Environmental factors interact with gene variants to influence patterns of alcohol use, abuse, adaptation, addiction, withdrawal, and relapse. Ethanol is a highly soluble small molecule that has subtle allosteric effects on many molecular processes in the CNS and not all of its many targets are known. Individual differences in how humans respond to ethanol are also not well understood. This project leverages the broad expertise of INIA to explore and test genetic, molecular, synaptic, cellular, and behavioral causes of alcohol consumption and the increased vulnerability following stressors. Our focus is on exploiting new high-resolution genomic resources (sequence data, SNPs, mRNA microarrays) to model networks of molecular and synaptic interactions in forebrain regions that have important roles in alcoholism. To ensure robust results we use two large genetic reference populations of rodents (BXD mice and HXB rats) and apply sophisticated statistical methods to generate hypotheses that are then subjected to rigorous experimental testing. We combine data from our own work with data from numerous other published studies using a systems genetics approach. This combined approach is made possible by our use of well studied genetic reference populations. We will define shared and unique genetic and synaptic factors that modulate ethanol use and the convergent effects of stress on ethanol addiction and relapse.
In Aim 1 (Data Generation) we generate normative expression data and networks for four key forebrain regions (medial prefrontal cortex, nucleus accumbens, bed nucleus of the stria terminalis, and the basolateral amygdala) from complementary genetic reference populations with different genetic structures (inbred Rl and hybrid RIX lines). We are acquiring gene expression data for 48 brain regions in C57BU6J and DBA/2J lines. Our goal is to extract robust networks that are cross-validated and that have strong prospects of generalizing to admixed human populations. Data will be made publicly available on the GeneNetwork (GN) site (www.genenetwork.org).
In Aim 2 (Model Construction) we develop open source programs and standard operating procedures to produce well defined and testable hypotheses. The INIA Models Work Group will be responsible for developing, testing, and using the INIA GeneNetwork (GN) and this software to construct explicit process diagrams and statistical models. We will integrate these models into GN for use and critique by INIA and NIAAA researchers.
In Aim 3 (Predictive Validation), members of INIA will experimentally manipulate sets of isogenic lines (BXD and RIX), predicting whether they will be high or low responders using INIA standard operating protocols. The synergy among genetic, transcriptome, electrophysiological, and experimental studies and data sets will allow us to test the role of complex interactions in the mesocorticolimbic system that contribute to alcoholism and maladaptive stress response.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01AA013499-10
Application #
8019580
Study Section
Special Emphasis Panel (ZAA1-DD (71))
Program Officer
Grandison, Lindsey
Project Start
2002-02-05
Project End
2012-01-31
Budget Start
2011-02-01
Budget End
2012-01-31
Support Year
10
Fiscal Year
2011
Total Cost
$339,071
Indirect Cost
Name
University of Tennessee Health Science Center
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
941884009
City
Memphis
State
TN
Country
United States
Zip Code
38163
Neuner, Sarah M; Garfinkel, Benjamin P; Wilmott, Lynda A et al. (2016) Systems genetics identifies Hp1bp3 as a novel modulator of cognitive aging. Neurobiol Aging 46:58-67
Alam, Gelareh; Miller, Diane B; O'Callaghan, James P et al. (2016) MPTP neurotoxicity is highly concordant between the sexes among BXD recombinant inbred mouse strains. Neurotoxicology 55:40-7
Lopez, Marcelo F; Miles, Michael F; Williams, Robert W et al. (2016) Variable effects of chronic intermittent ethanol exposure on ethanol drinking in a genetically diverse mouse cohort. Alcohol :
Shi, Xiao; Walter, Nicole A R; Harkness, John H et al. (2016) Genetic Polymorphisms Affect Mouse and Human Trace Amine-Associated Receptor 1 Function. PLoS One 11:e0152581
Porcu, Patrizia; O'Buckley, Todd K; Lopez, Marcelo F et al. (2016) Initial genetic dissection of serum neuroactive steroids following chronic intermittent ethanol across BXD mouse strains. Alcohol :
Wang, Xusheng; Pandey, Ashutosh K; Mulligan, Megan K et al. (2016) Joint mouse-human phenome-wide association to test gene function and disease risk. Nat Commun 7:10464
Delprato, A; Bonheur, B; Algéo, M-P et al. (2015) Systems genetic analysis of hippocampal neuroanatomy and spatial learning in mice. Genes Brain Behav 14:591-606
Bubier, Jason A; Phillips, Charles A; Langston, Michael A et al. (2015) GeneWeaver: finding consilience in heterogeneous cross-species functional genomics data. Mamm Genome 26:556-66
Padula, Audrey E; Griffin 3rd, William C; Lopez, Marcelo F et al. (2015) KCNN Genes that Encode Small-Conductance Ca2+-Activated K+ Channels Influence Alcohol and Drug Addiction. Neuropsychopharmacology 40:1928-39
Cook, Melloni N; Baker, Jessica A; Heldt, Scott A et al. (2015) Identification of candidate genes that underlie the QTL on chromosome 1 that mediates genetic differences in stress-ethanol interactions. Physiol Genomics 47:308-17

Showing the most recent 10 out of 105 publications