Figure 1
From: Dual barrier system against xenomitochondrial contamination in mouse embryos

Preimplantation development and metabolic profile of mouse embryos harbouring bovine mtDNAs. (A) Developmental arrest in the mouse embryos harbouring bovine mtDNAs (mtB-M embryos (n = 97); orange). Note that proportions of surviving embryos in mtB-M embryos from the 4-cell (4C) stage were significantly reduced compared to IVF embryos (n = 128; blue) and mtM-M embryos (mouse embryos with mitochondria derived from other mouse embryos (n = 59); grey). Data were analyzed after arcsine transformation. *p < 0.05 and **p < 0.01. (B, C) Production levels of cellular reactive oxygen species (ROS) at the 4C stage and 8C stage. IVF (4C: n = 23, 8C: n = 23), mtM-M (n = 4, 12), and mtB-M (n = 7, 18). The ROS level in the mtB-M embryos at the 4C stage was elevated compared to that in the IVF embryos (***p < 0.001). Bar graph shows mean ± standard error of the mean (S.E.M.). (D) Relative expression of mitochondrial respiratory chain (MRC) complex-related genes at the 4C stage. Ndufa3 for MRC complex I [IVF (n = 6) vs. mtB-M (n = 7)], Sdhd for MRC complex II (n = 4 vs. n = 4), Uqcr10 for MRC complex III (n = 6 vs. n = 7), Cox6b1 for MRC complex IV (n = 6 vs. n = 7), and Atp5h for MRC complex V (n = 4 vs. n = 4). Each value was normalised to H2afz expression. *p < 0.05. (E) The ATP contents (pmol / embryo) in IVF and mtB-M embryos. More than 50 embryos were measured for each cell stage, and then, values within mean ± 1 standard deviation were selected. Among them, 28 to 42 embryos were analyzed for each cell stage. The data for all embryos were represented in Fig. S2. *p < 0.05 and **p < 0.01. (F) The PDH activity in IVF (n = 18–33; blue), mtB-M (n = 15–21; orange) embryos, and presumptive 1C stage bovine (n = 9; white) embryos. *p < 0.05, **p < 0.01, and ***p < 0.001.