G‐protein γ7 subunit is selectively expressed in medium‐sized neurons and dendrites of the rat neostriatum

We used subtractive hybridization to isolate clones of γ7, a 68 residue G‐protein γ subunit. Northern blotting and in situ hybridization reveal that the γ7 subunit mRNA is expressed primarily in medium‐sized neurons of the neostriatum and nucleus accumbens and neurons of the olfactory tubercle, and at low levels in the dentate gyrus of the hippocampal formation and laminae II–III, and V of the neocortex. The γ7 mRNA is translocated into dendrites of neurons in the neostriatum and the dentate gyrus of the hippocampus. γ7 is expressed at relatively very low concentrations in peripheral tissues. The selective pattern of γ7 expression within the brain is highly reminiscent of those of the striatum‐enriched adenylyl cyclase ACST, dopamine receptors, and the α subunit of Golf, suggesting that, in striatum, γ7 may be a subunit of a Golfα‐containing G protein that couples dopamine receptors selectively to ACST.Copyright © 1994 Wiley‐Liss, Inc.

[1]  M. Erlander,et al.  Chromosomal mapping of mouse genes expressed selectively within the central nervous system. , 1994, Genomics.

[2]  P C Sternweis,et al.  Regulation of purified subtypes of phosphatidylinositol-specific phospholipase C beta by G protein alpha and beta gamma subunits. , 1993, The Journal of biological chemistry.

[3]  C. Verney,et al.  G(olf) and Gs in rat basal ganglia: possible involvement of G(olf) in the coupling of dopamine D1 receptor with adenylyl cyclase , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[4]  C J Marshall,et al.  Protein prenylation: a mediator of protein-protein interactions. , 1993, Science.

[5]  S. Snyder,et al.  Cloning and expression of an adenylyl cyclase localized to the corpus striatum , 1993, Nature.

[6]  G. Schultz,et al.  Selectivity in signal transduction determined by gamma subunits of heterotrimeric G proteins. , 1993, Science.

[7]  M. Simon,et al.  Subunits βγ of heterotrimeric G protein activate β2 isoform of phospholipase C , 1992, Nature.

[8]  M. Camps,et al.  Isozyme-selective stimulation of phospholipase C-β2 by G protein βγ-subunits , 1992, Nature.

[9]  J. Boyer,et al.  Beta gamma-subunit activation of G-protein-regulated phospholipase C. , 1992, The Journal of biological chemistry.

[10]  J. Cali,et al.  Selective tissue distribution of G protein gamma subunits, including a new form of the gamma subunits identified by cDNA cloning. , 1992, The Journal of biological chemistry.

[11]  J. Blank,et al.  Activation of cytosolic phosphoinositide phospholipase C by G-protein beta gamma subunits. , 1992, The Journal of biological chemistry.

[12]  M. Simon,et al.  G protein beta gamma subunits synthesized in Sf9 cells. Functional characterization and the significance of prenylation of gamma. , 1992, The Journal of biological chemistry.

[13]  P. Greengard,et al.  Developmental regulation of phosphoprotein gene expression in the caudate-putamen of rat: An in situ hybridization study , 1992, Neuroscience.

[14]  G. Schultz,et al.  Different β-subunits determine G-protein interaction with transmembrane receptors , 1992, Nature.

[15]  O. Steward,et al.  Getting the message from the gene to the synapse: sorting and intracellular transport of RNA in neurons , 1992, Trends in Neurosciences.

[16]  N. Aronson,et al.  Characterization of the cDNA and genomic sequence of a G protein gamma subunit (gamma 5) , 1992, Molecular and cellular biology.

[17]  K. Ray,et al.  The Drosophila G protein gamma subunit gene (D-G gamma 1) produces three developmentally regulated transcripts and is predominantly expressed in the central nervous system. , 1992, The Journal of biological chemistry.

[18]  B. Conklin,et al.  Hormonal stimulation of adenylyl cyclase through Gi-protein βγ subunits , 1992, Nature.

[19]  G. Schultz,et al.  Assignment of G-protein subtypes to specific receptors inducing inhibition of calcium currents , 1991, Nature.

[20]  L. Birnbaumer,et al.  Gamma-subunits of G proteins, but not their alpha- or beta-subunits, are polyisoprenylated. Studies on post-translational modifications using in vitro translation with rabbit reticulocyte lysates. , 1991, The Journal of biological chemistry.

[21]  C. Gerfen,et al.  D1 and D2 dopamine receptor-regulated gene expression of striatonigral and striatopallidal neurons. , 1990, Science.

[22]  R. Rozmahel,et al.  Human dopamine D1 receptor encoded by an intronless gene on chromosome 5 , 1990, Nature.

[23]  D. Grandy,et al.  Cloning and expression of human and rat Dt dopamine receptors , 1990, Nature.

[24]  M. Caron,et al.  Molecular cloning and expression of the gene for a human D1 dopamine receptor , 1990, Nature.

[25]  F. Bloom,et al.  Subtractive cDNA cloning of RC3, a rodent cortex‐enriched mRNA encoding a novel 78 residue protein , 1990, Journal of neuroscience research.

[26]  P. Greengard,et al.  Activation of NMDA receptors induces dephosphorylation of DARPP-32 in rat striatal slices , 1990, Nature.

[27]  C. Slaughter,et al.  Existence of two gamma subunits of the G proteins in brain. , 1989, The Journal of biological chemistry.

[28]  R. Aebersold,et al.  A G protein gamma subunit shares homology with ras proteins. , 1989, Science.

[29]  D. Clapham,et al.  G-protein βγ-subunits activate the cardiac muscarinic K+-channel via phospholipase A2 , 1989, Nature.

[30]  A. Brown,et al.  Recombinant alpha i-3 subunit of G protein activates Gk-gated K+ channels. , 1989, The Journal of biological chemistry.

[31]  A. Campagnoni,et al.  Regional expression of myelin protein genes in the developing mouse brain: In situ hybridization studies , 1988, Journal of neuroscience research.

[32]  D. Clapham,et al.  The βγ subunits of GTP-binding proteins activate the muscarinic K+ channel in heart , 1987, Nature.

[33]  S. Henikoff Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing. , 1984, Gene.

[34]  A. Feinberg,et al.  A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. , 1983, Analytical biochemistry.

[35]  T. Pasik,et al.  Ultrastructure of Golgi-impregnated and gold-toned spiny and aspiny neurons in the monkey neostriatum , 1980, Journal of neurocytology.

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

[37]  D. Sibley,et al.  Molecular biology of dopamine receptors. , 1992, Trends in pharmacological sciences.

[38]  B. Bloch,et al.  Ontogeny of D1 and DARPP-32 gene expression in the rat striatum: an in situ hybridization study. , 1992, Brain research. Molecular brain research.