Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.cellsig.2005.05.019
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dc.titleRhoA acts downstream of Wnt5 and Wnt11 to regulate convergence and extension movements by involving effectors Rho Kinase and Diaphanous: Use of zebrafish as an in vivo model for GTPase signaling
dc.contributor.authorZhu, S.
dc.contributor.authorLiu, L.
dc.contributor.authorKorzh, V.
dc.contributor.authorGong, Z.
dc.contributor.authorLow, B.C.
dc.date.accessioned2014-10-27T08:38:54Z
dc.date.available2014-10-27T08:38:54Z
dc.date.issued2006-03
dc.identifier.citationZhu, S., Liu, L., Korzh, V., Gong, Z., Low, B.C. (2006-03). RhoA acts downstream of Wnt5 and Wnt11 to regulate convergence and extension movements by involving effectors Rho Kinase and Diaphanous: Use of zebrafish as an in vivo model for GTPase signaling. Cellular Signalling 18 (3) : 359-372. ScholarBank@NUS Repository. https://doi.org/10.1016/j.cellsig.2005.05.019
dc.identifier.issn08986568
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/101598
dc.description.abstractGastrulation shapes the early embryos by forming three germ layers, ectoderm, mesoderm and endoderm. In vertebrates, this process requires massive cell rearrangement including convergence and extension (CE) movements that involve narrowing and lengthening of embryonic tissues as well as cell elongation. Such polarization and movements require precise reorganization and regulation of the cytoskeleton network and cell adhesion. Rho small GTPases are key regulators for dynamic actin cytoskeleton. However, the signaling mechanisms underlying their functions in CE remain to be further elucidated. We have cloned the zebrafish Danio rerio rhoA and by capitalizing on the specific functional knockdown using morpholinos against rhoA and the availability of CE mutants defective in Wnt signaling, we showed that rhoA morphants were reminiscent to noncanonical wnt mutants with serious disruption in CE movements. Injection of rhoA mRNA effectively rescued such defects in wnt5 and wnt11 mutants. Furthermore, CE defects in rhoA knockdown or wnt mutants can be suppressed through functional bypass after ectopic expression of the two mammalian Rho effectors, the Rho kinase and Diaphanous (mDia). These results provide the first evidence that the RhoA in vivo acts downstream of Wnt5 and Wnt11 to effect, without affecting cell fates, on the CE movements in zebrafish embryos. Significantly, it elicits such effect via both effectors, Rho kinase and Dia. These findings also support the versatility of the zebrafish as a model to further investigate the roles of various classes of small GTPases in regulating cell dynamics in vivo. © 2005 Elsevier Inc. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.cellsig.2005.05.019
dc.sourceScopus
dc.subjectConvergence extension
dc.subjectGastrulation
dc.subjectmDia
dc.subjectRho kinase
dc.subjectRhoA
dc.subjectWnt
dc.typeArticle
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.doi10.1016/j.cellsig.2005.05.019
dc.description.sourcetitleCellular Signalling
dc.description.volume18
dc.description.issue3
dc.description.page359-372
dc.description.codenCESIE
dc.identifier.isiut000233954800010
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