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. Author manuscript; available in PMC: 2008 Sep 18.
Published in final edited form as: Curr Biol. 2007 Sep 6;17(18):1586ā€“1594. doi: 10.1016/j.cub.2007.08.034

Figure 2. Systemic loss of Kif3a and/or Tg737 from adult mice results in a hyperphagia-induced obesity phenotype.

Figure 2

(A) Images of Kif3a-cKO (left) and Kif3a-cWT (right) females 16 weeks after administration of tamoxifen. These littermates were of equivalent weight at time of injection. (B) Tg737-cKO (left) and Tg737-cWT (right) females are also shown 16 weeks after tamoxifen administration. (C,D) Body weight analysis of (C) Kif3a-cWT and Kif3a-cKO and (D) Tg737-cWT and Tg737-cKO males and females after tamoxifen administration (week zero). The number of Kif3a-cKO and Kif3a-cWT females analyzed in this study changed at week 6 when several of the mice were used to evaluate fat pad and organ weight masses. Animals were 8ā€“12 weeks of age at the time of initial tamoxifen administration. (E,F) Weekly food intake analysis of (E) Kif3a-cKO and Kif3a-cWT males and (F) Tg737-cKO and Tg737-cWT males after initial tamoxifen administration (week 0). Several animals were euthanized in the course of the experiment for body composition and histological analyses. Kif3a-cWT controls that were not induced with tamoxifen are also shown in blue (E). (G) Body weight analysis in pair feeding studies of Kif3a-cKO males after administration of tamoxifen. Separate groups of Kif3a-cWT males were tested with or without tamoxifen to assess changes due to tamoxifen administration. (H) Kif3a-cWT and Kif3a-cKO males were administered tamoxifen and were diet restricted to 4.0 g/day for 8 subsequent weeks. At 8 weeks, all mice were then fed ad libitum (* = pā‰¤0.05, indicates the initial point of significant deviation between controls and mutants).