TheXenopusreceptor tyrosine kinase Xror2 modulates morphogenetic movements of the axial mesoderm and neuroectoderm via Wnt signaling

Development ◽  
2002 ◽  
Vol 129 (22) ◽  
pp. 5227-5239 ◽  
Author(s):  
Hiroki Hikasa ◽  
Mikihito Shibata ◽  
Ichiro Hiratani ◽  
Masanori Taira

The Spemann organizer plays a central role in neural induction, patterning of the neuroectoderm and mesoderm, and morphogenetic movements during early embryogenesis. By seeking genes whose expression is activated by the organizer-specific LIM homeobox gene Xlim-1 in Xenopusanimal caps, we isolated the receptor tyrosine kinase Xror2. Xror2 is expressed initially in the dorsal marginal zone, then in the notochord and the neuroectoderm posterior to the midbrain-hindbrain boundary. mRNA injection experiments revealed that overexpression of Xror2 inhibits convergent extension of the dorsal mesoderm and neuroectoderm in whole embryos, as well as the elongation of animal caps treated with activin, whereas it does not appear to affect cell differentiation of neural tissue and notochord. Interestingly, mutant constructs in which the kinase domain was point-mutated or deleted (named Xror2-TM) also inhibited convergent extension, and did not counteract the wild-type, suggesting that the ectodomain of Xror2 per se has activities that may be modulated by the intracellular domain. In relation to Wnt signaling for planar cell polarity, we observed: (1) the Frizzled-like domain in the ectodomain is required for the activity of wild-type Xror2 and Xror2-TM; (2) co-expression of Xror2 with Xwnt11, Xfz7, or both,synergistically inhibits convergent extension in embryos; (3) inhibition of elongation by Xror2 in activin-treated animal caps is reversed by co-expression of a dominant negative form of Cdc42 that has been suggested to mediate the planar cell polarity pathway of Wnt; and (4) the ectodomain of Xror2 interacts with Xwnts in co-immunoprecipitation experiments. These results suggest that Xror2 cooperates with Wnts to regulate convergent extension of the axial mesoderm and neuroectoderm by modulating the planar cell polarity pathway of Wnt.

Development ◽  
2012 ◽  
Vol 139 (5) ◽  
pp. 968-978 ◽  
Author(s):  
M. F. Chacon-Heszele ◽  
D. Ren ◽  
A. B. Reynolds ◽  
F. Chi ◽  
P. Chen

2008 ◽  
Vol 15 (1) ◽  
pp. 23-36 ◽  
Author(s):  
Shinji Yamamoto ◽  
Osamu Nishimura ◽  
Kazuyo Misaki ◽  
Michiru Nishita ◽  
Yasuhiro Minami ◽  
...  

2008 ◽  
Vol 13 (9) ◽  
pp. 965-975 ◽  
Author(s):  
Yosuke Funato ◽  
Tatsuo Michiue ◽  
Takeshi Terabayashi ◽  
Akira Yukita ◽  
Hiroki Danno ◽  
...  

2002 ◽  
Vol 2 ◽  
pp. 434-454 ◽  
Author(s):  
Jeffrey D. Axelrod ◽  
Helen McNeill

Epithelial cells and other groups of cells acquire a polarity orthogonal to their apical–basal axes, referred to as Planar Cell Polarity (PCP). The process by which these cells become polarized requires a signaling pathway using Frizzled as a receptor. Responding cells sense cues from their environment that provide directional information, and they translate this information into cellular asymmetry. Most of what is known about PCP derives from studies in the fruit fly,Drosophila. We review what is known about how cells translate an unknown signal into asymmetric cytoskeletal reorganization. We then discuss how the vertebrate processes of convergent extension and cochlear hair-cell development may relate toDrosophilaPCP signaling.


Sign in / Sign up

Export Citation Format

Share Document