Translocation of a store of maternal cytoplasmic c-myc protein into nuclei during early development

1989 ◽  
Vol 9 (12) ◽  
pp. 5395-5403
Author(s):  
M Gusse ◽  
J Ghysdael ◽  
G Evan ◽  
T Soussi ◽  
M Méchali
Keyword(s):  
Embryonic Development ◽  
Xenopus Laevis ◽  
Protein Content ◽  
Mature Oocyte ◽  
Gastrula Stage ◽  
Cleavage Stage ◽  
Midblastula Transition ◽  
Phosphorylation State ◽  
Growing Cell ◽  
Delayed Translation

The c-myc proto-oncogene is expressed as a maternal protein during oogenesis in Xenopus laevis, namely, in nondividing cells. A delayed translation of c-myc mRNA accumulated in early oocytes results in the accumulation of the protein during late oogenesis. The oocyte c-myc protein is unusually stable and is located in the cytoplasm, contrasting with its features in somatic cells. A mature oocyte contains a maternal c-myc protein stockpile of 4 x 10(5) to 6 x 10(5) times the level in a somatic growing cell. This level of c-myc protein is preserved only during the cleavage stage of the embryo. Fertilization triggers its rapid migration into the nuclei of the cleaving embryo and a change in the phosphorylation state of the protein. The c-myc protein content per nucleus decreases exponentially during the cleavage stage until a stoichiometric titration by the embryonic nuclei is reached during a 0.5-h period at the midblastula stage. Most of the maternal c-myc store is degraded by the gastrula stage. These observations implicate the participation of c-myc in the events linked to early embryonic development and the midblastula transition.

scholarly journals Translocation of a store of maternal cytoplasmic c-myc protein into nuclei during early development.

1989 ◽  
Vol 9 (12) ◽  
pp. 5395-5403 ◽  
Author(s):  
M Gusse ◽  
J Ghysdael ◽  
G Evan ◽  
T Soussi ◽  
M Méchali
Keyword(s):  
Embryonic Development ◽  
Xenopus Laevis ◽  
Protein Content ◽  
Mature Oocyte ◽  
Gastrula Stage ◽  
Cleavage Stage ◽  
Midblastula Transition ◽  
Phosphorylation State ◽  
Growing Cell ◽  
Delayed Translation

The c-myc proto-oncogene is expressed as a maternal protein during oogenesis in Xenopus laevis, namely, in nondividing cells. A delayed translation of c-myc mRNA accumulated in early oocytes results in the accumulation of the protein during late oogenesis. The oocyte c-myc protein is unusually stable and is located in the cytoplasm, contrasting with its features in somatic cells. A mature oocyte contains a maternal c-myc protein stockpile of 4 x 10(5) to 6 x 10(5) times the level in a somatic growing cell. This level of c-myc protein is preserved only during the cleavage stage of the embryo. Fertilization triggers its rapid migration into the nuclei of the cleaving embryo and a change in the phosphorylation state of the protein. The c-myc protein content per nucleus decreases exponentially during the cleavage stage until a stoichiometric titration by the embryonic nuclei is reached during a 0.5-h period at the midblastula stage. Most of the maternal c-myc store is degraded by the gastrula stage. These observations implicate the participation of c-myc in the events linked to early embryonic development and the midblastula transition.

A method for isolating uncontaminated nuclei from all stages of developing Xenopus laevis embryos*

Development ◽  
1978 ◽  
Vol 48 (1) ◽  
pp. 101-108
Author(s):  
F. Farzaneh ◽  
C. K. Pearson
Keyword(s):  
Embryonic Development ◽  
Xenopus Laevis ◽  
Protein Content ◽  
Early Cleavage ◽  
Histone Protein ◽  
Pigment Granules ◽  
Xenopus Laevis Embryos ◽  
Number Of Cells

A method for isolating nuclei from Xenopus laevis embryos has been developed. This procedure enables the isolation of nuclei, free from contamination with yolk and pigment granules, at all stages of embryonic development. Using this method the nuclear yield is 60–70% of the estimated number of cells in the embryo. The DNA, RNA, histone and non-histone protein content of these nuclei during embryogenesis (from early cleavage to the swimming tadpole stage) has been measured.

scholarly journals Structural and ultrastructural analysis of embryonic development ofProchilodus lineatus(Valenciennes, 1836) (Characiforme; Prochilodontidae)

Zygote ◽  
2006 ◽  
Vol 14 (3) ◽  
pp. 217-229 ◽  
Author(s):  
Alexandre Ninhaus-Silveira ◽  
Fausto Foresti ◽  
Alexandre de Azevedo
Keyword(s):  
Embryonic Development ◽  
Larval Stage ◽  
Cleavage Pattern ◽  
Optic Vesicle ◽  
Gastrula Stage ◽  
Cleavage Stage ◽  
Blastula Stage ◽  
Prochilodus Lineatus ◽  
The Third ◽  
High Mitotic Activity

SummaryThis survey was performed to characterize the embryogenesis ofProchilodus lineatus. Seven stages of embryo development were identified – zygote, cleavage, blastula, gastrula, segmentation, larval and hatching – after a period of incubation of 22 h (24 °C) or 14 h (28 °C). The following cleavage pattern was identified: the first plane was vertical (2 blastomeres); the second was vertical and perpendicular to the first (4 blastomeres); the third was vertical and parallel to the first (4 × 2); the fourth cleavage was vertical and parallel to the second (4 × 4); the fifth was vertical and parallel to the first (4 × 8); and the sixth cleavage was horizontal (64 blastomeres). At the blastula stage (3.0–4.0 h (24 °C); 1.66–2.0 h (28 °C)) irregular spaces were detected and periblast structuring was initiated. At the gastrula stage (4.0–8.0 h (24 °C); 3.0–6.0 h (28 °C)) the epiboly, convergence and cell movements, as well as the formation of embryonic layers, had begun. The segmentation stage (10.0–15.0 h (24 °C); 7.0–10.0 h (28 °C)) was characterized by a rudimentary formation of organs and systems (somites, optic vesicle and intestinal delimitation). The embryo at the larval stage (16.0–21.0 h (24 °C); 11.0–13.0 h (28 °C)) showed a free tail, more than 25 somites, an optic vesicle and a ready-to-hatch larval shape. The blastomeres at cleavage stage had disorganized nuclei indicating high mitotic activity. At gastrula, the blastomeres and the periblast had euchromatic nuclei and a large number of mitochondria and vesicles. The yolk was organized into globose sacs, which were dispersed into small pieces prior to absorption.

Expression of N-CAM precedes neural induction in Pleurodeles waltl (urodele, amphibian)

Development ◽  
1989 ◽  
Vol 106 (4) ◽  
pp. 675-683 ◽  
Author(s):  
J.P. Saint-Jeannet ◽  
F. Foulquier ◽  
C. Goridis ◽  
A.M. Duprat
Keyword(s):  
Monoclonal Antibody ◽  
Nervous System ◽  
Xenopus Laevis ◽  
Neural Induction ◽  
Gastrula Stage ◽  
Pleurodeles Waltl ◽  
Early Gastrula

The appearance and localization of N-CAM during neural induction were studied in Pleurodeles waltl embryos and compared with recent contradictory results reported in Xenopus laevis. A monoclonal antibody raised against mouse N-CAM was used. In the nervous system of Pleurodeles, it recognized two glycoproteins of 180 and 140×10(3) M(r) which are the Pleurodeles equivalent of N-CAM-180 and -140. Using this probe for immunohistochemistry and immunocytochemistry, we showed that N-CAM was already expressed in presumptive ectoderm at the early gastrula stage. In late gastrula embryos, a slight increase in staining was observed in the neurectoderm, whereas the labelling persisted in the noninduced ectoderm. When induced ectodermal cells were isolated at the late gastrula stage and cultured in vitro up to 14 days, a faint polarized labelling of cells was observed initially. During differentiation, the staining increased and became progressively restricted to differentiating neurons.

scholarly journals Embryonic development in Zungaro jahu

Zygote ◽  
2016 ◽  
Vol 25 (1) ◽  
pp. 17-31 ◽  
Author(s):  
Camila Marques ◽  
Francine Faustino ◽  
Bruno Bertolucci ◽  
Maria do Carmo Faria Paes ◽  
Regiane Cristina da Silva ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Embryonic Development ◽  
Egg Cell ◽  
Gastrula Stage ◽  
Transmission Electron ◽  
Larval Hatching ◽  
Morula Stage ◽  
Zygote Stage ◽  
Scanning Electron

SummaryThe aim of this study was to characterize the embryonic development of Zungaro jahu, a fresh water teleostei commonly known as ‘jaú’. Samples were collected at pre-determined times from oocyte release to larval hatching and analysed under light microscopy, transmission electron microscopy and scanning electron microscopy. At the first collection times, the oocytes and eggs were spherical and yellowish, with an evident micropyle. Embryo development took place at 29.4 ± 1.5°C and was divided into seven stages: zygote, cleavage, morula, blastula, gastrula, organogenesis, and hatching. The differentiation of the animal and vegetative poles occured during the zygote stage, at 10 min post-fertilization (mpf), leading to the development of the egg cell at 15 mpf. From 20 to 75 mpf, successive cleavages resulted in the formation of 2, 4, 8, 16, 32 and 64 blastomeres. The morula stage was observed between 90 and 105 mpf, and the blastula and gastrula stage at 120 and 180 mpf; respectively. The end of the gastrula stage was characterized by the presence of the yolk plug at 360 mpf. Organogenesis followed, with differentiation of the cephalic and caudal regions, elongation of the embryo by the cephalo-caudal axis, and somitogenesis. Hatching occurred at 780 mpf, with mean larval total length of 3.79 ± 0.11 mm.

The role of water-regulating mechanisms in the development of the haploid syndrome in Xenopus laevis

Development ◽  
1972 ◽  
Vol 28 (2) ◽  
pp. 449-462
Author(s):  
Louie Hamilton ◽  
P. H. Tuft
Keyword(s):  
Xenopus Laevis ◽  
Cell Number ◽  
Gastrula Stage ◽  
Tail Bud ◽  
Volume Changes ◽  
Membrane Area ◽  
Flow Through ◽  
The Difference ◽  
Haploid Embryos

The uptake of water by haploid and diploid sibling embryos of Xenopus laevis has been investigated by measuring the density changes which occur during the development of intact embryos from the blastula to the late tail-bud stage, and of explants from which most of the presumptive endoderm has been removed. The results show that up to the mid-gastrula stage there is no difference between the haploid and diploid embryos; but from then on, whereas the diploid volume increases steadily, the haploid gastrulae undergo a series of cyclical volume changes due to loss of fluid through the blastopore. It is concluded that this is the result of an excessive inflow of water through the haploid ectoderm, because it was found that the volume of haploid ectodermal explants increased much more rapidly than the volume of similar diploid explants. Excess flow through the haploid ectoderm also accounts for other characteristics of the haploid syndrome – microcephaly and lordosis. It is suggested that it is the doubling of the cell number in haploid embryos with the consequent 25% increase in aggregate cell membrane area which accounts for the difference between the uptake of water by the two types of embryos. It is also suggested that changes in the rate of water flow through the ectoderm and endoderm which are thought to account for the accumulation of water in the blastocoel and archenteron in the normal diploid embryo arise in a similar way.

Gene expression in Xenopus embryogenesis

Development ◽  
1985 ◽  
Vol 89 (Supplement) ◽  
pp. 113-124
Author(s):  
Igor B. Dawid ◽  
Susan R. Haynes ◽  
Milan Jamrich ◽  
Erzsebet Jonas ◽  
Seiji Miyatani ◽  
...  
Keyword(s):  
Gene Expression ◽  
Protein Synthesis ◽  
Xenopus Laevis ◽  
Cdna Cloning ◽  
Early Embryogenesis ◽  
Gene Activity ◽  
Complex Nature ◽  
Cdna Clones ◽  
Midblastula Transition ◽  
First Time

This article considers some aspects of the storage of macromolecules in the oocyte of Xenopus laevis and the activation of previously unexpressed genes during early embryogenesis. The large quantity and complex nature of poly(A)+ RNA accumulated in the egg provides the cleavage embryo with a supply of mRNA sufficient to sustain protein synthesis for several hours of development. Onset of gene activity at the midblastula transition (MBT) leads to the synthesis and accumulation of molecules of various RNA classes, including tRNAs, rRNAs, mRNAs and mitochondrial RNAs. At gastrulation the poly(A)+ RNA population is still qualitatively similar to that of the egg but some sequences not present in egg RNA have accumulated by this time. Through the use of a subtractive cDNA cloning procedure we have prepared a library of sequences that represent genes activated for the first time between MBT and gastrula. A study of several of these cDNA clones suggests that genes in this class are restricted in their activity to embryonic and tadpole stages.

The effect of egg rotation on the differentiation of primordial germ cells in Xenopus laevis

Development ◽  
1985 ◽  
Vol 90 (1) ◽  
pp. 79-99
Author(s):  
J. H. Cleine ◽  
K. E. Dixon
Keyword(s):  
Xenopus Laevis ◽  
Germ Cells ◽  
Germ Plasm ◽  
Primordial Germ Cells ◽  
Intermediate Zone ◽  
Gastrula Stage ◽  
Tail Bud ◽  
Axis Orientation ◽  
Early Gastrula ◽  
Number Of Cells

Eggs of X. laevis were rotated (sperm entrance point downwards) either through 90° (1×90 embryos) or 180° in two 90° steps (2×90 embryos) at approximately 25–30 min postfertilization after cooling to 13°C. The embryos were kept in their off-axis orientation and cooled until the early gastrula stage. Rotation resulted in relocation of egg constituents with slight changes in the distribution of outer cortical and subcortical components and major changes in inner constituents where the heavy yolk and cytoplasm appeared to reorient as a single coherent unit to maintain their relative positions with respect to gravity. Development of rotated embryos was such that regions of the egg which normally give rise to posterior structures instead developed into anterior structures and vice versa. Germ plasm was displaced in the vegetal-dorsal-animal direction (the direction of rotation) and was segregated into dorsal micromeres and intermediate zone cells in 2×90 embryos and dorsal macromeres and intermediate zone cells in 1×90 embryos. In consequence, at the gastrula stage, cells containing germ plasm were situated closer to the dorsal lip of the blastopore after rotation — in 2×90 gastrulas around and generally above the dorsal lip. Hence, in rotated embryos, the cells containing germ plasm were invaginated earlier during gastrulation and therefore were carried further anteriorly in the endoderm to a mean position anterior to the midpoint of the endoderm. The number of cells containing germ plasm in rotated embryos was not significantly different from that in controls at all stages up to and including tail bud (stage 25). However at stages 46, 48 and 49 the number of primordial germ cells was reduced in 1×90 embryos in one experiment of three and in 2×90 embryos in all experiments. We tested the hypothesis that the decreased number of primordial germ cells in the genital ridges was due to the inability of cells to migrate to the genital ridges from their ectopic location in the endoderm. When anterior endoderm was grafted into posterior endodermal regions the number of primordial germ cells increased slightly or not at all suggesting that the anterior displacement of the cells containing germ plasm was not the only factor responsible for the decreased number of primordial germ cells in rotated embryos. Other possible explanations are discussed.

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