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Fig. 2. Deletion of floxed Myog sequences using CMV-cre and
analysis of embryonic skeletal muscle at E18.5. (A) Southern genome
hybridization of yolk-sac DNA digested with EcoRI from embryos
resulting from a Myogflox/+;CMV-cre/+ intercross and
probed with Myog cDNA. Deletion of the floxed myogenin sequences
produced a 3 kb EcoRI fragment representing the
Myogflox
allele. The 4 kb EcoRI fragment
represents the wild-type allele (Myog+). Lanes 1 and 2
show DNA from Myogflox
/flox
embryos; lanes 3
and 4 show Myogflox
/+ embryos; and lanes 5 and 6
show wild-type embryos. (B) Diaphragms of E18.5 Myog+/-,
Myog-/- and Myogflox
/flox
embryos. The genotype is shown above each image. Scale bar: 100 µm.
(C) Hindlimb sections from E18.5 Myogflox
/+
and Myogflox
/flox
embryos immunostained with
polyclonal M225 anti-myogenin antibody. Arrows indicate positively stained
cells. Scale bar: 100 µm.