Please use this identifier to cite or link to this item: https://doi.org/10.1242/dev.01901
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dc.titleDepletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos
dc.contributor.authorReversade, B
dc.contributor.authorKuroda, H
dc.contributor.authorLee, H
dc.contributor.authorMays, A
dc.contributor.authorDe Robertis, E.M
dc.date.accessioned2020-10-27T09:47:26Z
dc.date.available2020-10-27T09:47:26Z
dc.date.issued2005
dc.identifier.citationReversade, B, Kuroda, H, Lee, H, Mays, A, De Robertis, E.M (2005). Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos. Development 132 (15) : 3381-3392. ScholarBank@NUS Repository. https://doi.org/10.1242/dev.01901
dc.identifier.issn09501991
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181088
dc.description.abstractTo address the patterning function of the Bmp2, Bmp4 and Bmp7 growth factors, we designed antisense morpholino oligomers (MO) that block their activity in Xenopus laevis. Bmp4 knockdown was sufficient to rescue the ventralizing effects caused by loss of Chordin activity. Double Bmp4 and Bmp7 knockdown inhibited tail development. Triple Bmp2/Bmp4/Bmp7 depletion further compromised trunk development but did not eliminate dorsoventral patterning. Unexpectedly, we found that blocking Spemann organizer formation by UV treatment or ?-Catenin depletion caused BMP inhibition to have much more potent effects, abolishing all ventral development and resulting in embryos having radial central nervous system (CNS) structures. Surprisingly, dorsal signaling molecules such as Chordin, Noggin, Xnr6 and Cerberus were not re-expressed in these embryos. We conclude that BMP inhibition is sufficient for neural induction in vivo, and that in the absence of ventral BMPs, Spemann organizer signals are not required for brain formation.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectbone morphogenetic protein 2
dc.subjectbone morphogenetic protein 4
dc.subjectchordin
dc.subjectnoggin
dc.subjectoligomer
dc.subjectosteogenic protein 1
dc.subjectanimal cell
dc.subjectanimal tissue
dc.subjectarticle
dc.subjectbrain development
dc.subjectcentral nervous system
dc.subjectcontrolled study
dc.subjectembryo
dc.subjectembryo development
dc.subjectembryo pattern formation
dc.subjectembryonic structures
dc.subjectgene activity
dc.subjectgene expression
dc.subjectin vivo study
dc.subjectinhibition kinetics
dc.subjectnerve cell
dc.subjectnervous system development
dc.subjectnonhuman
dc.subjectpriority journal
dc.subjectprotein depletion
dc.subjectprotein function
dc.subjectsignal transduction
dc.subjecttail
dc.subjectXenopus laevis
dc.subjectAnimals
dc.subjectBase Sequence
dc.subjectBody Patterning
dc.subjectBone Morphogenetic Proteins
dc.subjectBrain
dc.subjectEmbryo, Nonmammalian
dc.subjectGlycoproteins
dc.subjectIntercellular Signaling Peptides and Proteins
dc.subjectMolecular Sequence Data
dc.subjectMorphogenesis
dc.subjectMorpholines
dc.subjectProteins
dc.subjectSignal Transduction
dc.subjectTail
dc.subjectTransforming Growth Factor beta
dc.subjectXenopus laevis
dc.subjectXenopus Proteins
dc.subjectAnimalia
dc.subjectCerberus
dc.subjectXenopus laevis
dc.typeArticle
dc.contributor.departmentPAEDIATRICS
dc.description.doi10.1242/dev.01901
dc.description.sourcetitleDevelopment
dc.description.volume132
dc.description.issue15
dc.description.page3381-3392
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