Experiment
Multivariate approaches are used here to uncover the genetic architecture of anxiety related phenotypes. Novel QTL were detected on Chromosomes 3, 9, 13 and 17.
Genotype and phenotype data generated from combined results from (H1 x L1) and (H2 x L2) intercrosses of 1636 F2 DeFries mice, in previously published works (J:70479 and J88525), were used. Genetic mapping data was analyyzed using MAPMAKER software. Multivariate analyses were performed with Multi-QTL and JZ-MAPQTL.
Twenty-three phenotypes (Table 1) were analyzed jointly using Multi-QTL and obtained genome-wide significance threshold by permutation. Analysis detected LOD scores with p< 0.05 on 15 chromosomes (Table 2); 10 of which corresponded to those previoulsy identified by single-trait analysis on Chrs 1, 4, 7, 8, 11, 12, 14, 15, 18, and X. On 4 chromosomes, 3, 9, 13 and 17 only the multivariate analyses identified QTL.
Axtrb9, anxiety-related behaviors 9, mapped to Chromosome 17 with a LOD=22.5, p=0.0000. [Table 2].
Traits contributing to the Axtrb9 QTL were [Table 3]:
open field defecation, p=0.019;
activity in the center of the open field, p=0.002;
time spent in the center of the open field, p=0.011;
activity in the dark side of the light dark box, p=0.006;
transitions in the light dark box, p=0.006;
activity in the light side of the light dark box, p=0.010;
time spent on the light side of the light dark box, p=0.004;
latency in the light dark box, p=0.008;
closed entries in the elevated plus maze, p=0.000;
activity in the closed arm of the elevated plus maze, p=0.000; and
latency to enter the open arm of the elevated plus maze, p=0.028