The establishment of the oral-aboral axis in the ctenophore embryo

Development ◽  
1977 ◽  
Vol 42 (1) ◽  
pp. 237-260
Author(s):  
Gary Freeman

In a small percentage of normal embryos and in a higher percentage of embryos centrifuged prior to the first cleavage the positions of the polar bodies and the site of the first cleavage furrow do not coincide. These cases have been used to establish whether polar body formation sites or first cleavage initiation sites correlate best with the oral-aboral axis of the embryo. In all cases when the first cleavage is initiated at a site different from the site where the polar bodies were given off, the pattern of the first four cleavages is normal, the segregation of comb plate potential at these stages is normal, and the larvae that form are normal. The extent to which comb plate potential is localized along the oral-aboral axis of the embryo prior to the first cleavage, during the first cleavage and at the 2-cell stage was also examined. These experiments demonstrate that the oral-aboral axis is established at the time of the first cleavage, that cleavage plays a causal role in setting up the axis, and that comb plate-forming potential begins to be localized in the aboral region of the embryo at this time.

1935 ◽  
Vol s2-77 (308) ◽  
pp. 585-604
Author(s):  
MARGOT E. METEALFE

1. The somatic cells in both sexes of Phytophaga destructor Say contain four pairs of V-shaped chromosomes, the sex-group being indistinguishable in size or form. 2. The germ-cells in both sexes contain eight pairs of chromosomes. 3. The maturation of the egg follows the normal course of development, eight bivalents being formed. After polar body formation the female pronucleus has eight chromosomes. The polar bodies are never extruded from the egg. 4. Spermatogenesis is a complicated process, the details of which have not been satisfactorily determined. The growth stage appears to take place before the last spermatogonial division. No pairing of chromosome has been observed, and apparently no metaphase plate is formed at meiosis. Eeduction is effected by the expulsion of two buds each containing four chromosomes. Thus only one sperm is produced from each spermatocyte. 5. One or more sperms may enter the egg at fertilization. 6. The germ-line is differentiated from the soma at the eightcell stage. 7. At the fifth cleavage the somatic nuclei eliminate half their number of chromosomes, and are left with eight chromosomes. 8. Migration of the germ nuclei takes place at the sixteencell stage. 9. The relation of the chromosome numbers in the somatic and germ lines is discussed.


1990 ◽  
Vol 582 (1 Cytokinesis) ◽  
pp. 260-272 ◽  
Author(s):  
TAKASHI SHIMIZU

Development ◽  
1982 ◽  
Vol 69 (1) ◽  
pp. 215-222
Author(s):  
Ewa Borsuk

Diploid gynogenetic mouse embryos were produced in a three-step procedure: fertilization in vitro, suppression of the 2nd polar body formation by Cytochalasin B, and microsurgical removal of the male pronucleus. The operated eggs were transplanted to the oviduct of recipient females for 72 or 96 h. The overall recovery rate was 73%, but compacted morulae and blastocysts constituted only 28·6% of transplanted eggs. After 72 h blastocysts were rare (3·5%) but 24 h later their incidence increased to 21·2%. In eggs homozygous for T6 chromosome it was possible to prove karyologically that the male pronucleus was effectively removed and that the diploid genome was of purely maternal origin.


1993 ◽  
Vol 59 (12) ◽  
pp. 2017-2023 ◽  
Author(s):  
John Scarpa ◽  
Katsuhiko T.Wada ◽  
Akira Komaru

2015 ◽  
Vol 129 (3) ◽  
pp. 531-542 ◽  
Author(s):  
Zhihao Guo ◽  
Osamah Batiha ◽  
Mohammed Bourouh ◽  
Eric Fifield ◽  
Andrew Swan

2011 ◽  
Vol 49 (No. 3) ◽  
pp. 93-98 ◽  
Author(s):  
I. Petrová ◽  
M. Sedmíková ◽  
E. Chmelíková ◽  
D. Švestková ◽  
R. Rajmon

Porcine oocytes matured in vitro develop in various ways if they are further cultivated. In our studies these oocytes were cultivated for 1 to 5 days (in vitro aging). During the 1st day of aging, most of them remained at the stage of metaphase II (98%). Then many oocytes underwent the spontaneous parthenogenetic activation. The portion of activated oocytes reached its peak after 2 or 3 days of aging in vitro (39 or 45%). The portion of fragmented oocytes peaked at the same time (28%). During subsequent aging in vitro (i.e. day 4 or 5 of aging), the portion of lysed oocytes significantly increased (30 or 37%). The highest portion of spontaneously activated parthenogenetic embryos at a pronuclear stage (35%) was observed during the 2nd day of aging in vitro. These pronuclear embryos had mainly one polar body with two pronuclei (47% of all pronuclear embryos) or two polar bodies with one pronucleus (38% of all pronuclear embryos). During the 3rd and 5th day of in vitro aging, there was a significant increase in the portion of parthenogenetic embryos cleaved to the 2-cell or 3-cell stage. When considering the prolonged in vitro culture of porcine oocyte, only the first day of aging should be taken into account, since beyond this time significant changes, i.e. parthenogenesis, fragmentation or lysis, occurred in oocytes under in vitro conditions.  


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