scholarly journals Xbra3 Induces Mesoderm and Neural Tissue in Xenopus laevis

2000 ◽  
Vol 222 (2) ◽  
pp. 405-419 ◽  
Author(s):  
C.F. Strong ◽  
M.W. Barnett ◽  
D. Hartman ◽  
E.A. Jones ◽  
D. Stott
Keyword(s):  
1994 ◽  
Vol 127 (2) ◽  
pp. 521-535 ◽  
Author(s):  
S Dufour ◽  
J P Saint-Jeannet ◽  
F Broders ◽  
D Wedlich ◽  
J P Thiery

Cadherins, a family of Ca-dependent adhesion molecules, have been proposed to act as regulators of morphogenetic processes and to be major effectors in the maintenance of tissue integrity. In this study, we have compared the effects of the expression of two truncated cadherins during early neurogenesis in Xenopus laevis. mRNA encoding deleted forms of XB- and N-cadherin lacking most of the extracellular domain were injected into the four animal dorsal blastomeres of 32-cell stage Xenopus embryos. These truncated cadherins altered the cohesion of cells derived from the injected blastomeres and induced morphogenetic defects in the anterior neural tissue to which they chiefly contributed. Truncated XB-cadherin was more efficient than N-cadherin in inducing these perturbations. Moreover, the coexpression of both truncated cadherins had additive perturbation effects on neural development. The two truncated cadherins can interact with the three known catenins, but with distinct affinities. These results suggest that the adhesive signal mediated by cadherins can be perturbed by overexpressing their cytoplasmic domains by competing with different affinity with catenins and/or a common anchor structure. Therefore, the correct regulation of cadherin function through the cytoplasmic domain appears to be a crucial step in the formation of the neural tissue.


1993 ◽  
Vol 155 (1) ◽  
pp. 46-57 ◽  
Author(s):  
S.L. Wolda ◽  
C.J. Moody ◽  
R.T. Moon

2000 ◽  
Vol 227 (1) ◽  
pp. 183-196 ◽  
Author(s):  
Stephen Ribisi ◽  
Francesca V. Mariani ◽  
Emil Aamar ◽  
Teresa M. Lamb ◽  
Dale Frank ◽  
...  

2019 ◽  
Vol 42 ◽  
Author(s):  
Charles R. Gallistel

Abstract Shannon's theory lays the foundation for understanding the flow of information from world into brain: There must be a set of possible messages. Brain structure determines what they are. Many messages convey quantitative facts (distances, directions, durations, etc.). It is impossible to consider how neural tissue processes these numbers without first considering how it encodes them.


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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