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dc.contributor.authorAutorMuñoz-Montecinos, Carlos
dc.contributor.authorAutorRomero, Adrián
dc.contributor.authorAutorSepúlveda, Vania
dc.contributor.authorAutorVira, María Ángela
dc.contributor.authorAutorFehrmann-Cartes, Karen
dc.contributor.authorAutorMarcellini, Sylvain
dc.contributor.authorAutorAguilera, Felipe
dc.contributor.authorAutorCaprile, Teresa
dc.contributor.authorAutorFuentes, Ricardo
dc.contributor.otherCarreraFacultad de medicina veterinaria y agronomíaes
dc.date.accessionedFecha ingreso2022-02-22T19:53:10Z
dc.date.availableFecha disponible2022-02-22T19:53:10Z
dc.date.issuedFecha publicación2022
dc.identifier.citationReferencia BibliográficaFrontiers in Cell and Developmental Biology 9, 20 p.
dc.identifier.issnISSN2296-634X
dc.identifier.uriURLhttp://repositorio.udla.cl/xmlui/handle/udla/955
dc.identifier.uriURLhttps://www.frontiersin.org/journals/cell-and-developmental-biology
dc.description.abstractResumenThe vertebral column, or spine, provides mechanical support and determines body axis posture and motion. The most common malformation altering spine morphology and function is adolescent idiopathic scoliosis (AIS), a three-dimensional spinal deformity that affects approximately 4% of the population worldwide. Due to AIS genetic heterogenicity and the lack of suitable animal models for its study, the etiology of this condition remains unclear, thus limiting treatment options. We here review current advances in zebrafish phenogenetics concerning AIS-like models and highlight the recently discovered biological processes leading to spine malformations. First, we focus on gene functions and phenotypes controlling critical aspects of postembryonic aspects that prime in spine architecture development and straightening. Second, we summarize how primary cilia assembly and biomechanical stimulus transduction, cerebrospinal fluid components and flow driven by motile cilia have been implicated in the pathogenesis of AIS-like phenotypes. Third, we highlight the inflammatory responses associated with scoliosis. We finally discuss recent innovations and methodologies for morphometrically characterize and analyze the zebrafish spine. Ongoing phenotyping projects are expected to identify novel and unprecedented postembryonic gene functions controlling spine morphology and mutant models of AIS. Importantly, imaging and gene editing technologies are allowing deep phenotyping studies in the zebrafish, opening new experimental paradigms in the morphometric and three-dimensional assessment of spinal malformations. In the future, fully elucidating the phenogenetic underpinnings of AIS etiology in zebrafish and humans will undoubtedly lead to innovative pharmacological treatments against spinal deformities.es
dc.format.extentdc.format.extent20 páginas
dc.format.extentdc.format.extent1.623Mb
dc.format.mimetypedc.format.mimetypePDF
dc.publisherEditorFrontiers Media S.A.
dc.rightsDerechosCreative Commons Attribution License (CC BY).
dc.sourceFuentesFrontiers in Cell and Developmental Biology
dc.subjectPalabras ClavesReissner fiber
dc.subjectPalabras ClavesCSF-cNs
dc.subject.lcshdc.subject.lcshSpine
dc.subject.lcshdc.subject.lcshScoliosis
dc.subject.lcshdc.subject.lcshCerebrospinal fluid
dc.subject.lcshdc.subject.lcshInflammation
dc.subject.meshdc.subject.meshZebrafish
dc.subject.meshdc.subject.meshCilia
dc.titleTítuloTurning the Curve Into Straight: Phenogenetics of the Spine Morphology and Coordinate Maintenance in the Zebrafishes
dc.typeTipo de DocumentoArtículoes
dc.udla.catalogadordc.udla.catalogadorCBM
dc.udla.indexdc.udla.indexSCOPUS
dc.udla.indexdc.udla.indexSCOPUS
dc.identifier.doidc.identifier.doi10.3389/fcell.2021.801652
dc.udla.privacidaddc.udla.privacidadDocumento públicoes


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