Investigations into the molecular targets of drugs of abuse and their associated intracellular signaling pathways have yielded a wealth of information regarding the cellular perturbations associated with these drugs. The combined studies outlined in Projects I-IV will extend upon this existing knowledge with rigorous cell biological, molecular, biochemical, behavioral, and electrophysiological studies of neuronal cells upon drug treatment. These studies have the potential to provide greater insights into the causes of drug dependence as well as to elucidate possible novel targets for pharmacological intervention. The Scientific Core will be a center devoted to facilitating those experiments proposed in Projects I-IV that require the use of genetically modified animals, yeast two-hybrid screens, and various key biological reagents. The experiments outlined in these Projects require the creation and maintenance of large numbers of genetically modified animals. The creation and characterization of necessary transgenic mice, and the maintenance of these and all other genetically modified mice is Specific Aim I of the Core. To help identify and characterize novel protein-protein interactions relevant to signaling molecules targeted by drug of abuse, the Core will design and execute yeast two-hybrid screens in Specific Aim II. In addition, the Scientific Core will be a key source of various reagents needed for the experiments outlined in Projects I-IV. Key proteins, enzymes, and antibodies will be produced in Specific Aim III,while new polyclonal antibodies, including phosphorylation state- specific antibodies, will be produced in Specific Aim IV.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Program Projects (P01)
Project #
5P01DA010044-15
Application #
8022940
Study Section
Special Emphasis Panel (ZDA1)
Project Start
Project End
Budget Start
2010-02-01
Budget End
2011-01-31
Support Year
15
Fiscal Year
2010
Total Cost
$507,654
Indirect Cost
Name
Rockefeller University
Department
Type
DUNS #
071037113
City
New York
State
NY
Country
United States
Zip Code
10065
Li, Daniel; Musante, Veronica; Zhou, Wenliang et al. (2018) Striatin-1 is a B subunit of protein phosphatase PP2A that regulates dendritic arborization and spine development in striatal neurons. J Biol Chem 293:11179-11194
Seo, J-S; Zhong, P; Liu, A et al. (2018) Elevation of p11 in lateral habenula mediates depression-like behavior. Mol Psychiatry 23:1113-1119
Madero-Pérez, Jesús; Fdez, Elena; Fernández, Belén et al. (2018) Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation. Mol Neurodegener 13:3
Chang, Audrey N; Gao, Ning; Liu, Zhenan et al. (2018) The dominant protein phosphatase PP1c isoform in smooth muscle cells, PP1c?, is essential for smooth muscle contraction. J Biol Chem 293:16677-16686
Andrade, Erika C; Musante, Veronica; Horiuchi, Atsuko et al. (2017) ARPP-16 Is a Striatal-Enriched Inhibitor of Protein Phosphatase 2A Regulated by Microtubule-Associated Serine/Threonine Kinase 3 (Mast 3 Kinase). J Neurosci 37:2709-2722
Musante, Veronica; Li, Lu; Kanyo, Jean et al. (2017) Reciprocal regulation of ARPP-16 by PKA and MAST3 kinases provides a cAMP-regulated switch in protein phosphatase 2A inhibition. Elife 6:
Milosevic, Ana; Liebmann, Thomas; Knudsen, Margarete et al. (2017) Cell- and region-specific expression of depression-related protein p11 (S100a10) in the brain. J Comp Neurol 525:955-975
Ceglia, Ilaria; Lee, Ko-Woon; Cahill, Michael E et al. (2017) WAVE1 in neurons expressing the D1 dopamine receptor regulates cellular and behavioral actions of cocaine. Proc Natl Acad Sci U S A 114:1395-1400
Seo, J-S; Wei, J; Qin, L et al. (2017) Cellular and molecular basis for stress-induced depression. Mol Psychiatry 22:1440-1447
Nishi, Akinori; Matamales, Miriam; Musante, Veronica et al. (2017) Glutamate Counteracts Dopamine/PKA Signaling via Dephosphorylation of DARPP-32 Ser-97 and Alteration of Its Cytonuclear Distribution. J Biol Chem 292:1462-1476

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