First published online April 13, 2005
doi: 10.1242/10.1242/dev.01792
Development 132, 2225-2234 (2005)
Published by The Company of Biologists 2005
Hym-301, a novel peptide, regulates the number of tentacles formed in hydra
Toshio Takahashi1,*,
Masayuki Hatta2,
,
Seungshic Yum2,
,
Lydia Gee1,
Masahiro Ohtani3,
,
Toshitaka Fujisawa2 and
Hans R. Bode1,¶
1 Developmental Biology Center, University of California, Irvine, CA 92697,
USA
2 National Institute of Genetics, Mishima, Shizuoka 411-8540, Japan
3 Suntory Institute for Bioorganic Research, Osaka 618, Japan

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Fig. 1. (A) Nucleotide and deduced amino acid sequences of the Hym-301
gene. The predicted signal sequence is underlined and the Hym-301 is shown in
red. The asterisk indicates a stop codon.
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Fig. 2. Expression of the Hym-301 gene (dark blue) in an adult hydra using
whole-mount in situ hybridization.
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Fig. 3. Expression of Hym-301 gene (dark blue) during the stage of bud
formation. (A) Stage 0, (B) stage 1-2, (C) stage 2-3, (D) stage 3, (E) stage
4, (F) stage 5, (G) stage 6-7 and (H) stage 8.
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Fig. 4. Expression of Hym-301 gene (dark blue) during head regeneration.
(A) Six hours, (B) 12 hours, (C) 24 hours, (D) 48 hours, (E) 72 hours and (F)
96 hours.
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Fig. 5. Effect of Hym-301 on the number of tentacles formed (A), and the rate of
hypostome formation (B) during head regeneration. Both figures represent
regenerates treated with the Hym-301 peptide (black circles) and controls
(white circles). Each data point is the average value±s.e.m. for three
experiments. Fifteen to 20 regenerates were used in each of the
experiments.
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Fig. 6. Effect of Hym-301 dsRNA on the number of tentacles formed during
bud formation: Hym-301 dsRNA-treated buds (black circles), Luciferase
dsRNA-treated buds (triangles) and untreated control buds (white circles).
Each data point is the average value±s.e.m. for five experiments. In
each experiment, 10-20 animals were used.
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Fig. 7. Transient reduction of the level of Hym-301 RNA in developing buds
after the introduction of Hym-301 dsRNA as measured by RT-PCR. Levels
of EF1- served as the control.
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Fig. 8. Changes in the expression pattern of Hym-301 with time following
the addition of 2 mM LiCl as measured with in situ hybridization on whole
mounts.
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© The Company of Biologists Ltd 2005