Gene networks associated with conditional fear in mice identified using a systems genetics approach

被引:64
作者
Park, Christopher C. [1 ]
Gale, Greg D. [1 ]
de Jong, Simone [2 ,3 ]
Ghazalpour, Anatole [4 ]
Bennett, Brian J. [5 ]
Farber, Charles R. [4 ,8 ]
Langfelder, Peter [5 ]
Lin, Andy [1 ]
Khan, Arshad H. [1 ]
Eskin, Eleazar [5 ,6 ]
Horvath, Steve [5 ]
Lusis, Aldons J. [4 ,5 ]
Ophoff, Roel A. [2 ,3 ,5 ,7 ]
Smith, Desmond J. [1 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
[2] UMC Utrecht, Dept Med Genet, NL-3584 CG Utrecht, Netherlands
[3] UMC Utrecht, Rudolf Magnus Inst Neurosci, NL-3584 CG Utrecht, Netherlands
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med Cardiol, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA
[6] Univ Calif Los Angeles, Dept Comp Sci, Los Angeles, CA 90095 USA
[7] Univ Calif Los Angeles, David Geffen Sch Med, Ctr Neurobehav Genet, Los Angeles, CA 90095 USA
[8] Univ Virginia, Sch Med, Ctr Publ Hlth Genom, Charlottesville, VA 22908 USA
基金
美国国家卫生研究院;
关键词
QUANTITATIVE TRAIT LOCI; FALSE DISCOVERY RATE; CONTEXTUAL FEAR; EXPRESSION; MEMORY; TERM; HIPPOCAMPUS; DISSECTION; PLASTICITY; SOFTWARE;
D O I
10.1186/1752-0509-5-43
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Our understanding of the genetic basis of learning and memory remains shrouded in mystery. To explore the genetic networks governing the biology of conditional fear, we used a systems genetics approach to analyze a hybrid mouse diversity panel (HMDP) with high mapping resolution. Results: A total of 27 behavioral quantitative trait loci were mapped with a false discovery rate of 5%. By integrating fear phenotypes, transcript profiling data from hippocampus and striatum and also genotype information, two gene co-expression networks correlated with context-dependent immobility were identified. We prioritized the key markers and genes in these pathways using intramodular connectivity measures and structural equation modeling. Highly connected genes in the context fear modules included Psmd6, Ube2a and Usp33, suggesting an important role for ubiquitination in learning and memory. In addition, we surveyed the architecture of brain transcript regulation and demonstrated preservation of gene co-expression modules in hippocampus and striatum, while also highlighting important differences. Rps15a, Kif3a, Stard7, 6330503K22RIK, and Plvap were among the individual genes whose transcript abundance were strongly associated with fear phenotypes. Conclusion: Application of our multi-faceted mapping strategy permits an increasingly detailed characterization of the genetic networks underlying behavior.
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页数:15
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