KRATZER, Marie-Claire, Sarah F. S. BECKER, Anita GRUND, Anne MERKS, Jakub HARNOŠ, Vítězslav BRYJA, Klaudia GIEHL, Jubin KASHEF and Annette BORCHERS. The Rho guanine nucleotide exchange factor Trio is required for neural crest cell migration and interacts with Dishevelled. Development. Cambridge: Company Biologists Ltd., 2020, vol. 147, No 10, p. 1-15. ISSN 0950-1991. Available from: https://dx.doi.org/10.1242/dev.186338.
Other formats:   BibTeX LaTeX RIS
Basic information
Original name The Rho guanine nucleotide exchange factor Trio is required for neural crest cell migration and interacts with Dishevelled
Authors KRATZER, Marie-Claire, Sarah F. S. BECKER, Anita GRUND, Anne MERKS, Jakub HARNOŠ (203 Czech Republic, belonging to the institution), Vítězslav BRYJA (203 Czech Republic, belonging to the institution), Klaudia GIEHL, Jubin KASHEF and Annette BORCHERS (guarantor).
Edition Development, Cambridge, Company Biologists Ltd. 2020, 0950-1991.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10605 Developmental biology
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 6.868
RIV identification code RIV/00216224:14310/20:00114430
Organization unit Faculty of Science
Doi http://dx.doi.org/10.1242/dev.186338
UT WoS 000541757600011
Keywords in English GEF Trio; Neural crest cell migration; Xenopus; Dishevelled; Rho GTPases; Cadherin-11
Tags rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Marie Šípková, DiS., učo 437722. Changed: 5/11/2020 17:53.
Abstract
Directional migration during embryogenesis and tumor progression faces the challenge that numerous external signals need to converge to precisely control cell movement. The Rho guanine exchange factor (GEF) Trio is especially well suited to relay signals, as it features distinct catalytic domains to activate Rho GTPases. Here, we show that Trio is required for Xenopus cranial neural crest (NC) cell migration and cartilage formation. Trio cell-autonomously controls protrusion formation of NC cells and Trio morphant NC cells show a blebbing phenotype. Interestingly, the Trio GEF2 domain is sufficient to rescue protrusion formation and migration of Trio morphant NC cells. We show that this domain interacts with the DEP/C-terminus of Dishevelled (DVL). DVL - but not a deletion construct lacking the DEP domain - is able to rescue protrusion formation and migration of Trio morphant NC cells. This is likely mediated by activation of Reel, as we find that DVL rescues Rac1 activity in Trio morphant embryos. Thus, our data provide evidence for a novel signaling pathway, whereby Trio controls protrusion formation of cranial NC cells by interacting with DVL to activate Rac1.
Links
GA17-16680S, research and development projectName: Nové postupy pro určení aktivity dráhy planární buněčné polarity (PCP)
Investor: Czech Science Foundation
PrintDisplayed: 24/5/2024 06:29