Phosphorylation of Deoxyribonucleosides and DNA Synthesis during Embryogenesis of the Sea Urchin

The phosphorylation of thymidine, deoxycytidine, deoxyadenosine and deoxyguanosine was studied during the embryogenesis of the sea urchin Hemicentrotus pulcherrimus. [³H]Thymidine was taken up, phosphorylated and accumulated mostly as [³H]thymidine triphosphate in the early cleavage stage embryos. As the embryos developed, the formation of [³H]thymidine triphosphate decreased and most of the [³H]thymidine taken up by the blastulae remained be phosphorylated. When [³H]deoxycytidine was added to the cleaving embryos, the resultant labeled pool consisted of almost equal amounts of [³H]deoxycytidine monophosphate and [³H]deoxycytidine triphosphate. The formation of [³H]deoxycytidine monophosphate increased up to 10 hr following fertilization and then decreased, while the formation of [³H]deoxycytidine triphosphate decreased for 10 hr following fertilization and then gradually increased. [³H]Deoxyadenosine was rapidly phosphorylated to monophosphate derivative in the cleavage stage embryos. The formation of [³H]deoxyadenosine triphosphate increased rapidly after cleavage stage with a concomitant decrease of [³H]deoxyadenosine monophosphate. The activity of phosphorylation in [³H]deoxyguanosine to triphosphate derivative increased rapidly reaching a plateau 10 hr after fertilization. At this point, 80 % of the [³H]deoxyguanosine was recovered as [³H]deoxyguanosine triphosphate. Based on the above results, it was concluded that the profile of production of each deoxyribonucleoside triphosphate changed during the embryogenesis of the sea urchin, and the in vivo rate-limiting step of phosphorylation of the individual deoxyribonucleoside was assumed to be different.     

Changes in the Nitrogen Compounds of Xylem Sap of Mulberry (Morus alba L.) during Regrowth after Pruning

Changes in fresh and dry weights and total nitrogen in stemsections of mulberry (Morus alba L.) and seasonal fluctuationin the amounts of exudate, pH and nitrogen compounds in xylemsap from cut stems of the plant after pruning have been studied.The amount and concentrations of nitrogen compounds in the sapchanged during the experimental period, but nitrate-nitrogenand ammonia-nitrogen were constant constituents, and asparaginewas quantitatively the major organic nitrogen compound. Smalleramounts of glutamine, aspartic acid and glutamic acid were alsofound, but no ureides or alkaloids were detected. Relationshipsbetween growth and nitrogen in xylem sap of mulberry and therole and importance of asparagine in nitrogen metabolism arediscussed. Morus alba L., mulberry, asparagine, exudates, nitrogen, amino-acids, xylem sap, stem growth, aspartic acid, glutamic acid, ureides     

Neural Induction by Treatment with Ca2+-free Saline Solution in the Gastrula Ectoderm of Cynops pyrrhogaster and Inhibition of Neural Induction with Fetal Calf Serum

The relation between the inducing activity and the cell-dissociation effect of Ca²⁺-free (or Ca²⁺, Mg²⁺-free) saline solution (CF or CMF) on the early gastrula ectoderm was examined. In the culture medium containing no fetal calf serum (FCS), most ectoderm cells treated with CF or CMF died within a few days and only a few differentiated into epidermal cells. However, when the culture medium contained 2% FCS, ectoderm cells treated with CF or CMF differentiated into neural crest derivatives (NCDs), such as mesenchyme cells, pigment cells, and nerve cells. The frequency of the induction depended only on the duration of CF- or CMF-treatment. FCS alone had no inducing activity on ectoderm cells. On the contrary a high concentration of FCS gave an inhibitory effect on the induction. These results indicate that CF is a neuralizing factor and that CF-treated cells require FCS, not for induction, but for survival and differentiation. With CF, the maximum induction of NCDs required a longer duration than that necessary for complete cell-dissociation. This result suggests that the induction depends on some effects of CF other than cell-dissociation.     

Red and far-red reversible photoreactions on seed germination of Cucumis sativa

The effects of red and far-red light in seed germination ofCucumis sativa differs markedly with the degree of seed ripeningand the variety of seed; reciprocal hybrids are clearly maternal. (Received December 26, 1968; )     

Inactivation of Nitrate Reductase of the Yeast, Rhodotorula glutinis

Nitrate reductase (NR) from the yeast, Rhodotorula glutinis var. salinaria was composed of two enzymatic components, diaphorase and terminal nitrate reducing moieties. The enzyme used NADPH as electron donor and FAD as cofactor. The synthesis of nitrate reductase was promoted specifically by nitrate and repressed by ammonium and amino acids. Nitrate reductase from this yeast had an inactive as well as an active form. Inactive enzyme was reactivated by oxidation with ferricyanide in vitro. Hydroxylamine promoted the formation of inactive enzyme in vivo. Ammonium could neither promote the inactivation nor reduce the total level of nitrate reductase activity. Nitrate could protect nitrate reductase from inactivation caused by nitrogen starvation or hydroxylamine.     

Prey capture performance in hatchlings of two sibling Harmonia ladybird species in relation to maternal investment through sibling cannibalism

1. To elucidate the factors responsible for the evolution of host specialisation, prey capture performance in hatchlings of two sibling ladybird species, Harmonia yedoensis and H. axyridis, feeding on four aphid species was examined. Harmonia yedoensis is a specialist predator that preys only on pine aphids in the field, whereas H. axyridis is a generalist predator with a broad prey range. 2. In H. yedoensis, sibling cannibalism in each clutch was intense and predation against pine aphid as well as other aphid species was moderately successful. In contrast, the predation success rate of H. axyridis against pine aphid was quite low. 3. Moreover, it was experimentally shown that increased maternal investment enhanced prey capture performance against pine aphid in H. yedoensis but not in H. axyridis hatchlings, despite their increased body size due to maternal investment. 4. In addition, morphological and behavioural analysis showed that hatchlings of H. yedoensis had longer legs and a larger head capsule size and could walk faster than H. axyridis. 5. In summary, the interactive effects between a large amount of maternal investment and morphological specialisation of the first instars may enable H. yedoensis to capture the pine aphid efficiently, a highly elusive prey for ladybird hatchlings. The ability of H. yedoensis to utilise the three other aphid species in addition to the pine aphid suggests that a trade‐off in prey capture performance is not the main factor in the host specialisation of H. yedoensis.     

MITOTIC ACTIVITY AND CELL PROLIFERATION IN PRIMARY INDUCTION OF NEWT EMBRYO

Mitotic activity and cell proliferation of newt ( Triturus pyrrhogaster ) embryo were examined with special reference to primary induction.
Mitotic activity of gastrula ectoderm gradually decreases during gastrulation. The ectoderm, which is isolated from mid-gastrula (stage 12b) and cultured in vitro , also shows gradual decrease in mitotic activity during cultivation and the mitotic activity steeply decreases after 48 hr.
The ectoderm cultured with heterologous inductor (GPL-extract) shows a temporal suppression in mitotic activity. The ectoderm of the whole gastrula also shows a regional suppression where it is in contact with the chorda-mesoderm.
The number of the ectodermal cells increases about 2 times after 24 hr culture and to more than 3 times after 48 hr culture. Accordingly it is certain that the majority of the ectodermal cells divides at least one time in the course of 48 hr.
Histological examination of the ectoderm cultured together with the inductor reveals that differentiation of undifferentiated ectoderm to neural tissues is accomplished at least within 48 hr after cultivation with the inductor.
The present examination shows the possibility that the mitotic activity of the ectoderm may be temporarily suppressed by the inductor and that it then decreases along with neural cell differentiation after recovery of the activity.
The results also suggest that the determination of undifferentiated ectoderm to neural tissues occurs before the second cell division after the contact with the inductor and the events occurring during the first cell cycle after activating by the inducing stimulus are critical for the primary induction.