Hidemi Sato

Asynchronization of Cell Division is Concurrently Related with Ciliogenesis in Sea Urchin Blastulae

During the early development of the sea urchins, Temnopleurus toreumaticus, Temnopleurus hardwickii and Hemicentrotus pulcherrimus, the division synchrony in all blastomeres lasted only until the 4th cleavage and a regional synchrony or a graded activity of cell division appeared. In the midblastula stage prior to hatching, the regional synchrony vanished simultaneously with the formation of cilia, then the division proceeded asynchronously. The analysis of cell pedigrees confirmed that a variable extension of intercleavage times occurred after the ciliogenesis. In blastomeres derived from mesomeres of T. toreumaticus embryos, the mean intercleavage time extended from 48 min of the 8th cycle (pre‐ciliated) to 115 min of the 9th cycle (ciliated), and the coefficient of variation increased from 15% to 39%. We attempted a kinetic analysis of cell proliferation on the basis of the transition probability model of cell cycle control. We concluded that the minimum time required for the completion of the cell cycle was the decisive factor in the cell cycle succession of pre‐ciliated blastomeres, and that a sudden and sharp decrease in the transition probability of the ciliated blastomeres probably interpreted the abrupt slowing and asynchronization of the cleavage cycle at the time of ciliogenesis.

Isolation of the major basic nuclear protein and its localization on chromosomes of the dinoflagellate, Oxyrrhis marina.

Basic nuclear proteins were extracted from isolated nuclei of Oxyrrhis marina. The HPLC pattern of the extract showed a single major peak, which consisted of a major band with an apparent molecular mass of 23 kDa on an SDS‐PAGE gel. We designated this protein as Np23 because of its apparent molecular mass. The amino acid composition of this protein revealed its extremely basic nature with a high lysine content. Polyclonal antibodies were raised against Np23. Immunofluorescence microscopy showed that Np23 was localized within the nucleus of dividing and non‐dividing cells as well, and immuno‐electron microscopy showed that the protein was localized only on chromosomes. These data established that Np23 is the major basic chromosome protein of Oxyrrhis marina.

Analysis by polarizing microscopy of chromosomal structure among dinoflagellates and its phylogenetic involvement

Dinoflagellate chromosomes are highly interesting because of their condensed state, their lack of histone, and their ultrastructure reminiscent of that of bacterial nucleoid.

Distribution of Membrane‐Associated Calcium in Fertilized Sea Urchin Eggs during Mitosis*

The distribution of membrane‐associated calcium in dividing sea urchin eggs was examined with chlortetracycline as a fluorescent chelate probe. The fluorescence of bound chlortetracycline in fertilized eggs was initially evenly distributed, but began to gather around the nucleus in prophase, and formed a dumb‐bell shaped condensation enclosing the mitotic apparatus by metaphase. During anaphase and telophase, the fluorescence was observed in kinetochore‐to‐pole regions of the spindle, with little fluorescence in the interkinetochore region. The astral regions showed intense fluorescence. The distribution of the chlortetracycline‐fluorescence coincided with that of ER‐like membranes seen in electron micrographs. The distribution of the fluorescence was obscure and the birefringence of spindles disappeared on perfusion on perfusion of the cells in metaphase with 1 mM tetracaine, which is known to displace membrane‐bound calcium.

Ultrastructural Study of Asters Induced by Microinjection with Sperm Centriolar Fraction in Sea Urchin Eggs

Multiple asters can be artificially induced in sea urchin fertilized eggs by the microinjection of the centriolar fraction of sperm homogenate. Investigation was continued by the electron microscopy to determine whether the multi‐aster formation was due to the centrioles or the contaminants in the injected sperm fraction. Thirty three asters in 3 operated eggs were thoroughly examined, and we confirmed that the presence of centrioles in the central region of 26 asters. We considered that the rest of them might contained the centrioles in the sections lost during the preparation procedures. Fragmented axoneme, the plug of electron dense material, and the centriolar fossa, which were usually accompanied with the isolated centrioles, disappeared from the centrioles in these multiple asters. However, electron dense, amorphous materials were formed associating with the triplet blades and distributed around the centrioles. Many astral microtubules were terminated in these pericentriolar materials. Results obtained suggest that, although the pericentriolar material is acting as the microtubule organizing center, all multiple asters, except those derived from fertilization (2 asters per egg), are most likely induced by the injected centrioles and not by the contaminants.