The Transgenic Core provides all of our preclinical Projects (Projects 1-4) with state-of-the-art tools toenable manipulation of specific genes of interest in brain reward regions in the context of animal models ofdepression and antidepressant action. Centralizing these functions within a single Core derives substantialcost savings and ensures the proper and rigorous use of these approaches.First, numerous lines of transgenic and knockout mice, generated by Center investigators or obtained fromother laboratories, are required for the Center's research. The Core is responsible for breeding, genotyping,and maintaining the progeny for use by the individual Projects, as well as providing the appropriate controlmice. The Core is also be responsible for generating several new lines of transgenic and knockout micerequired for the proposed program of research. Prominent among the existing and proposed new mouselines are those that manipulate the expression of specific genes both temporally and spatially, i.e., inducibleand cell-targeted mutations. Our group has substantial experiencewith these methods, which include thetetracycline gene regulation system and the Cre-loxP system. Indeed, Core research has succeeded indeveloping truly inducible, cell-targeted gene knockouts in brain reward regions.Second, the Core provides Project investigators with vectors for viral-mediated gene transfer, an importanttool used in our research program. Center investigators have played a leading role nationally in these efforts,and now routinely use herpes simplex and adeno-associated viral vectors. This work includes viralexpression of Cre to induce highly localized knockouts in brain, and the expression of small hairpin RNA's toinduce knockdowns of genes via an RNA interference mechanism.We are very proud of the Core's achievements over the past 4 years, and we will work during the next Grantperiod to introduce further innovations in mouse mutagenesis and viral gene transfer for studies ofdepression.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Specialized Center (P50)
Project #
2P50MH066172-06
Application #
7333063
Study Section
Special Emphasis Panel (ZMH1-ERB-S (03))
Project Start
2007-08-01
Project End
2012-07-31
Budget Start
2007-08-09
Budget End
2008-07-31
Support Year
6
Fiscal Year
2007
Total Cost
$362,243
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Type
DUNS #
800771545
City
Dallas
State
TX
Country
United States
Zip Code
75390
Olausson, Peter; Kiraly, Drew D; Gourley, Shannon L et al. (2013) Persistent effects of prior chronic exposure to corticosterone on reward-related learning and motivation in rodents. Psychopharmacology (Berl) 225:569-77
Warren, Brandon L; Vialou, Vincent F; IƱiguez, Sergio D et al. (2013) Neurobiological sequelae of witnessing stressful events in adult mice. Biol Psychiatry 73:7-14
Nestler, Eric J (2013) Treating the brain deep down: Brain surgery for anorexia nervosa? Nat Med 19:678-9
Quinn, Jennifer J; Pittenger, Christopher; Lee, Anni S et al. (2013) Striatum-dependent habits are insensitive to both increases and decreases in reinforcer value in mice. Eur J Neurosci 37:1012-21
Golden, Sam A; Christoffel, Daniel J; Heshmati, Mitra et al. (2013) Epigenetic regulation of RAC1 induces synaptic remodeling in stress disorders and depression. Nat Med 19:337-44
Olausson, P; Venkitaramani, D V; Moran, T D et al. (2012) The tyrosine phosphatase STEP constrains amygdala-dependent memory formation and neuroplasticity. Neuroscience 225:1-8
Sanchez-Ortiz, Efrain; Yui, Daishi; Song, Dongli et al. (2012) TrkA gene ablation in basal forebrain results in dysfunction of the cholinergic circuitry. J Neurosci 32:4065-79
Russo, Scott J; Murrough, James W; Han, Ming-Hu et al. (2012) Neurobiology of resilience. Nat Neurosci 15:1475-84
Torregrossa, Mary M; Xie, Maylene; Taylor, Jane R (2012) Chronic corticosterone exposure during adolescence reduces impulsive action but increases impulsive choice and sensitivity to yohimbine in male Sprague-Dawley rats. Neuropsychopharmacology 37:1656-70
Lobo, Mary Kay; Nestler, Eric J; Covington 3rd, Herbert E (2012) Potential utility of optogenetics in the study of depression. Biol Psychiatry 71:1068-74

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