et al.  Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. , 1979, Biochemistry.

[5]  J. Watkins,et al.  Differentiation of kainate and quisqualate receptors in the cat spinal cord by selective antagonism with γ-D(and L)-glutamylglycine , 1981, Brain Research.

[6]  R. Doolittle,et al.  A simple method for displaying the hydropathic character of a protein. , 1982, Journal of molecular biology.

[7]  C. Cotman,et al.  Anatomical distributions of four pharmacologically distinct 3H-L-glutamate binding sites , 1983, Nature.

[8]  J. Devereux,et al.  A comprehensive set of sequence analysis programs for the VAX , 1984, Nucleic Acids Res..

[9]  G. Fagg,et al.  Acidic amino acid binding sites in mammalian neuronal membranes: their characteristics and relationship to synaptic receptors , 1984, Brain Research Reviews.

[10]  G. Fagg l-Glutamate, excitatory amino acid receptors and brain function , 1985, Trends in Neurosciences.

[11]  J. Changeux,et al.  Structure of the high-affinity binding site for noncompetitive blockers of the acetylcholine receptor: serine-262 of the delta subunit is labeled by [3H]chlorpromazine. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[12]  G. Heijne A new method for predicting signal sequence cleavage sites. , 1986 .

[13]  B. Meldrum,et al.  Distribution of [3H]kainic acid and binding sites in the rat brain: in vivo and in vitro receptor autoradiography , 1986, Neuroscience Letters.

[14]  P. Seeburg,et al.  Sequence and functional expression of the GABAA receptor shows a ligand-gated receptor super-family , 1987, Nature.

[15]  S. Heinemann,et al.  Functional expression of two neuronal nicotinic acetylcholine receptors from cDNA clones identifies a gene family. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[16]  P. Seeburg,et al.  Glycine vs GABA receptors , 1987, Nature.

[17]  Molecular neurobiology : recombinant DNA approaches , 1987 .

[18]  P. Seeburg,et al.  Molecular biology of the GABAA receptor: the receptor/channel superfamily , 1987, Trends in Neurosciences.

[19]  E. Gundelfinger,et al.  The strychnine-binding subunit of the glycine receptor shows homology with nicotinic acetylcholine receptors , 1987, Nature.

[20]  S. Nakanishi,et al.  cDNA eloping of bovine substance-K receptor through oocyte expression system , 1987, Nature.

[21]  S. Heinemann,et al.  Molecular Biology of the Neural and Muscle Nicotinic Acetylcholine Receptors , 1987 .

[22]  T. Bliss,et al.  NMDA receptors - their role in long-term potentiation , 1987, Trends in Neurosciences.

[23]  D. O. Hebb,et al.  The organization of behavior , 1988 .

[24]  E. Michaelis,et al.  Immune labeling and purification of a 71-kDa glutamate-binding protein from brain synaptic membranes. Possible relationship of this protein to physiologic glutamate receptors. , 1988, The Journal of biological chemistry.

[25]  E. Barnard,et al.  Single subunits of the GABAA receptor form ion channels with properties of the native receptor. , 1988, Science.

[26]  R. Wenthold,et al.  A kainic acid receptor from frog brain purified using domoic acid affinity chromatography. , 1988, The Journal of biological chemistry.

[27]  H. Sugiyama,et al.  Characterization of glutamate receptors induced in Xenopus oocytes after injection of rat brain mRNA , 1988, Neuroscience Research.

[28]  A. Ortega,et al.  Isolation, immunochemical characterization and localization of the kainate sub‐class of glutamate receptor from chick cerebellum. , 1988, The EMBO journal.

[29]  M. Cuénod,et al.  A kainate binding protein in pigeon cerebellum: Purification and localization by monoclonal antibody , 1988, Neuroscience Letters.

[30]  W. Huse,et al.  Lambda ZAP: a bacteriophage lambda expression vector with in vivo excision properties. , 1988, Nucleic acids research.

[31]  E. Wong,et al.  Solubilization of the N‐Methyl‐d‐Aspartate Receptor Channel Complex from Rat and Porcine Brain , 1989, Journal of neurochemistry.

[32]  M. Bennett,et al.  N-methyl-D-aspartate activates different channels than do kainate and quisqualate. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[33]  J. Henley,et al.  Solubilisation and Characterisation of a Putative Quisqualate‐Type Glutamate Receptor from Chick Brain , 1989, Journal of neurochemistry.

[34]  S. Halpain,et al.  Characterization and partial purification of a chloride- and calcium-dependent glutamate-binding protein from rat brain. , 1989, The Journal of biological chemistry.

[35]  R. Wenthold,et al.  Identification and characterization of the ligand binding subunit of a kainic acid receptor using monoclonal antibodies and peptide mapping. , 1989, The Journal of biological chemistry.

[36]  C. Cotman,et al.  The excitatory amino acid receptors: their classes, pharmacology, and distinct properties in the function of the central nervous system. , 1989, Annual review of pharmacology and toxicology.

[37]  R. Grantyn,et al.  Separation of quisqualate- and kainate-selective glutamate receptors in cultured neurons from the rat superior colliculus , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[38]  L. Swanson,et al.  Beta 3: a new member of nicotinic acetylcholine receptor gene family is expressed in brain. , 1989, The Journal of biological chemistry.

[39]  P. Seeburg,et al.  Type I and type II GABAA-benzodiazepine receptors produced in transfected cells. , 1989, Science.

[40]  S. Heinemann,et al.  The functional diversity of the neuronal nicotinic acetylcholine receptors is increased by a novel subunit: β4 , 1989, Neuron.

[41]  P. Seeburg,et al.  Two novel GABAA receptor subunits exist in distinct neuronal subpopulations , 1989, Neuron.

[42]  H. Betz,et al.  Functional expression in Xenopus oocytes of the strychnine binding 48 kd subunit of the glycine receptor. , 1989, The EMBO journal.