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Sizes of yolk platelets were measured in sections of oocytes and embryos in Xenopus. It was found that the average size of the largest group of platelets in cells differed between germ layers of neurulae. It was small (3 to 5 μm) in the ectoderm, medium-sized (5 to 8 µm) in the mesoderm, and large (over 8 μm) in the endoderm. Platelets of these size classes formed layers in egg, the yolk gradient, by the end of oocyte maturation. The yolk gradient contained products of the mitochondrial cloud and a part of the germinal vesicle material at certain positions. The layers of small, medium and large platelets in the egg changed their locations to distribute to the ectoderm, mesoderm and endoderm of neurulae, respectively. The yolk layers in the egg thus represented different prospective fates, and a figure describing the locations of these layers could be regarded as a fate map for the one-cell stage. Most of the marginal blastomeres of embryos at cleavage stages consisted of a few parts with different prospective fates. Results were discussed with reference to available fate maps for cleavage stage embryos.
Bauer,
The cleavage stage origin of Spemann's Organizer: analysis of the movements of blastomere clones before and during gastrulation in Xenopus.
1994, Pubmed,
Xenbase
Bauer,
The cleavage stage origin of Spemann's Organizer: analysis of the movements of blastomere clones before and during gastrulation in Xenopus.
1994,
Pubmed
,
Xenbase Brachet,
An old enigma: the gray crescent of amphibian eggs.
1977,
Pubmed
,
Xenbase Dale,
Fate map for the 32-cell stage of Xenopus laevis.
1987,
Pubmed
,
Xenbase Danilchik,
Differentiation of the animal-vegetal axis in Xenopus laevis oocytes. I. Polarized intracellular translocation of platelets establishes the yolk gradient.
1987,
Pubmed
,
Xenbase Danilchik,
Deep cytoplasmic rearrangements during early development in Xenopus laevis.
1991,
Pubmed
,
Xenbase Darnbrough,
Turnover and processing of poly(A) in full-grown oocytes and during progesterone-induced oocyte maturation in Xenopus laevis.
1979,
Pubmed
,
Xenbase Dreyer,
The fate of oocyte nuclear proteins during early development ofXenopus laevis.
1982,
Pubmed
,
Xenbase Dumont,
Oogenesis in Xenopus laevis (Daudin). I. Stages of oocyte development in laboratory maintained animals.
1972,
Pubmed
,
Xenbase Hainski,
Xenopus maternal RNAs from a dorsal animal blastomere induce a secondary axis in host embryos.
1992,
Pubmed
,
Xenbase Heasman,
The mitochondrial cloud of Xenopus oocytes: the source of germinal granule material.
1984,
Pubmed
,
Xenbase Hemmati-Brivanlou,
Follistatin, an antagonist of activin, is expressed in the Spemann organizer and displays direct neuralizing activity.
1994,
Pubmed
,
Xenbase Herkovits,
The ultrastructure of the dorsal yolk-free cytoplasm and the immediately surrounding cytoplasm in the symmetrized egg of Xenopus laevis.
1979,
Pubmed
,
Xenbase Imoh,
Behaviour of annulate lamellae during the maturation of oocytes in the newt, Cynops pyrrhogaster.
1982,
Pubmed Imoh,
Formation of germ layers and roles of the dorsal lip of the blastopore in normally developing embryos of the newt Cynops pyrrhogaster.
1988,
Pubmed KARASAKI,
Studies on amphibian yolk 1. The ultrastructure of the yolk platelet.
1963,
Pubmed Keller,
The function and mechanism of convergent extension during gastrulation of Xenopus laevis.
1985,
Pubmed
,
Xenbase Keller,
Vital dye mapping of the gastrula and neurula of Xenopus laevis. II. Prospective areas and morphogenetic movements of the deep layer.
1976,
Pubmed
,
Xenbase Keller,
Vital dye mapping of the gastrula and neurula of Xenopus laevis. I. Prospective areas and morphogenetic movements of the superficial layer.
1975,
Pubmed
,
Xenbase Keller,
An experimental analysis of the role of bottle cells and the deep marginal zone in gastrulation of Xenopus laevis.
1981,
Pubmed
,
Xenbase Moody,
Fates of the blastomeres of the 16-cell stage Xenopus embryo.
1987,
Pubmed
,
Xenbase Moody,
Fates of the blastomeres of the 32-cell-stage Xenopus embryo.
1987,
Pubmed
,
Xenbase Nakatzuji,
Studies on the gastrulation of amphibian embryos: Cell movement during gastrulation inXenopus laevis embryos.
1975,
Pubmed Neff,
Pattern formation in amphibian embryos prevented from undergoing the classical "rotation response" to egg activation.
1983,
Pubmed
,
Xenbase Neff,
Experimental analyses of cytoplasmic rearrangements which follow fertilization and accompany symmetrization of inverted Xenopus eggs.
1984,
Pubmed
,
Xenbase Nieuwkoop,
The formation of the mesoderm in urodelean amphibians : I. Induction by the endoderm.
1969,
Pubmed Nieuwkoop,
The Formation of the Mesoderm in Urodelean Amphibians : II. The origin of the dorso-ventral polarity of the mesoderm.
1969,
Pubmed Palecek,
Changes of the external and internal pigment pattern upon fertilization in the egg of Xenopus laevis.
1978,
Pubmed
,
Xenbase PASTEELS,
THE MORPHOGENETIC ROLE OF THE CORTEX OF THE AMPHIBIAN EGG.
1964,
Pubmed Selman,
The utilization of yolk platelets by tissues of Xenopus embryos studied by a safranin staining method.
1965,
Pubmed
,
Xenbase Slack,
Mechanism of anteroposterior axis specification in vertebrates. Lessons from the amphibians.
1992,
Pubmed Uchiyama,
Localization of activin and follistatin proteins in the Xenopus oocyte.
1994,
Pubmed
,
Xenbase Vincent,
Kinematics of gray crescent formation in Xenopus eggs: the displacement of subcortical cytoplasm relative to the egg surface.
1986,
Pubmed
,
Xenbase WALLACE,
STUDIES ON AMPHIBIAN YOLK. IV. AN ANALYSIS OF THE MAIN-BODY COMPONENT OF YOLK PLATELETS.
1963,
Pubmed WARD,
The origin of protein and fatty yolk in Rana pipiens. II. Electron microscopical and cytochemical observations of young and mature oocytes.
1962,
Pubmed Weeks,
A maternal mRNA localized to the vegetal hemisphere in Xenopus eggs codes for a growth factor related to TGF-beta.
1987,
Pubmed
,
Xenbase