To isolate new peptide signal molecules involved in regulating developmental processes in hydra, a novel screening project was developed. Peptides extracted from the tissue of Hydra magnipapillata were systematically purified to homogeneity using HPLC. A fraction of each purified peptide was examined by differential display-PCR for its ability to affect gene expression in hydra. Another fraction was used to determine the tentative structure using an amino acid sequence analyzer and͞or a mass spectrometer. Based on the results, peptides of potential interest were selected for chemical synthesis, followed by confirmation of the identity of the synthetic with the native peptides using HPLC. Using this approach, 286 peptides have been isolated, tentative amino acid sequences have been determined for 95 of them, and 19 synthetic peptides identical to native ones were produced. The 19 synthetic peptides were active in a variety of biological tests. For example, Hym-54 stimulated muscle contraction in adult polyps of hydra and sea anemone, Anthopleura fuscoviridis, and induced metamorphosis of planula, the larval stage, into polyps in a marine hydrozoan species, Hydractinia serrata. Another peptide, Hym-33H, inhibited nerve cell differentiation in hydra and induced tissue contraction in planula of Hydractinia serrata. The evidence obtained so far suggests that hydra contains a large number (>350) of peptide signal molecules involved in regulating developmental or other processes in cnidaria. These peptides can be isolated and their functions examined systematically with the new approach developed in this study.
Reef-building corals, which reproduce through simultaneous multispecies spawning, are thought to hybridize frequently, and it is hypothesized that they have evolved in repeated rounds of species separation and fusion. We conducted cross-fertilization experiments and molecular analyses with a number of mass-spawning coral species in the genus Acropora. A high rate of interspecific fertilization occurred between some species despite very different morphologies. The hybrid larvae developed normally and contained an allelic sequence transmitted from each parent, suggesting common diploid hybridization. Molecular phylogenetic analyses provided strong evidence for a gene pool shared between the hybridizing species. These reproductive and genetic characteristics are consistent with a species complex formed under the separation/fusion processes predicted for a reticulate evolutionary history.
The nucleation and growth process of anatase TiO 2 on several kinds of self-assembled monolayers (SAMs) in an aqueous solution has been evaluated in detail. Homogeneously nucleated TiO 2 particles and amino groups of SAM showed negative or positive potential in the solution, respectively. The adhesion of TiO 2 particles to the amino group surface by attractive electrostatic interaction caused rapid growth of TiO 2 thin films in the supersaturated solution at pH 2.8. On the other hand, TiO 2 was deposited on SAMs without the adhesion of TiO 2 particles regardless of the type of SAM in the solution at pH 1.5 whose degree of supersaturation is low as a result of a high concentration of H + . Additionally, the orientation of films deposited on all SAMs was shown to be improved by enlarging the reaction time regardless of the kind of SAM or pH. It is conjectured that the adsorption of anions to specific crystal planes caused c-axis orientation of anatase TiO 2 .
Micropatterning of anatase TiO 2 thin films by site-selective immersion was realized using a self-assembled monolayer (SAM) which has a pattern of hydrophilic and hydrophobic surfaces. A solution containing a Ti precursor contacted the hydrophilic surface during the experiment and briefly came into contact with the hydrophobic surface via our newly developed method. The solution on the hydrophilic surface was replaced with a fresh solution by the continuous movement of bubbles. Thus TiO 2 was deposited and a thin film was grown selectively on the hydrophilic surface. A TiO 2 thin film fabricated by the site-selective immersion method has no cracks and the feature edge acuity of its micropattern was much higher than that of the micropattern obtained by the lift-off process.
Hydra magnipapillata strains collected from various localities in Japan were induced to reproduce sexually.
From the survival data of the progeny, it was calculated that H. magnipapillata contained an average of between 3.5 and 4.0 lethal equivalent units of recessive deleterious genes per gamate (between 7.0 and 8.0 per animal).
Various types of developmental mutants were found among the offspring of crosses made between strains isolated from the same ponds. The mutant types isolated included mini strains, maxi strains, multi‐headed strains, nematocyst‐deficient strains, regeneration‐deficient strains and male sterile strains. The characters of these strains were stably transmissible to the successive progeny produced by budding. These strains therefore were propagated by budding and maintained as clonal lines to be used later for developmental studies.
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