scholarly journals Receptor Tyrosine Kinases ror1/2 and ryk Are Co-expressed with Multiple Wnt Signaling Components During Early Development of Sea Urchin Embryos

2021 ◽  
pp. 000-000
Author(s):  
C. Ka ◽  
S. Gautam ◽  
S. R. Marshall ◽  
L. P. Tice ◽  
M. Martinez-Bartolome ◽  
...  
Keyword(s):  
Wnt Signaling ◽  
Early Development ◽  
Sea Urchin ◽  
Tyrosine Kinases ◽  
Receptor Tyrosine Kinases ◽  
Sea Urchin Embryos ◽  
Signaling Components

Synthesis of nuclear and cytoplasmic proteins in the early development of fishes and echinoderms

Development ◽  
1971 ◽  
Vol 26 (3) ◽  
pp. 611-622
Author(s):  
Maya R. Krigsgaber ◽  
Alla A. Kostomarova ◽  
Tamara A. Terekhova ◽  
Tatiana A. Burakova
Keyword(s):  
Amino Acids ◽  
Early Development ◽  
Sea Urchin ◽  
Nuclear Volume ◽  
Sea Urchin Embryos ◽  
Cytoplasmic Proteins ◽  
Specific Activities ◽  
Strongylocentrotus Nudus ◽  
Silver Grains ◽  
Misgurnus Fossilis

Synthesis of nuclear and cytoplasmic proteins was studied biochemically and autoradiographically in early loach (Misgurnus fossilis) and sea-urchin (Strongylocentrotus nudus) embryos. After incubation with [14C]amino acids for 5–120 min the ratio of the specific activities of nuclear, mitochondrial and 12000 g supernatant proteins was shown to be equal approximately to 6:1:2 in loach embryos and to 8:4:3 in sea-urchin embryos independently of the duration of labelling. After incubation with [3H]amino acids the number of silver grains per unit section was on the average 2·4 times higher for nuclei than it was for cytoplasm at mid-blastula and mid-gastrula stages. At the mid-gastrula the vegeto-animal gradient of protein synthesis was found. A higher level of the synthesis of nuclear proteins as compared with that of cytoplasmic proteins appears to be related to an increase in the nuclear volume and the nucleo-cytoplasmic ratio during the early development of the loach and sea-urchin embryos.

The hierarchy of requirements for an elevated intracellular pH during early development of sea urchin embryos

Cell ◽  
1985 ◽  
Vol 40 (3) ◽  
pp. 657-666 ◽  
Author(s):  
François Dubé ◽  
Tobias Schmidt ◽  
Carl Hirschie Johnson ◽  
David Epel
Keyword(s):  
Intracellular Ph ◽  
Early Development ◽  
Sea Urchin ◽  
Sea Urchin Embryos

scholarly journals Proteolysis of the major yolk glycoproteins is regulated by acidification of the yolk platelets in sea urchin embryos

1992 ◽  
Vol 117 (6) ◽  
pp. 1211-1221 ◽  
Author(s):  
SK Mallya ◽  
JS Partin ◽  
MC Valdizan ◽  
WJ Lennarz
Keyword(s):  
Early Development ◽  
Sea Urchin ◽  
Ph Value ◽  
Total Protein Content ◽  
Developmentally Regulated ◽  
Cell Stage ◽  
Ph Optimum ◽  
Sea Urchin Embryos

The precise function of the yolk platelets of sea urchin embryos during early development is unknown. We have shown previously that the chemical composition of the yolk platelets remains unchanged in terms of phospholipid, triglyceride, hexose, sialic acid, RNA, and total protein content after fertilization and early development. However, the platelet is not entirely static because the major 160-kD yolk glycoprotein YP-160 undergoes limited, step-wise proteolytic cleavage during early development. Based on previous studies by us and others, it has been postulated that yolk platelets become acidified during development, leading to the activation of a cathepsin B-like yolk proteinase that is believed to be responsible for the degradation of the major yolk glycoprotein. To investigate this possibility, we studied the effect of addition of chloroquine, which prevents acidification of lysosomes. Consistent with the postulated requirement for acidification, it was found that chloroquine blocked YP-160 breakdown but had no effect on embryonic development. To directly test the possibility that acidification of the yolk platelets over the course of development temporally correlated with YP-160 proteolysis, we added 3-(2,4-dinitroanilo)-3-amino-N-methyldipropylamine (DAMP) to eggs or embryos. This compound localizes to acidic organelles and can be detected in these organelles by EM. The results of these studies revealed that yolk platelets did, in fact, become transiently acidified during development. This acidification occurred at the same time as yolk protein proteolysis, i.e., at 6 h after fertilization (64-cell stage) in Strongylocentrotus purpuratus and at 48 h after fertilization (late gastrula) in L. pictus. Furthermore, the pH value at the point of maximal acidification of the yolk platelets in vivo was equal to the pH optimum of the enzyme measured in vitro, indicating that this acidification is sufficient to activate the enzyme. For both S. purpuratus and Lytechinus pictus, the observed decrease in the pH was approximately 0.8 U, from 7.0 to 6.2. The trypsin inhibitor benzamidine was found to inhibit the yolk proteinase in vivo. By virtue of the fact that this inhibitor was reversible we established that the activity of the yolk proteinase is developmentally regulated even though the enzyme is present throughout the course of development. These findings indicate that acidification of yolk platelets is a developmentally regulated process that is a prerequisite to initiation of the catabolism of the major yolk glycoprotein.

Autonomous expression of tissue-specific genes in dissociated sea urchin embryos

Development ◽  
1989 ◽  
Vol 107 (2) ◽  
pp. 299-307 ◽  
Author(s):  
L. Stephens ◽  
T. Kitajima ◽  
F. Wilt
Keyword(s):  
Early Development ◽  
Sea Urchin ◽  
Single Cells ◽  
Cell Types ◽  
Cell Interactions ◽  
Cell Stage ◽  
Tissue Specific ◽  
Specific Transcript ◽  
Sea Urchin Embryos ◽  
Early Stages

The effects of disrupting cell interactions in early development were investigated by examining the accumulation of a primary mesenchyme specific transcript (SM50) and an aboral ectoderm-specific transcript (Spec 1) in cultures of sea urchin embryos that were dissociated at early stages and then cultured in CFSW. The expression of both SM50 and Spec 1 is temporally correct and remains restricted to the appropriate cell types, even if the embryo is dissociated as early as the 2-cell stage and maintained as a suspension of single cells. This result is consistent with the idea that the specificity of expression of these two genes, each characteristic of different lineages, is strongly regulated by information in the egg. Average SM50 expression is half that of intact embryos, but Spec 1 expression is very low, only 10–20% of intact controls, suggesting some differences in the response of the two genes to lack of close cell interactions.

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