Genome-Wide Association for Fear Conditioning in an Advanced Intercross Mouse Line

被引:38
作者
Parker, Clarissa C. [1 ]
Sokoloff, Greta [1 ]
Cheng, Riyan [1 ]
Palmer, Abraham A. [1 ,2 ]
机构
[1] Univ Chicago, Dept Human Genet, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Psychiat & Behav Neurosci, Chicago, IL 60637 USA
关键词
Advanced intercross lines; Fear conditioning; Fear learning; Genome-wide association; Post-traumatic stress disorder; Quantitative trait loci; POSTTRAUMATIC-STRESS-DISORDER; DIAZEPAM-BINDING INHIBITOR; MESSENGER-RNA EXPRESSION; QUANTITATIVE TRAIT LOCUS; GENE-EXPRESSION; NEUROTROPHIC FACTOR; IMMOBILIZATION STRESS; SYNAPTIC PLASTICITY; SUBSPECIFIC ORIGIN; RECEPTOR-BINDING;
D O I
10.1007/s10519-011-9524-8
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Fear conditioning (FC) may provide a useful model for some components of post-traumatic stress disorder (PTSD). We used a C57BL/6J x DBA/2J F-2 intercross (n = 620) and a C57BL/6J x DBA/2J F-8 advanced intercross line (n = 567) to fine-map quantitative trait loci (QTL) associated with FC. We conducted an integrated genome-wide association analysis in QTLRel and identified five highly significant QTL affecting freezing to context as well as four highly significant QTL associated with freezing to cue. The average percent decrease in QTL width between the F-2 and the integrated analysis was 59.2%. Next, we exploited bioinformatic sequence and expression data to identify candidate genes based on the existence of non-synonymous coding polymorphisms and/or expression QTLs. We identified numerous candidate genes that have been previously implicated in either fear learning in animal models (, , , , , and ) or PTSD in humans (, and ); other identified genes may represent novel findings. The integration of F-2 and AIL data maintains the advantages of studying FC in model organisms while significantly improving resolution over previous approaches.
引用
收藏
页码:437 / 448
页数:12
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