Circadian gene variants and the skeletal muscle circadian clock contribute to the evolutionary divergence in longevity across Drosophila populations

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 1.
Figure 1.

Drosophila long-lived O lines are protected from age-related skeletal muscle functional decay. (A) Lifespan extension in the O lines versus B3. B3 flies had a median lifespan of 42 d (n = 180), whereas O1 (n = 273) and O3 (n = 213) flies had a median lifespan of 72 and 76 d, respectively (P < 0.05). (B) With aging, the B3 line displays a progressive increase in the ratio of flies unable to climb, as estimated with negative geotaxis assays (P < 0.05), whereas the O lines are partly protected. (C,D) Analysis of spontaneous locomotion indicates that, although there is no substantial difference in young age (1 wk old) (C), O lines have increased spontaneous locomotion and rhythmicity in old age (6 wk old) (D), compared with the parental B3 strain (P < 0.05; n[batches of 10 flies] = 10). (E,F) Flight defects arise with aging in B3 but less so in the O lines, as also demonstrated by the flight index (F), which is calculated considering all classes of flyers shown in E; n = 100–102, SEM, (***) P < 0.001. (G) Jump ability declines with aging in B3 flies but not in O1 and O3 flies; n = 25, SEM, (***) P < 0.001.

This Article

  1. Genome Res. 29: 1262-1276

Preprint Server