Literature DB >> 6087160

DARPP-32, a dopamine-regulated neuronal phosphoprotein, is a potent inhibitor of protein phosphatase-1.

H C Hemmings, P Greengard, H Y Tung, P Cohen.   

Abstract

The neurotransmitter dopamine has been demonstrated by biochemical, histochemical and immunocytochemical techniques to be unevenly distributed in the mammalian central nervous system. DARPP-32 (dopamine- and cyclic-AMP-regulated phosphoprotein of molecular weight 32,000) is a neuronal phosphoprotein that displays a regional distribution in the mammalian brain very similar to that of dopamine-containing nerve terminals, being highly concentrated in the basal ganglia. The state of phosphorylation of DARPP-32 can be regulated by dopamine and by cyclic AMP in intact nerve cells, suggesting a role for this phosphoprotein in mediating certain of the effects of dopamine on dopaminoceptive cells. The observation that many of the physical and chemical properties of purified DARPP-32 resemble those of phosphatase inhibitor-1 (inhibitor-1), a widely distributed inhibitor of protein phosphatase-1, suggests that DARPP-32 might also function as a phosphatase inhibitor. We report here that DARPP-32 inhibits protein phosphatase-1 at nanomolar concentrations. Moreover, like inhibitor-1, DARPP-32 is effective as an inhibitor in its phosphorylated but not its dephosphorylated form. Thus, the basal ganglia of mammalian brain contain a region-specific neuronal phosphoprotein that is a protein phosphatase inhibitor.

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Year:  1984        PMID: 6087160     DOI: 10.1038/310503a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  173 in total

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2.  Striatal-enriched protein tyrosine phosphatase expression and activity in Huntington's disease: a STEP in the resistance to excitotoxicity.

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3.  Calcineurin mediates alpha-adrenergic stimulation of Na+,K(+)-ATPase activity in renal tubule cells.

Authors:  A Aperia; F Ibarra; L B Svensson; C Klee; P Greengard
Journal:  Proc Natl Acad Sci U S A       Date:  1992-08-15       Impact factor: 11.205

4.  Activation of Aurora-A kinase by protein phosphatase inhibitor-2, a bifunctional signaling protein.

Authors:  David L Satinover; Craig A Leach; P Todd Stukenberg; David L Brautigan
Journal:  Proc Natl Acad Sci U S A       Date:  2004-06-01       Impact factor: 11.205

Review 5.  Protein phosphatases and their regulation in the control of mitosis.

Authors:  Satoru Mochida; Tim Hunt
Journal:  EMBO Rep       Date:  2012-03       Impact factor: 8.807

6.  Molecular identification of human G-substrate, a possible downstream component of the cGMP-dependent protein kinase cascade in cerebellar Purkinje cells.

Authors:  S Endo; M Suzuki; M Sumi; A C Nairn; R Morita; K Yamakawa; P Greengard; M Ito
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-02       Impact factor: 11.205

7.  Nerve agent exposure elicits site-specific changes in protein phosphorylation in mouse brain.

Authors:  Hongwen Zhu; Jennifer J O'Brien; James P O'Callaghan; Diane B Miller; Qiang Zhang; Minal Rana; Tiffany Tsui; Youyi Peng; John Tomesch; Joseph P Hendrick; Lawrence P Wennogle; Gretchen L Snyder
Journal:  Brain Res       Date:  2010-04-25       Impact factor: 3.252

8.  Calcineurin in the postnatal striatum of the rat: an immunohistochemical study.

Authors:  S Goto; A Hirano
Journal:  Exp Brain Res       Date:  1989       Impact factor: 1.972

9.  Inhibition of Ca2+/calmodulin-dependent protein kinase II by arachidonic acid and its metabolites.

Authors:  D Piomelli; J K Wang; T S Sihra; A C Nairn; A J Czernik; P Greengard
Journal:  Proc Natl Acad Sci U S A       Date:  1989-11       Impact factor: 11.205

10.  Mechanisms of antagonistic action of internal Ca2+ on serotonin-induced potentiation of Ca2+ currents in Helix neurones.

Authors:  P G Kostyuk; E A Lukyanetz
Journal:  Pflugers Arch       Date:  1993-06       Impact factor: 3.657

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