Extended Data Fig. 2: Metabolic analysis and breeding performance of control and mutant TrnE mouse models. | Nature Aging

Extended Data Fig. 2: Metabolic analysis and breeding performance of control and mutant TrnE mouse models.

From: Age-dependent accumulation of mitochondrial tRNA mutations in mouse kidneys linked to mitochondrial kidney diseases

Extended Data Fig. 2

a, Summary of birth rates and mutation load for in vivo DdCBE editing at three sites. bd, Metabolic assessment in 20-week-old and 75-week-old mice. O2 consumption (b) and CO2 elimination (c) are shown for daytime and nighttime. Locomotion (d) is shown as ped meters and total meters (mean ± SEM, n = 9 (20w, control), n = 4–5 (20w, high-mutant TrnE), n = 8 (75w, control and high-mutant TrnE). Unpaired two-tailed Student’s t-test e, Breeding performance (pup number per litter) of TrnE mutant mothers (n = 43) with varying mutation loads, showing no obvious effect on female fertility. The black line (y = mx + c) represents the line of best fit with 95% confidence intervals (gray). f, Total pup number in a 6-month fertility test of control (TrnE 0–17%, n = 4) and high-mutant (TrnE 72–81%, n = 5) TrnE females (mean ± SD, unpaired two-tailed Student’s t-test). g, Male fertility comparison between WT and TrnE high-mutant group. Total pup number over 6 months is shown as the accumulation of litter index. h, Testis weight comparison between control and TrnE high-mutant groups at different ages (3, 8, 24, 50, and 75 weeks) (mean ± SD, n = 3 (3w), n = 5 (8w), n = 7 (24w), n = 8–9 (50w) and n = 6–7 (75w). Unpaired two-tailed Student’s t-test).

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