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Fig. 3. Morpholino oligonucleotides (MOs) targeted to the FGF8
mRNA. (A) Schematic of FGF8 gene diagramming the position
of the MOs (red); FGF8b-specific alternatively spliced region (dark
blue). (B) RT-PCR analysis of explants from embryos injected as
indicated above the lanes. EF1
, loading control; explants were
examined for xbra expression. F8b (FGF8b with the
UTRs) (200 pg) induces xbra in explants (lane 4); co-injection of 40
ng of XlMOF8 effectively inhibits this effect (lane 6); xbra
expression is rescued with injection of FGF8b-cds (does not have the
MOF8 target sequence) (lane 7); FGF4 induction of xbra
expression is unaffected by the MOF8 (lane 8). (C) XlMOF8 was designed
to bind the translational start region of X. laevis FGF8. (D)
Nucleotide sequence that MOSAF8a and MOSDF8 bind, respectively; MO sequence is
in red. (E) Schematic of MOSDF8 and MOSAF8a effects on splicing.
(F) RTPCR of X. laevis whole embryos injected as indicated;
MOSAF8a (160, 120, 80 ng); MOSDF8 (170, 85, 43 ng); red brackets indicate
MOSDF8 induced alternative splicing products that lead to premature
termination; MOSAF8a results in a loss of the FGF8a but not
FGF8b spliceform. (G) RTPCR of X. tropicalis embryos
demonstrating the efficacy of MOSAF8a (32, 16 ng) and MOSDF8 (68, 34, 17
ng).