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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


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Hym-301, a novel peptide, regulates the number of tentacles formed in hydra

Toshio Takahashi1,*, Masayuki Hatta2,{dagger}, Seungshic Yum2,{ddagger}, 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-{alpha} 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