Rescue of the cei maternal-effect cellularization defect by transgenic copies of Tol2-EF1a-aurB.

1Genotype of the females generating the clutch: absence or presence of the Tol2-EF1��-aurB transgene (tg(?) or tg(+), respectively) in a cei/cei homozygous mutant background. Numbered rows indicate results from individual sibling adult females, derived from four independent founder males, which have been genotyped for the presence or absence of the transgene according to Materials and Methods. Results from the two categories of females have been pooled in the rows labeled ��total tg(?)�� and ��total tg(+)�� (highlighted in gray).2Fraction of embryos exhibiting cellularization defects of various severities at the 1,000-cell stage, according to the classification presented in Figure 1O�CR. For clarity, percentages have been rounded off to the nearest digit, with the exception of values under 1.0, which have been rounded off to the nearest decimal.