Functional Heterogeneity of Gephyrins

Postsynaptic clustering of the glycine receptor requires the cytoplasmic protein gephyrin, which interacts with the receptor beta subunit. Several variants of gephyrin are generated by alternative splicing and differ by the presence of short amino acid sequences (cassettes) in the N-terminal half of the molecule. In this work, seven isoforms of gephyrin were cloned from adult rat spinal cord, some of then containing new cassettes. The relationships between gephyrin structure and recognition of glycine receptor beta subunit were analyzed. This was carried out by GST-pulldown assays using the beta subunit cytoplasmic loop and cotransfection experiments of GFP-tagged gephyrins with an alpha1 subunit bearing the gephyrin-binding site of the beta subunit. Data demonstrated that not all gephyrin molecules can bind to the beta subunit. Identified cassettes modulate this interaction. It is thus concluded that the function of gephyrin in synapse formation can rely on a structure acquired through cassette combinations.

[1]  J. Meier,et al.  Formation of glycine receptor clusters and their accumulation at synapses. , 2000, Journal of cell science.

[2]  C. Lévêque,et al.  Direct interaction between synaptotagmin and the intracellular loop I-II of neuronal voltage-sensitive sodium channels. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[3]  H. Schindelin,et al.  Crystal Structure of the Gephyrin-related Molybdenum Cofactor Biosynthesis Protein MogA from Escherichia coli * , 2000, The Journal of Biological Chemistry.

[4]  J. Brandstätter,et al.  Loss of Postsynaptic GABAA Receptor Clustering in Gephyrin-Deficient Mice , 1999, The Journal of Neuroscience.

[5]  W. Sieghart,et al.  Synaptic Control of Glycine and GABAA Receptors and Gephyrin Expression in Cultured Motoneurons , 1999, The Journal of Neuroscience.

[6]  J. Anderson,et al.  Protein modules as organizers of membrane structure. , 1999, Current opinion in cell biology.

[7]  S. Snyder,et al.  Interaction of RAFT1 with gephyrin required for rapamycin-sensitive signaling. , 1999, Science.

[8]  R. Huganir,et al.  Organization and regulation of proteins at synapses. , 1999, Current opinion in cell biology.

[9]  M. Kneussel,et al.  Hydrophobic Interactions Mediate Binding of the Glycine Receptor β‐Subunit to Gephyrin , 1999, Journal of neurochemistry.

[10]  J. Reiss,et al.  The neurotransmitter receptor-anchoring protein gephyrin reconstitutes molybdenum cofactor biosynthesis in bacteria, plants, and mammalian cells. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[11]  J. Kirsch,et al.  Incorporation of a gephyrin‐binding motif targets NMDA receptors to gephyrin‐rich domains in HEK 293 cells , 1999, The European journal of neuroscience.

[12]  N. Brandon,et al.  GABAA-receptor-associated protein links GABAA receptors and the cytoskeleton , 1999, Nature.

[13]  G. Feng,et al.  Dual requirement for gephyrin in glycine receptor clustering and molybdoenzyme activity. , 1998, Science.

[14]  Bernhard Lüscher,et al.  Postsynaptic clustering of major GABAA receptor subtypes requires the γ2 subunit and gephyrin , 1998, Nature Neuroscience.

[15]  M. Giustetto,et al.  Localization of the clustering protein gephyrin at GABAergic synapses in the main olfactory bulb of the rat , 1998, The Journal of comparative neurology.

[16]  T. Sasaki,et al.  Interactions of drebrin and gephyrin with profilin. , 1998, Biochemical and biophysical research communications.

[17]  P. Seeburg,et al.  Interaction of ion channels and receptors with PDZ domain proteins , 1997, Current Opinion in Neurobiology.

[18]  H. Wässle,et al.  Synaptogenesis in the rat retina: subcellular localization of glycine receptors, GABAA receptors, and the anchoring protein gephyrin , 1997, The Journal of comparative neurology.

[19]  Richard L. Huganir,et al.  GRIP: a synaptic PDZ domain-containing protein that interacts with AMPA receptors , 1997, Nature.

[20]  C. Barnes,et al.  Homer: a protein that selectively binds metabotropic glutamate receptors , 1997, Nature.

[21]  C. Richter-Landsberg,et al.  Expression and mRNA splicing of glycine receptor subunits and gephyrin during neuronal differentiation of P19 cells in vitro, studied by RT-PCR and immunocytochemistry. , 1997, Brain research. Developmental brain research.

[22]  J. Sanes Genetic analysis of postsynaptic differentiation at the vertebrate neuromuscular junction , 1997, Current Opinion in Neurobiology.

[23]  J. Schiemann,et al.  Molybdenum co-factor biosynthesis: the Arabidopsis thaliana cDNA cnx1 encodes a multifunctional two-domain protein homologous to a mammalian neuroprotein, the insect protein Cinnamon and three Escherichia coli proteins. , 1995, The Plant journal : for cell and molecular biology.

[24]  J. Kirsch,et al.  Targeting of Glycine Receptor Subunits to Gephyrin-Rich Domains in Transfected Human Embryonic Kidney Cells , 1995, Molecular and Cellular Neuroscience.

[25]  J. Sanes,et al.  Failure of postsynaptic specialization to develop at neuromuscular junctions of rapsyn-deficient mice , 1995, Nature.

[26]  Dieter Langosch,et al.  Identification of a gephyrin binding motif on the glycine receptor β subunit , 1995, Neuron.

[27]  J. Kirsch,et al.  The postsynaptic localization of the glycine receptor-associated protein gephyrin is regulated by the cytoskeleton , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[28]  M. Shelton,et al.  The Drosophila molybdenum cofactor gene cinnamon is homologous to three Escherichia coli cofactor proteins and to the rat protein gephyrin. , 1994, Genetics.

[29]  A. Triller,et al.  Gephyrin antisense oligonucleotides prevent glycine receptor clustering in spinal neurons , 1993, Nature.

[30]  J. Kirsch,et al.  Widespread expression of gephyrin, a putative glycine receptor-tubulin linker protein, in rat brain , 1993, Brain Research.

[31]  J. Kirsch,et al.  Distribution of Gephyrin Transcripts in the Adult and Developing Rat Brain , 1993, The European journal of neuroscience.

[32]  G. Multhaup,et al.  Primary structure and alternative splice variants of gephyrin, a putative glycine receptor-tubulin linker protein , 1992, Neuron.

[33]  D. Langosch,et al.  The 93-kDa glycine receptor-associated protein binds to tubulin. , 1991, The Journal of biological chemistry.

[34]  G. Multhaup,et al.  Cloning and expression of the 58 kd β subunit of the inhibitory glycine receptor , 1990, Neuron.

[35]  H. Korn,et al.  gamma-Aminobutyric acid-containing terminals can be apposed to glycine receptors at central synapses , 1987, The Journal of cell biology.

[36]  C. Becker,et al.  The Mr 93,000 polypeptide of the postsynaptic glycine receptor complex is a peripheral membrane protein. , 1987, Biochemistry.

[37]  R. Wenthold,et al.  Identification of glycinergic synapses in the cochlear nucleus through immunocytochemical localization of the postsynaptic receptor , 1986, Brain Research.

[38]  S D Fuller,et al.  Intracellular sorting and basolateral appearance of the G protein of vesicular stomatitis virus in Madin-Darby canine kidney cells , 1985, The Journal of cell biology.

[39]  H. Korn,et al.  Distribution of glycine receptors at central synapses: an immunoelectron microscopy study , 1985, The Journal of cell biology.

[40]  David E. Misek,et al.  Biogenesis of epithelial cell polarity: Intracellular sorting and vectorial exocytosis of an apical plasma membrane glycoprotein , 1984, Cell.

[41]  F. Pfeiffer,et al.  Purification by affinity chromatography of the glycine receptor of rat spinal cord. , 1982, The Journal of biological chemistry.

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

[43]  J. Kirsch,et al.  Collybistin, a newly identified brain-specific GEF, induces submembrane clustering of gephyrin , 2000, Nature Neuroscience.

[44]  A. Triller,et al.  Biology of the postsynaptic glycine receptor. , 1997, International review of cytology.

[45]  S. Froehner Regulation of ion channel distribution at synapses. , 1993, Annual review of neuroscience.