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Resolution: standard / high Figure 5.
MommeD mutants show abnormal embryonic development. Timed matings and intercrosses of MommeD mutants. (a)WizMommeD30 mice; data show the number of mice observed (and in brackets the percentage) at 10.5
days post-coitum (dpc), 12.5 dpc, 14.5 dpc and at weaning. Representative embryos
are shown. (b)Rif1MommeD18 mice; data show the number of mice observed (and in brackets the percentage) at 10.5
to 12.5 dpc, 14.5 dpc and at weaning. na, not applicable. (c)Rlf mutants; data show the number of mice observed (and in brackets the percentage).
Embryonic weights were measured from intercrosses of RlfMommeD34 and RlfMommeD28 mice. Homozygous embryos from both had a significant increase in weight variation
at 17.5 dpc or 16.5 dpc, respectively. Weights for each litter were normalized to
the average weight of wild-type embryos in that litter. Each data point represents
an individual. Homozygotes were smaller than wild-type littermates at one week after
birth. ns, not significant. (d)Setdb1MommeD13 and Setdb1MommeD17 mice; data show the number of mice observed (and in brackets the percentage). (e)Smarcc1MommeD19 and Smarcc1MommeD19 mated to wild-type mice revealed incomplete penetrance of heterozygous lethality
after birth. Data show the number of mice (and in brackets the percentage). Weights
of 17.5 dpc Smarcc1MommeD19 embryos and pups were, on average, less than that of wild-type littermates (T-test,
P < 0.0001) and showed greater variation (F-test, P < 0.05). Weights in each litter were normalized to the average weight of wild-type
embryos in that litter. Each data point represents an individual. (f)Smarca4MommeD39 heterozygotes showed reduced viability. Data show the number of mice and in brackets
the percentage. Heterozygotes were smaller than their wild-type littermates. Smarc4MommeD39/+ weighed less (T-test, P < 0.0001) and weights were more variable (F-test, P<0.0001) than wild types. Weights
in each litter were normalized to the average weight of wild-type embryos in that
litter. Each data point represents an individual.
Daxinger et al. Genome Biology 2013 14:R96 doi:10.1186/gb-2013-14-9-r96 |