4.5 Article

Quantitative trait loci for physical activity traits in mice

Journal

PHYSIOLOGICAL GENOMICS
Volume 32, Issue 3, Pages 401-408

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/physiolgenomics.00241.2007

Keywords

genetics; locomotion; linkage mapping

Funding

  1. Intramural NIH HHS Funding Source: Medline
  2. NCI NIH HHS [U01 CA105417-04, U01 CA105417] Funding Source: Medline
  3. NIAMS NIH HHS [AR-050085, R01 AR050085] Funding Source: Medline
  4. NIA NIH HHS [AG-022417, R15 AG022417] Funding Source: Medline
  5. NIDDK NIH HHS [DK-61635, R01 DK076050, R15 DK061635, DK-076050, R01 DK076050-02] Funding Source: Medline

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The genomic locations and identities of the genes that regulate voluntary physical activity are presently unknown. The purpose of this study was to search for quantitative trait loci (QTL) that are linked with daily mouse running wheel distance, duration, and speed of exercise. F-2 animals (n = 310) derived from high active C57L/J and low active C3H/HeJ inbred strains were phenotyped for 21 days. After phenotyping, genotyping with a fully informative single-nucleotide polymorphism panel with an average intermarker interval of 13.7 cM was used. On all three activity indexes, sex and strain were significant factors, with the F2 animals similar to the high active C57L/J mice in both daily exercise distance and duration of exercise. In the F2 cohort, female mice ran significantly farther, longer, and faster than male mice. QTL analysis revealed no sex-specific QTL but at the 5% experimentwise significance level did identify one QTL for duration, one QTL for distance, and two QTL for speed. The QTL for duration (DUR13.1) and distance (DIST13.1) colocalized with the QTL for speed (SPD13.1). Each of these QTL accounted for similar to 6% of the phenotypic variance, whereas SPD9.1 (chromosome 9, 7 cM) accounted for 11.3% of the phenotypic variation. DUR13.1, DIST13.1, SPD13.1, and SPD9.1 were subsequently replicated by haplotype association mapping. The results of this study suggest a genetic basis of voluntary activity in mice and provide a foundation for future candidate gene studies.

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