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Fig. 6. A new phenotype (`ciuffo') results from loss of function of both
ß-catenin genes. (A-D) The `ciuffo' phenotype is apparent in
ichabod embryos injected with 3 mM MO1 (B) and wild-type embryos
injected with 3 mM MO1 and 3 mM MO2 (D). Uninjected ichabod (A) and
wild-type (C) embryos are shown for comparison. (E-H) Co-injection of
ß-catenin-1* RNA (ß-catenin-1
RNA with an altered ribosome binding region that will not bind to MO1) into
ichabod embryos can suppress the `ciuffo' phenotype produced by MO1
injection. In comparison with uninjected ichabod embryos, which
develop to C1 phenotypes (E), injection of 1 mM MO1 transforms approximately
two-thirds of the embryos into `ciuffo' phenotypes (F), injection of the RNA
alone causes rescue to wild-type and less ventralized C2-C4 phenotypes (G),
but co-injection of both MO1 and RNA results in embryos with the original
severe C1 phenotype and with C1a phenotype (H). Each of these panels shows a
group of representative embryos of one of four repeats of this experiment,
which all gave consistent results. (I-Z) Hindbrain and anterior neural
markers and neuronal markers are not expressed in ichabod embryos
(J,M,S) but are expressed in 3 mM MO1-injected ichabod (`ciuffo')
embryos (K,N,T). The posterior neural marker hox6b6 is expressed in
some ichabod embryos (P) and in `ciuffo' embryos (Q). Wild-type
embryos are shown as positive controls (I,L,O,R). The following probes were
used: krox20 (I-K), emx1 (L-N), hoxb6b (O-Q) and
islet1 (R-T). All three types of embryos express myoD (U-Z),
although the expression is radialized in both ichabod (V) and
`ciuffo' (Z) embryos compared with wild type (U). Embryos in A-H and L-N are
at 24 hpf and those in I-K,O-V are at 22 hpf. For I-Z, probes are indicated in
the lower left corner and type of embryo in the lower right corner of each
panel.
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