scholarly journals Localization and functional role of a 41 kDa collagenase/gelatinase activity expressed in the sea urchin embryo

2002 ◽  
Vol 44 (4) ◽  
pp. 345-356 ◽  
Author(s):  
Janice Mayne ◽  
John J. Robinson
Keyword(s):  
Sea Urchin ◽  
Functional Role ◽  
Gelatinase Activity ◽  
Sea Urchin Embryo

Autonomous and non-autonomous differentiation of ectoderm in different sea urchin species

Development ◽  
1995 ◽  
Vol 121 (5) ◽  
pp. 1497-1505 ◽  
Author(s):  
A.H. Wikramanayake ◽  
B.P. Brandhorst ◽  
W.H. Klein
Keyword(s):  
Sea Urchin ◽  
Strongylocentrotus Purpuratus ◽  
Protein A ◽  
Cellular Interactions ◽  
V Protein ◽  
Lytechinus Pictus ◽  
Sea Urchin Embryo ◽  
Oral Ectoderm ◽  
Temporal And Spatial

During early embryogenesis, the highly regulative sea urchin embryo relies extensively on cell-cell interactions for cellular specification. Here, the role of cellular interactions in the temporal and spatial expression of markers for oral and aboral ectoderm in Strongylocentrotus purpuratus and Lytechinus pictus was investigated. When pairs of mesomeres or animal caps, which are fated to give rise to ectoderm, were isolated and cultured they developed into ciliated embryoids that were morphologically polarized. In animal explants from S. purpuratus, the aboral ectoderm-specific Spec1 gene was activated at the same time as in control embryos and at relatively high levels. The Spec1 protein was restricted to the squamous epithelial cells in the embryoids suggesting that an oral-aboral axis formed and aboral ectoderm differentiation occurred correctly. However, the Ecto V protein, a marker for oral ectoderm differentiation, was detected throughout the embryoid and no stomodeum or ciliary band formed. These results indicated that animal explants from S. purpuratus were autonomous in their ability to form an oral-aboral axis and to differentiate aboral ectoderm, but other aspects of ectoderm differentiation require interaction with vegetal blastomeres. In contrast to S. purpuratus, aboral ectoderm-specific genes were not expressed in animal explants from L. pictus even though the resulting embryoids were morphologically very similar to those of S. purpuratus. Recombination of the explants with vegetal blastomeres or exposure to the vegetalizing agent LiCl restored activity of aboral ectoderm-specific genes, suggesting the requirement of a vegetal induction for differentiation of aboral ectoderm cells.(ABSTRACT TRUNCATED AT 250 WORDS)

Specification of endoderm and mesoderm in the sea urchin

Zygote ◽  
1999 ◽  
Vol 8 (S1) ◽  
pp. S41-S41 ◽  
Author(s):  
David R. McClay
Keyword(s):  
Sea Urchin ◽  
Wnt Pathway ◽  
Special Significance ◽  
Nuclear Entry ◽  
Cell Stage ◽  
Animal Pole ◽  
Secondary Axis ◽  
Sea Urchin Embryo ◽  
Vegetal Pole

It has long been recognized that micromeres have special significance in early specification events in the sea urchin embryo. Micromeres have the ability to induce a secondary axis if transferred to the animal pole at the 16-cell stage of sea urchin embryos (Hörstadius, 1939). Without micromeres an isolated animal hemisphere develops into an ectodermal ball called a dauer blastula. Addition of micromeres to an animal half rescues a normal pluteus larva, including endoderm (Hörstadius, 1939). Despite these well-known experiments, however, neither the molecular basis of that induction nor the endogenous inductive role of micromeres in development was known. In recent experiments we learned that if one eliminates micromeres from the vegetal pole at the 16-cell stage the resulting embryo makes no secondary mesenchyme. Earlier it had been found that β-catenin is crucial for specification events that lead to mesoderm and endoderm (Wikra-manayake et al., 1998; Emily-Fenouil et al., 1998; Logan et al., 1999). We noticed that at the 16-cell stage β-catenin enters the nuclei of micromeres, then enters the nuclei of macromeres at the 32-cell stage (Logan et al., 1999). Since nuclear entry of β-catenin is known to be important for its signalling function in the Wnt pathway, we asked whether β-catenin functions in the micromere induction pathway.

Lim1-related homeobox gene (HpLim1) expressed in sea urchin embryo

Zygote ◽  
1999 ◽  
Vol 8 (S1) ◽  
pp. S71-S72
Author(s):  
Keiko Mitsunaga-Nakatsubo ◽  
Takahiko Kawasaki ◽  
Koichi Takeda ◽  
Koji Akasaka ◽  
Hiraku Shimada
Keyword(s):  
Sea Urchin ◽  
Expression Patterns ◽  
Homeobox Gene ◽  
Mesoderm Induction ◽  
Over Expression ◽  
Lim Domains ◽  
Sea Urchin Embryo ◽  
Cell Type Specific ◽  
Islet 1

A characteristic cysteine-rich motif, LIM domain, was first detected in three different transcription factors: lin-11, Islet-1 and mec-3. A feature shared by these genes is the presence of two LIM domains linked to a DNA-binding homeodomain (Sánchez-García et al., 1994). LIM homeodomain (LHX) proteins have been reported to be implicated in a variety of developmental processes (Dawid et al., 1998).Expression patterns of LHX genes have been analysed in a wide variety of organisms and reported to be cell-type specific (Dawid et al., 1998). In vertebrates, they are expressed in organiser equivalent regions at the gastrula stage, suggesting their involvement in mesoderm induction (Taira et al., 1992; Barnes et al., 1994; Toyama et al., 1995). Hrlim, an ascidian Lim3, zygotically expresses in the endoderm lineage before gastrulation, suggesting that it is involved in the endoderm determination (Wada et al., 1995).Here, cDNA cloning of the Lim1-related homeobox gene (HpLim1) of the sea urchin, Hemicentrotus pulcherrimus, is described together with the spatially as well as temporally regulated expression of HpLim1 during sea urchin development. A possible role of HpLiml in sea urchin development is also discussed based on its spatial pattern of expression and on the result of an over-expression study.

scholarly journals A precise regulation of presenilin expression is required for the sea urchin early development

2021 ◽  
Author(s):  
Odile Bronchain ◽  
Laetitia Philippe-Caraty ◽  
Vincent Anquetil ◽  
Brigitte Ciapa
Keyword(s):  
Sea Urchin ◽  
Crucial Role ◽  
Senile Plaques ◽  
Ciliated Cells ◽  
Cellular Functions ◽  
Aβ Peptides ◽  
Multiple Substrates ◽  
Sea Urchin Embryo ◽  
Secretase Activity

Presenilins or PSENs homologues are widely expressed across eukaryotes. Two PSEN are expressed in humans where they play a crucial role in Alzheimer's disease (AD). Each PSEN can be part of the γ-secretase complex that has multiple substrates such as Notch or the amyloid precursor protein (AβPP) which gives the Aβ peptides composing the senile plaques during AD. PSENs also interact with various proteins independently of their γ-secretase activity. They can then be involved in numerous cellular functions, which makes their role in a given cell and/or organism complex to decipher. We settled the sea urchin embryo as a new model to study the role of PSEN. PSEN is present in unduplicated form and highly similar to that of humans. Our results suggest that its expression must be precisely tuned to control the course of the first mitotic cycles and the associated Cai transients, gastrulation execution and, probably in association with ciliated cells, the establishment of the pluteus. We suggest that it would be relevant to study the role of PSEN within the GRN deciphered in the sea urchin.

scholarly journals PERAN EKOLOGI BULU BABI DALAM KOMUNITAS RUMPUT LAUT DI PERAIRAN PESISIR KEMA KABUPATEN MINAHASA UTARA

2011 ◽  
Vol 7 (1) ◽  
pp. 1
Author(s):  
Ruddy D Moningkey
Keyword(s):  
Sea Urchin ◽  
Functional Role ◽  
Food Preference ◽  
Negative Impact ◽  
Sea Urchins ◽  
Gut Contents ◽  
Seagrass Bed ◽  
Transect Line ◽  
Feeding Periodicity

A study on the functional role of the sea urchin, Salmacis belli, on seagrass bed near the coast of Kema, North Minahasa Regency, was done by analyzing the gut contents, the food preference, and the feeding periodicity. Sea urchins and plants were collected from the seagrass bed by snorkeling along a 100 M transect line with 30 quadrates randomly placed. The feeding periodicity was determined from the gut index in 24 hours with 3 hour intervals.  The results showed that the sea urchin S. belli fed mainly on seagrass Thallasia hemprichii, Enhalus acoroides and Halimeda opuntioa. The feeding periodicity data indicated that the sea urchins actively fed in the day. The grazing capacity of the sea urchin was not affected by their body size.  In high density, sea urchins could potentially cause negative impact on the seagrass bed (i.e., destruction of the meadow).

Identification and characterization of gelatin-cleavage activities in the apically located extracellular matrix of the sea urchin embryo

2000 ◽  
Vol 78 (4) ◽  
pp. 455-462 ◽  
Author(s):  
Justin Flood ◽  
Janice Mayne ◽  
John J Robinson
Keyword(s):  
Extracellular Matrix ◽  
Sea Urchin ◽  
Inhibitory Effect ◽  
Divalent Metal Ions ◽  
Gelatinase Activity ◽  
Sea Urchin Embryo ◽  
Phenylmethyl Sulfonyl Fluoride ◽  
Sulfonyl Fluoride ◽  
Identification And Characterization

We have identified and partially characterized several gelatinase activities associated with the sea urchin extraembryonic matrix, the hyaline layer. A previously identified 41-kDa collagenase/gelatinase activity was generally not found to be associated with isolated hyaline layers but was dissociated from the surface of 1-h-old embryos in the absence of Ca2+ and Mg2+. While hyaline layers, freshly prepared from 1-h-old embryos, were devoid of any associated gelatinase activities, upon storage at 4°C for 4 days, a number of gelatin-cleavage activities appeared. Comparative analysis of these activities with the 41-kDa collagenase/gelatinase revealed that all species were inhibited by ethylenediamine tetraacetic acid but were refractory to inhibition with the serine protease inhibitors, phenylmethyl sulfonyl fluoride and benzamidine. In contrast, the largely Zn2+ specific chelator 1,10-phenanthroline had markedly different effects on the gelatinase activities. While several of the storage-induced, hyaline-layer-associated gelatinase activities were inhibited, the 41-kDa collagenase/gelatinase was refractory to inhibition as was a second gelatinase species with an apparent molecular mass of 45 kDa. We also examined the effects of a series of divalent metal ions on the gelatin-cleavage activities. In both qualitative and quantitative assays, Ca2+ was the most effective activator while Mn2+, Cu2+, Cd2+, and Zn2+ were all inhibitory. In contrast, Mg2+ had a minimal inhibitory effect on storage-induced gelatinase activities but significantly inhibited the 41-kDa collagenase/gelatinase. These results identify several distinct gelatin-cleavage activities associated with the sea urchin extraembryonic hyaline layer and point to diversity in the biochemical nature of these species.Key words: gelatinase, sea urchin, extracellular matrix.

The role of sea urchin embryo BMP-1 in skeleton assembly

1996 ◽  
Vol 15 (3) ◽  
pp. 150 ◽  
Author(s):  
L.G. Huggins ◽  
S-P. Hwang ◽  
W.J. Lennarz
Keyword(s):  
Sea Urchin ◽  
Sea Urchin Embryo
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