Structure of Four Acidic Oligosaccharides from the Jelly Coat Surrounding the Eggs of Xenopus Laevis

2008 ◽  
Vol 231 (2) ◽  
pp. 434-439
Author(s):  
Yves Plancke ◽  
Jean-Michel Wieruszeski ◽  
Catherine Alonso ◽  
Benoni Boilly ◽  
Gérard Strecker
Keyword(s):  
2006 ◽  
Vol 52 (1) ◽  
pp. 113-120 ◽  
Author(s):  
Andrea N. Edginton ◽  
Claude Rouleau ◽  
Gerald R. Stephenson ◽  
Herman J. Boermans

2000 ◽  
Vol 352 (2) ◽  
pp. 449-463 ◽  
Author(s):  
Yann GUERARDEL ◽  
Ossarath KOL ◽  
Emmanuel MAES ◽  
Tony LEFEBVRE ◽  
Bénoni BOILLY ◽  
...  

Eggs from Xenopus laevis are surrounded by several layers of jelly that are needed for proper fertilization. Jelly coat is composed of high-molecular-mass glycoconjugates to which are bound many globular proteins. O-glycans released from the jelly coat of X. laevis have been partially described in previous studies. In this study, we compared the glycosylation pattern of the egg jelly coat isolated from six specimens of X. laevis. The O-glycans were released from jelly coats by alkali/borohydride treatment. Structural characterization was performed through a combination of one- and two-dimensional 1H-NMR and methylation analysis. This allowed the description of a new family of sulphated O-glycans present in jelly coats of all X. laevis. However, the jelly O-glycans showed a low extent of polymorphism between specimens. This intra-specific variability was restricted to the terminal substitution of O-linked oligosaccharides. The differential expression of two glycosyltransferase [an α-(1 → 4) galactosyltransferase and an α-(1 → 3) fucosyltransferase] activities resulted in the characterization of four phenotypes of X. laevis. Furthermore, electrophoretic analysis suggested that the high-molecular-mass fraction of jelly coat was mostly composed of mucin-type glycoproteins. Blot analysis with lectins confirmed that the glycan variability was borne by these mucin-type components. However, fertilization assays suggested that the glycan polymorphism had no repercussion on egg fertilizability.


Biochemistry ◽  
1975 ◽  
Vol 14 (14) ◽  
pp. 3101-3107 ◽  
Author(s):  
Edward C. Yurewicz ◽  
Gene Oliphant ◽  
Jerry L. Hedrick

1974 ◽  
Vol 11 (5) ◽  
pp. 534-542 ◽  
Author(s):  
Jerry L. Hedrick ◽  
Alan J. Smith ◽  
Edward C. Yurewicz ◽  
Gene Oliphant ◽  
Don P. Wolf
Keyword(s):  

1995 ◽  
Vol 231 (2) ◽  
pp. 434-439 ◽  
Author(s):  
Yves Plancke ◽  
Jean-Michel Wieruszeski ◽  
Catherine Alonso ◽  
Benoni Boilly ◽  
Gerard Strecker
Keyword(s):  

Author(s):  
Darcy B. Kelley ◽  
Martha L. Tobias ◽  
Mark Ellisman

Brain and muscle are sexually differentiated tissues in which masculinization is controlled by the secretion of androgens from the testes. Sensitivity to androgen is conferred by the expression of an intracellular protein, the androgen receptor. A central problem of sexual differentiation is thus to understand the cellular and molecular basis of androgen action. We do not understand how hormone occupancy of a receptor translates into an alteration in the developmental program of the target cell. Our studies on sexual differentiation of brain and muscle in Xenopus laevis are designed to explore the molecular basis of androgen induced sexual differentiation by examining how this hormone controls the masculinization of brain and muscle targets.Our approach to this problem has focused on a highly androgen sensitive, sexually dimorphic neuromuscular system: laryngeal muscles and motor neurons of the clawed frog, Xenopus laevis. We have been studying sex differences at a synapse, the laryngeal neuromuscular junction, which mediates sexually dimorphic vocal behavior in Xenopus laevis frogs.


1956 ◽  
Vol 23 (3) ◽  
pp. 265-273 ◽  
Author(s):  
A. C. J. Burgers ◽  
G. J. van Oordt

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