Faculty Opinions recommendation of Distinct PAR-1 proteins function in different branches of Wnt signaling during vertebrate development.

Author(s):  
Andreas Wodarz
Author(s):  
Eliza Zylkiewicz ◽  
Sergei Y. Sokol ◽  
Stefan Hoppler

2005 ◽  
Vol 73 (7) ◽  
pp. 323-329 ◽  
Author(s):  
Barbara K. Brott ◽  
Sergei Y. Sokol

Development ◽  
2002 ◽  
Vol 129 (10) ◽  
pp. 2317-2327 ◽  
Author(s):  
Motoyuki Itoh ◽  
Tetsuhiro Kudoh ◽  
Michael Dedekian ◽  
Cheol-Hee Kim ◽  
Ajay B. Chitnis

We have identified a novel Iroquois (Iro) gene, iro7, in zebrafish. iro7 is expressed during gastrulation along with iro1 in a compartment of the dorsal ectoderm that includes the prospective midbrain-hindbrain domain, the adjacent neural crest and the trigeminal placodes in the epidermis. The iro1 and iro7 expression domain is expanded in headless and masterblind mutants, which are characterized by exaggerated Wnt signaling. Early expansion of iro1 and iro7 expression in these mutants correlates with expansion of the midbrain-hindbrain boundary (MHB) domain, the neural crest and trigeminal neurons, raising the possibility that iro1 and iro7 have a role in determination of these ectodermal derivatives. A knockdown of iro7 function revealed that iro7 is essential for the determination of neurons in the trigeminal placode. In addition, a knockdown of both iro1 and iro7 genes uncovered their essential roles in neural crest development and establishment of the isthmic organizer at the MHB. These results suggest a new role for Iro genes in establishment of an ectodermal compartment after Wnt signaling in vertebrate development. Furthermore, analysis of activator or repressor forms of iro7 suggests that iro1 and iro7 are likely to function as repressors in establishment of the isthmic organizer and neural crest, and Iro genes may have dual functions as repressors and activators in neurogenesis.


Development ◽  
2000 ◽  
Vol 127 (3) ◽  
pp. 457-467 ◽  
Author(s):  
S.M. Lee ◽  
S. Tole ◽  
E. Grove ◽  
A.P. McMahon

The mechanisms that regulate patterning and growth of the developing cerebral cortex remain unclear. Suggesting a role for Wnt signaling in these processes, multiple Wnt genes are expressed in selective patterns in the embryonic cortex. We have examined the role of Wnt-3a signaling at the caudomedial margin of the developing cerebral cortex, the site of hippocampal development. We show that Wnt-3a acts locally to regulate the expansion of the caudomedial cortex, from which the hippocampus develops. In mice lacking Wnt-3a, caudomedial cortical progenitor cells appear to be specified normally, but then underproliferate. By mid-gestation, the hippocampus is missing or represented by tiny populations of residual hippocampal cells. Thus, Wnt-3a signaling is crucial for the normal growth of the hippocampus. We suggest that the coordination of growth with patterning may be a general role for Wnts during vertebrate development.


2005 ◽  
Vol 8 (6) ◽  
pp. 829-841 ◽  
Author(s):  
Olga Ossipova ◽  
Sangeeta Dhawan ◽  
Sergei Sokol ◽  
Jeremy B.A. Green

2021 ◽  
Vol 118 (12) ◽  
pp. e2013239118
Author(s):  
Lorenzo Rella ◽  
Euclides E. Fernandes Póvoa ◽  
Jonas Mars ◽  
Annabel L. P. Ebbing ◽  
Luc Schoppink ◽  
...  

Members of the Wnt family of secreted glycoproteins regulate cell migration through distinct canonical and noncanonical signaling pathways. Studies of vertebrate development and disease have shown that these pathways can have opposing effects on cell migration, but the mechanism of this functional interplay is not known. In the nematode Caenorhabditis elegans, a switch from noncanonical to canonical Wnt signaling terminates the long-range migration of the QR neuroblast descendants, providing a tractable system to study this mechanism in vivo. Here, we show that noncanonical Wnt signaling acts through PIX-1/RhoGEF, while canonical signaling directly activates the Slt–Robo pathway component EVA-1/EVA1C and the Rho GTPase–activating protein RGA-9b/ARHGAP, which are required for migration inhibition. Our results support a model in which cross-talk between noncanonical and canonical Wnt signaling occurs through antagonistic regulation of the Rho GTPases that drive cell migration.


2010 ◽  
Vol 34 (8) ◽  
pp. S41-S41
Author(s):  
Yang Bi ◽  
Yun He ◽  
Tingyu Li ◽  
Tao Feng ◽  
Tongchuan He

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