Molecular biology of the sea urchin embryo

Science ◽  
1982 ◽  
Vol 217 (4554) ◽  
pp. 17-26 ◽  
Author(s):  
E. Davidson ◽  
B. Hough-Evans ◽  
R. Britten
Development ◽  
1989 ◽  
Vol 107 (Supplement) ◽  
pp. 1-2
Author(s):  
R. R. Kay ◽  
J. C. Smith

The importance of cell–cell interactions in embryonic development was first described by Driesch (1891), who showed that any of the blastomeres of the 2-cell or 4-cell sea-urchin embryo is capable of forming a complete embryo if cultured in isolation; this implied that in normal development each blastomere is aware of the other and will only form a half- or quarter-embryo, as appropriate. And it was only ten years later that Spemann (1901) discovered the phenomenon of embryonic induction, recently reviewed by Gurdon (1987) and defined as an interaction in which the differentiation of one group of cells is affected by a signal from an adjacent group. Thus the significance of cell signalling during development has been appreciated for almost a century, but, as has frequently been remarked, progress in the molecular analysis of the phenomenon has been slow compared with that in the younger disciplines of, for example, immunology and molecular biology.


1999 ◽  
Vol 212 (2) ◽  
pp. 503-510 ◽  
Author(s):  
Ikuko Yazaki ◽  
Brian Dale ◽  
Elisabetta Tosti

Zygote ◽  
2008 ◽  
Vol 16 (1) ◽  
pp. 73-78 ◽  
Author(s):  
M. Alvarez ◽  
J. Nnoli ◽  
E.J. Carroll ◽  
V. Hutchins-Carroll ◽  
Z. Razinia ◽  
...  

SummaryThe 330 kDa fibrillar glycoprotein hyalin is a well known component of the sea urchin embryo extracellular hyaline layer. Only recently, the main component of hyalin, the hyalin repeat domain, has been identified in organisms as widely divergent as bacteria and humans using the GenBank database and therefore its possible function has garnered a great deal of interest. In the sea urchin, hyalin serves as an adhesive substrate in the developing embryo and we have recently shown that exogenously added purified hyalin from Strongylocentrotus purpuratus embryos blocks a model cellular interaction in these embryos, archenteron elongation/attachment to the blastocoel roof. It is important to demonstrate the generality of this result by observing if hyalin from one species of sea urchin blocks archenteron elongation/attachment in another species. Here we show in three repeated experiments, with 30 replicate samples for each condition, that the same concentration of S. purpuratus hyalin (57 μg/ml) that blocked the interaction in living S. purpuratus embryos blocked the same interaction in living Lytechinus pictus embryos. These results correspond with the known crossreactivity of antibody against S. purpuratus hyalin with L. pictus hyalin. We propose that hyalin–hyalin receptor binding may mediate this adhesive interaction. The use of a microplate assay that allows precise quantification of developmental effects should help facilitate identification of the function of hyalin in organisms as divergent as bacteria and humans.


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