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Fig. 6. Severely affected EomesN/+;
NodalLacZ/+ double heterozygotes fail to rotate the PD
axis. (A,A') Nodal expression normally confined to the
posterior epiblast at E6.5, (B,B') persists throughout the
entire proximal epiblast of EomesN/+;
NodalLacZ/+ double heterozygous embryos. (C-F)
AVE-markers (Hex and Cer) remain localized to the distal tip
of double heterozygous mutant embryos. (G-L) Consequently posterior
marker genes (cripto, Eomes and brachyury) are expressed throughout
the proximal epiblast. (M,N) Spc4 is expressed at
normal levels in the ExE of mutant embryos, which fails to be displaced
proximally. (O-P') From late gastrulation stages onwards, double
heterozygous mutants show gross disturbances of germ layer formation, and
massive cell accumulations of mesenchymal cells within in the amniotic cavity
(arrowhead in P', lacZ staining) and severe constrictions
between the embryonic and extra-embryonic regions of the embryo (arrows in P).
(Q-T) At E7.5, the mesoderm marker Fgf8 is widely expressed in
mutants, whereas Cer1, which marks newly formed DE, fails to be
expressed.