(Downloading may take up to 30 seconds.
If the slide opens in your browser, select File -> Save As to save it.)
Click on image to view larger version.

Fig. 5. The missense mutation F110S does not affect cell proliferation.
(A,B) Expression of prim1 mRNA in wild-type zebrafish
embryos at the eight cell stage (A) and 2 dpf (B). The maternal expression of
prim1 is observed (A). The prim1 gene is predominantly
expressed in regions with high cell proliferation rate, such as the eyes and
tectum at 2 dpf (B). (C,D) Plastic sections of wild-type retinas
labeled with prim1 RNA probe at 2 dpf (C) and 3 dpf (D). The
prim1 gene is expressed in the CMZ of the neural retina, suggesting
that this gene is expressed in the proliferating cells of the retina.
(E,F) Labeling of wild-type (E) and piy mutant (F)
retinas with anti-phosphorylated histone H3 antibody (red, arrowheads). All
nuclei are counterstained with Sytox Green (green). (G) Percentage of
retinal cells that are dividing in wild-type (blue bar) and piy
mutant (red bar) retinas at 24 hpf and 32 hpf. (H,I) BrdU
labeling (red) of wild-type (H) and piy mutant (I) retinas.
(J) Percentage of retinal area that is BrdU-positive in wild-type (blue
bar) and piy mutant (red bar) retinas at 24 hpf and 32 hpf.
(K,L) Representative traces from FACS analyses after propiduim
isodide staining of dissociated cells from wild-type (black line) and
piy mutant (green line) heads at 38 hpf (K) and 48 hpf (L). The
traces are divided into four regions, M1, M2, M3 and M4, which represent cells
with <2N, 2N, 2N-4N and 4N DNA, respectively. (M,N) Bar graph
showing summary of FACS results from wild-type sibling and piy
homozygous mutant dissociated cell pools at 38 hpf (M) and 48 hpf (N). The
piy mutant embryos (light green) contain fewer G1/postmitotic cells
and more apoptotic cells than wild type. However, there is no significant
difference in the ratio of S/G2/M cells between wild-type and piy
mutant embryos. (O) Proliferation rate of yeast pri1-1 mutant
cells transformed with wild-type prim1, F110S mutated prim1
and control vector at 37°C. The proliferation rate of the yeast
pri1-1 mutant cells transformed with the F110S mutant prim1
(pink) is not significantly different from that of the yeast pri1-1
mutant cells transformed with the wild-type prim1 (blue), whereas the
proliferation rate of the yeast pri1-1 mutant cells transformed with
the control vector (yellow) is low.