This proposal seeks to provide Edward S. Brodkin, M.D. with a five-year period of supervised research training that will enable him to become an independent investigator, with a research focus on the genetic dissection of aggressive behaviors in mice. The candidate will gain training and experience in high resolution genetic mapping of quantitative trait loci (QTLs), candidate gene analysis, and mutagenesis methods. Background: Aggressive behaviors are a major source of morbidity and mortality in patients with severe neuropsychiatric disorders. A propensity towards aggression is substantially heritable in mammals. Genetic dissections of aggressive behaviors in mice can identify biological pathways that underlie mammalian aggression and that may be involved in the pathophysiology of human psychiatric disorders. Dr. Brodkin has previously identified aggression QTLs on chromosome 10 (Aggr1) and chromosome X (Aggr2) in NZB/B1NJ and A/J mice; however he has had no previous experience with high-resolution (fine) mapping of QTLs, candidate gene analysis, or mutagenesis methodologies. Training in these methodologies is important for the candidate's career development and is necessary for his future research independence.
Specific Aims of Research Plan: 1. Fine-mapping aggression QTLs. Using NZB/B1NJ and AJ mice as progenitor strains, interval-specific congenic strains will be bred for the Aggr1 and Aggr2 QTL intervals and will be used to fine map the QTL intervals. 2. Candidate gene analysis. Within the finely mapped QTL intervals, candidate genes that are expressed in brain will be sequenced in the progenitor strains to look for functional polymorphisms. Expression level of the candidate genes in brain regions will be compared in the progenitor strains. 3. Initiation of mutagenesis studies of aggressive behaviors. ENU mutagenesis and gene-trap studies of aggressive behaviors in mice will be initiated. ENVIRONMENT: The training will be conducted at the Center for Neurobiology and Behavior, Department of Psychiatry, University of Pennsylvania School of Medicine. RESEARCH CAREER DEVELOPMENT: The candidate will take relevant courses at Penn and elsewhere and will attend research meetings. Dr. Wade Berrettini will be the mentor, and Drs. Maja Bucan, Russell Buono, Thomas Ferraro, and Irwin Lucki will provide additional consultation in genetics and behavioral analysis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Clinical Investigator Award (CIA) (K08)
Project #
1K08MH068586-01
Application #
6675250
Study Section
Mammalian Genetics Study Section (MGN)
Program Officer
Wynne, Debra K
Project Start
2003-07-01
Project End
2008-06-30
Budget Start
2003-07-01
Budget End
2004-06-30
Support Year
1
Fiscal Year
2003
Total Cost
$179,582
Indirect Cost
Name
University of Pennsylvania
Department
Psychiatry
Type
Schools of Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Dow, H C; Kreibich, A S; Kaercher, K A et al. (2011) Genetic dissection of intermale aggressive behavior in BALB/cJ and A/J mice. Genes Brain Behav 10:57-68
Gillihan, Seth J; Rao, Hengyi; Brennan, Lauretta et al. (2011) Serotonin transporter genotype modulates the association between depressive symptoms and amygdala activity among psychiatrically healthy adults. Psychiatry Res 193:161-7
Gillihan, Seth J; Rao, Hengyi; Wang, Jiongjiong et al. (2010) Serotonin transporter genotype modulates amygdala activity during mood regulation. Soc Cogn Affect Neurosci 5:1-10
Halene, T B; Ehrlichman, R S; Liang, Y et al. (2009) Assessment of NMDA receptor NR1 subunit hypofunction in mice as a model for schizophrenia. Genes Brain Behav 8:661-75
Potenza, Marc N; Brodkin, Edward S; Yang, Bao-Zhu et al. (2008) Quantitative trait locus analysis identifies rat genomic regions related to amphetamine-induced locomotion and Galpha(i3) levels in nucleus accumbens. Neuropsychopharmacology 33:2735-46
Brodkin, Edward S (2008) Social behavior phenotypes in fragile X syndrome, autism, and the Fmr1 knockout mouse: theoretical comment on McNaughton et al. (2008). Behav Neurosci 122:483-9
Rao, Hengyi; Gillihan, Seth J; Wang, Jiongjiong et al. (2007) Genetic variation in serotonin transporter alters resting brain function in healthy individuals. Biol Psychiatry 62:600-6
Brodkin, Edward S (2007) BALB/c mice: low sociability and other phenotypes that may be relevant to autism. Behav Brain Res 176:53-65
Crowley, James J; Brodkin, Edward S; Blendy, Julie A et al. (2006) Pharmacogenomic evaluation of the antidepressant citalopram in the mouse tail suspension test. Neuropsychopharmacology 31:2433-42
Sankoorikal, Geena Mary V; Kaercher, Kristin A; Boon, Catherine J et al. (2006) A mouse model system for genetic analysis of sociability: C57BL/6J versus BALB/cJ inbred mouse strains. Biol Psychiatry 59:415-23

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